COVID-19’s Biological Politics

Because SARS-CoV-2 D614G (aspartic acid-to-glycine) mutation links precisely to the VSV of ebola vaccine, a Pubmed search ‘ebola aspartic glycine,’ yielded no references. Next, an ‘ebola mutations’ search yielded Niemann-Pick references, so a refined search was attempted: ‘Niemann-Pick aspartic glycine,’ which indeed retrieved a D-to-G mutation:

2011 Dartmouth Medical School, Niemann-Pick D1005G
’This change is in the cysteine-rich luminal loop of the NPC1 protein and is highly similar to commonly occurring human mutations....late-onset, slowly progressing forms of NPC disease that comprise the large majority of cases.’

To verify a link to COVID-19, a search ‘cysteine-rich covid-19’ yielded a coagulopathy link:

Nov 2020 Rome: Cysteine-Rich Coagulopathy
’....The pattern was present in both human and bat coronavirus S proteins....a positive role of cysteine palmitoylation in cell fusion has been reported for influenza virus HA proteins, while a negative role was observed for Vesicular Stomatitis virus (VSV)....Intriguingly, the CAF-motif occurs in proteins such as coagulation factor X, von Willebrand factor, platelet endothelial aggregation receptor 1, and some pro-thrombin activator venom toxins that are involved in the coagulation process. The identification of a common pattern could suggest a new function of the S protein in the pathological effects of SARS-CoV-2.’
 
The late-onset form of NPC disease, above, links to coagulopathy, and we have already mentioned coagulation factor XII in relation to Alzheimer’s disease in posts # 338-9 of this thread. It is thus interesting that the French Henri Mondor variant does not contain the D614G mutation, whilst it does contain two Alzheimer’s-like mutations.

18 Ap 2021 Posts #338 & 339
’....Alzheimer’s fibrinogen blood coagulation system.’

Furthermore, the Mondor variant’s two Alzheimer-like mutations are N501Y, which we have already mentioned in this thread, and A653V. The latter Mondor mutation is similar to C-19’s A483V Alzheimer-like mutation, which can be compared with late-onset coagulopathy of NPC disease, because it causes early-onset Alzheimer’s from 26-36 years of age.
 
Then in post #340, Ft. Detrick studies were linked to hantavirus and coagulation factor XII:

Post #340
 
Fauci got a lotta explaining to do.

DOC #2286 [Bioweapon Recipe]


DOC DUMP ARCHIVES:
LEOPOLD NIH FOIA Anthony Fauci Emails – DocumentCloud


La de da

"British professor Angus Dalgleish - best known for creating the world's first 'HIV vaccine', and Norwegian virologist Dr. Birger Sørensen - chair of pharmaceutical company, Immunor, who has published 31 peer-reviewed papers and holds several patents, wrote that while analyzing virus samples last year, the pair discovered "unique fingerprints" in the form of "six inserts" created through gain-of-function research at the Wuhan Institute of Virology in China."
 
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Yes, LBT, we’d like to know about the inserts, because retroviral elements can naturally integrate into the coronavirus genome, without human manipulation. Fauci likely was involved in early HIV vaccine research, and all that Rand Paul has to do in public is to mention the D614G mutation, that precisely links to ebola vaccine.

Furthermore, Fort Detrick’s study on increased potency of the venom of one of the suspected hosts of SARS-CoV-2, Bungarus, is problematic, because a subspecies of this genus, B. wanghaotingi, has apparently not yet been sequenced. This subspecies may occur near to RaTG13. Thus, Bungarus as intermediate host of SARS-CoV-2 cannot yet be ruled out. One important thing to do is to document the precise geographical location of C-19’s closest relative, RaTG13, from Yunnan Province.

We mentioned Daszak’s work, which goes back to 2011, in conjunction with the nasty Kunming animal market, not the Wuhan seafood market, on 13 Feb 2020. Daszak is co-author of the second entry of post #404:

Post #404
 
In the video, Fauci gets the 614 mutation backwards. This was surprising due to the fact that mutating to glycine seemed more primitive than mutating to an aspartic acid. Fauci mentions this D614G mutation, but never links it to ebola vaccine as we have done in this thread. Indeed, this D-to-G mutation occurs not only in HIV-1, but also HIV-2, which many consider to be an older virus. Fauci’s apparent “mistake” begins at timepoint 6:45 in the youtube video, and he makes a point to reify this mutation:

Fauci / D614G Mutation / Timepoint 6:45


2013: Osaka, Japan / TRIM HIV-1 Aspartic Acid to Glycine Substitution
 
Note that in Fig.1 at position 249 in the TRIM5 report, above, the chart shows that African Green monkey is glycine (G) and human MT4 is aspartic acid (D), and that ‘ human TRIM5alpha with 249D may lose the flexibility required for optimal recognition of retroviral capsid protein.’

This is quite comparable with the COVID-19 D614G mutation found in the B.1.351 South Africa variant, P.1 Japan-Brazil, B.1.427 & B.1.429 California, and all Indian variants (B.1.617-B.1.617.3).
 
An Italian report is among the few linking TRIM5 with COVID-19:

Mar 2021 Italy: TRIM5 / COVID-19
’TRIM5’

Similar to human TRIM5, a bat can also fail in its defense by TRIM5:

Sep 2020 Australia, Colorado, Singapore: Yinpterochiropteran Bat / TRIM5
’....Viral nuclear import was significantly decreased, and this deficit was substantially rescued by cyclosporine treatment....However, saturation with HIV-1 virus-like particles did not relieve the restriction at all. P. Alecto TRIM5 was inactive against HIV-1, although it blocked the gammaretrovirus N-tropic murine leukemia virus.’
 
