COVID-19
COVID-19, Hygiene Theatre, Masks, and Lockdowns “Solid Science” or Science Veneer?
From the Fraser Institute
By Kenneth P. Green
Nearly two and a half years since COVID-19 overturned much of the world, vigorous debate
still exists over whether or not governments “got COVID-19 right.” That is, despite more
than two years for analysis and retrospective studies, it is unclear if governments—any governments—implemented the best policies (or even 2nd best policies) as the COVID pandemic exploded in 2020, and as it unfolded through 2021 and 2022.
This situation is troubling, as the world will undoubtedly face similar, and perhaps more severe pandemic challenges again in the future. Society needs to know what worked and what did not work, not only with regard to vaccines, but with regard to the many other interventions government deployed to fight the COVID epidemic.
One key dispute regarding what went right or what went wrong with regard to COVID policies revolves around whether or not the public policies promulgated by governments and public health authorities were science- or evidence-based. Governments, regulatory bodies, and public health institutions around the world were not only unified, but strident in their proclamations that policies were “following the science.” Skeptics of such pronouncements were given little attention at the time, and were more often than not simply attacked as being peddlers of misinformation, or dis-information, and were squelched in public discourse. This did not, however, settle the dispute.
In fact, the battle lines over this question—whether governments were actually following the science or evidence available at the time, or were merely asserting that they were doing so—have only hardened since the pandemic struck in 2020. Even as this essay is being written, for example, a war is raging across Twitter (now “X”) between a prominent COVID vaccine researcher (Peter Hotez), and people who question whether his representation of his work is honest. The questioners seek a public debate, but the scientist involved (backed by many other prominent colleagues) have declared the very idea of societal debate to be anathema to the idea of science itself. The “Twitter war” over this dispute has drawn in one of the world’s richest men (Elon Musk), one of the world’s loudest populist broadcasters (Joe Rogan), and a host of high-level scientists and heads of scientific agencies (Mikhail, 2023).
This dynamic, of public accusations of obstruction, and demonizing of those making the accusations, bodes poorly for the prospects of improving future policy by learning from experience. It also bodes poorly for future confidence in governmental policy responses to threatening situations. It seems self-evident that the public will be less likely to follow governmental recommendations or guidance in future if the consensus develops that they cannot be trusted when they claim to be telling the truth, or following the evidence, or, as such truth-telling was cast in this case, “following the science.”
So what is the answer? Were governments following the science or the evidence extant at the time of COVID’s emergence and progression through the population, or were they following the science selectively, creating more of a veneer of science than a solid policy foundation of science?
Let’s examine this question by examining the two highly controversial, major non-pharmaceutical interventions, or NPIs, imposed during the COVID pandemic. NPIs implemented throughout the COVID-19 outbreak were policies intended to slow or limit the spread of the virus, and to reduce risk of infection via measures of physical separation including: enhanced hygiene, social distancing (keeping separate from others at a distance of 2 meters), erecting physical air/particle barricades, wearing gloves, donning masks, accepting voluntary and involuntary isolation, and a variety of restrictions on assemblage, including closures of parks, businesses, schools, and houses of worship, etc.
Gathering restrictions/closures (bars, businesses, churches, schools)
Several articles have looked into the question of “what the science said” about gathering restrictions imposed in response to COVID-19: closures of businesses, schools, public gatherings, etc., as that science already existed in 2020, and before.
The Cochrane Library, a respected clearinghouse of scientific and medical information,
published one such retrospective look at “the science” conducted in mid-2020, and entitled Quarantine Alone or in Combination with Other Public Health Measures to Control COVID-19: A Rapid Review (Nussbaumer-Streit, 2020; for simplicity, Nussbaumer).
Nussbaumer searched for studies related to quarantine efficacy on the PubMed, Ovid MEDLINE, WHO Global Index Medicus, Embase, and CINAHL databases on June 23, 2020, only about six months into the pandemic. Nussbaumer specifically searched for “Cohort studies, case-control studies, time series, interrupted time series, case series, and mathematical modelling studies that assessed the effect of any type of quarantine to control COVID-19.” The authors even included studies on SARS (Severe Acute Respiratory Syndrome) and MERS (Middle East Respiratory Syndrome) for indirect evidence that might apply to COVID-19. The net was cast widely. Nussbaumer identified 51 studies that met their criteria for inclusion in their analysis. Ten were modeling studies on COVID19; 15 were modelling studies of SARS and MERS; and the team found four observational studies
on SARS and MERS.
