COVID-19’s Biological Politics

From Flutrackers today, artificial intelligence is being now being used:

AI / ECG
’....Infection with SARS-CoV-2 results in electrocardiographic changes that permit the artificial intelligence-enhanced ECG to be used as a rapid screening test.’
 
We will list the ACE2 binding mutations in comparison with other coronavirus genomes. For the HIV dynamics connection, the reader can scroll down to the paragraphs under “Mutant Frequency Under neutral Drift is Liklely to Lead to Escape from Single and Double Antibody Combinations.”

1.) Y453F
2.) Y508H
3.) N440K
4.) E484K
5.) Q493K
6.) R346S
7.) N439K
8.) E484Q
9.) L452R
10.) K444Q
11.) F490S
12.) S494P
13.) R346K
14.) N450D
15.) V483A
16.) K444T
17.) V445A
18.) E484A
19.) Q493R
20.) F490L
21.) K444N
22.) A475V
23.) V445E
24.) L455F
25.) G446V
26.) V445G
27.) E484D
28.) F486V
29.) G485D
30.) F456V
31.) L455R
....
First, what is the evolutionary cost of harboring nAb-evading RBD mutations? Second, given the evolutionary cost, how likely is it that SARS-CoV-2 patients will harbor viruses with pre-existing nAb-evvading RBD mutations as their dominant viral sequence? Third, how rapidly will such nAb-evading RBD mutations become fixed in the population once nAb vaccines and therapies are widely deployed?’
 
We will list the ACE2 binding mutations in comparison with other coronavirus genomes. For the HIV dynamics connection, the reader can scroll down to the paragraphs under “Mutant Frequency Under neutral Drift is Liklely to Lead to Escape from Single and Double Antibody Combinations.”

1.) Y453F
2.) Y508H
3.) N440K
4.) E484K
5.) Q493K
6.) R346S
7.) N439K
8.) E484Q
9.) L452R
10.) K444Q
11.) F490S
12.) S494P
13.) R346K
14.) N450D
15.) V483A
16.) K444T
17.) V445A
18.) E484A
19.) Q493R
20.) F490L
21.) K444N
22.) A475V
23.) V445E
24.) L455F
25.) G446V
26.) V445G
27.) E484D
28.) F486V
29.) G485D
30.) F456V
31.) L455R
....
First, what is the evolutionary cost of harboring nAb-evading RBD mutations? Second, given the evolutionary cost, how likely is it that SARS-CoV-2 patients will harbor viruses with pre-existing nAb-evvading RBD mutations as their dominant viral sequence? Third, how rapidly will such nAb-evading RBD mutations become fixed in the population once nAb vaccines and therapies are widely deployed?’

Why would ACE2 receptors want to accept any spike protein except the one used by exosomes?

If ACE2 receptors are so flexible, then how flexible will our immune system be after being sensitized to attack one particular spike protein?
 
We now link the Chinese large spotted civet to Yunnan, and a liver fluke of civets to the first reported case of cholangiocarcinoma in a COVID-19 patient in Illinois. There is also a thrombotic link:

Illinois: COVID-19 / Thrombotic Microangiopathy / Cholangiocarcinoma / Gemcitabine

Aug 2021 Thailand: Opisthorchis viverrini as Risk Factor for Cholangiocarcinoma

2012: Opisthorchis: Unarguable Cancer Risk Factor

Yunnan: Viverra megaspila Large Spotted Civet (Map)

Therefore, the COVID-19 cholangiocarcinoma case in Illinois links to a parasite of the Yunnan Large Spotted Civet, Viverra megaspila.
 
SARS-CoV-2’s closest relative came from the Mojiang copper mine, Yunnan. We have already mentioned in this thread the Mengla filovirus (ebola-Marburg family) from Rousettus fruit bat in Yunnan. The second-most common cancer in this Rousettus bat was cholangiocarcinoma:

Rousettus aegypticus Iron Storage Disease / Cholangiocarcinoma
 
Why would ACE2 receptors want to accept any spike protein except the one used by exosomes?

If ACE2 receptors are so flexible, then how flexible will our immune system be after being sensitized to attack one particular spike protein?
There are clues to sensitivity in the cited article.
 
France is now rebelling against vaccine mandates, as seen in this video:

 
The earliest SARS-CoV-2 was in humans was early November, 2019.

