UPDATE 29. August 2021: EXCLUSIVE: U.S. Scientists Continue Their Treachery in Assisting China’s Biowarfare Program Unabated

UPDATE 28. August 2021: mRNA Vaccines: The Silent Weapon

UPDATE 06. June 2021: The Individuals Behind Obama’s Jan 2017 Memo Re-Authorizing Funding for ‘Gain of Function’ R&D Were the Same Individuals Who Lied and Claimed COVID Wasn’t Created in a Lab - Anthony Fauci, Peter Daszak, Ralph Baric, David Franz, Gigi Kwik Gronvall, Thomas Inglesby, W. Ian Lipkin, Kanta Subbarao must immediately be indicted and stand trial.

UPDATE 02. June 2021: How the University of Minnesota May Have Contributed to China’s Biowarfare Program

UPDATE 12. May 2021: BOMBSHELL: Chinese military planned aerosolized bioweapon development and deployment to “cause the enemy’s medical system to collapse”

UPDATE 09. May 2021: Chinese Military Discussed Weaponizing COVID In 2015 'To Cause Enemy's Medical System To Collapse'

UPDATE 05. May 2021: The origin of COVID: Did people or nature open Pandora’s box at Wuhan?

RE-UPLOAD 27. January 2021: Proof Dr. Fauci Owns COVID-19

ICYMI: Mandatory Vaccination Programs Violate the Nuremberg Code | Objective: Health – The Nuremberg Code and Mandatory Vaccinations + Depopulation by Forced Vaccination—Article from 2011

Bio-warfare & Weaponization of Medicine Amid Covid

Image result for Bio Warfare VirusBy TNA - 16. January 2021

In this explosive interview with Senior Editor Alex Newman of The New Americanmagazine, former president of the Association of American Physicians and Surgeons (AAPS) Dr. Lee Merrit explains her belief that America is currently facing what appears to be biological warfare.

Whether the Communist Chinese released the COVID-19 virus on purpose or by accident is impossible to know, but the implications are enormous.

And when it comes to the new vaccines, Dr. Merrit, a former military doctor who studied biological warfare, reviews previous animal studies on the technology underlying the vaccines and paints a dire picture.

However, even though modern medical schools do not often teach it, there are ways to treat viral infections that are time-tested and effective, she concludes.

Dr. Lee Merritt:  So, let me point out, we have never made it through an animal study successfully for this type of virus. We have never done this in humans before, at least we haven’t, maybe the Chinese have. I’ll talk about that in a second but we don’t really have a track record of success.

This vaccine was rolled out to distribution centers before they even made a show of caring about FDA approving it. Do you realize it went out for distribution? In Nebraska it was in the distribution center within days before the FDA said they were going to approve it. What?

Alex Newman [AN]: Do you get the sense that medicine is being weaponized against our freedom, and that this coronavirus is being used to trample our rights? You’re not alone. We have a very special guest her name is Dr. Lee Merritt. In brief, Dr. Merrick started her medical career at age four doing house calls with her father.

Dr. Lee Merritt:  In 1980 graduated from the University of Rochester School of Medicine and Dentistry in New York, where she was elected to life membership in the Alpha Omega Alpha Honor Medical Society.

Dr. Merritt completed an Orthopaedic Surgery Residency in the United States Navy and served 9 years as a Navy physician and surgeon before returning to Rochester, where she was the only woman to be appointed as the Louis A. Goldstein Fellow of Spinal Surgery.

Dr. Merritt has been in the private practice of Orthopaedic and Spinal Surgery since 1995,  served on the Board of the Arizona Medical Association, and is past president of the Association of American Physicians and Surgeons.

She has had a long interest in wellness and fitness, and has been Fellowship Certified by the American Academy of Anti-Aging Medicine.  At age 63 she won a female bodybuilding championship in Physique class.

As a lifelong advocate of free market, patient-centered medicine Dr. Merritt had the opportunity to appear on the John Stossel show to speak against Obamacare.  More recently she has appeared on numerous radio programs discussing Covid-19, the futility of mask mandates, and other lies and omissions from the medical “technocrats”.  Her recent speech at Doctors for Disaster Preparedness on “Sars-CoV2 and the Rise of Medical Technocracy” has been widely viewed on YouTube, and forwarded on by Dr. Mercola—one of her medical heroes.

She is married and the proud mother of two sons, one of whom carries on the four generation medical tradition as a General Surgeon, and the other with a real job as an Electrical Engineer.  In her spare time, Dr. Merritt raises chickens, gardens and enjoys a rural Midwest lifestyle. https://drleemerritt.com


— Dr. Lee Merritt (Video)

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AN: Tell us your thoughts on covid and how it seems like the perfect excuse to take our rights, shut down our businesses, destroy our economy, overrule our personal bodily integrity. Now, they’re talking about a mandatory vaccines. What are your thoughts on this covid? Does the virus really justify the level of hysteria we’ve seen, and the massive expansion of government power we’ve seen?

DR: The simple answer is no it does not, and when I gave my talk in August at the Doctors for Disaster Preparedness, the talk was ‘SARS-COV 2 and the Rise of Medical Technocracy’ https://youtu.be/sjYvitCeMPc I had come up with an idea years before that. Literally I had started thinking about a talk for them a couple years earlier because I go to the meetings periodically, and my talk was on the weaponization of medicine. The problem is by the time I actually was ready to give the talk I had to change things so rapidly because they already did it.

I believe we’re at war, we’re in an unconventional, unrestricted war, the kind that the military Chinese generals talked about 30 years ago, and I’m not saying this is just coming from China but that’s the approximate militarization of this.

My thought, before all this happened when I was just theoretically thinking about this, was warfare changed over time. We started just hitting each other with clubs, then we went to set piece battles, and then we as Americans kind of pioneered guerrilla warfare shooting behind trees that the British thought was unsportsmanlike, and so on. In our lifetime, what I call military conflict 4.0, and I made this up before I ever heard people now talking about 5th generation warfare but that’s really what we’re talking about.

04:03 mins 4.0 was when we were fighting say IsIs, or the Taliban, or Al Qaeda. You knew maybe who the enemy was, by the Geneva convention they appeared like a standing army, they had uniforms, they had training, they used group tactics and things, but you weren’t 100% sure who the enemy was because you didn’t know who was funding them, who was sending them weapons, who was really doing the training. So, there was plausible deniability but what if you could take it the next step further. What I called, and what some other people called warfare 5.0, what if you had a weapon that was so stealth that not only did you not know who the enemy was, you didn’t even know you were being attacked so it looked like nature? That’s really what we’re in.

What they’ve done, and this is again my thinking, know how this thing came about. One of the things I learned, which was confirmed by a Taiwanese engineer on an airplane I was on one night. He said the reason they didn’t get hit badly with this virus is they figured out right away, not to listen to Chinese Communist Party propaganda news. They don’t listen to them. What they do is they have a whole department that screens their social media, and when they see something get censored, they start looking at it because that must be the truth. That’s something we should start appreciating here in America today.

I believed early in February this was a biologically manipulated bio weapon because the minute anybody popped up with data suggesting that they were censored. I think there’s a host of evidence that shows coronavirus is a naturally occurring, very benign virus that doesn’t even give most people the cold. At the most it gives you a common cold, it doesn’t kill you, doesn’t make you very sick, but what they’ve done is make it the transmission device.

Think about years ago when we first came into the nuclear age. We couldn’t easily distribute nuclear weapons, we had to drop them onto Japanese cities of Hiroshima and Nagasaki. We had to take them in a plane but now we have the guidance missile technology. We had a lot of bio weapons over the years. The one I was very worried about was smallpox. Most of these bioweapons were either hard to distribute or there was treatment for them and the problem here is distribution. Remember the anthrax thing? It came out in envelopes, went to congress, it’s hard to distribute anthrax. It might be deadly to some people but it’s hard to distribute.

So, let’s make a missile, and that missile is coronavirus, which is a huge, highly transmissible, very small particle virus. It can’t be masked away no matter what the propaganda is. You can’t hide from it behind a plastic little screen that costs businesses too much money. It’s just incredibly transmissible and it’s very benign. Now, add to that basically the warhead, and the warhead is a little protein they tacked on that attaches to your Ace2 pathway. Humans have these Ace2 pathways, somewhat genetically determined. When you put on this hook or spike protein, it gets into these Ace2 pathways, which now is in your heart, in your lungs, in your testicle, in your brain. It can kill you

I believe what happened here is it was let out purposely but I can’t prove that. It was either accidentally released or it was let out purposely but whatever happened, when it first came out, like many viruses, I believe it was worse, the first generation was more deadly. It did kill a lot of people in Wuhan, it did kill people in Lombardy. I know there’s a problem when doctors are dying, and doctors and nurses in Lombardy were dying. If we can’t save ourselves, we’re in trouble .

It first came out in Lombardy, went to New York that was probably first generation virus, and it did kill a bunch of people initially. Like most viruses, almost all viruses I know of, as they pass through the human host they get weaker. This is just adaptive advantage. If you’re the Napoleon of viruses and you want to take over the world, you don’t kill every host or you’re not going to spread, so what you do is you become less deadly, more transmissible. That’s what this has done over time. That’s my belief about the big picture here, but as soon as this thing came out it became easy to piggyback onto things.

If this was a planned release then we’re talking about planned warfare. If it was an accidental release then we’re talking about warfare that was piggybacked onto this accidental release because what they’ve done is they used it to create fear and fear is an incredible psychological manipulator of populations.

They’ve taken down our economy, they’re taking down our generation of children with these stupid masks, they’re damaging us in all sorts of ways. It’s a psyop at this point. We  were shut down, we were sitting at home, and our response is to study. I found out we had treatment for viruses going back into the late 1970s. I graduated medical school in 1980, my son graduated just recently, and he’s a general surgeon. I asked him if he ever heard in his entire medical education, all the fellowship, all stuff you’re doing, have you ever heard we could treat viruses with these antimicrobial agents? No, he never heard it. I called my friend in Florida, 40-year internal medicine professor, a real medicine doctor. I asked him the same question and he never heard that. So, this is the biggest lie.

They lied to us for 40 years about this treatment. So, here’s the big picture. If you bring out a virus like this, we’re talking about vaccines and things, why do we have vaccines? We have vaccines because we didn’t have treatment for smallpox and it was a very deadly disease that made sense to have a vaccine. We didn’t have treatment for polio initially so it made sense to have a vaccine, but this. Even without doing anything, this disease has a 99.991% chance of survival than last viral season I’ll call it a viral season because it really isn’t just a flu season anymore. In the last winter season including New York and elsewhere that was the overall survival in the world, as opposed to a standard viral flu season it’s 99.992%.

#1 it’s not that all deadly

#2 we actually have a treatment for this that works extremely well.

In spite of all the propaganda and attempts to falsify medical literature, which they got caught at, and attempts to dismiss anything they don’t agree with. Why would they hide treatment? I came up with two reasons:

1] Your $69 billion vaccine industry goes to zero if you have an effective treatment for all these viral airborne diseases. So mumps, measles blah blah blah.

AN: You’re talking about things like chloroquine and hydroxychloroquine and ivermectin.

DR: These are called lysosomotropic agents, and one of my friends called me he’s an anesthesiologist trained in India. He was so excited when we first heard about it before Trump said anything. I first thought they said they didn’t want to go along with this because orange man bad, they just didn’t want anything that Trump said but we actually knew about it beforehand and it’s much bigger than anything to do with Trump. So he called and said “I think I know how these things work” because he got out his old textbook of infectious disease and biochemistry basically from India and he figured it out. I said if that’s the way it works we should be able to find other medications. Then I found the term lysosomatropic agents and I started looking for these and it turns out there are a number of them.

They don’t want you to know because the $69 billion vaccine industry goes to zero. Even more than that if we are at bio warfare right now, as a part of this multi-dimensional warfare, if you have a treatment in your back pocket they cannot terrorize you with viruses. That’s important because the way they’ve made this experimental treatment, it’s not a vaccine but whatever this thing is, this RNA thing, it doesn’t prevent transmission by their own admission. Even if it did, it is created to act on the warhead part of this deal, the spike protein. So, next year these guys, and these bio weapons, which is one of the other things I learned sadly, is there are these bio weaponeers all over the country. We literally have funded them

14:00 mins We funded a PLA [People’s Liberation Army, CCP] virologist to come and work in our army bio weapons lab, which is the height of insanity or treason.

Under Clinton’s administration it was completely illegal to have non-aligned foreign students, so if you were from Iran or some place that was not our ally you couldn’t even work in a biology lab with lesser pathogens. Suddenly, we’ve gone from that stance to under the Obama administration actually funding PLA Chinese Communist virologists to work in our bio weapons lab.

We have more bio weaponeers than I anticipated. I knew the soviets had them but I didn’t realize how many were in the world. They can now create another little thing to go on this coronavirus. They’ve got  missile technology to put whatever they want on there, and every year you’d have to have a different vaccine. So even if you believe this type of vaccine will work, which I don’t, even if you believe that, it’s not a permanent solution. Viruses are all around us, they’re part of nature, we lived with them for millennia, we’ll live them for them hopefully if we survive all this for another few millennia but now we need a solution that doesn’t involve a vaccine of any kind.

We have those solutions, we have treatment and we have prevention, and each of us can improve our immune system.

22:42 mins I will make this military point. This is a perfect binary weapon. There’s no way I know exactly what that m-RNA is programmed to, neither do most doctors. The doctors can’t get at that data, except the guys at the very top of this project they know. They say it’s to the spike protein but how do we prove it? We don’t know.

So, if I were China, and I wanted to take down our military that’s easy, we’ve seen it happen. I make it to a something, something l could hook onto this coronavirus, like the spike protein or another protein. I just make an m-RNA to that, I know it doesn’t exist in nature so nobody’s gonna die from a vaccine, and then two years later I release whatever it is I made, the  counterpart, and it causes this immune enhancement death. It’s a delayed death that’s what binary poisons are. I give you part one and then I can walk away, and then you accidentally get in contact with part two and you die and you can’t trace it. That’s not a hypothetical threat.

AN: There was a leak, of members of the Communist Chinese Party out of Shanghai and there were hundreds of them working in Pfizer, and AstraZeneca and GlaxoSmithKline, the companies making these vaccines, which is absolutely terrifying.

DR: But, we’re going to trust them, they’re acting in our best interest.

AN: Where do we go from here D. Merritt? What are your concerns about what’s on the horizon? I’ve talked to doctors who’ve said maybe we’re coming up to a covid 2021, some variation a coronavirus mutation.