Nussbaumer found that while modeling studies were uniform in predicting that quarantine, in a variety of forms, would effectively reduce transmission of SARS, MERS, or COVID-19, the quality of evidence from these modeling studies was characterized as having low certainty or very low certainty, and the studies were, primarily, as the authors themselves noted, “modeling studies that make parameter assumptions based on the current, fragmented knowledge.”1
1 The four observational studies identified suggested quarantine was effective as a control strategy for SARS and MERS. However, Nussbaumer deemed them unlikely to be reflective of COVID-19 controls.
School closures
As discussed in a separate essay on the issue of school closures and educational performance (McPherson and Green, 2023), the question of whether school closures reduced either children’s risk directly, or society’s risk of COVID-contagion vie exposure to children, remains an important and particularly contentious area of debate. We are still trying to assess the damage done to children’s educational attainment in the nearly three years of intermittent school closures in Canada, and it will be some time before the extent of that damage is well understood. Longer term impacts on children’s mental health and social development will likely take many years to ascertain.
When COVID-19 struck in 2020, understanding how school closures related to the spread of a virus through school populations were based mostly on studies of Influenza pandemics that preceded COVID.
In another Cochrane Library review of studies on school closures published as of December 2020, the team of Krishnaratne et al. surveyed research on the issue of school closures published in “the Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE, Embase, and the Educational Resources Information Center, as well as COVID-19-specific databases, including the Cochrane COVID-19 Study Register and the WHO COVID-19 Global literature on coronavirus disease” (2022). They found 38 unique studies in their analysis, 33 of which were modeling studies, three of which were observational studies, one study that was described as “quasi-experimental,” and one “experimental study with modelling components.”
Krishnaratne et al. concluded that
- a broad range of measures implemented in the school setting can have positive impacts
on the transmission of SARS-CoV-2, and on healthcare utilisation outcomes related
to COVID-19. The certainty of the evidence for most intervention-outcome combinations is very low, and the true effects of these measures are likely to be substantially
different from those reported here. Measures implemented in the school setting may
limit the number or proportion of cases and deaths, and may delay the progression
of the pandemic. However, they may also lead to negative unintended consequences,
such as fewer days spent in school (beyond those intended by the intervention).
(Krishnaratne et al., 2022)
This aligns with by another review of the literature published in the British Medical Journal in 2023. In that paper, Hume et al. characterized the findings of 26 systemic reviews pertinent to the school-transmission question. They conclude, “We found evidence that both school closures and in-school mitigations may have had a beneficial impact on reducing COVID-19 transmission in the community. However, the GRADE [a measure of research quality] certainty was very low in both outcomes. We also found that school closures may have had negative impacts on children, including reduced learning, increased anxiety and increased rates of obesity. However, GRADE certainties were low or very low in these outcomes. Overall, confidence in the included SRs was generally low or critically low” (Hume, et al., 2023).
Other studies pre-dating COVID-19 also raised questions about the potential utility of school closures. One of the more interesting studies on the question from much farther back—a decade back, in fact—came out of University College London, by a research
team that included Neil M. Ferguson, the same researcher whose initial modeling of COVID-19 shaped the world’s response to the pandemic. That study concluded regarding school closures for Influenza, “Although some health benefits can be expected, there is
still substantial debate about if, when, and how school closure policy should be used. There is no consensus on the scale of the benefits to be expected, and recent reviews highlighted the lack of evidence for social distancing measures such as school closure. Even if benefits are substantial, they must be weighed against the potential high economic and social costs of proactively closing schools, which also can have negative effects on key workers since, for example, many doctors and nurses are also parents” (Cauchemez et al, 2009).
- “School closures may have had negative impacts on children, including reduced learning, increased anxiety and increased rates of obesity.”
Enhanced Hygiene: Hand-washing, mask-wearing, and social distancing
The Cochrane Library has again been a world leader in performing retrospective reviews of the effectiveness (and state of knowledge) regarding interventions intended to manage the COVID-19 pandemic.