Jul 2020 SARS-CoV-2 ORF8 Deletions
’....significantly increased replicative fitness....the lack of ORF8 mays assist host immune evasion....The emergence of ORF8 deletion variants may also impact vaccination strategies....The dated tree demonstrates the intra- and intercontinental dissemination of wild-type (WT) viruses, whereas all del.382 viruses from Singapore and Taiwan are closely related (99.9%)....del.382 viruses emerged between the middle of Dec 2019 and early Jan 2020. The introductions of SARS-CoV-2 into humans occurred early Nov 2019, suggesting that the viruses were present in humans approximately one month before the outbreak was detected.’
 
Post #637 is from an Obama-Biden funded facility, DUKE-NUS. As we compile a list of military connections to Wuhan, it was Bottlecap who first pointed to the funding by these two stupid and arrogant psychopaths:

Post #27
 
Post #673 (rather) is an Obama-Biden funded facility. Singapore linked to Taiwan in the 99.9% identity of the viral strains that were in place in Homo sapiens in Nov 2019, though there is questioning due as to the contribution of each of these variants for their deletions in SARS-CoV-2 ORFs. Delta is not only not the new kid on the block, the Alpha variant B.1.1.7 is just as interresting.
 
Here is a webpage of current variants to assist the reader in analyzing mutations as they arise, in conjunction with the eight coronavirus spike sequences shown in post #518 of this thread:

SARS-CoV-2 Variants of Concern as of 5 Aug 2021
 
There is concern by some recipients of thew J&J vaccine as to efficacy. J&J uses human adenovirus, and AstraZeneca uses chimp adenovirus:

Delta Sparks Fear For J&J Recipients
’....suggested it was less effective against the Delta variant....The AstraZeneca vaccine is a viral vector vaccine, the same technology used by the J&J vaccine.’

Already posted in message #554, this viral-vector technology is the same one funded by the Obama-Biden administration, and links North Carolina To Singapore:

’....Nicholas School of the Environment, Durham, North Carolina; Emerging Infectious Disease Programme, Duke-NUS Medical School, Singapore....from 2012 to 2018....’
 
Linking to J&J and AstraZeneca adenovirus-vectored vaccines in more comprehensively listing military connections, two references from the report in post #677:
’....reference #6: Adenovirus 4 and 7 Vaccine: New Body Armor for U.S. Marine Corps Officer Trainees (2019)....Reference #10: Human Adenovirus Type 7 Outbreak in Police Training Center, Malaysia, 2011.’

Earlier in this thread (post #555), we linked 2019 also to the discovery of an ebola-related virus from China: ‘A New Disturbing Ebola Related Virus from Bats in China: ‘ 8 Jan 2019....a professor at the Duke-NUS Medical School in Singapore....George Mason University, Manassas, Virginia....American University, Washington, D.C.’
 
The first adenovirus ever isolated from a North American bat was the Jan 2017 report from Kentucky:
 
Speculation is that this report from India is correct: the earliest SARS-CoV-2 ancestor was from a pig rather than a bat.

Dec 2020 India / Zoonotic Evolution
’....The evolutionary tree of SARS-CoV-2 revealed that Porcine Reproductive and Respiratory Syndrome Virus 2 (PRRSV-2), which belongs to the beta Arterivirus genus from the Arteriviridae family is possibly the most ancient ancestral origin of SARS-CoV-2 and other Coronaviridae.’

Minnesota now being the U.S. hotspot for the Delta variant, links to Minnesota PRRSV:

Ap 1992 University of Minnesota Department of Veterinary Diagnostic Medicine
’A syndrome of reproductive failure and respiratory disease of unknown etiology was first recognized in 1987-1988 in swine herds in North Carolina, Iowa, and Minnesota. A similar syndrome has been recognized in Germany, The Netherlands, England, Belgium, and Spain.’

1989 Indiana: PRRSV Outbreak
’....An outbreak of Porcine Reproductive and Respiratory Syndrome (PRRS), formerly called swine infertility and reproductive syndrome or mystery swine disease, occurred on 18 farms in Wabash County, Indiana, in spring of 1989. An extensive diagnostic investigation conducted at Purdue Animal Disease Diagnostic Laboratory and diagnostic testing at a number of other laboratories did not result in a conclusive etiologic diagnosis.’

’Retrospective serological studies indicate that PRRSV first appeared in North America in 1979, in Asia in 1985, in Europe in 1987, and the virus was subsequently disseminated to swine populations throughout the world. PRRSV is most similar genetically to LDV (lactate dehydrogenase-elevating virus).’
(MacLachlan NJ, et al, Arterivirus Pathogenesis and Immune Response, Ch. 21, Nidoviruses, ASM Press, Washington, D.C. 2008)
 

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