DR: Don’t’ even worry about that. They’re saying it’s more transmissible, which is like saying I was going 95 on the freeway but now I’m going to go 97. This is so transmissible. Making it a little bit worse is not going to be the problem. Lethality is what you worry about and we’re not talking about that. They could come out with something else but again, if you come out with something that’s based on these airborne viruses like corona we pretty much have a treatment, which is the hydroxychloroquine or ivermectin. What we need to do is take back our world from the virology bad boys by having a supply of ivermectin and hydroxychloroquine available. Two hydroxychloroquine plants burned down and they say oh no they weren’t hydroxychloroquine plants. They made the precursors to hydroxychloroquine, so you’re being lied to at every turn.

We need to stand up now. Governor Ricketts in Nebraska is one of five governors who’s not restricted hydroxychloroquine in any way. Everybody needs to ring their governor to stop signing this stuff brought to us by medical universities that are all being paid by Fauci and the NIH. Let’s give your people the ability to defend themselves.

There are five or six things in my office: NAC, vitamin C, vitamin D, zinc, selenium and quercetin. If you do that you can improve your immune response and your own ability to fight this off and not get terribly sick.

It’s possible they are going to come around with more dangerous things in the future and then we need more than that, so that’s why we have to  get the truth out, people have to spread the news that we have treatment and patients are getting it.

27:03 mins I would just make this point to doctors.

I get it if you’re in training and you can’t speak out, you’re stuck, I don’t fault you. I do fault everybody above that taking money from Fauci, the people who are taking money from the NIH, who are willing to take that money and push remdesivir and kill people, not because they’re necessarily killing them with remdesivir but they’re killing them by omitting treatment early on as outpatient that works, and the doctors below those who are out of training, they have to make a moral decision here because we should be prophylaxing people in nursing homes. We could be saving lives for five dollars a week, we could be saving a lot of these old people but they don’t want to. They’re considered kind of not contributory to society that’s where the Nazis went with this.

People considered not worthy of living, we have to get over that because the doctors who are making the choice to be quiet because they got a mortgage, they got two kids and they don’t want to lose their university salary. It’s time to rethink your position. I think everybody in the medical community, we need to man up and be honest here.

The information’s out there, don’t tell me there’s no evidence. They’re lying to you about the evidence. If you really make any effort on the internet you can find the evidence and if not you can go to American’s front line doctors https://aflds.com or you can go to the Association of American Physicians and Surgeons https://aapsonline.org  and many other organizations speaking up now. There’s The Barrington Declaration https://gbdeclaration.org and https://www.sott.net has good articles.

If you want to get out of the pandemic right now it’s easy, turn off your tv, take off your mask, reopen your business, and live your life. Hug your relatives  go see your old relatives, have neighborhood parties because let me tell you, we cannot live in a basement .

Even if you think masks work don’t do this to your children. How many decades are going to do this? Live every winter, every year in a mask from now on? NO, not doing that.

▶️ Our “uncensored” video content can be viewed at TheNewAmerican.com as well as these other sites.



Alex Newman is a senior editor for The New American. He can be reached at or through Liberty Sentinel Media. Follow him on Twitter @ALEXNEWMAN_JOU or on Facebook.



Proof Dr. Fauci Owns COVID-19

Re-upload 27. January 2021



EXCLUSIVE: U.S. Scientists Continue Their Treachery in Assisting China’s Biowarfare Program Unabated

By Lawrence Sellin and Anna Chen - 29. August 2021

On June 9, 2020, the former Chair of Harvard University’s Chemistry and Chemical Biology Department, Dr. Charles Lieber, was indicted on charges of making false statements to federal authorities regarding his participation in China’s Thousand Talents Program.

China’s Thousand Talents Program is one of the most prominent Chinese talent recruitment plans designed to attract, recruit and cultivate high-level scientific talent in furtherance of China’s scientific development, economic prosperity and national security.  These talent recruitment efforts seek to lure Chinese overseas talent and foreign experts to bring their knowledge and experience to China, and they often reward individuals for stealing proprietary information.

Beginning in 2011, Lieber became a “Strategic Scientist” at China’s Wuhan University of Technology and later became a contractual participant in the Thousand Talents Plan from at least 2012 through 2015.

Accusations of lying to federal investigators aside, Lieber may have significantly contributed to China’s biological warfare program.

Geng-feng Zheng is a professor of chemistry at Fudan University in Shanghai, China. He received a Ph.D. degree in Chemistry in 2007 from Harvard University under the guidance of Dr. Charles Lieber and completed postdoctoral training at Northwestern University.

Zheng is an expert in nanotechnologies and, together with Lieber in 2004, began to investigate the use of nanowire field effect transistors to detect single viruses.

The collaboration between Zheng and Lieber continued even after 2010, when Zheng became a professor at Fudan University, together producing no less than eleven scientific publications on nanowire technologies.

But the collaboration did not end there. In accordance with China’s practice of “scientific chain migration,” Zheng’s student at Fudan University, An-Qi Zhang, continued the work with Lieber on nano-bioelectronics.

In 2016, An-Qi Zhang, Geng-feng Zheng and Charles Lieber published a book “Nanowires – Building Blocks for Nanoscience and Nanotechnology.”

China’s People’s Liberation Army’s (PLA) biosensor program is based on nanotechnologies, in particular, nanowire field effect transistor biosensors.

Since 2016, there has been a massive expansion of fused military-civilian research in China after it was mandated by the Chinese Communist Party’s Thirteenth Five-Year Plan.

A key figure in China’s military-civilian biosensor program is Mao-sheng Yao of Peking University.

Mao-sheng Yao is an expert in the surveillance and measurement of microorganisms in the environment, who, incidentally, was entirely educated in U.S. universities, receiving a Master’s degree from the University of Alabama, a doctoral degree from Rutgers University and postdoctoral training at Yale University.

In 2018, during a kick-off seminar entitled “Bioaerosol Detection Technology Strategic Collaboration,” Mao-sheng Yao announced a fused military-civilian research program with the PLA’s National Bio-protection Engineering Center, Institute of Medical Support Technology, Institute of Systems Engineering, Academy of Military Sciences in Tianjin, led by Jian-cheng Qi.

Mao-sheng Yao and Geng-feng Zheng, Charles Lieber’s former student, have conducted collaborative research on nanowire bio-detection, co-authoring a publication in 2018.

Also in 2018, Jian-cheng Qi’s research group at the PLA’s National Bio-protection Engineering Center in Tianjin published an article entitled “Applications of silicon nanowire FET biosensors to bacterial and viral detection.”

In December 2019, Mao-sheng Yao was granted a Chinese patent entitled “Method for rapidly detecting pathogenic microorganisms in air and respiratory tract on site.”

It is important to note that Jian-cheng Qi’s research group at the PLA’s National Bio-protection Engineering Center has operated under Major General Wei Chen, presumed chief of China’s biowarfare program, who took command in Wuhan after the outbreak of COVID-19, a response highlighted in Chinese news reports and no doubt including stolen U.S. technologies. Jian-cheng Qi was part of her team in Wuhan.

The massive infiltration of U.S. virus research programs by China’s People’s Liberation Army and the hemorrhaging of American skills and knowledge into China’s biowarfare program remain unaddressed.



Lawrence Sellin, Ph.D. is retired from an international career in business and medical research with 29 years of service in the US Army Reserve and a veteran of Afghanistan and Iraq. His email address is .


Joe Hoft is the twin brother of TGP's founder, Jim Hoft, and a contributing editor at TGP. Joe's reporting is often months ahead of the Mainstream media as was observed in his reporting on the Mueller sham investigation, the origins of the China coronavirus, and 2020 Election fraud. Joe was a corporate executive in Hong Kong for a decade and has years of experience in finance, IT, operations and auditing around the world. The knowledge gained in his career provide him with a unique perspective of current events in the US and globally. He has ten degrees or designations and is the author of three books. His new book: 'In God We Trust: Not in Lying Liberal Lunatics' is out now - please take a look and buy a copy. @joehoft


mRNA Vaccines: The Silent Weapon

By Dr. Igor Shepherd - 28. August 2021

My seven-year medical studies in the Soviet Army under the Strategic Rocket Force sector included large WMD-oriented military field exercises. I learned tactics of global warfare, including weapons of mass destruction and their effects on populations and enemy forces. The Soviet Army had a powerful biological defense system, and to be a successful military medical doctor I was required to know more than traditional medicine—I had to stay abrupt on the combat of “silent weaponry,” because this type of covert biowarfare was crucial in extermination of enemies (peoples of western free nations) and globalizing communism.

Under Soviet rule, biowarfare was set up to be carried out through either tactical or strategic methods. In a tactical event, the military aggressor would use bio-agents during ground battlefield against enemy troops. With strategic warfare, the civilian population would be the main focus for destruction. Bio-agents, as bomblets, would be dropped onto large populated areas using cruise missiles or through aerosol dispersal off aircraft. This type of silent warfare allowed the enemy to quickly take over a country’s infrastructure and economy, and incapacitate the population without a messy drawn-out military invasion.

Americans should be concerned about silent warfare, because most nations, including the US, no longer follow the very Bioweapon Treaty that was put in place to protect the world and whole populations against maniacal bio-genocide.

Worldwide Bioweapons Treaty Violations

After WWII, Americans ramped up their bio-research in order to counter the Soviet threat, and weaponized both incapacitating and lethal biological agents. In 1969, President Nixon stalled the biological research program, allowing the Soviet Union to roll forward as the running wheel of WMD in the world. This caused the US to backpedal, and redirect billions to fund bio-defense efforts and projects related to biological weapons. As bio-production escalated worldwide, the threat to humanity once again caused a stir.

That global threat is what brought about the 1975 Bioweapons Treaty under the Convention. It was established to prohibit the development, production and stockpiling of biological and toxin weapons. One hundred and eighty-three nations signed on, including Russia and China.

Compromise started prior to the finalization of the treaty when Russia refused to sign unless the verification provisions were removed. The verification process was crucial because it would compel nations to identify the number of civilian facilities and allow regular inspections. Russia had no intention of sanctioning inspections inside their research labs or displaying their enormous bio-stash. The US and UK caved in to Russia’s ridiculous ultimatum, and allowed the treaty to remove the verification process.

This move opened the door to lack of transparency and constant violations of the treaty, putting entire nations under constant threat. This is why it is important to understand that under this treaty gene-splicing and DNA manipulation used in the recent CRISPR technology and Covid-19 mRNA vaccines is illegal. All mRNA vaccine makers are in violation of this Biological Weapons Treaty, and getting away with it, thus allowing bioweapon development and production to move forward at the pace of a high-speed rail.

mRNA Technology is Not New

Messenger RNA technology in Covid vaccines is not new, even though our leaders have been spinning this mistruth since day one. The Soviets began developing mRNA sequencing almost four decades ago. They were the first to develop “designer” bio-agents under a classified program called Project Factor, one of many classified programs using recombinant DNA (rDNA) technology, known as DNA genetic engineering. Their gene-sequencing included messenger RNA (mRNA), and microRNA (miRNA), and carried the capability of creating horrific epidemics against enemy populations, even severe and debilitating multiple sclerosis.

DNA is the molecule that contains the genetic code of organisms like plants, animals, and bacteria, and is the hereditary material in humans and almost all other organisms. DNA is in each cell in the organism and directs the cells on what proteins to make. Messenger RNA is naturally located within all of our cells and is in charge of carrying out messages from the DNA that lies inside the nucleus of the cell. In the nucleus, the proteins are made from the mRNA sequence in a process known as translation. Both DNA and mRNA are molecules within a cell that are known as nucleic acids. MicroRNA regulates many mRNAs, and equally, a mRNA is regulated by several miRNAs in the production of bioweapons.

The molecules within the cells make up specific genetic codes for each individual’s life, and is the “instruction manual” in keeping the human body functioning properly. Our human genome is what makes the human species human, and gives each one of us our own unique and specific genetic code, which is truly an amazing wonder because everything from eye color to why we have thin or thick lips is locked up inside that code. If our code was modified in any way and genetically changed from its original version, then the chances of losing our humanness becomes a certainty. This is why bioweapons in the wrong hands can dramatically alter human life as we know it.

Through lab-created modified pathogens, using rDNA and mRNA, Soviet scientists decided to rival God. By plugging genes and combining segments of DNA from one type of organism with the gene of another organism, they created more deadly, contagious, environmentally stable and pathogenic novel strains of the various microorganisms. These included multi-drug-resistant anthrax, genetically modified super plague, chimeric variations of smallpox, and German measles. They also found the way to effectively hijack the body’s natural immune processes by producing overstimulation of the immune system through the “reprogramming” of the human immune system responses to those manmade-modified external pathogens. The over stimulation of the body’s immune system was purposed to cause serious immunological reactions and remove the body’s responsibility to release antibodies when the body decided to do so. Once the immune system was continuously in overdrive and self-exhausted (similar example of self-exhaust would be like a cancer patient whose immune system gets depleted from chemo-therapy), the body weakened and became susceptible to mild infections, like a cold, and could no longer fight off infections. For the Soviets, this breakthrough became important “silent warfare” for mass destruction.

Does this “reprogramming” of the immune system sound familiar? It should. The Covid-19 vaccines utilize the same mRNA technology of reprogramming the body’s immune system as Russia used in producing bioweapons for silent warfare against civilians. Unlike traditional vaccines, mRNA vaccines do not carry real pathogens, and works by “tricking” the body into thinking it is under attack with a real virus. The body becomes like a computer, and is instructed to develop the pathogenic proteins itself, “reprogramming” the human body to produce its own antibodies. The proteins become independent and do not gather to form a virus like traditional vaccines. The immune system then detects these viral proteins and starts to produce a defensive response to them. The final result, though, has altered the body’s natural responses, and dangerous pathological immune reactions are induced, including systemic inflammation and stimulation of auto-reactive antibodies, resulting in a cytokine storm or death. Worse, these harmful outcomes might not show up for months or years. This is why the initial side effects of many Covid vaccinated individuals were severe, and developed in days and weeks after the injection. The overstimulated immune system caused by the mRNA Covid-19 vaccines certainly blueprints Russia’s silent weapons of warfare.

Silent Warfare

The Covid vaccine companies insist mRNA does not alter DNA, but I do not buy it. They have their reasons for bypassing the traditional vaccine method and going with the bioweapon technology, and I do not think it has anything to do with ensuring the health of populations, otherwise they would have taken the time to follow proper testing protocols for their “new” vaccines at the onset, and not been rash in ignoring the abundant reports of injuries and deaths caused so far with the vaccinated. And so, should we blindly trust them after knowing mRNA technology was initially developed and used by the Soviets to harm and destroy whole populations? Should we trust them knowing there is no known proper gauge for short or long-term side effects and what fatalities might occur up ahead? Do we ignore the fact Covid vaccine ingredients use aborted fetal cells which could potentially initiate cancer and autoimmune system shifts within the vaccinated? Do we close our eyes to the toxic and non-biodegradable synthetic materials, such as polyethylene glycol (PEG), used to make the vaccines, knowing PEG’s cause disruption to cellular function and provoke severe neuropsychiatric symptoms in offspring?