In 2020, the research team of Jefferson et al. searched the extant scientific literature and
published its findings in the Cochrane Library’s Physical Interventions to Interrupt or Reduce the Spread of Respiratory Viruses. Searching an array of medical and scientific literature indices and databases, the Jefferson team amassed a total of 67 studies which met the criteria for inclusion in their retrospective analysis of the evidence regarding enhanced hygiene (hand-washing and mask-wearing). All of these studies pre-dated the COVID-19 pandemic and focused on previous disease outbreaks of influenza, including the highly virulent H1:N1 variant that wrought worldwide havoc in 2009.
As there is unusually contentious debate over Cochrane’s research on this topic (a fairly vicious battle between the “masks don’t work” and “masks do work” tribes), it is best to read the team’s conclusions in the authors’ own words:
- The high risk of bias in the trials, variation in outcome measurement, and relatively low compliance with the interventions during the studies hamper drawing firm conclusions and generalising the findings to the current COVID-19 pandemic. There is uncertainty about the effects of face masks. The low-moderate certainty of the evidence means our confidence in the effect estimate is limited, and that the true effect may be different from the observed estimate of the effect. The pooled results of randomized trials did not show a clear reduction in respiratory viral infection with the use of medical/surgical masks during seasonal influenza. There were no clear differences between the use of medical/surgical masks compared with N95/P2 respirators in healthcare workers when used in routine care to reduce respiratory viral infection. Hand hygiene is likely to modestly reduce the burden of respiratory illness. Harms associated with physical interventions were under-investigated. (Jefferson et al., 2020: 2–3).
Team Jefferson would update this research in 2023, amassing an expanded set of 78 randomized clinical trials involving physical interventions that had been conducted prior to the time of search (Jefferson et al., 2023). Most of those studies were also conducted prior to the COVID-19 outbreak, and studied the effectiveness of physical interventions against various types of influenza. However, six of the studies included in the 2023 review were conducted during the COVID-19 pandemic.
I’ll also reproduce this latest summary of findings from Jefferson et al. in the authors’ own
words:
- There is uncertainty about the effects of face masks. The low to moderate certainty
of evidence means our confidence in the effect estimate is limited, and that the true
effect may be different from the observed estimate of the effect. The pooled results
of RCTs did not show a clear reduction in respiratory viral infection with the use of
medical/surgical masks. There were no clear differences between the use of medical/
surgical masks compared with N95/P2 respirators in healthcare workers when used in
routine care to reduce respiratory viral infection. Hand hygiene is likely to modestly
reduce the burden of respiratory illness, and although this effect was also present
when ILI [Influenza-Like Illness] and laboratory-confirmed influenza were analysed
separately, it was not found to be a significant difference for the latter two outcomes.
Harms associated with physical interventions were under-investigated. (Jefferson et
al., 2023: 3).
Discussion
Governments and government policies were deeply involved in the development, definition, and deployment of both pharmaceutical and non-pharmaceutical interventions throughout the COVID pandemic, far more directly than was routinely seen in past public health crises or in contagious disease outbreaks. Whereas in the past one might have consulted with one’s doctor to get an idea about what to do to protect one’s health, there was no need for that in 2020: government pronouncements at the highest levels of health care bureaucracy were loud, clear, and insistent from the earliest days of the COVID pandemic.
At the time, governments, regulatory agencies, and a vast panoply of public health authorities asserted that they were, in all cases, diligently “following the science” in the policy guidances and prescriptions they wrote for society. “Following the science” became a constant refrain in explaining everything government did. It was also a bludgeon when used in the negative: “not following the science” was applied to anyone critical of what government did. And despite the fact that science is generally a relatively slow process of theory, experimentation, and publication of findings, somehow, as of January 2020, “the science” took to changing on a daily, even hourly basis.
Despite government assertions that they were following the science, reviews of the literature on the subject extant at the time suggest that governments were selectively interpreting the studies that already existed.
In fact, studies regarding the effectiveness of the measures governments adopted to fight COVID were relatively few in number, were mostly in the past tense as of 2020, were largely characterized as having mixed results, were highly uncertain, and were primarily driven by computer models.
The “consensus” of reviews of the literature extant at the time, conducted both during 2020 and afterward, come to basically the same conclusions. Specifically, they find with regard to the non-pharmaceutical interventions of enhanced hygiene, mask-wearing, and restrictions on gathering that while these NPIs might have helped, they might also have harmed, but that there was no strong evidence one way or the other.