Now analyzing the HIV-1 inserts mentioned in post #404, which study states: ‘....it is unlikely for a virus to have acquired such unique insertions naturally in a short duration of time.’ We are still searching for the amount of time the authors are talking about, and indeed they are identical to HIV-1: ‘....the insert 1 (6 amino acid residues) and insert 2 (6 amino acid residues) in the spike glycoproptein of 2019-nCoV are 100% identical to residues mapped to HIV-1 gp120.’
 
It was a dead give-away for the CDC to change their webpage for the P.1 variant at position 417, because it shows that the virus was using either aspartic acid or threonine. Originally published as K417N/T, it is highly unlikely to be a typo, and because of the threonine, is a link to (other members [italics]) of the coronavirus family. They removed the asparagine, and the new change is ‘K417T.’
 
From post #404, Sorenson and Andres Susrud both work at Immunor (Norway), and Dalgleish is Professor of Oncology at St. George’s University, London. All three own shares or have stock options in the company.
 
CDC, having removed the fentanyl evidence (N) at position 417 of the P.1 Brazil-Japan variant from their webpage, now links to Public Health England at position 417:

18 hours ago, Portugal Removed From UK Green List
’....On the so-called “Nepal mutation,” Public Health England told BBC it was “aware of reports linking Nepal to Delta (VOC-21Apr-02) with the additional mutation K417N....PHE said “We are investigating K417N to better understand its significance.” ‘

Thus, the N (asparagine) that the CDC removed from their page only differs from D (aspartic acid) of the D614G mutation, by a single hydrogen atom. The significance is that asparagine is the residue that shows how COVID-19 mimics the increased potency of fentanyl at the mu-opioid receptor. Janssen Pharmaceutica, a division of Johnson & Johnson, is the origin of fentanyl.
 
The full title of the article is COVID-19 Severity Linked to Gut Bacteria in First-of-Its-Kind Study. We will take a closer look at the bacteria mentioned: Ruminococcus gnavus, R. torques and Bacterioides dorie, because they may point to an intermediate host-reservoir in nature (‘unusually higher volumes’).
 
Bacteroides, above, links COVID-19 to Hashimoto’s thyroiditis

Jul 2020 Singapore

Ruminococcus torques biota increase found in Hashimoto’s
2018 China
 
While searching for the actual env retroviral excerpt found in The Nidoviruses, a May 2021 report links env to HIV-1 and COVID-19, recalling that Sorenson, et al, inserts (above) are for gp120 env of HIV-1:

May 2021 Env / HIV-1 / SARS-CoV-2, NIH, Duke Human Vaccine Institute, Perelman School of Medicine, Boston Children’s Hospital, Beth Israel Deaconess, Harvard Medical School, Swarthmore College, Memorial Sloan-Kettering, Institute of Macromolecular Chemistry, Prague
’....Here we describe HIV-1 Env Fab-dimerized glycan (FDG)-reactive bnAbs without Vh-swapped domains from SHIV (simian human immunodeficiency virus)-infected macaques. FDG also recognized cell-surface glycans on diverse pathogens, including yeast and SARS-CoV-2 spike.’
 
Moving along the trajectory linked to Africa, there are now two major world viruses whose natural reservoirs have apparently not been found.
In a special issue of Ecology of Virus Emergence From Wildlife, there is an Eco Health Alliance connection for African coronaviruses:

18 May 2021 Overview of Bat and Wildlife Coronavirus Surveillance in Africa: A Framework for Global Investigations
’....Eco Health Alliance, New York....’
 
Yes, LBT, we’d like to know about the inserts, because retroviral elements can naturally integrate into the coronavirus genome, without human manipulation. Fauci likely was involved in early HIV vaccine research, and all that Rand Paul has to do in public is to mention the D614G mutation, that precisely links to ebola vaccine.

Furthermore, Fort Detrick’s study on increased potency of the venom of one of the suspected hosts of SARS-CoV-2, Bungarus, is problematic, because a subspecies of this genus, B. wanghaotingi, has apparently not yet been sequenced. This subspecies may occur near to RaTG13. Thus, Bungarus as intermediate host of SARS-CoV-2 cannot yet be ruled out. One important thing to do is to document the precise geographical location of C-19’s closest relative, RaTG13, from Yunnan Province.

We mentioned Daszak’s work, which goes back to 2011, in conjunction with the nasty Kunming animal market, not the Wuhan seafood market, on 13 Feb 2020. Daszak is co-author of the second entry of post #404:

Post #404

That D614 keeps appearing again and again and again which should send up some blaring red flags.
 
Yes, LBT, the D614G mutation is primitive, because it goes to glycine rather than what Fauci said, aspartic acid. Rand Paul’s D614G question to Fauci connects the dots to Africa for ebola, because the Kansas cow is the basis for ebola vaccine, not a cow from Indiana. The D614G mutation precisely causes increased replication of the VSV virus from the Kansas cow.

A major clue to COVID-19’s origins was published by India on 20 Oct 2020, at the precise location where COVID-19’s closest relative, RaTG13, was found:

20 Oct 2020 India: Lethal Pneumonia in Miners, Tongguan, Mojiang County, Yunnan
’....A Master’s thesis (in the Chinese language) was found on the ckni.net website which described in detail the severe illness of the miners.’
 

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