> Within the scientific community, one thing leapt off the page. Wade quoted one of the world’s most famous microbiologists, Dr. David Baltimore, saying that he believed the furin cleavage site “was the smoking gun for the origin of the virus.” Baltimore, a Nobel Laureate and pioneer in molecular biology, was about as far from Steve Bannon and the conspiracy theorists as it was possible to get. His judgment, that the furin cleavage site raised the prospect of gene manipulation, had to be taken seriously.
Furin cleavage sites have evolved and are present in multiple coronaviruses:
- HCoV-OC43 (infects humans)
- HCoV-HKU1 (infects humans)
- MHV-A59
- ChRCoV-HKU24
- BtCoV-ENT
- BtNeCoV-PML-PHE1
- BtCoV-HKU4
- BtCoV-HKU5
- MERS-CoV
- BtHpCoV-Zhejiang2013
- SARS-CoV-2
Phylogenetic analysis suggests that it has evolved independently at least 6 times that we know of.
https://www.sciencedirect.com/science/article/pii/S187350612...
After that article was published a team in Thailand found furin cleavage sites in sarbecoviruses closely related to SARS-CoV-2 called RacCS203 (91.5% similarity to SARS-CoV-2) and RmYN02 (93.3% similarity to SARS-CoV-2)
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7873279/
Furin cleavage sites are common, nature understands how to utilize that trick very well, and continuously has re-discovered it.
Because per se it does not prove the claim of bioengineering.
You are of course more likely correct about the alignment issue, I can't find my source now, and the above is probably much stronger evidence. For the alignment you'd have to be a virologist, probably one specializing in coronaviruses, to be able to really judge this. Of course a whole bunch of biologists have shifted their focus to coronaviruses in the last year and a half.
The closest genetic match is only 3.8% similar. When it only has 29,903 base pairs, that's 1,136 mutations. I'm no bioscientist but my friends who are tell me that's a lot of changes, and that experiments might change a few base pairs or proteins at a time. A lab leak theory doesn't explain how gain of function study resulted in so many mutations, unless they were blasting these viruses with radiation, and what would be the point of that? Radiation mutations would cause too many changes to do useful science.
Everyone keeps looking at bats but the closest bat coronavorus is 20 years of evolution away. SARS and MERS came from palm covets and dromedary camels respectively, so what's the deal?
Every time I read about this I keep thinking "huh that's sketchy but circumstantial" and I've yet to find an answer to how the lab would've gotten to this point, undiscovered, with no published papers or research or notes or preprints anywhere
Or explicitly creating chimeric coronaviruses, which has been the state of the are for some time. Here's https://pubmed.ncbi.nlm.nih.gov/26552008/ one of the sources of smoke on this, a 2015 paper co-authored by the Bat Woman (2nd to last author), the key sentence from the abstract:
Using the SARS-CoV reverse genetics system, we generated and characterized a chimeric virus expressing the spike of bat coronavirus SHC014 in a mouse-adapted SARS-CoV backbone.
Have you read the fine article? It cites more than a few papers.
The mutations on covid 19 are Really Different compared to the known and studied viruses. If it was a lab leak of an engineered chimera, you'd be able to see that A proteins came from virus X and B proteins came from virus Y and Z, but that hasn't been shown to be the case. From what I understand there are a bunch of smaller mutations across a lot of proteins resulting in something that doesn't really line up with known and studied genomes.
This paper actually goes through and compares the DNA of covid 19 against several other studied viruses: https://www.nature.com/articles/s41579-020-00459-7
So still nothing to point out to bioengineering in my opinion.
I guess I don't find the argument "we can't figure out how to reconstruct SARS-COV-2 from known viruses" very convincing on either side.
Sitting in a cave somewhere implies not being studied, right? Which is more the "natural mutation" thing.
Sitting in some government lab is a different story and depends on belief in scientific institutions to do science and publish peer reviewed papers and all that jazz.
Keep in mind there is an estimated 1.5 million viruses that have not been identified yet. There might very well be a virus in nature which is the 'missing link'.
It doesn't have to be crispr introducing reach mutation.
