Dr Steven Quay Profile picture
Aug 23, 2023 1 tweets 3 min read Read on X
A simplified explanation of SARS-CoV-2 even @hiltzikm can understand, since it is definitely not @elonmusk level rocket science.

1. A Zoonosis is a 3 'body' event: an animal, a microbe (hereafter we'll just say virus), and a human. Study each element to understand the origin.

2. A laboratory-acquired infection a/k/a lab leak, is a singularity: 1 animal, 1 pure virus, 1 human.

3. A natural spillover has diversity: a diversity of animals that are infected, viruses that are cousins of each other, and many humans.

4. A natural spillover has two stages: the first stage is when an animal virus tries to infect a human for the first time. Usually not very successful, asymptomatic infections, since it is coming from an animal host and is not adapted for humans. But it still leaves an immunological record. Then stage two, it is good enough when it infects humans to be able to support human-to-human transmission. An epidemic is now possible.

5. SARS-CoV-2 has all of the hallmarks of a singularity.

6. No animal has ever been found infected with the ancestral virus anywhere in the world. 40,000 tested. In SARS1 and MERS, 90%+ of animals near the first human infections had the virus. While the Wuhan seafood market clearly had animals that could be infected with SARS2, none of them were infected. The environmental specimens which contained SARS2 also contained human genetic material consistent with a human infection. The fact these susceptible animals were there where the virus was circulating but DID not get infected is actually good evidence the market was a human-to-human super spreader event.

7. The virus sequences in natural infections are cousins of each other, since they have been infecting the animal hosts for months or even years. This is called posterior diversity and both SARS1 and MERS had a year or more of posterior diversity as evidence of having been in the animal host.

SARS2 has NO posterior diversity. Every one of the billion human infections can trace its sequence to a single virus, just like a vaccine with respect to sequence purity.

8. Finally, a natural spillover can be detected in stored blood specimens after an antibody test exists for the infection. SARS1 antibodies were found in 20% of market workers and 2-3% of the general population near where it broke out. In >36,000 blood samples from Wuhan, not a single seroconversion as this is called. No evidence of ever having been in humans in the past.

9. Now was it a virus from nature that leaked or an engineered virus? Two facts support engineered.

10. Human-to-human infection was perfected on day 1. Yet there is no evidence in the blood of Wuhan citizens of how it learned to be so good at human cell infection. We know this can be accomplished by serial passage in human cells or mice that have genetically modified lungs to simulate humans.

11. The most important genetic feature that increased infectivity was the furin cleavage site, coded, in part, by a 6 letter code, CGG-CGG. When you examine the genetic diversity of the ancestry of SARS2, the subgenus sarbecovirus, that split from the other betacoronaviruses about 1100 AD, there has never been a furin cleavage site in any related virus in that entire time. There has also never been the use of that same 6 letters to code for an arginine dimer in that entire time either. But the CGG-CGG can be found used routinely in lab engineering.

So two rarities on top of each other: a protein feature never seen, coded by an RNA sequence whose name has never been spoken a/k/a used.

A definite Lord Voldemort moment.

12. Scientists, including from the Wuhan Institute of Virology, wrote a grant proposal before 2019 to actually do steps 10 and 11 above.

This is like looking at the Google search history of a suspected murderer and finding searches for how to hide a murder.

So that's it!

If any of this is confusing or you don't understand it, please drop your comment below.

But if you feel like using foul language @hiltzikm resist the urge:

some people still believe you are a journalist.

• • •

Missing some Tweet in this thread? You can try to force a refresh
 

Keep Current with Dr Steven Quay

Dr Steven Quay Profile picture

Stay in touch and get notified when new unrolls are available from this author!

Read all threads

This Thread may be Removed Anytime!

PDF

Twitter may remove this content at anytime! Save it as PDF for later use!

Try unrolling a thread yourself!

how to unroll video
  1. Follow @ThreadReaderApp to mention us!

  2. From a Twitter thread mention us with a keyword "unroll"
@threadreaderapp unroll

Practice here first or read more on our help page!