Should we believe our leaders when they insist these “secretly-patented” mRNA vaccines are safe, even after knowingly receiving reports that the Covid-19 vaccinations resulted in injuries and deaths caused by blood coagulation, pathological thrombus formation, Bell’s Palsy, cardiac disorders, heart inflammation, neurological mayhem, paralysis, Guillain-Barre’s Syndrome, and numerous miscarriages? The creators of the Covid-19 vaccines expect numerous injuries and fatalities ahead. You cannot mess with this type of bio-technology and be “clueless” regarding end results. This is why the pharmaceutical giants made sure they would be free of legal ramifications for harmful effects and deaths.

The evidence of global warfare is everywhere—from the dictatorial global alliances being formed between nations, to the violations of civil rights, to the imprisonment of citizens inside their own homes, to the destruction of private businesses, to the extreme rules of mask wearing, to the cruel new laws denying unvaccinated Americans the right to work, eat at restaurants, or attend theaters—these are not normal responses to a pandemic, especially one with a 0.1% to 0.5% fatality rate. These are the responses of a communist despotism. By mandating these bio-vaccines, they are forcing us to play Russian Roulette, but instead of one bullet in the six-chamber shooter, there are five.

The communist-patterned pandemic responses forced on free Americans is inconceivable, and I find it worrisome that our own American government and the US Department of Defense is knee-deep in partnerships with China regarding Covid-19 vaccine research and development. DOD’s bioweapon research and expert sectors, BARDA, DARPA, and DTRA, have all been heavily involved with the vaccine conglomerates, as well as China’s military, the People’s Liberation Army. To trust the health of our nation’s citizens to a country who is an active enemy of American ideals, and who cannot adequately secure their own bioweapon laboratories is treasonable.

Messenger RNA technology, because it involves genetic engineering, can be used in any Covid or flu vaccine today for rapid global depopulation through sterility measures or immunological complications, for racial extermination, to modify human sexual composition and create non-genders, for behavioral modifications, or to undergo chromosomal integration or insertional mutagenesis, leading to random insertions of genetic codes into the host of cellular genomes (inducing tumors). The idea of vaccines as a dispersal method to annihilate or debilitate millions of people unknowingly, with their consent, is a brilliant strategy of warfare. The very means with which should help eliminate a pandemic and save lives is instead used as a “kill” device.

Because the masses have accepted vaccinations as preventive medicine for decades, most would reject the possibility that a vaccine could be used as a bioweapon against them. Nonetheless, strong evidence of a global “coup” is piling up as more and more citizens become alarmed that this pandemic is less about health and safety, and more about the restructuring and destruction of our laws, economy, civil rights, and freedoms—everything that occurs during an enemy takeover, and not during a pandemic. And with no enforced treaty to protect civilians against biological weapons of mass destruction, silent warfare against all of humanity becomes today’s reality.






Copyright © Igor Shepherd


PROLOG: Anthony Fauci, Peter Daszak, Ralph Baric, David Franz, Gigi Kwik Gronvall, Thomas Inglesby, W. Ian Lipkin, Kanta Subbarao must immediately be indicted and stand trial.

The Individuals Behind Obama’s Jan 2017 Memo Re-Authorizing Funding for ‘Gain of Function’ R&D Were the Same Individuals Who Lied and Claimed COVID Wasn’t Created in a Lab

By Lawrence Sellin - 06. June 2021

The same government medical professionals and doctors whose signatures supported Obama re-authorizing funding for the creation of SARS biological weapons were the ones in early 2020 to do all they could to push the lie that the China coronavirus happened in nature and was related to bat soup served at a Wuhan, China wet market.  

The Conservative Treehouse reported yesterday:

Eleven Days before leaving office President Obama’s administration re-authorized funding for the creation of biological weapons using SARS viruses. However, essentially this re-authorization was only kickstarting funding within the U.S. because the funding of weaponization of SARS-CoV-2 never actually stopped in 2014…

…This exception [from 2014] essentially permitted the Pentagon to continue funding the creation of SARS as a biological weapon in Wuhan, China, under the auspices of national security.  Which is exactly what the defense department did: “Grants from the Pentagon included $6,491,025 from the Defense Threat Reduction Agency (DTRA) from 2017 to 2020” (link).

The Treehouse provided the following timeline:

♦ October 17, 2014 – U.S. funding of SARS to create a biological weapon was paused due to the extreme risk of a pandemic.  However, the pause allowed agencies within the U.S. government to continue funding if they determined “the research is urgently necessary to protect the public health or national security.”

♦ 2014 through 2020 the Pentagon continued funding research in Wuhan, China. Fear of discovery would explain why many top officials in the U.S. Defense Department were against the Trump administration [with increased severity after the COVID pandemic began].

♦ May 2016 – [An Election Year] “after thorough deliberation and extensive input from domestic and international stakeholders, the NSABB [National Science Advisory Board for Biosecurity] issued its recommendations. NSABB’s central finding was that studies that are expected to enhance PPP have potential benefits to public health but also entail significant risks. NSABB recommended that such studies warranted additional scrutiny prior to being funded.”  Anthony Fauci is on the NSABB.

♦ January 9, 2017 – [Four Days after the Susan Rice oval office meeting with Obama, Biden, Comey, et al] The Obama Administration re-authorizes funding for the creation of SARS biological weapons.  “Adoption of these recommendations will satisfy the requirements for lifting the current moratorium on certain life sciences research that could enhance a pathogen’s virulence and/or transmissibility to produce a potential pandemic pathogen (an enhanced PPP).

Below is the May 2016 document evaluating proposed oversight for Gain of Function Research.  This is a much larger document than the later January 2017 memo.

What is interesting in this longer May 2016 document is the people who were involved. Go towards the end, starting at Appendix E. – Ralph Baric, David Franz, Gigi Kwik Gronvall, Thomas Inglesby, W. Ian Lipkin, Kanta Subbarao, all people who support gain of function.

Baric, Gronvall, and Inglesby were involved in the initial Jan-Feb 2020 cover-up of the origin of COVID with Daszak and Fauci. It’s in their emails.  Kanta Subbarao joined the now infamous ‘The Lancet’ article labeling the lab origin a conspiracy theory. Ian Lipkin got a medal from the Chinese government in January 2020.

NSABB Final Report Recommendations Evaluation Oversight Proposed Gain of Function Research May 2016 by Jim Hoft on Scribd

The longer NSABB Report (May 2016) is what the shorter January 9, 2017, announcement below is based on.  The key sentence in the January 9, 2017 announcement is:

Agencies that adopt a review mechanism consistent with the provisions specified below will have satisfied the requirements for lifting that agency’s moratorium on certain gain-of-function research”

Below is the final Guidance on Gain of Function from January 9, 2017:

p3co-Finalguidancestatement Jan 9 2017 by Jim Hoft on Scribd



Col. Lawrence Sellin, Ph.D. is retired from an international career in business and medical research with 29 years of service in the US Army Reserve and a veteran of Afghanistan and Iraq. His email address is .


Joe Hoft is the twin brother of TGP's founder, Jim Hoft. His posts have been retweeted by President Trump and have made the headlines at the Drudge Report. Joe worked as a corporate executive in Hong Kong and traveled the world for his work, which gives him a unique perspective of US and global current events. He has ten degrees or designations and is the author of three books. His new book: 'In God We Trust: Not in Lying Liberal Lunatics' is out now - please take a look and buy a copy. @joehoft


How the University of Minnesota May Have Contributed to China’s Biowarfare Program

By Lawrence Sellin and Anna Chen - 02. June 2021

The COVID-19 virus was created in a laboratory and it was part of China’s biowarfare program.

The Chinese Communist Party (CCP) has overall responsibility for that program, which is executed by the People’s Liberation Army (PLA).

The biowarfare program consists of three levels.

The first level is the core, secret military level.

Layered on top of the core level are China’s universities, civilian research institutions and medical companies.

Everyone needs to understand that, in China, there is no difference between military and civilian research. The fusion of those research and development sectors was mandated by the 2016 CCP Thirteenth Five-Year Plan.

It is the middle layer that has allowed the PLA to access international knowledge and skills, particularly from the U.S., all of which has contributed to the advancement of China’s virus research programs, including bioweapons development.

A potential example of the PLA gaining access to U.S. knowledge, skills and funding is the laboratory of Fang Li, who graduated from Beijing University and received a Ph.D. from Yale University.

Fang Li has been a frequent research collaborator with Zheng-Li Shi, the “bat woman” of the Wuhan Institute of Virology and Shibo Jiang, a graduate of China’s military medical universities and a long-time and extensive collaborator with China’s People’s Liberation Army.

But Fang Li also appears to have connections with what is believed to be part of China’s core military and secret biowarfare program.

Fang Li obtained a faculty position at the University of Minnesota and has been continuously funded by Dr. Anthony Fauci’s National Institute of Allergy and Infectious Diseases.

After establishing himself at the University of Minnesota and as an example of the CCP’s “scientific chain migration,” Fang Li began inviting Chinese researchers into his laboratory, mainly from Wuhan University and Huazhong Agricultural University, also in Wuhan.

From Wuhan University were Yang Yang (now at Iowa State University), Lang ChenYushun Wan, and Jian Shang, who also acts as an official recruiterfor Fang Li, presumably seeking more CCP researchers.

From Huazhong Agricultural University were Guiqing Peng and Ye Gang.

In an earlier Gateway Pundit article, we emphasized the importance of Chinese veterinary and agricultural research as contributors to a biowarfare program, one element being the Military Veterinary Research Institute in Changchun, led by General Ningyi Jin, shown below giving a lecture at Huazhong Agricultural University in 2018.

For over 20 years, the Huazhong Agricultural University directly collaboratedwith the Military Veterinary Research Institute on its J-203-1-01 project “Research and Application of Key Technologies for the Prevention and Control of Important Animal Viral Diseases.”

At one time there was a 4th PLA Veterinary School in Wuhan before it merged with the Military Veterinary Research Institute in Changchun.

Little trace of the 4th PLA Veterinary School remains on the internet, but if you search it plus “Wuhan,” the results yield Huazhong Agricultural University and its animal testing facility.

In our May 25, 2021 Gateway Pundit article, we identified the Wuhan University Animal Biosafety Level Three (ABSL-3) testing facility as a potential origin of the COVID-19 pandemic, a consequence of the non-human primate tests being conducted there.

All the PLA-connected facilities shown on the map were within the epicenter of the early outbreak at the beginning of the COVID-19 pandemic.

Fang Li, together with the “bat woman” Zheng-Li Shi of the Wuhan Institute of Virology, conducted detailed collaborative research involving an analysis and artificial manipulation of coronavirus spike proteins, structures regulating human infectivity.

It is yet to be determined how much of Fang Li’s research may have found its way into China’s biological warfare program via his extensive collaboration with Wuhan research institutions and their links to the People’s Liberation Army.


Lawrence Sellin, Ph.D. is retired from an international career in business and medical research with 29 years of service in the US Army Reserve and a veteran of Afghanistan and Iraq. His email address is .


Joe Hoft is the twin brother of TGP's founder, Jim Hoft. His posts have been retweeted by President Trump and have made the headlines at the Drudge Report. Joe worked as a corporate executive in Hong Kong and traveled the world for his work, which gives him a unique perspective of US and global current events. He has ten degrees or designations and is the author of three books. His new book: 'In God We Trust: Not in Lying Liberal Lunatics' is out now - please take a look and buy a copy. @joehoft


PROLOGUE: It is for us still difficult to understand that - though we spoke and warned together with Prof. Francis Boyle and few others since over year of the bio-weapon component in SARS-CoV-2 - it is only now that wider circles start to realize what really is going on. But better now than never. 

BOMBSHELL: Chinese military planned aerosolized bioweapon development and deployment to “cause the enemy’s medical system to collapse”

By  - 12. May 2021

Image: BOMBSHELL: Chinese military planned aerosolized bioweapon development and deployment to “cause the enemy’s medical system to collapse”

During the investigation into the origins of SARS-CoV-2, the U.S. State Department obtained a 263-page document revealing the true intent of senior Chinese public health officials and top scientists with the Chinese People’s Liberation Army (PLA). This document has been vetted and confirmed authentic by digital forensic specialists who worked for the US, Australian and Canadian governments.

Five years before the pandemic emerged in Wuhan, Chinese military scientists were preparing for a third World War and communicating strategies on how to weaken their opponents using freeze-dried, aerosolized bioweapons. In the documents, the PLA openly discuss using a bioweapon that “could cause the enemy’s medical system to collapse.” They discussed how a successful bioweapon could turn hospitals into battlefields, causing a surge of hospitalizations, and burdening medical systems to the point of collapse.

The monsters behind bioterrorism, medical experimentation, and human rights violations must be hunted down and tried

The documents are authored by ten highly trained Chinese defense experts who are affiliated with the Air Force Medical University in Xi’an, which is under the command of the PLA. The documents are titled, “The Unnatural Origin of SARS and New Species of Man-Made Viruses as Genetic Bioweapons.” The documents clearly show that China is engaged in advanced biowarfare. “Following developments in other scientific fields, there have been major advances in the delivery of biological agents,” the documents state. Even more revealing, the documents discuss new technologies for freeze-drying micro-organisms to make it “possible to store biological agents and aerosolize them during attacks.”

The documents even reveal the best time to release a bio-weapon: “Bioweapon attacks are best conducted during dawn, dusk, night or cloudy weather because intense sunlight can damage the pathogens,” it states. “Biological agents should be released during dry weather. Rain or snow can cause the aerosol particles to precipitate. A stable wind direction is desirable so that the aerosol can float into the target area.”

In the beginning of the pandemic, WHO believed that SARS-CoV-2 proliferated via asymptomatic spread. That hypothesis was outlandish, overcautious, and did not coincide with the science of viral load. This Chinese military propaganda led to lock downs and the crippling of people’s livelihoods, education systems and economies. After “asymptomatic spread” was later debunked by WHO and scientists from around the world, many still wondered how so many people around the world were suddenly suffering from a severe cytokine storm inside their bodies. A bioweapon that can be freeze dried and aerosolized to target medical systems can be deployed stealthily in hospitals and in nursing homes around the world, where the weakest immune systems reside. This is where almost all of the death is occurring. Is the world under attack from an aerosolized bioweapon, that is spread through the skies?

