Yuri Deigin Profile picture
Mar 5, 2021 13 tweets 4 min read Read on X
1/12

Ok, here goes nothing. Remember this little thing called a furin cleavage site? You know, the one that made SARS2 into a real promiscuous little virus? Well, as some have pointed out before, the strategy of inserting a furin cleavage site was not only
2/12

investigated by coronavirologists previously as a tool to expand virus tropism, but also by other virologists as a tool to actually ATTENUATE a virus. In other words, a vaccine strategy.

Getting goosebumps yet? I am.
3/12

So how could this be a vaccine strategy? Well, the idea, as I understand it, was to take a virus, insert some FCSs into it in key places, but do so in a cell culture that do NOT normally have furin, and thus the virus won’t get cut in such cells. But then if you infect
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an animal with such virus, it will get into the cells, trigger an immune reaction which will produce antibodies, but the virus won’t be able to effectively replicate because the newly created virus proteins will get diced up by furin that is well present in animal cells.
5/12

Sounds great on paper, doesn’t it?

So what’s a good place to insert a new FCS in a coronavirus that won’t affect it too much? I mean, you need the virus to remain viable in culture and infective enough to get into cells. So, any obvious candidate spots?
6/12

Oh, oh, I know! Why not insert it in the Spike, at the spot where other CoVs have one natively, but none of the SARS-like CoVs do? They must not have one for a reason, right? It probably makes them non-viable or something – there’s gotta be evolutionary pressure against it.
7/12

Oh, oh, you know what else we can do to make our vaccine safer? It seems that if we have a polybasic cleavage site like RxRR, then furin normally cuts after RR. So And that is where other proteases normally cleave the S1/S2 junction, even without a FCS –
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after the R already present at the junction. But what if we insert not RxRR, but RRxR? Would that maybe change the cleavage direction, leaving S2 with a little xRR overhang and thus interfering with its membrane fusion and attenuating it further? Worth a try.
9/12

Ok, let’s do a literature search on FCS insertion into viruses. Oh look, there is a 2013 Chinese paper whose authors have done so – they inserted RIRR into their construct. Image
10/12

Oh, look, there’s CGG coding for the first R. Where did I see it before? Hmm Oh right, in SARS2 where RRAR is coded by CGG CGG GCA CGT.

ncbi.nlm.nih.gov/pmc/articles/P… Image
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Btw, one of the authors of that paper, Shibo Jiang, has subsequently co-authored a paper in 2015 with Shi Zhengli and Ralph Baric on – guess what – the role of FCS in the tropism of CoVs:

jvi.asm.org/content/89/17/… Image
12/12

Waaaait a second. So could it be that SARS2 is an undercooked bat virus vaccine candidate that has escaped from a lab??? You know, like that time in 1977 when a temperature-sensitive H1N1 vaccine candidate escaped from a lab and caused a global pandemic?

Holy shit. 💣💥
Oh crap, seems I forgot to mention this nice little patent that I was pointed to by @nicholsonbaker8:

patentimages.storage.googleapis.com/f9/34/81/515c1… Image

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More from @ydeigin

Dec 18
🧵 Covid Origins: Lab leak critics claim the coincidence of a novel coronavirus emerging near the Wuhan Institute of Virology is dwarfed by the “counter-coincidence” of it first being noticed at a wildlife market. But the market was actually one of the most likely places for a lab-leaked virus to get noticed.

Here’s a clip from my podcast with @robertwrighter and a deep dive in the thread below:
Basically, if we imagine the map of Wuhan as a “probability landscape”, where each location has an inherent probability that a roaming lab-leaked virus would get noticed if it got there, the Huanan seafood market would dominate that landscape like Mount Everest.
Now, let’s walk through the thought experiment: How would a lab-leaked virus get noticed in Wuhan in late 2019?
Read 16 tweets
Nov 29
Some critics of the Covid lab leak hypothesis say the SARS2 furin cleavage site is unlikely to have been engineered because in previous cases of creating novel FCSes in coronaviruses virologists have never inserted an FCS but rather created them in place via point mutations. But!
A close collaborator of Zhengli Shi and the Wuhan Institute of Virology, Shibo Jiang, in 2013 published a paper creating a furin cleavage site in a non-CoV synthetic vector via a 12-nt insertion (note the CGG codon for the leading arginine): Image
In 2016-17, WIV has created a novel reverse genetics system ("backbone") for the WIV1 virus, and Shibo Jiang subsequently coauthored a paper with Lei-Ping Zeng, the author of that backbone. (Lanying Du, another key collaborator of both WIV and Shibo Jiang, was also on the paper. She was also the editor for the 2013 paper inserting the RIRR FCS):

pmc.ncbi.nlm.nih.gov/articles/PMC70…
Read 20 tweets
Jul 13
🚀 More amazing partial reprogramming news! This time from @davidasinclair — he mentioned some unpublished animal results for:

- *reversing* Alzheimer’s symptoms
- hearing loss
- ALS
- glaucoma (anticipating clinical trials in 2025!)
- rejuvenating skin, kidneys and liver
Great to hear that the FDA is ok with Tet-inducible (via rtTA3) partial reprogramming gene therapies, and that Life Bio is so close to the clinic. They presented encouraging results in monkeys in an eye stroke model (NIAON); I didn’t know they also tried a glaucoma monkey model.