Thus, it’s safe to say that while governments did not actively lie about “following the science,” they most certainly misrepresented “the science” in that they exaggerated certainty (a constant problem of government), they chose to believe models over observational studies, they only acknowledged half the science (about slowing transmission, not about causing harm to people economically and socially), and they spoke in tones of absolute certainty that denied the essence of science. That essence understands that knowledge is provisional, that this was a novel virus, and that there was, in fact, no
solid reason to find prior research outcomes dispositive in terms of giving guidance about what to do.
In acting with such certainty, governments not only did harm to their own future credibility, but they did harm to the credibility of public health institutions, biomedical institutions, pharmaceutical institutions, and others that governments chose to use as fig-leaves to obscure what were, in very large measure, arbitrary choices that governments made based on fragmentary, cherry-picked, model-dominated studies that mostly pre-existed the COVID pandemic. At the same time, governments also suppressed dissent among and elevated the authoritarian voices and managers of those institutions.
In an ideal world, there would be some process by which our public health agencies, at least, could come to recognize and admit how badly they managed to “follow the science” on COVID-19, and how vast was the gulf between their expressions of absolute certainty and what the scientific literature showed at the time was, in fact, a sea of uncertainty. Until such a “truth and reconciliation” process takes place, it is hard to see how public trust in public health institutions might be restored.
About the author
Kenneth P. Green is a Fraser Institute senior fellow and author of over 800 essays and articles on public policy, published by think tanks, major newspapers, and technical and trade journals in North America. Mr. Green holds a doctoral degree in environmental science and engineering from UCLA, a master’s degree in molecular genetics from San Diego State University, and a bachelors degree in general biology from UCLA.
Brownstone Institute
The Deplorable Ethics of a Preemptive Pardon for Fauci
From the Brownstone Institute
Anthony “I represent science” Fauci can now stand beside Richard “I am not a crook” Nixon in the history books as someone who received the poison pill of a preemptive pardon.
While Nixon was pardoned for specific charges related to Watergate, the exact crimes for which Fauci was pardoned are not specified. Rather, the pardon specifies:
Baseless and politically motivated investigations wreak havoc on the lives, safety, and financial security of targeted individuals and their families. Even when individuals have done nothing wrong – and in fact have done the right things – and will ultimately be exonerated, the mere fact of being investigated and prosecuted can irreparably damage reputations and finances.
In other words, the dying breath of the Biden administration appears to be pardoning Fauci for crimes he didn’t commit, which would seem to make a pardon null and void. The pardon goes further than simply granting clemency for crimes. Clemency usually alleviates the punishment associated with a crime, but here Biden attempts to alleviate the burden of investigations and prosecutions, the likes of which our justice system uses to uncover crimes.
It’s one thing to pardon someone who has been subjected to a fair trial and convicted, to say they have already paid their dues. Gerald Ford, in his pardon of Richard Nixon, admitted that Nixon had already paid the high cost of resigning from the highest office in the land. Nixon’s resignation came as the final chapter of prolonged investigations into his illegal and unpresidential conduct during Watergate, and those investigations provided us the truth we needed to know that Nixon was a crook and move on content that his ignominious reputation was carve d into stone for all of history.
Fauci, meanwhile, has evaded investigations on matters far more serious than Watergate. In 2017, DARPA organized a grant call – the PREEMPT call – aiming to preempt pathogen spillover from wildlife to people. In 2018 a newly formed collaborative group of scientists from the US, Singapore, and Wuhan wrote a grant – the DEFUSE grant – proposing to modify a bat sarbecovirus in Wuhan in a very unusual way. DARPA did not fund the team because their work was too risky for the Department of Defense, but in 2019 Fauci’s NIAID funded this exact set of scientists who never wrote a paper together prior or since. In late 2019, SARS-CoV-2 emerged in Wuhan with the precise modifications proposed in the DEFUSE grant submitted to PREEMPT.
It’s reasonable to be concerned that this line of research funded by Fauci’s NIAID may have caused the pandemic. In fact, if we’re sharp-penciled and honest with our probabilities, it’s likely beyond reasonable doubt that SARS-CoV-2 emerged as a consequence of research proposed in DEFUSE. What we don’t know, however, is whether the research proceeded with US involvement or not.
Congress used its constitutionally-granted investigation and oversight responsibilities to investigate and oversee NIAID in search of answers. In the process of these investigations, they found endless pages of emails with unjustified redactions, evidence that Fauci’s FOIA lady could “make emails disappear,” Fauci’s right-hand-man David Morens aided the DEFUSE authors as they navigated disciplinary measures at NIH and NIAID, and there were significant concerns that NIAID sought to obstruct investigations and destroy federal records.