The world population, including the Chinese people, must be liberated from these monsters of bioterrorism, bioweapon research and deadly medial experimentation on human populations. Freedom fighters around the world must stand up and face the evil that seeks to control, mislead and defraud medical systems, putting people’s lives at risk. Fraudulent diagnostic tests are part of the bio-terror, misleading medical authorities as people are imprisoned, isolated and stripped of their dignity and basic human rights.

Chinese propaganda is alive and well in the Western media, as knowledge on viable treatments are withheld, natural immune therapy protocols blacklisted. The asymptomatic spread deception underpins all motivations to lock people down and restrict human interaction, covering up the real issue at hand: the bioweapon is engineered to be aerosolized anywhere, anytime to target competing nations, exploit the most vulnerable, and take down hospital systems. To make matters worse, coronavirus gain-of-function research continues in Wuhan to this day, with U.S. taxpayer money paving the way for future waves of bio-terrorism and medical experimentation. Many CCP assets operate in the United States and they include Dr. Anthony Fauci and Dr. Peter Daszak.

Peter Daszak an asset of the CCP who misled the world to cover up bio-terrorism trail

Bio-weapon research was thwarted in the United States in 2014, after a ban was placed on the highly-unethical, coronavirus gain-of function research. But under the direction of Anthony Fauci, the National Institute of Allergy and Infectious Disease (NIAID) continued the research through grants assigned to Peter Daszak at New York’s Eco Health Alliance.

After receiving NIH grants worth $3.7 million in 2014, Eco Health Alliance began funneling payments to CCP scientists working in Wuhan. The first $666,442 installment was received by the CCP in June of 2014. The project was code-named “Understanding the Risk of Bat Coronavirus Emergence.” By May of 2019, Eco Health had wired six installments to CCP scientists, each payment worth more than half a million dollars. Daszak met repeatedly with Wuhan Institute of Virology’s Shi Zhengli, who conducted gain-of-function research in participation with U.S. universities for years.

It came as no surprise that Daszak was granted investigator status as part of the World Health Organization’s “investigation” into the origins of SARS-CoV-2. In early 2020, WHO quickly concluded that SARS-CoV-2 was of natural origin; any assertion otherwise was written off as “conspiracy theory.” Following in the footsteps of communist China, American Big Tech companies colluded with WHO and scrubbed any information about the bio-weapon origin of SARS-CoV-2, even though the release could have been accidental in Wuhan and intentional in other air spaces around the world. It came as no surprise that this “global consensus” on the origins of covid-19 was drafted by Dr. Peter Daszak himself, the man who funneled money to the CCP to engineer coronaviruses.

On February 19, 2020, a group of virologists wrote to the Lancet, calling on governments around the world to stand with the CCP: “We stand together to strongly condemn conspiracy theories suggesting that COVID-19 does not have a natural origin.” The letter declared there were “no competing interests,” but it turned out that the letter was organized and drafted by Peter Daszak. He tried to assure the world of facts he could never verify. There are at least three known laboratory tactics for virus engineering that leave no trace of evidence behind. Serial passage is the repeated transfer of viruses from one culture of cells to another. Other sly methods include the “no-see-um” or “seamless” approach which conceal any evidence that the virus was manipulated.

How could the accidental bioweapon release theory be so easily thrown out as “conspiracy?” Worse, Daszak made these broad assertions before anyone could be sure of what really happened or could continue to occur. Now there is proof that the hospitalizations and deaths taking place around the world are the result of careful planning and execution by Chinese military scientists, whose intent to exploit human immune systems and harm medical systems is now known. Daszak is complicit in trying to cover up these crimes against humanity, and his collaboration with the CCP, is at the very least, a conflict of interest that should forever bar him from having any authority on the matter. All monsters, assets and collaborators behind the continued bioterrorism, human rights abuses and medical experimentation must be hunted down and tried for war crimes.

Sources include:








Chinese Military Discussed Weaponizing COVID In 2015 'To Cause Enemy's Medical System To Collapse'

By Tyler Durden - 09. May 2021

In 2015, Chinese military scientists discussed how to weaponze SARS coronaviruses, five years before the COVID-19 pandemic emerged in Wuhan, China - where CCP scientists were collaborating with a US-funded NGO on so-called 'gain of function' research to make bat coronaviruses infect humans more easily.

In a 263-page document, written by People's Liberation Army scientists and senior Chinese public health officials and obtained by the US State Department during its investigation into the origins of COVID-19, PLA scientists note how a sudden surge of patients requiring hospitalization during a bioweapon attack "could cause the enemy’s medical system to collapse," according to The Weekend Australian (a subsidiary of News Corp).

It suggests that SARS coronaviruses could herald a "new era of genetic weapons," and noted that they can be "artificially manipulated into an emerging human ­disease virus, then weaponized and unleashed in a way never seen before."

The chairmen of the British and Australian foreign affairs and intelligence committees, Tom ­Tugendhat and James Paterson, say the document raises major concerns about China’s lack of transparency over the origins of COVID-19.

The Chinese-language paper, titled The Unnatural Origin of SARS and New Species of Man-Made Viruses as Genetic Bioweapons, outlines China’s progress in the research field of biowarfare.

“Following developments in other scientific fields, there have been major advances in the delivery of biological agents,” it states.

“For example, the new-found ability to freeze-dry micro-organisms has made it possible to store biological agents and aerosolise them during attacks.”

Ten of the authors are scientists and weapons experts affiliated with the Air Force Medical ­University in Xi’an, ranked “very high-risk” for its level of defence research, including its work on medical and psychological sciences, according to the Australian Strategic Policy Institute’s ­Defence Universities Tracker.

The Air Force Medical University, also known as the Fourth Medical University, was placed under the command of the PLA under President Xi Jinping’s military reforms in 2017. The editor-in-chief of the paper, Xu Dezhong, reported to the top leadership of the Chinese Military Commission and Ministry of Health during the SARS epidemic of 2003, briefing them 24 times and preparing three reports, according to his online ­biography. -The Australian

The editor-in-chief of the paper, Xu Dezhong, reported to the top leadership of the Chinese Military Commission and Ministry of Health on the SARS epidemic of 2003. (via The Australian)

"We were able to verify its ­authenticity as a document authored by the particular PLA ­researchers and scientists," according to Robert Potter, a digital forensics specialist who has worked for the US, Australian and Canadian governments - and has previously analyzed leaked Chinese government documents, according to the report. "We were able to locate its genesis on the Chinese internet."

Former US Secretary of State Mike Pompeo and his chief China adviser, Miles Yu, referenced the document in a February op-ed in the Wall Street Journal, writing that "A 2015 PLA study treated the 2003 SARS coronavirus outbreak as a ‘contemporary genetic weapon’ launched by foreign forces."

And according to Peter Jennings, executive director of the Australian Strategic Policy Institute, "There is no clear distinction for research capability because whether it’s used offensively or defensively is not a decision these scientists would take," adding "If you are building skills ostensibly to protect your military from a biological attack, you’re at the same time giving your military a capacity to use these weapons ­offensively. You can’t separate the two."

The study also examines the optimum conditions under which to release a bioweapon. “Bioweapon attacks are best conducted during dawn, dusk, night or cloudy weather because intense sunlight can damage the pathogens,” it states. “Biological agents should be released during dry weather. Rain or snow can cause the aerosol particles to precipitate.

“A stable wind direction is ­desirable so that the aerosol can float into the target area.”

Among the most bizarre claims by the military scientists is their theory that SARS-CoV-1, the virus that caused the SARS epidemic of 2003, was a man-made bioweapon, deliberately unleashed on China by “terrorists”. -The Australian

News of the document follows a May 3 report that the Wuhan Institute of Virology was working with the Chinese government in a team which comprised five military and civil experts, "who conducted research at WIV labs, military labs, and other civil labs leading to “the discovery of animal pathogens [biological agents that causes disease] in wild animals," according to the Epoch Times.

And as we noted in March, the US National Institutes of Health (NIH) - headed by Dr. Anthony Fauci, "had funded a number of projects that involved WIV scientists, including much of the Wuhan lab's work with bat coronaviruses."

In 2017, Fauci's agency resumed funding a controversial grant to genetically modify bat coronaviruses in Wuhan, China without the approval of a government oversight body, according to the Daily Caller. For context, in 2014, the Obama administration temporarily suspended federal funding for gain-of-function research on bat coronaviruses. Four months prior to that decision, the NIH effectively shifted this research to the Wuhan Institute of Virology (WIV) via a grant to nonprofit group EcoHealth Alliance, headed by Peter Daszak. 

Peter Daszak, president of EcoHealth Alliance

The NIH's first $666,442 installment of EcoHealth's $3.7 million grant was paid in June 2014, with similar annual payments through May 2019 under the "Understanding The Risk Of Bat Coronavirus Emergence" project.

Notably, the WIV "had openly participated in gain-of-function research in partnership with U.S. universities and institutions" for years under the leadership of Dr. Shi 'Batwoman' Zhengli, according to the Washington Post's Josh Rogin.

EcoHealth Alliance president Peter Daszak toasts with WIV's 'Batwoman' Shi Zhengli  

So now we have a 2015 document from the Chinese military describing using COVID as a bioweapon - four years before the COVID-19 pandemic breaks out just miles away from a Chinese lab working to make bat COVID more transmissible to humans, and you're a conspiracy theorist peddling 'debunked lies' if you think they might be related.

And for those who say 'COVID-19 couldn't be man-made because a laboratory-created virus would have tell-tale signs of manipulation' - au contraire. As Nicholas Wade noted three days ago in the Bulletin of the Atomic Scientists, "newer methods, called “no-see-um” or “seamless” approaches, leave no defining marks. Nor do other methods for manipulating viruses such as serial passage, the repeated transfer of viruses from one culture of cells to another. If a virus has been manipulated, whether with a seamless method or by serial passage, there is no way of knowing that this is the case. "

It's as if the painfully obvious answer was right in front of us, only to be shrouded in propaganda by China-friendly politicians, big tech, and news outlets running cover for what should be the easiest game of connect-the-dots on the planet. Luckily, what was taboo as recently as a year ago will soon be exposed for the world to see, thanks to The Bulletin Of Atomic Scientists which earlier this week dared to open The Wuhan Virus "Pandora's Box"...


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Tyler Durden


The origin of COVID:

Did people or nature open Pandora’s box at Wuhan?

By Nicholas Wade - 05. May 2021

Members of the World Health Organization (WHO) team investigating the origins of the COVID-19 coronavirus arrive by car at the Wuhan Institute of Virology on February 3. (Photo by HECTOR RETAMAL/AFP via Getty Images)

Members of the World Health Organization (WHO) team investigating the origins of the COVID-19 coronavirus arrive by car at the Wuhan Institute of Virology on February 3. (Photo by HECTOR RETAMAL/AFP via Getty Images)

The COVID-19 pandemic has disrupted lives the world over for more than a year. Its death toll will soon reach three million people. Yet the origin of pandemic remains uncertain: The political agendas of governments and scientists have generated thick clouds of obfuscation, which the mainstream press seems helpless to dispel.

In what follows I will sort through the available scientific facts, which hold many clues as to what happened, and provide readers with the evidence to make their own judgments. I will then try to assess the complex issue of blame, which starts with, but extends far beyond, the government of China.

By the end of this article, you may have learned a lot about the molecular biology of viruses. I will try to keep this process as painless as possible. But the science cannot be avoided because for now, and probably for a long time hence, it offers the only sure thread through the maze.

The virus that caused the pandemic is known officially as SARS-CoV-2, but can be called SARS2 for short. As many people know, there are two main theories about its origin. One is that it jumped naturally from wildlife to people. The other is that the virus was under study in a lab, from which it escaped. It matters a great deal which is the case if we hope to prevent a second such occurrence.

I’ll describe the two theories, explain why each is plausible, and then ask which provides the better explanation of the available facts. It’s important to note that so far there is no direct evidence for either theory. Each depends on a set of reasonable conjectures but so far lacks proof. So I have only clues, not conclusions, to offer. But those clues point in a specific direction. And having inferred that direction, I’m going to delineate some of the strands in this tangled skein of disaster.

A tale of two theories. After the pandemic first broke out in December 2019, Chinese authorities reported that many cases had occurred in the wet market — a place selling wild animals for meat — in Wuhan. This reminded experts of the SARS1 epidemic of 2002, in which a bat virus had spread first to civets, an animal sold in wet markets, and from civets to people. A similar bat virus caused a second epidemic, known as MERS, in 2012. This time the intermediary host animal was camels.

The decoding of the virus’s genome showed it belonged a viral family known as beta-coronaviruses, to which the SARS1 and MERS viruses also belong. The relationship supported the idea that, like them, it was a natural virus that had managed to jump from bats, via another animal host, to people. The wet market connection, the major point of similarity with the SARS1 and MERS epidemics, was soon broken: Chinese researchers found earlier cases in Wuhan with no link to the wet market. But that seemed not to matter when so much further evidence in support of natural emergence was expected shortly.

Wuhan, however, is home of the Wuhan Institute of Virology, a leading world center for research on coronaviruses. So the possibility that the SARS2 virus had escaped from the lab could not be ruled out. Two reasonable scenarios of origin were on the table.

From early on, public and media perceptions were shaped in favor of the natural emergence scenario by strong statements from two scientific groups. These statements were not at first examined as critically as they should have been.

“We stand together to strongly condemn conspiracy theories suggesting that COVID-19 does not have a natural origin,” a group of virologists and others wrote in the Lancet on February 19, 2020, when it was really far too soon for anyone to be sure what had happened. Scientists “overwhelmingly conclude that this coronavirus originated in wildlife,” they said, with a stirring rallying call for readers to stand with Chinese colleagues on the frontline of fighting the disease.

Contrary to the letter writers’ assertion, the idea that the virus might have escaped from a lab invoked accident, not conspiracy. It surely needed to be explored, not rejected out of hand. A defining mark of good scientists is that they go to great pains to distinguish between what they know and what they don’t know. By this criterion, the signatories of the Lancet letter were behaving as poor scientists: They were assuring the public of facts they could not know for sure were true.

It later turned out that the Lancet letter had been organized and drafted by Peter Daszak, president of the EcoHealth Alliance of New York. Daszak’s organization funded coronavirus research at the Wuhan Institute of Virology. If the SARS2 virus had indeed escaped from research he funded, Daszak would be potentially culpable. This acute conflict of interest was not declared to the Lancet’s readers. To the contrary, the letter concluded, “We declare no competing interests.”