"But they also reported that it was 96.2% identical to a coronavirus sequence in their possession called RaTG13, which was previously detected in “Yunnan province.” They concluded that RaTG13 was the closest known relative to SARS-CoV-2.
In the following months, as researchers around the world hunted for any known bat virus that might be a progenitor of SARS-CoV-2, Shi Zhengli offered shifting and sometimes contradictory accounts of where RaTG13 had come from and when it was fully sequenced. Searching a publicly available library of genetic sequences, several teams, including a group of DRASTIC researchers, soon realized that RaTG13 appeared identical to RaBtCoV/4991—the virus from the cave where the miners fell ill in 2012 with what looked like COVID-19.
In July, as questions mounted, Shi Zhengli told Science magazine that her lab had renamed the sample for clarity. But to skeptics, the renaming exercise looked like an effort to hide the sample’s connection to the Mojiang mine."
Also, "circumstantial" doesn't mean weak. It means "pertaining to circumstance". For example, the fact that the virus's origins are in the same area as the lab would be circumstantial evidence that it was created in that lab.
Many circumstances can point to a conclusion. Even the phrase "the smoking gun" which has been bandied about in the discussion of this article, is an example of circumstantial evidence. Circumstantial evidence is opposed by direct evidence, which would be eyewitnesses, video/photos of the thing taking place, etc. And eyewitness is actually one of the weakest forms of evidence because memory is faulty. So circumstantial evidence is usually the evidence that convicts a criminal.
To illustrate that, I like to point to my two favorite circumstantial convictions, Hans Reiser and Scott Peterson.
They convicted Scott Peterson based on buying porn, a dye job, and selling cars.
The convicted Hans Reiser of first degree murder of his wife, Nina, despite not even having any direct evidence that she was in fact dead. They only found the body after Reiser himself led them to Nina's body in exchange for pleading guilty to second-degree murder.
A cleaned car, a missing seat, and some books on murder investigations were the evidence they used. Entirely circumstantial. And they deduced that Nina was murdered from those same circumstances.
You don't get there by splicing an ACE2 spike onto an RaTG13 backbone and passing it through a dozen mice. That gives you something that still looks similar to RaTG13 and infects mice.
The ACE2 spike also looks most similar to a previously unknown ACE2-binding spike protein found in malaysian pangolins.
So WIV would have had to have discovered that pangolin spike-protein, kept it secret, spliced it into an RaTG13 backbone, then not used mice but passed it through a species like that had a human-like ACE2 for a decade and millions of animals.
An alternative hypothesis is that Charles Darwin did that experiment.
That does not mean it doesn't exist, just that we haven't found it.
We didn't know of any other sarbecoviruses that had furin cleavage sites, then we found them in bats in Thailand, then the goalposts moved to how this paricular furin cleavage site is weird.
Once a decade passes and we find animals with beta-coronviruses which have the same kinds of furin cleavage sites, I'm sure the goalposts will move again.
That likely did happen, but Charles Darwin was the geneticist that executed the gain of function experiment via serial passage through that many animals.
> Have you read the fine article? It cites more than a few papers.
Yes, i read it. The ability to construct bibliographic references is also a fairly widely-held and unimpressive skill.
>There are several curious features about this insert but the oddest is that of the two side-by-side CGG codons. Only 5 percent of SARS2’s arginine codons are CGG, and the double codon CGG-CGG has not been found in any other beta-coronavirus. https://thebulletin.org/2021/05/the-origin-of-covid-did-peop...
According to the article, the database of sequences for the WIV samples had been deleted before the pandemic became widespread, so there was no way to verify this, but also somewhat suspicious.
>you then do not get SARS-CoV-2 out of passing that through mice, you get a mouse virus. You'd need to pass it serially through something with a human-like ACE2 like minks.
From the article:
>Using the gene-editing technology known as CRISPR, the researchers had engineered mice with humanized lungs, then studied their susceptibility to SARS-CoV-2. As the NSC officials worked backward from the date of publication to establish a timeline for the study, it became clear that the mice had been engineered sometime in the summer of 2019, before the pandemic even started.
So, it's likely they had mice with humanized lung and ACE2 receptors, no?