Such obstructive actions did not inspire confidence in the innocence of Anthony Fauci or the US scientists he funded in 2019. On the contrary, Fauci testified twice under oath saying NIAID did not fund gain-of-function research of concern in Wuhan…but then we discovered a 2018 progress report of research NIAID funded in Wuhan revealing research they funded had enhanced the transmissibility of a bat SARS-related coronavirus 10,000 times higher than the wild virus. That is, indisputably, gain-of-function research of concern. Fauci thus lied to the American public and perjured himself in his testimony to Congress, and Senator Rand Paul (R-KY) has referred Fauci’s perjury charges to the Department of Justice.
What was NIAID trying to preempt with their obstruction of Congressional investigations? What is Biden trying to preempt with his pardon of Fauci? Why do we not have the 2019 NIAID progress report from the PI’s who submitted DEFUSE to PREEMPT and later received funding from NIAID?
It is deplorable for Biden to preemptively pardon Fauci on his last day in office, with so little known about the research NIAID funded in 2019 and voters so clearly eager to learn more. With Nixon’s preemptive pardon, the truth of his wrongdoing was known and all that was left was punishment. With Fauci’s preemptive pardon, the truth is not yet known, NIAID officials in Fauci’s orbit violated federal records laws in their effort to avoid the truth from being known, and Biden didn’t preemptively pardon Fauci to grant clemency and alleviate punishment, but to stop investigations and prosecutions the likes of which could uncover the truth.
I’m not a Constitutional scholar prepared to argue the legality of this maneuver, but I am an ethical human being, a scientist who contributed another grant to the PREEMPT call, and a scientist who helped uncover some of the evidence consistent with a lab origin and quantify the likelihood of a lab origin from research proposed in the DEFUSE grant. Any ethical human being knows that we need to know what caused the pandemic, and to deprive the citizenry of such information from open investigations of NIAID research in 2019 would be to deprive us of critical information we need to self-govern and elect people who manage scientific risks in ways we see fit. As a scientist, there are critical questions about bioattribution that require testing, and the way to test our hypotheses is to uncover the redacted and withheld documents from Fauci’s NIAID in 2019.
The Biden administration’s dying breath was to pardon Anthony Fauci not for the convictions for crimes he didn’t commit (?) but to avoid investigations that could be a reputational and financial burden for Anthony Fauci. A pardon to preempt an investigation is not a pardon; it is obstruction. The Biden administration’s dying breath is to obstruct our pursuit of truth and reconciliation on the ultimate cause of 1 million Americans’ dying breaths.
To remind everyone what we still need to know, it helps to look through the peephole of what we’ve already found to inspire curiosity about what else we’d find if only the peephole could be widened. Below is one of the precious few emails investigative journalists pursuing FOIAs against NIAID have managed to obtain from the critical period when SARS-CoV-2 is believed to have emerged. The email connects DEFUSE PI’s Peter Daszak (EcoHealth Alliance), Ralph Baric (UNC), Linfa Wang (Duke-NUS), Ben Hu (Wuhan Institute of Virology), Shi ZhengLi (Wuhan Institute of Virology) and others in October 2019. The subject line “NIAID SARS-CoV Call – October 30/31” connects these authors to NIAID.
It is approximately in that time range – October/November 2019 – when SARS-CoV-2 is hypothesized to have entered the human population in Wuhan. When it emerged, SARS-CoV-2 was unique among sarbecoviruses in having a furin cleavage site, as proposed by these authors in their 2019 DEFUSE grant. Of all the places the furin cleavage site could be, the furin cleavage site of SARS-CoV-2 was in the S1/S2 junction of the Spike protein, precisely as proposed by these authors.
In order to insert a furin cleavage site in a SARS-CoV, however, the researchers would’ve needed to build a reverse genetic system, i.e. a DNA copy of the virus. SARS-CoV-2 is unique among coronaviruses in having exactly the fingerprint we would expect from reverse genetic systems. There is an unusual even spacing in the cutting/pasting sites for the enzymes BsaI and BsmBI and an anomalous hot-spot of silent mutations in precisely these sites, exactly as researchers at the Wuhan Institute of Virology have done for other coronavirus reverse genetic systems. The odds of such an extreme synthetic-looking pattern occurring in nature are, conservatively, about 1 in 50 billion.