Peter Daszak, a member of the World Health Organization (WHO) team investigating the origins of the COVID-19 coronavirus, talks on his cellphone at the Hilton Wuhan Optics Valley in Wuhan. (Photo by HECTOR RETAMAL/AFP via Getty Images)

Peter Daszak, a member of the World Health Organization (WHO) team investigating the origins of the COVID-19 coronavirus, talks on his cellphone at the Hilton Wuhan Optics Valley in Wuhan. (Photo by HECTOR RETAMAL/AFP via Getty Images)

Virologists like Daszak had much at stake in the assigning of blame for the pandemic. For 20 years, mostly beneath the public’s attention, they had been playing a dangerous game. In their laboratories they routinely created viruses more dangerous than those that exist in nature. They argued that they could do so safely, and that by getting ahead of nature they could predict and prevent natural “spillovers,” the cross-over of viruses from an animal host to people. If SARS2 had indeed escaped from such a laboratory experiment, a savage blowback could be expected, and the storm of public indignation would affect virologists everywhere, not just in China. “It would shatter the scientific edifice top to bottom,” an MIT Technology Review editor, Antonio Regalado, said in March 2020.

A second statement that had enormous influence in shaping public attitudes was a letter (in other words an opinion piece, not a scientific article) published on 17 March 2020 in the journal Nature Medicine. Its authors were a group of virologists led by Kristian G. Andersen of the Scripps Research Institute. “Our analyses clearly show that SARS-CoV-2 is not a laboratory construct or a purposefully manipulated virus,” the five virologists declared in the second paragraph of their letter.

Unfortunately, this was another case of poor science, in the sense defined above. True, some older methods of cutting and pasting viral genomes retain tell-tale signs of manipulation. But newer methods, called “no-see-um” or “seamless” approaches, leave no defining marks. Nor do other methods for manipulating viruses such as serial passage, the repeated transfer of viruses from one culture of cells to another. If a virus has been manipulated, whether with a seamless method or by serial passage, there is no way of knowing that this is the case. Andersen and his colleagues were assuring their readers of something they could not know.

The discussion part of their letter begins, “It is improbable that SARS-CoV-2 emerged through laboratory manipulation of a related SARS-CoV-like coronavirus.” But wait, didn’t the lead say the virus had clearly not been manipulated? The authors’ degree of certainty seemed to slip several notches when it came to laying out their reasoning.

The reason for the slippage is clear once the technical language has been penetrated. The two reasons the authors give for supposing manipulation to be improbable are decidedly inconclusive.

First, they say that the spike protein of SARS2 binds very well to its target, the human ACE2 receptor, but does so in a different way from that which physical calculations suggest would be the best fit. Therefore the virus must have arisen by natural selection, not manipulation.

If this argument seems hard to grasp, it’s because it’s so strained. The authors’ basic assumption, not spelt out, is that anyone trying to make a bat virus bind to human cells could do so in only one way. First they would calculate the strongest possible fit between the human ACE2 receptor and the spike protein with which the virus latches onto it. They would then design the spike protein accordingly (by selecting the right string of amino acid units that compose it). Since the SARS2 spike protein is not of this calculated best design, the Andersen paper says, therefore it can’t have been manipulated.

But this ignores the way that virologists do in fact get spike proteins to bind to chosen targets, which is not by calculation but by splicing in spike protein genes from other viruses or by serial passage. With serial passage, each time the virus’s progeny are transferred to new cell cultures or animals, the more successful are selected until one emerges that makes a really tight bind to human cells. Natural selection has done all the heavy lifting. The Andersen paper’s speculation about designing a viral spike protein through calculation has no bearing on whether or not the virus was manipulated by one of the other two methods.

The authors’ second argument against manipulation is even more contrived. Although most living things use DNA as their hereditary material, a number of viruses use RNA, DNA’s close chemical cousin. But RNA is difficult to manipulate, so researchers working on coronaviruses, which are RNA-based, will first convert the RNA genome to DNA. They manipulate the DNA version, whether by adding or altering genes, and then arrange for the manipulated DNA genome to be converted back into infectious RNA.

Only a certain number of these DNA backbones have been described in the scientific literature. Anyone manipulating the SARS2 virus “would probably” have used one of these known backbones, the Andersen group writes, and since SARS2 is not derived from any of them, therefore it was not manipulated. But the argument is conspicuously inconclusive. DNA backbones are quite easy to make, so it’s obviously possible that SARS2 was manipulated using an unpublished DNA backbone.

And that’s it. These are the two arguments made by the Andersen group in support of their declaration that the SARS2 virus was clearly not manipulated. And this conclusion, grounded in nothing but two inconclusive speculations, convinced the world’s press that SARS2 could not have escaped from a lab. A technical critique of the Andersen letter takes it down in harsher words.

Science is supposedly a self-correcting community of experts who constantly check each other’s work. So why didn’t other virologists point out that the Andersen group’s argument was full of absurdly large holes? Perhaps because in today’s universities speech can be very costly. Careers can be destroyed for stepping out of line. Any virologist who challenges the community’s declared view risks having his next grant application turned down by the panel of fellow virologists that advises the government grant distribution agency.

The Daszak and Andersen letters were really political, not scientific, statements, yet were amazingly effective. Articles in the mainstream press repeatedly stated that a consensus of experts had ruled lab escape out of the question or extremely unlikely. Their authors relied for the most part on the Daszak and Andersen letters, failing to understand the yawning gaps in their arguments. Mainstream newspapers all have science journalists on their staff, as do the major networks, and these specialist reporters are supposed to be able to question scientists and check their assertions. But the Daszak and Andersen assertions went largely unchallenged.

Doubts about natural emergence. Natural emergence was the media’s preferred theory until around February 2021 and the visit by a World Health Organization (WHO) commission to China. The commission’s composition and access were heavily controlled by the Chinese authorities. Its members, who included the ubiquitous Daszak, kept asserting before, during, and after their visit that lab escape was extremely unlikely. But this was not quite the propaganda victory the Chinese authorities may have been hoping for. What became clear was that the Chinese had no evidence to offer the commission in support of the natural emergence theory.

This was surprising because both the SARS1 and MERS viruses had left copious traces in the environment. The intermediary host species of SARS1 was identified within four months of the epidemic’s outbreak, and the host of MERS within nine months. Yet some 15 months after the SARS2 pandemic began, and after a presumably intensive search, Chinese researchers had failed to find either the original bat population, or the intermediate species to which SARS2 might have jumped, or any serological evidence that any Chinese population, including that of Wuhan, had ever been exposed to the virus prior to December 2019. Natural emergence remained a conjecture which, however plausible to begin with, had gained not a shred of supporting evidence in over a year.

And as long as that remains the case, it’s logical to pay serious attention to the alternative conjecture, that SARS2 escaped from a lab.

Why would anyone want to create a novel virus capable of causing a pandemic? Ever since virologists gained the tools for manipulating a virus’s genes, they have argued they could get ahead of a potential pandemic by exploring how close a given animal virus might be to making the jump to humans. And that justified lab experiments in enhancing the ability of dangerous animal viruses to infect people, virologists asserted.

With this rationale, they have recreated the 1918 flu virus, shown how the almost extinct polio virus can be synthesized from its published DNA sequence, and introduced a smallpox gene into a related virus.

These enhancements of viral capabilities are known blandly as gain-of-function experiments. With coronaviruses, there was particular interest in the spike proteins, which jut out all around the spherical surface of the virus and pretty much determine which species of animal it will target. In 2000 Dutch researchers, for instance, earned the gratitude of rodents everywhere by genetically engineering the spike protein of a mouse coronavirus so that it would attack only cats.


The spike proteins on the coronavirus’s surface determine which animal it can infect. Image credit: CDC.gov

Virologists started studying bat coronaviruses in earnest after these turned out to be the source of both the SARS1 and MERS epidemics. In particular, researchers wanted to understand what changes needed to occur in a bat virus’s spike proteins before it could infect people.

Researchers at the Wuhan Institute of Virology, led by China’s leading expert on bat viruses, Shi Zheng-li or “Bat Lady,” mounted frequent expeditions to the bat-infested caves of Yunnan in southern China and collected around a hundred different bat coronaviruses.

Shi then teamed up with Ralph S. Baric, an eminent coronavirus researcher at the University of North Carolina. Their work focused on enhancing the ability of bat viruses to attack humans so as to “examine the emergence potential (that is, the potential to infect humans) of circulating bat CoVs [coronaviruses].” In pursuit of this aim, in November 2015 they created a novel virus by taking the backbone of the SARS1 virus and replacing its spike protein with one from a bat virus (known as SHC014-CoV). This manufactured virus was able to infect the cells of the human airway, at least when tested against a lab culture of such cells.

The SHC014-CoV/SARS1 virus is known as a chimera because its genome contains genetic material from two strains of virus. If the SARS2 virus were to have been cooked up in Shi’s lab, then its direct prototype would have been the SHC014-CoV/SARS1 chimera, the potential danger of which concerned many observers and prompted intense discussion.

“If the virus escaped, nobody could predict the trajectory,” said Simon Wain-Hobson, a virologist at the Pasteur Institute in Paris.

Baric and Shi referred to the obvious risks in their paper but argued they should be weighed against the benefit of foreshadowing future spillovers. Scientific review panels, they wrote, “may deem similar studies building chimeric viruses based on circulating strains too risky to pursue.” Given various restrictions being placed on gain-of function (GOF) research, matters had arrived in their view at “a crossroads of GOF research concerns; the potential to prepare for and mitigate future outbreaks must be weighed against the risk of creating more dangerous pathogens. In developing policies moving forward, it is important to consider the value of the data generated by these studies and whether these types of chimeric virus studies warrant further investigation versus the inherent risks involved.”

That statement was made in 2015. From the hindsight of 2021, one can say that the value of gain-of-function studies in preventing the SARS2 epidemic was zero. The risk was catastrophic, if indeed the SARS2 virus was generated in a gain-of-function experiment.

Inside the Wuhan Institute of Virology. Baric had developed, and taught Shi, a general method for engineering bat coronaviruses to attack other species. The specific targets were human cells grown in cultures and humanized mice. These laboratory mice, a cheap and ethical stand-in for human subjects, are genetically engineered to carry the human version of a protein called ACE2 that studs the surface of cells that line the airways.

Shi returned to her lab at the Wuhan Institute of Virology and resumed the work she had started on genetically engineering coronaviruses to attack human cells. How can we be so sure?

A May 20, 2020, photo of the Wuhan Institute of Virology in Wuhan, where research on bat coronaviruses was conducted. (Photo by Kyodo News via Getty Images)

Because, by a strange twist in the story, her work was funded by the National Institute of Allergy and Infectious Diseases (NIAID), a part of the US National Institutes of Health (NIH). And grant proposals that funded her work, which are a matter of public record, specify exactly what she planned to do with the money.

The grants were assigned to the prime contractor, Daszak of the EcoHealth Alliance, who subcontracted them to Shi. Here are extracts from the grants for fiscal years 2018 and 2019. (“CoV” stands for coronavirus and “S protein” refers to the virus’s spike protein.)

“Test predictions of CoV inter-species transmission. Predictive models of host range (i.e. emergence potential) will be tested experimentally using reverse genetics, pseudovirus and receptor binding assays, and virus infection experiments across a range of cell cultures from different species and humanized mice.

“We will use S protein sequence data, infectious clone technology, in vitro and in vivo infection experiments and analysis of receptor binding to test the hypothesis that % divergence thresholds in S protein sequences predict spillover potential.”

What this means, in non-technical language, is that Shi set out to create novel coronaviruses with the highest possible infectivity for human cells. Her plan was to take genes that coded for spike proteins possessing a variety of measured affinities for human cells, ranging from high to low. She would insert these spike genes one by one into the backbone of a number of viral genomes (“reverse genetics” and “infectious clone technology”), creating a series of chimeric viruses. These chimeric viruses would then be tested for their ability to attack human cell cultures (“in vitro”) and humanized mice (“in vivo”). And this information would help predict the likelihood of “spillover,” the jump of a coronavirus from bats to people.

The methodical approach was designed to find the best combination of coronavirus backbone and spike protein for infecting human cells. The approach could have generated SARS2-like viruses, and indeed may have created the SARS2 virus itself with the right combination of virus backbone and spike protein.

It cannot yet be stated that Shi did or did not generate SARS2 in her lab because her records have been sealed, but it seems she was certainly on the right track to have done so. “It is clear that the Wuhan Institute of Virology was systematically constructing novel chimeric coronaviruses and was assessing their ability to infect human cells and human-ACE2-expressing mice,” says Richard H. Ebright, a molecular biologist at Rutgers University and leading expert on biosafety.

“It is also clear,” Ebright said, “that, depending on the constant genomic contexts chosen for analysis, this work could have produced SARS-CoV-2 or a proximal progenitor of SARS-CoV-2.” “Genomic context” refers to the particular viral backbone used as the testbed for the spike protein.

The lab escape scenario for the origin of the SARS2 virus, as should by now be evident, is not mere hand-waving in the direction of the Wuhan Institute of Virology. It is a detailed proposal, based on the specific project being funded there by the NIAID.

Even if the grant required the work plan described above, how can we be sure that the plan was in fact carried out? For that we can rely on the word of Daszak, who has been much protesting for the last 15 months that lab escape was a ludicrous conspiracy theory invented by China-bashers.

On December 9, 2019, before the outbreak of the pandemic became generally known, Daszak gave an interview in which he talked in glowing terms of how researchers at the Wuhan Institute of Virology had been reprogramming the spike protein and generating chimeric coronaviruses capable of infecting humanized mice.

“And we have now found, you know, after 6 or 7 years of doing this, over 100 new SARS-related coronaviruses, very close to SARS,” Daszak says around minute 28 of the interview. “Some of them get into human cells in the lab, some of them can cause SARS disease in humanized mice models and are untreatable with therapeutic monoclonals and you can’t vaccinate against them with a vaccine. So, these are a clear and present danger….

“Interviewer: You say these are diverse coronaviruses and you can’t vaccinate against them, and no anti-virals — so what do we do?

“Daszak: Well I think…coronaviruses — you can manipulate them in the lab pretty easily. Spike protein drives a lot of what happen with coronavirus, in zoonotic risk. So you can get the sequence, you can build the protein, and we work a lot with Ralph Baric at UNC to do this. Insert into the backbone of another virus and do some work in the lab. So you can get more predictive when you find a sequence. You’ve got this diversity. Now the logical progression for vaccines is, if you are going to develop a vaccine for SARS, people are going to use pandemic SARS, but let’s insert some of these other things and get a better vaccine.” The insertions he referred to perhaps included an element called the furin cleavage site, discussed below, which greatly increases viral infectivity for human cells.

In disjointed style, Daszak is referring to the fact that once you have generated a novel coronavirus that can attack human cells, you can take the spike protein and make it the basis for a vaccine.

