COVID-19’s Biological Politics

Infectious SV40 survived the vaccine inactivation treatments, and conservative estimates indicate that up to 30 million people (children and adults) in the United States may have been exposed to live SV40 from 1955 through 1963 when administered potentially contaminated polio vaccines


ah!
~S~
Yes, SV40 was not killed by the formaldehyde used in the polio vaccine:
 
Trying another URL:
childrenshealthdefense.org/defender/chimpanzees-children-origins-respiratory-synctial-virus/

To retrieve the RSV article in post #2,284, click on that URL (search) and type either 'coryza' or 'rsv'....the article is titled, From Chimpanzees to Children.

Mason-Pfizer virus (#2,284) is a retrovirus, SV40 is a polyomavirus, so comparisons must find some commonality. As will be shown, the coronavirus link is the synctial link between the two:

(1978) Mason-Pfizer / SV40 / Synctia Formation
The entire article is not available at Pubmed, so a search elsewhere may retrieve it.


It's much more interesting. Chloroquine and the furin cleavage site are implicated.
 
The RSV article @ Childrenshealthdefense.org is historically quite comprehensive. RSV is (Pneumoviridae), and to properly compare, the addition of Nipah (Paramyxoviridae) and ebola (Filoviridae) (all three are Mononegavirales) must be included for this investigative trajectory that links furin and chloroquine, one that shows why hydroxychloroquine may not be effective regardless of the time-window of administration. As Dr. Quay has said, Nipah is 60 times more dangerous than SARS2.
 
Most recent, US Right to Know:

6 Dec 2023 Visual Timeline
 
SV40, continued

Nov 2023
'....A Pfizer spokesperson: " specific, non-infectious parts of the SV40 sequence, which are commonly used in the pharmaceutical industry are present in starting material used by Pfizer and BioNTech," '
 
Unlike Kory's X, Kory's Rumble is current and the comments can be seen:

Pierre Kory, Spike Protein Shedding
 
Synctium Formation in Coronaviruses

It's easy to see why GoF experiments would focus on the furin cleavage site.

'Of all natural MHV (mouse hepatitis virus) isolates, MHV-2 is the only strain with an uncleaved spike protein. Isolated mutants of MHV-2, which, in contrast to the parental virus, were capable of inducing synctium formation, appeared to have acquired this ability through a single mutation restoring an apparently lost cleavage site.
....
Interestingly, mutants of MHV-2 carrying a proper furin cleavage site appeared to have lost their sensitivity both to lysosomotropic agents (ex., chloroquine) and to cathepsin inhibitors.'
(Bosch and Rottier, Nidovirus Entry Into Cells, in Nidoviruses, ASM Press, 2008)

Virus entry into cells can be promoted by inhibition of such things as chloroquine and leupeptin. Thus, synctium formation does link to the absence and presence of furin cleavage sites, which target the S1-S2 junction.

If the reader understands the next paragraph, they will have gained much insight into GoF experiments, hydroxychloroquine and furin cleavage sites.

'As this cleavage induces cell-cell fusion, it is conceivable that cathepsin L also targets the Si-S2 junction. This is consistent with the already-mentioned rescue of SARS-CoV entry inhibition by leupeptin and lysosomotropic agents (ex., chloroquine) by trypsin treatment of cell-bound virions, as well as with the formation of synctia in SARS-CoV spike protein-expressing cells and in MHV-2-infected cells that is observed after introduction of a furin cleavage site at the S1-S2 junction of these spike proteins.
....
One might argue that all spike proteins, including those of group 1 coronaviruses, originally contained a furin cleavage site. Spike protein cleavage during biogenesis might have been unfavorable for some coronaviruses, as it could lead to spike inactivation through S1-S2 dissociation.

Viruses with uncleaved spikes might thus have benefitted somehow from the loss of furin cleavage. This idea is supported by the presence of what has been suggested to be a vestigial furin cleavage site (DRTRG) approximately in the middle of the TGEV spike protein.'
(ibid.)

This last statement is noteworthy considering the RGD motif of Dr. Quay's Twitter page showing the Chinese military virus, ZC45. TGEV is the pig coronavirus that can subsist on stainless steel surfaces and remain viable for up to 28 days. For the RGD motif, see this thread, post #2,288.
(USMB search 'rgd motif')
 
Hunter Biden's Metabiota and Pig Viruses

Previous posts have laid the foundation for further scrutiny of Metabiota's PEDV virus collected in Laos. This is the virus that was GoF manipulated by the Chinese @ the Huazhong lab.

In the previous post, 'Viruses with uncleaved spikes might thus have benefitted somehow....' continues:

'Viruses like this might have become furin protease independent while becoming dependent on the extracellular environment or after endocytosis, an adjustment might also have occurred to MHV-2 and SARS-CoV.

Similarly, the spike protein of porcine epidemic diarrhea virus (PEDV; strain CV777), a group 1 coronavirus, lacks the minimal furin recognition sequence in its ectodomain, yet the protein was found in a cleaved form in the gut of infected pigs.'
(Nidoviruses, Ch. 11)

This is the Huazhong lab and its GoF experiment on the Metabiota virus, PEDV:

PEDV / Furin
 
Hanson and Quay, a 1 hour podcast on origins, lockdowns and vaccines. @6:10: 'Fauci will testify in January.'
 
Points in the podcast:

8:01 Scott Atlas, lockdowns

8:40 Stanford faculty senate voted to censor Atlas

10:55 Oxford epidemiologist Neil Ferguson (in W C-U, RFK Jr. mentions Ferguson on p. 360-1, 363,367,382 & 447)
 
Podcast timepoint 39 m 30 s, furin cleavage site "tunnel" military lateral invasion
 
Podcast timepoints
45 m 15 s, 14 Feb 2020, 80,000 Chinese and those under 20 yrs

51 m WHO and law

52 m 45 s tracking the human
 
So in Jardine's comments and replies above, there is a NASA link to shedding (see this thread, post #2,307).
 
In the VAERS video, the term "throttling" comes up at timepoint 21 minutes 50 seconds. This concept is comparable to Musk's fascist machine on X, which we have already described, an ahistorical "wax museum" type of mechanism.
 

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