Image
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PS: while Life Bio seems closest to human clinical trials among partial reprogramming companies, others aren’t far behind:

- Turn Bio with their skin therapy
- we at YouthBio with our Alzheimer’s therapy
Read 6 tweets
May 8
🧵 I wrote a new Medium article about how Ralph Baric's January 2024 testimony provides new insights into the origins of COVID-19. Check out the article here:

yurideigin.medium.com/why-ralph-bari…
2/
Highlights:

- Ralph Baric confirmed that DEFUSE proposed inserting novel furin cleavage sites into live viruses, inspired by feline coronaviruses
- SARS-CoV-2’s furin cleavage sites is identical to the one found in several lethal feline coronavirus strains
- Ralph Baric strongly believes WIV had unpublished viruses and viral reverse genetics systems
- Most plausible Covid origin is the result of research on identifying new SARS-like viruses and developing broad vaccines against them
3/
Quick Summary:

Ralph Baric’s January 2024 testimony provided crucial insights into the DEFUSE grant proposal, a collaborative project involving EcoHealth and the Wuhan Institute of Virology (WIV), and the research interests of WIV prior to the Covid outbreak. The pre-Covid landscape of coronavirology research saw intense US-China collaboration aimed at creating broad-spectrum vaccines for SARS- and MERS-like viruses. Key players like Baric, along with researchers Lanying Du, Yusen Zhou, Fang Li, and Shibo Jiang, focused on overcoming challenges such as antibody-dependent enhancement (ADE). By 2018–2019, as collaboration between Baric and his counterparts shifted, WIV became central in SARS-like virus research.

Drawing on Baric’s testimony, I argue that the emergence of SARS-CoV-2 in Wuhan wasn’t coincidental but a likely result of research at WIV. In particular, I outline how WIV researchers, after a post-2018 shift in focus, concentrated on identifying SARS-like viruses with spike proteins 10–25% different from SARS1, capable of evading SARS1-based antibodies, and potentially causing ADE. They were plausibly inspired by Baric’s ideas on furin cleavage sites and his work with Fang Li on SARS and MERS spike cleavage, leading them to engineer furin cleavage sites into novel SARS-like strains. Baric’s testimony suggests that feline coronaviruses inspired this suggestion, and the identical furin cleavage sites in lethal feline coronavirus strains and SARS-CoV-2 strongly indicate that the WIV could have inserted such a site into a SARS-CoV-2 precursor to extend their research from MERS to novel SARS-like coronaviruses. This suggests the emergence of SARS-CoV-2 was not a coincidence but a potential result of this focused research.
Read 39 tweets
May 2
I was curious to hear Peter Dazsak mention at the @COVIDSelect hearing that prior to the Covid outbreak, he actually met with Dr. (Yi-Gang) Tong who was working on a SARS-like CoV found in pangolin samples. In his Feb 2020 paper, Dr. Tong mentions that they isolated this virus long before the outbreak and routinely cultured it at BSL2. More info in the thread below.

PS: Daszak erroneously claiming in 2020
that WIV didn’t have live bats goes to show that he could well be unaware of what other research relevant to Covid origins WIV was engaged in.
While Dr. Tong's lab is in Beijing, he did collaborate with WIV and EcoHealth previously, e.g. in 2018 on a SADS-CoV paper titled "Fatal swine acute diarrhoea syndrome caused by an HKU2-related coronavirus of bat origin":

pubmed.ncbi.nlm.nih.gov/29618817/
But I am more intrigued about the collaboration between Yi-Gang Tong and Yusen Zhou, the author of the Feb 2020 Covid vaccine patent who died a few months later under mysterious circumstances. They both hail from the same "State Key Laboratory of Pathogen and Biosecurity" at the Beijing Institute of Microbiology and Epidemiology. Here is their joint 2016 paper:

ijbs.com/v12p1104.htm
Read 10 tweets
Apr 22
4 years after my first Medium article on Covid origins, I wrote another one. In it, I make the case that SARS-CoV-2 is precisely the virus WIV was hunting for in 2019.



Below is a thread on the key points:yurideigin.medium.com/sars-cov-2-is-…
2/

In 2018, WIV started looking for SARS-like viruses that were 10–25% different from SARS1 in their spike but could still enter human cells, and escape SARS1-based antibodies. SARS2 fits those criteria like a glove.
3/

Moreover, as I will show below, precisely because SARS2 or its BANAL-like progenitor could evade SARS1-based vaccines and antibodies, such strains would have been prioritized and likely turned into full-genome synthetic backbones.
Read 97 tweets

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