COVID-19’s Biological Politics

Article in post #1,780 has a link for this report:
Balamurali & Ambati
'....The presence in SARS-CoV-2 of a 19-nt RNA sequence encoding an FCS (furin cleavage site) at amino acid 681 of its spike protein with 100% identity to the reverse complement of a proprietary MSH3 mRNA sequence is highly unusual.'
 
More on Artificiality

This came from Henan Province:
'@ 24 Jan....'Chinese scientists accidentally uploaded a sample from 2019 (pre-covid) that contained a spike protein with 100% match to SARS2 without the furin cleavage site. Basically confirming the virus was artificially created in a laboratory.'
 
Massey says it's not seen in nature:

' Several amino acids use almost entirely a single codon. These include V, Y, L, K, I, H, G. This is never seen in nature.

Though what is seen in nature is the coronavirus particular use of branched-chain amino acids, V, L, and I:

29 Nov 2021 Post#874 Branched-Chain Modus Operandae
 
She is talking about RaTG13 that came from the Mojiang mine. It can't infect humans. There were sick Mojiang miners shuffling into the Kunming Hospital while Fauci was testifying to the U.S. Senate on "Dual Use." Bizarre.

She says...."Teamwork. This ought to rattle some cages."
 
Fau Chi's Marionette Army

Many have questioned the worth and effectiveness of GoF.

150 American Scientists Call for GoF Continuance
 
Post-"vax" questioners have been silenced.
From Dr. McCullough's page:

'....biomarkers....'
 
Thusfar, the first furin cleavage site we have noticed from North America is from a phlebovirus from the American dog tick, Dermacentor variabilis, Heckscher State Park, Long Island, New York. This is not far from Fire Island, a homosexual playground which brings up the possibility that humans and dogs via tick-bite could influence the evolution of this FCS in a phlebovirus.

This occurrence links to Yong-Zhen Zhang's (first to sequence SARS2) SFTS Chinese phlebovirus from the Asian longhorned tick, Haemaphysalis longicornis, related to fatal American Heartland virus.

American Dog Tick Phlebovirus / Furin Cleavage Site
'....Heckscher State Park, Suffolk County, New York....'

The reader can view the furin cleavage site 'RRAR' @ line #18:
 
The furin cleavage site virus from Long Island, New York, was collected in Ap 2013, so this should be synchronized with Zheng-Li Shi's Wuhan Institute of Virology sampling in the Mojiang copper mine during that year, and the origins of RaTG13 with 96% similarity to SARS2.
 
Stuxnet virus - biological version
Stuxnet apparently in 2010. We have found an RGD motif, again from a phlebovirus, collected from the tick that vectors Lyme disease, Ixodes scapularis, from 2008 from the same Heckscher State Park.

Thus begins an archive of (American RGDs & FCSs [italics]).
 
So just where on the spike protein of SARS2 does the ivermectin bind? The RGD motif is located at positions 403-5.

'Moreover, (ivermectin) the drug prevents blood clots through binding to spike protein, and also deters the spike protein from binding to CD147 on red blood cells, which would otherwise trigger clumping.'
(Kennedy, The Real Anthony Fauci, p. 40)

So if Dr. Burgdorfer, discoverer of the Lyme disease agent were still alive, what would he say about the RGD motif of the phlebovirus from I. scapularis?

'In a bit of twisted logic, Federal officials continued to encourage doctors to use the suddenly-dangerous drug (hcq) without restriction for lupus, rheumatoid arthritis, Lyme and malaria.'
(Kennedy, op cit pp. 25-6)
 
Jikky is exposing pharma agents:


' You can't put an expression of concern on a hypothesis paper - it's an hypothesis!....ivermectin's mechanism in COVID-19....'
 
During these tick-virus surveys, also found were mononegavirales-like viruses. Marburg, ebola, and Chinese Mengla viruses are Mononegavirales:

Deer Tick, Ixodes scapularis Mononegavirales-Like Virus
'....collected 2008....'

At Marburg, German itself, they were producing artificial virus-like particles for targeting cancer:
Virus-Like Particles / RGD Motif / Melanoma
'....AVP technology is a useful approach for generating highly efficient and specific non-viral vectors for melanoma targeting.'

So further proof that the RGD motif of the SARS2 spike at positions 403-5, whether in "vaccines" or the virus itself are toxic, is here:

NIH Bethesda, Md. / Mechanism of Ad5 Vaccine Immunity and Toxicity / Ebola, etc. / RGD Motif
'....Mutant CAR and RGD rAd vectors target several DC and mononuclear subsets and induce both adaptive immunity and toxicity.'

Therefore, we are interested in those genomes susceptible to the toxic SARS2 spike rather than those who have thusfar shown no reactions to it.
 
Sputnik News: EcoHealthAlliance / Ukraine Biolabs
'....EcoHealthAlliance has been engaged in research on coronavirus strain transmission mechanisms since at least 2015.'

A more correct date is 17 Ap 2011, when EHA's Daszak and Zheng-Li Shi (Wuhan Institute of Virology) collected RsSHC014 in Yunnan, which virus was then manipulated in Baric's North Carolina bat lab to produce the disturbing and dangerous, potentially vaccine-thwarting recombinant mentioned in the report by Sorensen and Dalgleish.
 

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