The virus did not emerge in Bangkok, Hanoi, Bago, Kunming, Guangdong, or any of the myriad other places with similar animal trade networks and greater contact rates between people and sarbecovirus reservoirs. No. The virus emerged in Wuhan, the exact place and time one would expect from DEFUSE.
With all the evidence pointing the hounds towards NIAID, it is essential for global health security that we further investigate the research NIAID funded in 2019. It is imperative for our constitutional democracy, for our ability to self-govern, that we learn the truth. The only way to learn the truth is to investigate NIAID, the agency Fauci led for 38 years, the agency that funded gain-of-function research of concern, the agency named in the October 2019 call by DEFUSE PI’s, the agency that funded this exact group in 2019.
A preemptive pardon prior to the discovery of truth is a fancy name for obstruction of justice. The Biden administration’s dying breath must be challenged, and we must allow Congress and the incoming administration to investigate the possibility that Anthony Fauci’s NIAID-supported research caused the Covid-19 pandemic.
Republished from the author’s Substack
COVID-19
BREAKING: Days before Trump Inauguration HHS fires doctor in charge of gain of function research project
Dr. Daszak will likely be protected by the DoD & CIA from additional penalties.
By John Leake
HHS Formally Debars EcoHealth Alliance, President Peter Daszak Fired.
On January 17, 2025—just three days before President Trump is to be sworn in—Congress issued a press release with the following statement:
Today, after an eight-month investigation, the U.S. Department of Health and Human Services (HHS) cut off all funding and formally debarred EcoHealth Alliance Inc. (EcoHealth) and its former President, Dr. Peter Daszak, for five years based on evidence uncovered by the Select Subcommittee on the Coronavirus Pandemic.
As far as I can tell, the New York Times did not report this story, though the New York Post did.
More interesting than the superficial news reporting is the HHS ACTION REFERRAL MEMORANDUM recommending that Dr. Peter Daszak be barred from participating in United States Federal Government procurement and nonprocurement programs.
The Memorandum also states:
Dr. Peter Daszak was the President and Chief Executive Officer of EHA from 2009 until his termination, effective January 6, 2025. Dr. Daszak was the Project Director (PD)/Principal Investigator (PI) for Grant Number 1R01AI110964-01.
I am not sure what to make of this document, which is written in such an arcane and convoluted style that it challenges the attention span of even the most focused reader.
I have been researching this story for four years, and I found the following paragraphs the most intriguing:
9. In a letter dated May 28, 2016, the NIAID contacted EHA concerning possible GoF research based on information submitted in its most recent Year 2 RPPR. The NIAID notified EHA that GoF research conducted under Grant Number 5R01AI110964-03 would be subject to the October 17, 2014, United States Federal Government funding pause, and that per the funding pause announcement, new United States Federal Government funding would not be released for GoF research projects that may be reasonably anticipated to confer attributes to influenza, MERS, or SARS viruses such that the virus would have enhanced pathogenicity and/or transmissibility in mammals via the respiratory route. In the letter, the NIAID requested that EHA provide a determination within 15 days of the date of the letter as to whether EHA’s research under Grant Number 5R01AI110964-03 did or did not include GoF work subject to the funding pause.
10. In a letter dated June 8, 2016, EHA provided a response to the NIAID’s May 28, 2016 letter. EHA explained that the goal of its proposed work was to construct MERS and MERS-like chimeric CoVs in order to understand the potential origins of MERSCoV in bats by studying bat MERS-like CoVs in detail. EHA stated that it believed it was highly unlikely that the proposed work would have any pathogenic potential, but that should any of these recombinants show evidence of enhanced virus growth greater than certain specified benchmarks involving log growth increases, or grow more efficiently in human airway epithelial cells, EHA would immediately: (1) stop all experiments with the mutant, (2) inform the NIAID Program Officer of these results, and (3) participate in decision-making trees to decide appropriate paths forward.
11. Based on the information provided by EHA, the NIAID concluded that the proposed work was not subject to the GoF research pause. In a letter dated July 7, 2016, however, the NIAID informed EHA that should any of the MERS-like or SARS-like chimeras generated under the grant show evidence of enhanced virus growth greater than 1 log over the parental backbone strain, EHA must stop all experiments with these viruses and provide the NIAID Program Officer and Grants Management Specialist, and WIV Institutional Biosafety Committee, with the relevant data and information related to these unanticipated outcomes.
