3-24-21 Interview with
Dr. R. Ebright of Rutgers U., New JerseyRegarding the inspection personnel, at least one member of the WHO mission team, Ecohealth Alliance President Dr. Peter Daszak, seems to have conflicts of interest that should have disqualified him from being part of an investigation of the origins of the COVID-19 pandemic.
Yes. Daszak was the contractor who funded the laboratory at WIV that potentially was the source of the virus (with subcontracts from $200 million from the US Department of State and $7 million from the US National Institutes of Health), and he was a collaborator and co-author on research projects at the laboratory.
Dr. Ebright, you are a microbiologist and molecular biologist, what light can you shed on this matter from your fields of expertise?
Microbiologists and molecular biologists are as qualified as virologists to assess the relevant science and science policies. Virology is a subset, not a superset, of microbiology and molecular biology. The sequencing, sequence analysis, cell culture, animal-infection studies, and other laboratory procedures used by virologists are not materially different from the procedures used by other microbiologists and molecular biologists.
Dr. Ralph Baric, who is considered the US leading expert in coronavirus, so he probably is the world one, says that is possible to engineer a virus in a lab without leaving a trace of the manipulation.
The fact that the genome sequence of this virus shows no signatures of human manipulation rules out the kinds of gain-of-function (GoF) research that leave signatures. But this does not rule out kinds of GoF research that do not leave signatures.
What went wrong for the Cambridge Working Group thesis during the 2014-2016 USA official moratorium and deliberative process on Gain-of-Function Research of Concern (GoFRoC)?
The Director of the National Institute of Allergy and Infectious Diseases (NIAID) and the Director of the National Institutes of Health (NIH) have systematically thwarted efforts by the White House, the Congress, scientists, and science policy specialists to regulate GoF research of concern and even to require risk-benefit review for projects involving GoF research of concern.
In 2014, the Obama White House implemented a “Pause” in federal funding for GoF research of concern. However, the document announcing the Pause stated in a footnote that: “An exception from pause may be obtained if head of funding agency determines research is urgently necessary to protect public health or national security”. 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.
In 2017, the Trump Administration announced a Potential Pandemic Pathogens Control and Oversight (P3CO) Framework that implemented a requirement for risk-benefit review of GoF research of concern. However, the P3CO Framework relies on the funding agency to flag and forward proposals for risk-benefit review. Unfortunately, the NIAID Director and the NIH Director have declined to flag and forward proposals for risk-benefit review, thereby nullifying the P3CO Framework. https://www.independentsciencenews.org/commentaries/an-interview-with-richard-ebright-anthony-fauci-francis-collins-systematically-thwarted/
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