More from @quay_dr

Aug 28, 2023
Interesting how the envelope (A) and spike (E) genes of SARS-CoV-2 & RaTG13 but not the membrane or nucleocapsid genes segregate outside all bat CoVs with respect to codon usage?

This is behavior of a synthetic gene, constructed for improved laboratory amplification. Image


Every single bat CoV hates the CGG codon. Every. single. one.

So which bat virus would recombine to make SARS-CoV-2? There isn't one ncbi.nlm.nih.gov/pmc/articles/P…
Image
Let's look at every furin cleavage site in the non-SARS-CoV-2 related viruses. Can we find even one CGG?

No. Image
Read 5 tweets
Oct 20, 2022
Restriction Site Analysis of SARS-CoV-2 demonstrates the signature of a synthetic virus

The likelihood SARS-CoV2 is a natural sarbecovirus is less that one in a billion based on this analysis

Prior publication purposely delayed.
1/10
2/10
Two hypotheses of SARS-CoV-2 origin:
• A spillover from an animal host somewhere outside a laboratory
• A laboratory-related accident

• Finding features within the genome to address these would advance the investigation without requiring the cooperation of third-parties
Read 11 tweets
Jun 13, 2022
1/ Here is a thread of the slides from my recent YouTube video on the evidence against a market origin of SARS-CoV-2. #COVID19 #COVID #SARSCoV #OriginOfCovid
2/
3/
Read 18 tweets
Sep 15, 2021
Facts
1. CoV outbreak near CoV research institute (the John Stewart effect) of CoV found >1000 km to the south in nature but 96% match at WIV
2. No animal from market, city, province, or all of China with CoV. 80,000 tested
3. Single 'Virus Zero' with no posterior diversity
4. No pre-epidemic seroconversion. 9000+ tested
5. Spike Protein S1/S2 furin site never seen before in >1000 sarbecoviruses
6. CCG-CCG codon dimer never seen before in >1000 sarbecoviruses.
7. Recombination across subgenera to solve #5 & #6 either prohibited or rare.
8. RBD pre-adapted w best amino acid, 99.5%: Replacing every 1 of 200 amino acids of receptor binding region (3800 alternative AAs) leads to a poorer RBD.

9. WIV is only place in world combining 'gain-of-opportunity' CoV collection from nature and 'gain-of-function' research
Read 6 tweets
May 27, 2021
For the non-scientist who might be confused by the CoV-2 origin debate, a proper sentence by a scientist has two parts. The first part is the data, the observation; the second part is the conclusion that follows from the data.

Examples: #COVID19
Based on testing 80,000 animals and finding no CoV-2 in any of them, one can conclude from statistics that the prevalence of CoV-2 where the testing was done must be less than 0.0004%.
Given that the zoonoses, SARS1 and MERS, had >85% positive tests in markets, the likelihood CoV-2 is a zoonosis like SARS1 or MERS is less than 1 in a 1,000,000.
Read 4 tweets
Mar 23, 2021
I agree this is not an example of codon optimization for the same reason; it is done over a larger region.

But natural selection in betacoronaviruses has NEVER produced a -CGG-CGG- dimer codon pair. Repeating: there has never been this codon dimer in a coronavirus from nature.
So after scanning 580,000 betacoronavirus codons you suddenly have a -CGG-CGG- cannot be waved away with the 'sh#@' happens hypothesis. Remember, codons have a matching tRNA so putting the two rarest codons together is going to slow/stall transcription.
So we have a functional furin site that has never been seen in a betacoronavirus before that is coded for by a codon dimer that has never been seen before.
Read 7 tweets

Did Thread Reader help you today?

Support us! We are indie developers!


This site is made by just two indie developers on a laptop doing marketing, support and development! Read more about the story.

Become a Premium Member ($3/month or $30/year) and get exclusive features!

Become Premium

Don't want to be a Premium member but still want to support us?

Make a small donation by buying us coffee ($5) or help with server cost ($10)

Donate via Paypal

Or Donate anonymously using crypto!

Ethereum

0xfe58350B80634f60Fa6Dc149a72b4DFbc17D341E copy

Bitcoin

3ATGMxNzCUFzxpMCHL5sWSt4DVtS8UqXpi copy

Thank you for your support!

Follow Us!

:(