One can only imagine Daszak’s reaction when he heard of the outbreak of the epidemic in Wuhan a few days later. He would have known better than anyone the Wuhan Institute’s goal of making bat coronaviruses infectious to humans, as well as the weaknesses in the institute’s defense against their own researchers becoming infected.

But instead of providing public health authorities with the plentiful information at his disposal, he immediately launched a public relations campaign to persuade the world that the epidemic couldn’t possibly have been caused by one of the institute’s souped-up viruses. “The idea that this virus escaped from a lab is just pure baloney. It’s simply not true,” he declared in an April 2020 interview.

The safety arrangements at the Wuhan Institute of Virology. Daszak was possibly unaware of, or perhaps he knew all too well, the long history of viruses escaping from even the best run laboratories. The smallpox virus escaped three times from labs in England in the 1960’s and 1970’s, causing 80 cases and 3 deaths. Dangerous viruses have leaked out of labs almost every year since. Coming to more recent times, the SARS1 virus has proved a true escape artist, leaking from laboratories in Singapore, Taiwan, and no less than four times from the Chinese National Institute of Virology in Beijing.

One reason for SARS1 being so hard to handle is that there were no vaccines available to protect laboratory workers. As Daszak mentioned in the December 19 interview quoted above, the Wuhan researchers too had been unable to develop vaccines against the coronaviruses they had designed to infect human cells. They would have been as defenseless against the SARS2 virus, if it were generated in their lab, as their Beijing colleagues were against SARS1.

A second reason for the severe danger of novel coronaviruses has to do with the required levels of lab safety. There are four degrees of safety, designated BSL1 to BSL4, with BSL4 being the most restrictive and designed for deadly pathogens like the Ebola virus.

The Wuhan Institute of Virology had a new BSL4 lab, but its state of readiness considerably alarmed the State Department inspectors who visited it from the Beijing embassy in 2018. “The new lab has a serious shortage of appropriately trained technicians and investigators needed to safely operate this high-containment laboratory,” the inspectors wrote in a cable of January 19, 2018.

The real problem, however, was not the unsafe state of the Wuhan BSL4 lab but the fact that virologists worldwide don’t like working in BSL4 conditions. You have to wear a space suit, do operations in closed cabinets, and accept that everything will take twice as long. So the rules assigning each kind of virus to a given safety level were laxer than some might think was prudent.

Before 2020, the rules followed by virologists in China and elsewhere required that experiments with the SARS1 and MERS viruses be conducted in BSL3 conditions. But all other bat coronaviruses could be studied in BSL2, the next level down. BSL2 requires taking fairly minimal safety precautions, such as wearing lab coats and gloves, not sucking up liquids in a pipette, and putting up biohazard warning signs. Yet a gain-of-function experiment conducted in BSL2 might produce an agent more infectious than either SARS1 or MERS. And if it did, then lab workers would stand a high chance of infection, especially if unvaccinated.

Much of Shi’s work on gain-of-function in coronaviruses was performed at the BSL2 safety level, as is stated in her publications and other documents. She has said in an interview with Science magazine that “[t]he coronavirus research in our laboratory is conducted in BSL-2 or BSL-3 laboratories.”

“It is clear that some or all of this work was being performed using a biosafety standard — biosafety level 2, the biosafety level of a standard US dentist’s office — that would pose an unacceptably high risk of infection of laboratory staff upon contact with a virus having the transmission properties of SARS-CoV-2,” Ebright says.

“It also is clear,” he adds, “that this work never should have been funded and never should have been performed.”

This is a view he holds regardless of whether or not the SARS2 virus ever saw the inside of a lab.

Concern about safety conditions at the Wuhan lab was not, it seems, misplaced. According to a fact sheet issued by the State Department on January 15, 2021, “The U.S. government has reason to believe that several researchers inside the WIV became sick in autumn 2019, before the first identified case of the outbreak, with symptoms consistent with both COVID-19 and common seasonal illnesses.”

David Asher, a fellow of the Hudson Institute and former consultant to the State Department, provided more detail about the incident at a seminar. Knowledge of the incident came from a mix of public information and “some high end information collected by our intelligence community,” he said. Three people working at a BSL3 lab at the institute fell sick within a week of each other with severe symptoms that required hospitalization. This was “the first known cluster that we’re aware of, of victims of what we believe to be COVID-19.” Influenza could not completely be ruled out but seemed unlikely in the circumstances, he said.

Comparing the rival scenarios of SARS2 origin. The evidence above adds up to a serious case that the SARS2 virus could have been created in a lab, from which it then escaped. But the case, however substantial, falls short of proof. Proof would consist of evidence from the Wuhan Institute of Virology, or related labs in Wuhan, that SARS2 or a predecessor virus was under development there. For lack of access to such records, another approach is to take certain salient facts about the SARS2 virus and ask how well each is explained by the two rival scenarios of origin, those of natural emergence and lab escape. Here are four tests of the two hypotheses. A couple have some technical detail, but these are among the most persuasive for those who may care to follow the argument.

1) The place of origin. Start with geography. The two closest known relatives of the SARS2 virus were collected from bats living in caves in Yunnan, a province of southern China. If the SARS2 virus had first infected people living around the Yunnan caves, that would strongly support the idea that the virus had spilled over to people naturally. But this isn’t what happened. The pandemic broke out 1,500 kilometers away, in Wuhan.

Beta-coronaviruses, the family of bat viruses to which SARS2 belongs, infect the horseshoe bat Rhinolophus affinis, which ranges across southern China. The bats’ range is 50 kilometers, so it’s unlikely that any made it to Wuhan. In any case, the first cases of the COVID-19 pandemic probably occurred in September, when temperatures in Hubei province are already cold enough to send bats into hibernation.

What if the bat viruses infected some intermediate host first? You would need a longstanding population of bats in frequent proximity with an intermediate host, which in turn must often cross paths with people. All these exchanges of virus must take place somewhere outside Wuhan, a busy metropolis which so far as is known is not a natural habitat of Rhinolophus bat colonies. The infected person (or animal) carrying this highly transmissible virus must have traveled to Wuhan without infecting anyone else. No one in his or her family got sick. If the person jumped on a train to Wuhan, no fellow passengers fell ill.

It’s a stretch, in other words, to get the pandemic to break out naturally outside Wuhan and then, without leaving any trace, to make its first appearance there.

For the lab escape scenario, a Wuhan origin for the virus is a no-brainer. Wuhan is home to China’s leading center of coronavirus research where, as noted above, researchers were genetically engineering bat coronaviruses to attack human cells. They were doing so under the minimal safety conditions of a BSL2 lab. If a virus with the unexpected infectiousness of SARS2 had been generated there, its escape would be no surprise.

2) Natural history and evolution. The initial location of the pandemic is a small part of a larger problem, that of its natural history. Viruses don’t just make one time jumps from one species to another. The coronavirus spike protein, adapted to attack bat cells, needs repeated jumps to another species, most of which fail, before it gains a lucky mutation. Mutation — a change in one of its RNA units — causes a different amino acid unit to be incorporated into its spike protein and makes the spike protein better able to attack the cells of some other species.

Through several more such mutation-driven adjustments, the virus adapts to its new host, say some animal with which bats are in frequent contact. The whole process then resumes as the virus moves from this intermediate host to people.

In the case of SARS1, researchers have documented the successive changes in its spike protein as the virus evolved step by step into a dangerous pathogen. After it had gotten from bats into civets, there were six further changes in its spike protein before it became a mild pathogen in people. After a further 14 changes, the virus was much better adapted to humans, and with a further four, the epidemic took off.

But when you look for the fingerprints of a similar transition in SARS2, a strange surprise awaits. The virus has changed hardly at all, at least until recently. From its very first appearance, it was well adapted to human cells. Researchers led by Alina Chan of the Broad Institute compared SARS2 with late stage SARS1, which by then was well adapted to human cells, and found that the two viruses were similarly well adapted. “By the time SARS-CoV-2 was first detected in late 2019, it was already pre-adapted to human transmission to an extent similar to late epidemic SARS-CoV,” they wrote.

Even those who think lab origin unlikely agree that SARS2 genomes are remarkably uniform. Baric writes that “early strains identified in Wuhan, China, showed limited genetic diversity, which suggests that the virus may have been introduced from a single source.”

A single source would of course be compatible with lab escape, less so with the massive variation and selection which is evolution’s hallmark way of doing business.

The uniform structure of SARS2 genomes gives no hint of any passage through an intermediate animal host, and no such host has been identified in nature.

Proponents of natural emergence suggest that SARS2 incubated in a yet-to-be found human population before gaining its special properties. Or that it jumped to a host animal outside China.

All these conjectures are possible, but strained. Proponents of a lab leak have a simpler explanation. SARS2 was adapted to human cells from the start because it was grown in humanized mice or in lab cultures of human cells, just as described in Daszak’s grant proposal. Its genome shows little diversity because the hallmark of lab cultures is uniformity.

Proponents of laboratory escape joke that of course the SARS2 virus infected an intermediary host species before spreading to people, and that they have identified it — a humanized mouse from the Wuhan Institute of Virology.

3) The furin cleavage site. The furin cleavage site is a minute part of the virus’s anatomy but one that exerts great influence on its infectivity. It sits in the middle of the SARS2 spike protein. It also lies at the heart of the puzzle of where the virus came from.

The spike protein has two sub-units with different roles. The first, called S1, recognizes the virus’s target, a protein called angiotensin converting enzyme-2 (or ACE2) which studs the surface of cells lining the human airways. The second, S2, helps the virus, once anchored to the cell, to fuse with the cell’s membrane. After the virus’s outer membrane has coalesced with that of the stricken cell, the viral genome is injected into the cell, hijacks its protein-making machinery and forces it to generate new viruses.

But this invasion cannot begin until the S1 and S2 subunits have been cut apart. And there, right at the S1/S2 junction, is the furin cleavage site that ensures the spike protein will be cleaved in exactly the right place.

The virus, a model of economic design, does not carry its own cleaver. It relies on the cell to do the cleaving for it. Human cells have a protein cutting tool on their surface known as furin. Furin will cut any protein chain that carries its signature target cutting site. This is the sequence of amino acid units proline-arginine-arginine-alanine, or PRRA in the code that refers to each amino acid by a letter of the alphabet. PRRA is the amino acid sequence at the core of SARS2’s furin cleavage site.

Viruses have all kinds of clever tricks, so why does the furin cleavage site stand out? Because of all known SARS-related beta-coronaviruses, only SARS2 possesses a furin cleavage site. All the other viruses have their S2 unit cleaved at a different site and by a different mechanism.

How then did SARS2 acquire its furin cleavage site? Either the site evolved naturally, or it was inserted by researchers at the S1/S2 junction in a gain-of-function experiment.

Consider natural origin first. Two ways viruses evolve are by mutation and by recombination. Mutation is the process of random change in DNA (or RNA for coronaviruses) that usually results in one amino acid in a protein chain being switched for another. Many of these changes harm the virus but natural selection retains the few that do something useful. Mutation is the process by which the SARS1 spike protein gradually switched its preferred target cells from those of bats to civets, and then to humans.

Mutation seems a less likely way for SARS2’s furin cleavage site to be generated, even though it can’t completely be ruled out. The site’s four amino acid units are all together, and all at just the right place in the S1/S2 junction. Mutation is a random process triggered by copying errors (when new viral genomes are being generated) or by chemical decay of genomic units. So it typically affects single amino acids at different spots in a protein chain. A string of amino acids like that of the furin cleavage site is much more likely to be acquired all together through a quite different process known as recombination.

Recombination is an inadvertent swapping of genomic material that occurs when two viruses happen to invade the same cell, and their progeny are assembled with bits and pieces of RNA belonging to the other. Beta-coronaviruses will only combine with other beta-coronaviruses but can acquire, by recombination, almost any genetic element present in the collective genomic pool. What they cannot acquire is an element the pool does not possess. And no known SARS-related beta-coronavirus, the class to which SARS2 belongs, possesses a furin cleavage site.

Proponents of natural emergence say SARS2 could have picked up the site from some as yet unknown beta-coronavirus. But bat SARS-related beta-coronaviruses evidently don’t need a furin cleavage site to infect bat cells, so there’s no great likelihood that any in fact possesses one, and indeed none has been found so far.

The proponents’ next argument is that SARS2 acquired its furin cleavage site from people. A predecessor of SARS2 could have been circulating in the human population for months or years until at some point it acquired a furin cleavage site from human cells. It would then have been ready to break out as a pandemic.

If this is what happened, there should be traces in hospital surveillance records of the people infected by the slowly evolving virus. But none has so far come to light. According to the WHO report on the origins of the virus, the sentinel hospitals in Hubei province, home of Wuhan, routinely monitor influenza-like illnesses and “no evidence to suggest substantial SARSCoV-2 transmission in the months preceding the outbreak in December was observed.”

So it’s hard to explain how the SARS2 virus picked up its furin cleavage site naturally, whether by mutation or recombination.

That leaves a gain-of-function experiment. For those who think SARS2 may have escaped from a lab, explaining the furin cleavage site is no problem at all. “Since 1992 the virology community has known that the one sure way to make a virus deadlier is to give it a furin cleavage site at the S1/S2 junction in the laboratory,” writes Steven Quay, a biotech entrepreneur interested in the origins of SARS2. “At least 11 gain-of-function experiments, adding a furin site to make a virus more infective, are published in the open literature, including [by] Dr. Zhengli Shi, head of coronavirus research at the Wuhan Institute of Virology.”

4) A question of codons. There’s another aspect of the furin cleavage site that narrows the path for a natural emergence origin even further.

As everyone knows (or may at least recall from high school), the genetic code uses three units of DNA to specify each amino acid unit of a protein chain. When read in groups of 3, the 4 different kinds of DNA unit can specify 4 x 4 x 4 or 64 different triplets, or codons as they are called. Since there are only 20 kinds of amino acid, there are more than enough codons to go around, allowing some amino acids to be specified by more than one codon. The amino acid arginine, for instance, can be designated by any of the six codons CGU, CGC, CGA, CGG, AGA or AGG, where A, U, G and C stand for the four different kinds of unit in RNA.

Here’s where it gets interesting. Different organisms have different codon preferences. Human cells like to designate arginine with the codons CGT, CGC or CGG. But CGG is coronavirus’s least popular codon for arginine. Keep that in mind when looking at how the amino acids in the furin cleavage site are encoded in the SARS2 genome.

Now the functional reason why SARS2 has a furin cleavage site, and its cousin viruses don’t, can be seen by lining up (in a computer) the string of nearly 30,000 nucleotides in its genome with those of its cousin coronaviruses, of which the closest so far known is one called RaTG13. Compared with RaTG13, SARS2 has a 12-nucleotide insert right at the S1/S2 junction. The insert is the sequence T-CCT-CGG-CGG-GC. The CCT codes for proline, the two CGG’s for two arginines, and the GC is the beginning of a GCA codon that codes for alanine.

