Ralph Steven Baric (born 1954) is William R. Kenan Jr. Distinguished Professor in the Department of Epidemiology, and professor in the Department of Microbiology and Immunology at The University of North Carolina at Chapel Hill.
Baric's work involves coronaviruses, including gain of function research aimed at devising effective vaccines against coronaviruses.[1] Baric has warned of emerging coronaviruses presenting as a significant threat to global health, due to zoonosis.[2][3] Baric's work has drawn criticism from some scientists and members of the public related to chimeric virus experiments conducted at UNC-Chapel Hill.[4]
In 2015, with Shi Zhengli of the Wuhan Institute of Virology, he published an article titled "A SARS-like cluster of circulating bat coronaviruses shows potential for human emergence," which describes their work in generating and characterizing a chimeric virus which added the spike of a bat coronavirus (SHC014) onto the backbone of a mouse-adapted SARS-CoV (rMA15).[12] The research related to this article drew criticism from other scientists due to fears that the SHC014-rMA15 chimeric virus could have pandemic potential.[13] This concern was renewed and echoed by members of the public during the COVID-19 pandemic.
SUMMARY: The Sars-Cov-2 virus that causes COVID-19 contains genetic fragments of HIV. This post will show that numerous scientific studies created recombinant viruses containing genes from HIV. Thus, it should not surprise anyone that a lab-engineered pathogen such as Sars-Cov-2 is a recombinant carrier of HIV genes and expresses HIV peptides such as Gp120 or Gag.
I also explain that Sars-Cov-2 matches Ralph Baric’s description of his “perfect bioweapon” - a medium pathogenicity designer recombinant virus whose purpose is to create fear.
You may have heard that Sars-Cov-2 contains certain genes from HIV, which causes AIDS. Those genes encode proteins that go into Covid-19’s “spike protein.” Thus, anyone who had Covid or received the Covid vaccine containing the same spike protein was exposed to the HIV peptides on the spike.
Fact Checks Describe this as a Baseless Conspiracy Theory
The press made significant efforts to discredit the “HIV genes in Sars-CoV-2” theory.
NIH Funded Similar Coronavirus Recombinations
Scientists experimented with putting HIV and SIV (Simian Immunodeficiency Virus) bits into coronaviruses in the past, and the NIH supported such work.
In this 2008 grant, Amy Sims, who worked with Ralph Baric at UNC, describes her idea to put bits of Simian Immunodeficiency Virus (SIV, a precursor of HIV) into a human common cold virus OC43. (you probably had a few colds caused by OC43, which causes one-third of common colds). Amy then experimented with infecting monkeys with it.
There were numerous other attempts to add HIV genes to measles, poxviruses, and coronaviruses, specifically:
As all HIV vaccines failed, and most made their recipients paradoxically more susceptible to becoming infected with HIV, the above-described 2008 work did not lead to a working HIV vaccine. In addition, Amy’s discussion of “mucosal immunity” against HIV seems to be at odds with the fact that HIV is blood-borne and is passed through contaminated drug needles, razors, or sexual acts where blood is exchanged (such as unprotected anal sex).
Adding bits and parts of HIV to viruses was the bread and butter of virology.Thus, the fact-checks that deny the possibility that HIV inserts in SARS-Cov-2 were engineered are less than truthful.
Here’s Luc Montagnier, a pioneer in the field of HIV, who coincidentally died soon after giving this interview, explaining that Sars-Cov-2 was engineered:
And lastly, here’s a brand-new Mar 24 interview with Robert Redfield, former director of the CDC who also worked on HIV and HIV vaccines with Anthony Fauci and Debora Birx, explaining that Sars-Cov-2 is a product of mostly US-based research:
Ralph Baric Described His Perfect Bioweapon
Ralph Baric has devoted a lot of thinking to biological weapons.
Ralph shows that recombinant pathogens combining genes from several pathogens will likely be the future bioweapon. He then explains that high pathogenicity is NOT necessary for a perfect bioweapon: instead, what is important is that the bioweapon creates fear...
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