Note that various statements in the above paragraphs are inconsistent with what Baric et al. state in their 2015 paper A SARS-like cluster of circulating bat coronavirus shows potential for human emergence—a research paper funded by the NIAID EcoHealth Grant “Understanding the Risk of Bat Coronavirus Emergence.”
As the authors state in the section on Biosafety and biosecurity:
Reported studies were initiated after the University of North Carolina Institutional Biosafety Committee approved the experimental protocol (Project Title: Generating infectious clones of bat SARS-like CoVs; Lab Safety Plan ID: 20145741; Schedule G ID: 12279). These studies were initiated before the US Government Deliberative Process Research Funding Pause on Selected Gain-of-Function Research Involving Influenza, MERS and SARS Viruses (http://www.phe.gov/s3/
dualuse/Documents/gain-of- function.pdf). This paper has been reviewed by the funding agency, the NIH. Continuation of these studies was requested, and this has been approved by the NIH.
As I noted in my series of essays titled The Great SARS-CoV-2 Charade, one of the silliest lies told by Dr. Anthony Fauci has been his insistence that NIAID did not approve Gain-of-Function work by EcoHealth.
Fauci has repeatedly asserted this in a loud and vexed tone, as though he is outraged by the mere proposition. And yet, Ralph Baric and his colleagues—including Zhengli-Li Shi at the Wuhan Institute of Virology—plainly state in their 2015 paper that their Gain-of-Function experiments, performed in Baric’s UNC lab and Zhengli-Li Shi’s lab in Wuhan, were grandfathered in, given that they were funded before the 2014 Pause.
Another statement (in paragraph 11 of the recent HHS Action Referral Memo) that deserves special scrutiny is the following:
In a letter dated July 7, 2016, however, the NIAID informed EHA that should any of the MERS-like or SARS-like chimeras generated under the grant show evidence of enhanced virus growth greater than 1 log over the parental backbone strain, EHA must stop all experiments with these viruses and provide the NIAID Program Officer and Grants Management Specialist, and WIV Institutional Biosafety Committee, with the relevant data and information related to these unanticipated outcomes.
Again, it’s tough to interpret this statement, given that Baric et al. had, by the own admission, already generated chimeras that “replicate efficiently in primary human airway cells and achieve in vitro titers equivalent to epidemic strains of SARS-CoV.”
Let’s review what Baric et al. state in their Abstract about the functionality of the chimeric virus (named SHCOI4-MA15) they claimed to have generated. Using humanized mice (genetically modified to have primary human airway cells) as their experimental animals, the authors state:
Using the SARS-CoV reverse genetics system2, we generated and characterized a chimeric virus expressing the spike of bat coronavirus SHC014 in a mouse-adapted SARS-CoV backbone.
The results indicate that group 2b viruses encoding the SHC014 spike in a wild-type backbone can efficiently use multiple orthologs of the SARS receptor human angiotensin converting enzyme II (ACE2), replicate efficiently in primary human airway cells and achieve in vitro titers equivalent to epidemic strains of SARS-CoV. Additionally, in vivo experiments demonstrate replication of the chimeric virus in mouse lung with notable pathogenesis.
To this day, no legal authority that I am aware of has investigated the question: What became of the the chimeras SHC014-MA15 and WIV1-MA15? The latter chimera was documented by Baric et al. in their March 2016 paper titled SARS-like WIV1-CoV poised for human emergence—a chimera “that replaced the SARS spike with the WIV1 spike within the mouse-adapted backbone.”
What did the Wuhan Institute of Virology do with these chimeras? Did its researchers continue to modify and experiment with these chimeras?
Another exceedingly silly claim made by U.S. government officials—including members of Congress—is that the true origin of SARS-CoV-2 is likely to remain a mystery, given that the Chinese government and military will almost certainly never agree to perform a full and transparent investigation of their Wuhan Institute of Virology.
What did the U.S. government expect when it agreed to share cutting edge American biotechnology with the Wuhan Institute of Virology, which has long been known to be run by the Chinese military?
One grows weary of our U.S. government officials evading responsibility by pretending to be imbeciles or by revealing themselves to be true imbeciles.
If you found this post informative, please consider becoming a paid subscriber to our Substack. Penetrating the smoke and mirror show performed by the abominable U.S. government requires a great deal of time and effort.
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