There are several curious features about this insert but the oddest is that of the two side-by-side CGG codons. Only 5 percent of SARS2’s arginine codons are CGG, and the double codon CGG-CGG has not been found in any other beta-coronavirus. So how did SARS2 acquire a pair of arginine codons that are favored by human cells but not by coronaviruses?

Proponents of natural emergence have an up-hill task to explain all the features of SARS2’s furin cleavage site. They have to postulate a recombination event at a site on the virus’s genome where recombinations are rare, and the insertion of a 12-nucleotide sequence with a double arginine codon unknown in the beta-coronavirus repertoire, at the only site in the genome that would significantly expand the virus’s infectivity.

“Yes, but your wording makes this sound unlikely — viruses are specialists at unusual events,” is the riposte of David L. Robertson, a virologist at the University of Glasgow who regards lab escape as a conspiracy theory. “Recombination is naturally very, very frequent in these viruses, there are recombination breakpoints in the spike protein and these codons appear unusual exactly because we’ve not sampled enough.”

Robertson is correct that evolution is always producing results that may seem unlikely but in fact are not. Viruses can generate untold numbers of variants but we see only the one-in-a-billion that natural selection picks for survival. But this argument could be pushed too far. For instance, any result of a gain-of-function experiment could be explained as one that evolution would have arrived at in time. And the numbers game can be played the other way. For the furin cleavage site to arise naturally in SARS2, a chain of events has to happen, each of which is quite unlikely for the reasons given above. A long chain with several improbable steps is unlikely to ever be completed.

For the lab escape scenario, the double CGG codon is no surprise. The human-preferred codon is routinely used in labs. So anyone who wanted to insert a furin cleavage site into the virus’s genome would synthesize the PRRA-making sequence in the lab and would be likely to use CGG codons to do so.

“When I first saw the furin cleavage site in the viral sequence, with its arginine codons, I said to my wife it was the smoking gun for the origin of the virus,” said David Baltimore, an eminent virologist and former president of CalTech. “These features make a powerful challenge to the idea of a natural origin for SARS2,” he said. [1]

A third scenario of origin. There’s a variation on the natural emergence scenario that’s worth considering. This is the idea that SARS2 jumped directly from bats to humans, without going through an intermediate host as SARS1 and MERS did. A leading advocate is the virologist David Robertson who notes that SARS2 can attack several other species besides humans. He believes the virus evolved a generalist capability while still in bats. Because the bats it infects are widely distributed in southern and central China, the virus had ample opportunity to jump to people, even though it seems to have done so on only one known occasion. Robertson’s thesis explains why no one has so far found a trace of SARS2 in any intermediate host or in human populations surveilled before December 2019. It would also explain the puzzling fact that SARS2 has not changed since it first appeared in humans — it didn’t need to because it could already attack human cells efficiently.

One problem with this idea, though, is that if SARS2 jumped from bats to people in a single leap and hasn’t changed much since, it should still be good at infecting bats. And it seems it isn’t.

“Tested bat species are poorly infected by SARS-CoV-2 and they are therefore unlikely to be the direct source for human infection,” write a scientific group skeptical of natural emergence.

Still, Robertson may be onto something. The bat coronaviruses of the Yunnan caves can infect people directly. In April 2012 six miners clearing bat guano from the Mojiang mine contracted severe pneumonia with COVID-19-like symptoms and three eventually died. A virus isolated from the Mojiang mine, called RaTG13, is still the closest known relative of SARS2. Much mystery surrounds the origin, reporting and strangely low affinity of RaTG13 for bat cells, as well as the nature of 8 similar viruses that Shi reports she collected at the same time but has not yet published despite their great relevance to the ancestry of SARS2. But all that is a story for another time. The point here is that bat viruses can infect people directly, though only in special conditions.

So who else, besides miners excavating bat guano, comes into particularly close contact with bat coronaviruses? Well, coronavirus researchers do. Shi says she and her group collected more than 1,300 bat samples during some eight visits to the Mojiang cave between 2012 and 2015, and there were doubtless many expeditions to other Yunnan caves.

Imagine the researchers making frequent trips from Wuhan to Yunnan and back, stirring up bat guano in dark caves and mines, and now you begin to see a possible missing link between the two places. Researchers could have gotten infected during their collecting trips, or while working with the new viruses at the Wuhan Institute of Virology. The virus that escaped from the lab would have been a natural virus, not one cooked up by gain of function.

The direct-from-bats thesis is a chimera between the natural emergence and lab escape scenarios. It’s a possibility that can’t be dismissed. But against it are the facts that 1) both SARS2 and RaTG13 seem to have only feeble affinity for bat cells, so one can’t be fully confident that either ever saw the inside of a bat; and 2) the theory is no better than the natural emergence scenario at explaining how SARS2 gained its furin cleavage site, or why the furin cleavage site is determined by human-preferred arginine codons instead of by the bat-preferred codons.

Where we are so far. Neither the natural emergence nor the lab escape hypothesis can yet be ruled out. There is still no direct evidence for either. So no definitive conclusion can be reached.

That said, the available evidence leans more strongly in one direction than the other. Readers will form their own opinion. But it seems to me that proponents of lab escape can explain all the available facts about SARS2 considerably more easily than can those who favor natural emergence.

It’s documented that researchers at the Wuhan Institute of Virology were doing gain-of-function experiments designed to make coronaviruses infect human cells and humanized mice. This is exactly the kind of experiment from which a SARS2-like virus could have emerged. The researchers were not vaccinated against the viruses under study, and they were working in the minimal safety conditions of a BSL2 laboratory. So escape of a virus would not be at all surprising. In all of China, the pandemic broke out on the doorstep of the Wuhan institute. The virus was already well adapted to humans, as expected for a virus grown in humanized mice. It possessed an unusual enhancement, a furin cleavage site, which is not possessed by any other known SARS-related beta-coronavirus, and this site included a double arginine codon also unknown among beta-coronaviruses. What more evidence could you want, aside from the presently unobtainable lab records documenting SARS2’s creation?

Proponents of natural emergence have a rather harder story to tell. The plausibility of their case rests on a single surmise, the expected parallel between the emergence of SARS2 and that of SARS1 and MERS. But none of the evidence expected in support of such a parallel history has yet emerged. No one has found the bat population that was the source of SARS2, if indeed it ever infected bats. No intermediate host has presented itself, despite an intensive search by Chinese authorities that included the testing of 80,000 animals. There is no evidence of the virus making multiple independent jumps from its intermediate host to people, as both the SARS1 and MERS viruses did. There is no evidence from hospital surveillance records of the epidemic gathering strength in the population as the virus evolved. There is no explanation of why a natural epidemic should break out in Wuhan and nowhere else. There is no good explanation of how the virus acquired its furin cleavage site, which no other SARS-related beta-coronavirus possesses, nor why the site is composed of human-preferred codons. The natural emergence theory battles a bristling array of implausibilities.

The records of the Wuhan Institute of Virology certainly hold much relevant information. But Chinese authorities seem unlikely to release them given the substantial chance that they incriminate the regime in the creation of the pandemic. Absent the efforts of some courageous Chinese whistle-blower, we may already have at hand just about all of the relevant information we are likely to get for a while.

So it’s worth trying to assess responsibility for the pandemic, at least in a provisional way, because the paramount goal remains to prevent another one. Even those who aren’t persuaded that lab escape is the more likely origin of the SARS2 virus may see reason for concern about the present state of regulation governing gain-of-function research. There are two obvious levels of responsibility: the first, for allowing virologists to perform gain-of-function experiments, offering minimal gain and vast risk; the second, if indeed SARS2 was generated in a lab, for allowing the virus to escape and unleash a world-wide pandemic. Here are the players who seem most likely to deserve blame.

  1. Chinese virologists. First and foremost, Chinese virologists are to blame for performing gain-of-function experiments in mostly BSL2-level safety conditions which were far too lax to contain a virus of unexpected infectiousness like SARS2. If the virus did indeed escape from their lab, they deserve the world’s censure for a foreseeable accident that has already caused the deaths of three  million people. True, Shi was trained by French virologists, worked closely with American virologists and was following international rules for the containment of coronaviruses. But she could and should have made her own assessment of the risks she was running. She and her colleagues bear the responsibility for their actions.

I have been using the Wuhan Institute of Virology as a shorthand for all virological activities in Wuhan. It’s possible that SARS2 was generated in some other Wuhan lab, perhaps in an attempt to make a vaccine that worked against all coronaviruses. But until the role of other Chinese virologists is clarified, Shi is the public face of Chinese work on coronaviruses, and provisionally she and her colleagues will stand first in line for opprobrium.

2. Chinese authorities. China’s central authorities did not generate SARS2, but they sure did their utmost to conceal the nature of the tragedy and China’s responsibility for it. They suppressed all records at the Wuhan Institute of Virology and closed down its virus databases. They released a trickle of information, much of which may have been outright false or designed to misdirect and mislead. They did their best to manipulate the WHO’s inquiry into the virus’s origins, and led the commission’s members on a fruitless run-around. So far they have proved far more interested in deflecting blame than in taking the steps necessary to prevent a second pandemic.

3. The worldwide community of virologists. Virologists around the world are a loose-knit professional community. They write articles in the same journals. They attend the same conferences. They have common interests in seeking funds from governments and in not being overburdened with safety regulations.

Virologists knew better than anyone the dangers of gain-of-function research. But the power to create new viruses, and the research funding obtainable by doing so, was too tempting. They pushed ahead with gain-of-function experiments. They lobbied against the moratorium imposed on Federal funding for gain-of-function research in 2014, and it was raised in 2017.

The benefits of the research in preventing future epidemics have so far been nil, the risks vast. If research on the SARS1 and MERS viruses could only be done at the BSL3 safety level, it was surely illogical to allow any work with novel coronaviruses at the lesser level of BSL2. Whether or not SARS2 escaped from a lab, virologists around the world have been playing with fire.

Their behavior has long alarmed other biologists. In 2014 scientists calling themselves the Cambridge Working Group urged caution on creating new viruses. In prescient words, they specified the risk of creating a SARS2-like virus. “Accident risks with newly created ‘potential pandemic pathogens’ raise grave new concerns,” they wrote. “Laboratory creation of highly transmissible, novel strains of dangerous viruses, especially but not limited to influenza, poses substantially increased risks. An accidental infection in such a setting could trigger outbreaks that would be difficult or impossible to control.”

When molecular biologists discovered a technique for moving genes from one organism to another, they held a public conference at Asilomar in 1975 to discuss the possible risks. Despite much internal opposition, they drew up a list of stringent safety measures that could be relaxed in future — and duly were — when the possible hazards had been better assessed.

When the CRISPR technique for editing genes was invented, biologists convened a joint report by the US, UK and Chinese national academies of science to urge restraint on making heritable changes to the human genome. Biologists who invented gene drives have also been open about the dangers of their work and have sought to involve the public.

You might think the SARS2 pandemic would spur virologists to re-evaluate the benefits of gain-of-function research, even to engage the public in their deliberations. But no. Many virologists deride lab escape as a conspiracy theory, and others say nothing. They have barricaded themselves behind a Chinese wall of silence which so far is working well to allay, or at least postpone, journalists’ curiosity and the public’s wrath. Professions that cannot regulate themselves deserve to get regulated by others, and this would seem to be the future that virologists are choosing for themselves.

4. The US role in funding the Wuhan Institute of Virology. From June 2014 to May 2019, Daszak’s EcoHealth Alliance had a grant from the National Institute of Allergy and Infectious Diseases (NIAID), part of the National Institutes of Health, to do gain-of-function research with coronaviruses at the Wuhan Institute of Virology. Whether or not SARS2 is the product of that research, it seems a questionable policy to farm out high-risk research to unsafe foreign labs using minimal safety precautions. And if the SARS2 virus did indeed escape from the Wuhan institute, then the NIH will find itself in the terrible position of having funded a disastrous experiment that led to death of more than 3 million worldwide, including more than half a million of its own citizens.

The responsibility of the NIAID and NIH is even more acute because for the first three years of the grant to EcoHealth Alliance, there was a moratorium on funding gain-of-function research. Why didn’t the two agencies therefore halt the federal funding, as apparently required to do so by law? Because someone wrote a loophole into the moratorium.

The moratorium specifically barred funding any gain-of-function research that increased the pathogenicity of the flu, MERS, or SARS viruses. But then a footnote on page 2 of the moratorium document states that “[a]n exception from the research pause may be obtained if the head of the USG funding agency determines that the research is urgently necessary to protect the public health or national security.”

This seems to mean that either the director of the NIAID, Anthony Fauci, or the director of the NIH, Francis Collins, or maybe both, would have invoked the footnote in order to keep the money flowing to Shi’s gain-of-function research.

“Unfortunately, the NIAID director and the NIH director exploited this loophole to issue exemptions to projects subject to the Pause—preposterously asserting the exempted research was ‘urgently necessary to protect public health or national security’ — thereby nullifying the Pause,” Ebright said in an interview with Independent Science News.

When the moratorium was ended in 2017, it didn’t just vanish but was replaced by a reporting system, the Potential Pandemic Pathogens Control and Oversight (P3CO) Framework, which required agencies to report for review any dangerous gain-of-function work they wished to fund.

According to Ebright, both Collins and Fauci “have declined to flag and forward proposals for risk-benefit review, thereby nullifying the P3CO Framework.”

In his view, the two officials, in dealing with the moratorium and the ensuing reporting system, “have systematically thwarted efforts by the White House, the Congress, scientists, and science policy specialists to regulate GoF [gain-of-function] research of concern.”

Possibly the two officials had to take into account matters not evident in the public record, such as issues of national security. Perhaps funding the Wuhan Institute of Virology, which is believed to have ties with Chinese military virologists, provided a window into Chinese biowarfare research. But whatever other considerations may have been involved, the bottom line is that the National Institutes of Health was supporting gain-of-function research, of a kind that could have generated the SARS2 virus, in an unsupervised foreign lab that was doing work in BSL2 biosafety conditions. The prudence of this decision can be questioned, whether or not SARS2 and the death of 3 million people were the result of it, which emphasizes the need for some better system of control.

In conclusion. If the case that SARS2 originated in a lab is so substantial, why isn’t this more widely known? As may now be obvious, there are many people who have reason not to talk about it. The list is led, of course, by the Chinese authorities. But virologists in the United States and Europe have no great interest in igniting a public debate about the gain-of-function experiments that their community has been pursuing for years.

Nor have other scientists stepped forward to raise the issue. Government research funds are distributed on the advice of committees of scientific experts drawn from universities. Anyone who rocks the boat by raising awkward political issues runs the risk that their grant will not be renewed and their research career will be ended. Maybe good behavior is rewarded with the many perks that slosh around the distribution system. And if you thought that Andersen and Daszak might have blotted their reputation for scientific objectivity after their partisan attacks on the lab escape scenario, look at the second and third names on this list of recipients of an $82 million grant announced by the National Institute of Allergy and Infectious Diseases in August 2020.

The US government shares a strange common interest with the Chinese authorities: Neither is keen on drawing attention to the fact that Shi’s coronavirus work was funded by the US National Institutes of Health. One can imagine the behind-the-scenes conversation in which the Chinese government says, “If this research was so dangerous, why did you fund it, and on our territory too?” To which the US side might reply, “Looks like it was you who let it escape. But do we really need to have this discussion in public?”

Fauci is a longtime public servant who served with integrity under President Trump and has resumed leadership in the Biden Administration in handling the COVID-19 epidemic. Congress, no doubt understandably, may have little appetite for hauling him over the coals for the apparent lapse of judgment in funding gain-of-function research in Wuhan.

To these serried walls of silence must be added that of the mainstream media. To my knowledge, no major newspaper or television network has yet provided readers with an in-depth news story of the lab escape scenario, such as the one you have just read, although some have run brief editorials or opinion pieces. One might think that any plausible origin of a virus that has killed three million people would merit a serious investigation. Or that the wisdom of continuing gain-of-function research, regardless of the virus’s origin, would be worth some probing. Or that the funding of gain-of-function research by the NIH and NIAID during a moratorium on such funding would bear investigation. What accounts for the media’s apparent lack of curiosity?

The virologists’ omertà is one reason. Science reporters, unlike political reporters, have little innate skepticism of their sources’ motives; most see their role largely as purveying the wisdom of scientists to the unwashed masses. So when their sources won’t help, these journalists are at a loss.

Another reason, perhaps, is the migration of much of the media toward the left of the political spectrum. Because President Trump said the virus had escaped from a Wuhan lab, editors gave the idea little credence. They joined the virologists in regarding lab escape as a dismissible conspiracy theory. During the Trump administration, they had no trouble in rejecting the position of the intelligence services that lab escape could not be ruled out. But when Avril Haines, President Biden’s director of national intelligence, said the same thing, she too was largely ignored. This is not to argue that editors should have endorsed the lab escape scenario, merely that they should have explored the possibility fully and fairly.

People round the world who have been pretty much confined to their homes for the last year might like a better answer than their media are giving them. Perhaps one will emerge in time. After all, the more months pass without the natural emergence theory gaining a shred of supporting evidence, the less plausible it may seem. Perhaps the international community of virologists will come to be seen as a false and self-interested guide. The common sense perception that a pandemic breaking out in Wuhan might have something to do with a Wuhan lab cooking up novel viruses of maximal danger in unsafe conditions could eventually displace the ideological insistence that whatever Trump said can’t be true.

And then let the reckoning begin.


[1] This quotation was added to the article after initial publication.


The first person to take a serious look at the origins of the SARS2 virus was Yuri Deigin, a biotech entrepreneur in Russia and Canada. In a long and brilliant essay, he dissected the molecular biology of the SARS2 virus and raised, without endorsing, the possibility that it had been manipulated. The essay, published on April 22, 2020, provided a roadmap for anyone seeking to understand the virus’s origins. Deigin packed so much information and analysis into his essay that some have doubted it could be the work of a single individual and suggested some intelligence agency must have authored it. But the essay is written with greater lightness and humor than I suspect are ever found in CIA or KGB reports, and I see no reason to doubt that Deigin is its very capable sole author.

In Deigin’s wake have followed several other skeptics of the virologists’ orthodoxy. Nikolai Petrovsky calculated how tightly the SARS2 virus binds to the ACE2 receptors of various species and found to his surprise that it seemed optimized for the human receptor, leading him to infer the virus might have been generated in a laboratory. Alina Chan published a paper showing that SARS2 from its first appearance was very well adapted to human cells.

One of the very few establishment scientists to have questioned the virologists’ absolute rejection of lab escape is Richard Ebright, who has long warned against the dangers of gain-of-function research. Another is David A. Relman of Stanford University. “Even though strong opinions abound, none of these scenarios can be confidently ruled in or ruled out with currently available facts,” he wrote. Kudos too to Robert Redfield, former director of the Centers for Disease Control and Prevention, who told CNN on March 26, 2021 that the “most likely” cause of the epidemic was “from a laboratory,” because he doubted that a bat virus could become an extreme human pathogen overnight, without taking time to evolve, as seemed to be the case with SARS2.

Steven Quay, a physician-researcher, has applied statistical and bioinformatic tools to ingenious explorations of the virus’s origin, showing for instance how the hospitals receiving the early patients are clustered along the Wuhan №2 subway line which connects the Institute of Virology at one end with the international airport at the other, the perfect conveyor belt for distributing the virus from lab to globe.

In June 2020 Milton Leitenberg published an early survey of the evidence favoring lab escape from gain-of-function research at the Wuhan Institute of Virology.

Many others have contributed significant pieces of the puzzle. “Truth is the daughter,” said Francis Bacon, “not of authority but time.” The efforts of people such as those named above are what makes it so.



Depopulation by Forced Vaccination—Article from 2011


Mandatory Vaccination Programs Violate the Nuremberg Code

Objective: Health – The Nuremberg Code and Mandatory Vaccinations

O:H headerBy SOTT.net

At the end of World War II, after witnessing the atrocities of the Nazi concentration camps and forced human experimentation, some pre-eminent doctors of the time were brought together to come up with a code of ethics in human medical experimentation, to make sure nothing like this ever happens again. Informed consent, the core of the Nuremberg Code, has rightly been viewed as the protection of subjects’ human rights, and while it was never written into law, it came to influence the creation of the Universal Declaration on Bioethics and Human Rights by the United Nations.

With the looming threat of mandatory vaccinations on the horizon, these documents become all the more vital and important for every citizen to be aware of their rights and what one can do in the face of medical tyrrany. On this episode of Objective:Health, we discuss the Nuremberg Code, the Universal Declaration on Bioethics and Human Rights and how these documents are more pertinent now than ever before.

YouTube sucks, so check us out on Brighteon and lbry.tv!

For other health-related news and more, you can find us on:

♥Twitter: https://twitter.com/objecthealth
♥Facebook: https://www.facebook.com/objecthealth/
♥Brighteon: https://www.brighteon.com/channel/objectivehealth

♥And you can check out all of our previous shows (pre YouTube) here.

Running Time: 00:34:30

Download: MP3 — 31.6 MB



Cyborg-like Singer Poppy with creepy predictions since 2016

Poppy predicting COVID-19

•Jul 26, 2020


please breathe

Typical_ Nick!

Typical_ Nick!

you forgot to include the one from 2019, where she said: “The scary mask is coming.”

Estelle Pretorius

Estelle Pretorius

When she asks what rhymes with breath - I think she means death

Janthran Quentai

Janthran Quentai

she also released an album at the start of 2020 with songs like "don't go outside" and "scary mask" on it

Poki Pineapple

Poki Pineapple

Hmm... it feels like she was preparing us, year by year.. Breath rhymes with death, a lot of masks.. Though the first mask clip WAS posted in 2017, when the wild fires were the absolute worst, so.. CREEPY!


Not less creepy - the BUSINESSINSIDER


Deadly plague could potentially be released as a cloud above a city, killing thousands, according to bioterrorism experts

The CDC categorizes plague as one of the biological weapons agents of highest concern — along with anthrax, smallpox, and viral fevers like Ebola.

Plague is one of the oldest bioweapons out there.

When two cases of plague popped up in New Mexico in June , they served as a reminder that the black death — yes, the plague — is still around.

The infection affects a handful of people in the US every year and between a few hundred and a few thousand annually around the world. Most people survive a plague infection these days, since it can almost always be treated with antibiotics.

But researchers, bioweapons experts, and governments still worry that the plague could be turned into a deadly bioweapon, especially if someone with terroristic intent were to find or engineer a strain that couldn't be treated with common drugs.

The plague bacteria, Yersinia pestis, mutates regularly like any other organism. Drug-resistant strains have emerged several times in the wild. For that reason, as Stat News' Eric Boodman explains in a profile of wildlife biologist and plague detective David Wagner, there's always a scramble to identify plague strains when they emerge.

By analyzing the bacteria, researchers can see if the bacteria has picked up antibiotic-resistant genes and check whether the strain is wild or engineered.

Today, the CDC categorizes plague as one of the biological weapons agents of highest concern along with anthrax, smallpox, and viral fevers like Ebola and Marburg.

The scariest scenarios would involve an aerosolized version of the plague released like a cloud above a city or in a crowded area. The bacteria could be dumped from an airplane or even blown by a big fan, which would spark an outbreak of the pneumonic form of the illness — one that spreads rapidly through the air.

In 1970, World Health Organization researchers estimated that releasing a 50 kg aerosol cloud of plague bacteria over a city of 5 million could cause 150,00o plague cases, with between 80 and 100,000 hospitalizations and 36,000 deaths. That's assuming that antibiotics worked, which is the case for all known wild strains circulating today.

Generally, bites from fleas carrying Y. pestis spread bubonic or septicemic forms of the plague, both of which cause fever and weakness. Bubonic plague results in painfully swollen lymph nodes; septicemic plague happens when the infection gets in the blood and causes skin and tissue to turn black and die. It can appear on its own or develop from bubonic plague.

Untreated patients with either of these conditions can develop pneumonic plague, the most serious form of the disease, which happens when the infection gets into the lungs. (There are also rare Y. pestis strains that first infect the lungs, which causes a patient to leap straight to the most contagious form of the disease). When an infected person coughs, droplets of the bacteria enter the air and can survive there for an hour or so. People in close contact with the patient are therefore most likely to be infected by these droplets, and in a nightmare scenario those individuals could further spread .

As Boodman writes, plague is actually one of the oldest bioweapons out there:

"After all, the bacteria were being used as weapons long before anyone even knew to call them bacteria. Plague-infected corpses were catapulted over walls. Venetians plotted to distill deadly liquid from swollen lymph nodes. Japanese planes sprinkled a rainfall of infected fleas. If those with nefarious motives and technical expertise wanted to weaponize the bacteria today, they could."

As Johns Hopkins public health researchers note, both the US and Soviet Union developed ways to create the aerosolized version of the plague in the 1950s and 1960s.

The thought of any type of biological warfare between countries is scary, but journalist Wendy Orent describes an even more worrisome possibility in her history of the illness, "Plague: The Mysterious Past and Terrifying Future of the World's Most Dangerous Disease." According to the book, Dr. Ken Alibek, a Kazakh defector from a Soviet biological weapons project, has suggested that the program was able to produce plague weapons resistant to at least 10 common antibiotics. And that was before the modern advances in genetics that exist today.

There's currently no plague vaccine, according to the CDC, so we can only hope that such an untreatable strain is never seen.

If drug-resistant plague were released as a weapon, humans would risk reliving the terrifying history of the Middle Ages. As a Scottish account from then says, "[i]t generated such horror that children did not dare to visit their dying parents, nor parents their children, but fled for fear of contagion as if from leprosy or a serpent."


10 Scariest Biological Weapons

Aren’t all bio-weapons scary? Definitely. But these 10 are particularly troublesome once they’re released from labs and unleashed on an unsuspecting public.



Anthrax Spores was first tested as a biological warfare agent by Unit 731 of the Japanese Kwantung Army in Manchuria during the 1930s; some of this testing involved intentional infection of prisoners of war, thousands of whom died. Anthrax, designated at the time as Agent N, was also investigated by the Allies in the 1940s.



The British considered using smallpox as a biological warfare agent at the Siege of Fort Pitt during the French and Indian Wars (1754–63) against France and its Native American allies. Although it is not clear whether the actual use of smallpox had official sanction. It has also been alleged that smallpox was used as a weapon during the American Revolutionary War (1775–83).



North Korea is suspected of producing TB. The world’s second biggest infectious killer. Tuberculosis may infect any part of the body, but most commonly occurs in the lungs (known as pulmonary tuberculosis). Extrapulmonary TB occurs when tuberculosis develops outside of the lungs, although extrapulmonary TB may coexist with pulmonary TB as well.



Plague was used during the Second Sino-Japanese War as a bacteriological weapon by the Imperial Japanese Army. These weapons were provided by Shirō Ishii’s units and used in experiments on humans before being used on the field. For example, in 1940, the Imperial Japanese Army Air Service bombed Ningbo with fleas carrying the bubonic plague.



As a biological weapons agent, the Ebola virus is feared for its high case-fatality rate. Because of its rarity, the disease may not be diagnosed corrected at the onset of an outbreak. Reports suggested that the Ebola virus was researched and weaponized by the former Soviet Union’s biological weapons program Biopreparat. Dr. Ken Alibek, former the First Deputy Director of Biopreparat, speculated that the Russians had aerosolized the Ebola virus for dissemination as a biological weapon. The Japanese terrorist group Aum Shinrikyo reportedly sent members to Zaire during an outbreak to harvest the virus.

Image result for Bio Warfare Virus



During World War II, the Japanese biological weapons program known as Unit 731 located in Pingfan Manchuria (24 kilometers south of Harbin) experimented with Vibrio cholera as a weapons agent. It was reported that the Japanese dropped cholera and typhus cultures into more than 1,000 Chinese wells and reportedly caused 10,000 cases in 1941. However, an estimated 1,700 of the deaths were Japanese soldiers, a testimony to the difficulty of protecting one’s own troops from biological agents and controlling infections.



Botulinum toxin is one of the deadliest toxins known, and is produced by the bacterium Clostridium botulinum. Botulism causes death by respiratory failure and paralysis. Furthermore, the toxin is readily available worldwide due to its cosmetic applications in injections.



Being able to destroy an entire city in less than a second with the push of a button is one way to measure destructive power, but being able to selectively and slowly decimate a population with disease and infection is so unconventionally brutal that it has to top the list. That’s Chimera Viruses!



While advanced nuclear and bombs are scary and powerful, if you’re going for painful slow, mentally devastating destruction sometimes launching the diseased riddled bodies of prisoners that you’ve executed back over the city walls is the most sadistic way to go about decimating a population.



Tularemia doesn’t transfer between human hosts and can be easily treated with antibiotics or prevented with a vaccine. It does, however, spread very rapidly between animal hosts and humans or when used in aerosol form. It is this factor, not its mortality rate, that earned F. tularensis a Category A biological weapon ranking. It is especially virile in aerosol form. Due to these factors, the United States, Britain, Canada and the Soviet Union all worked to create weaponized tularemia after the close of World War II.