BC ALL
Saved by @BillyBostickson

1. The same “gang” of the Proximal Origin paper
https://t.co/Xmp20I58AQ
in action again (only Lipkin is missing, who knows why) to push once more faulty arguments in support of SARS2’s natural

 2. The newly identified Cambodian, Thai and Japan sequences are presented as evidence that some odd features of the SARS2’s genome are natural because present in other natural viruses, as RaTG13 and pangolin CoV were used in The Proximal paper.
3. First the FCS. @ydeigin and I wrote a preprint where we show that the claimed partial FCS insertion in RmYN02 is highly doubtful and the same applies to the new bat CoV sequences
https://t.co/0Goapx6cXj
https://t.co/5Z4Ndca98t
4. They present again only an amino acid biased alignment as in the Zhou paper
https://t.co/i9OZchD4LT
“adjusted by visual inspection” to push their false conclusion that all these CoVs have a partial FCS insertion at the S1/S2 junction and the FCS of SARS2 is therefore natural
5. SARS2 remains the only Sarbecovirus with a functioning FCS, as we describe here:
https://t.co/viqvfzv1Xa
and that can be easily inserted with the Seamless technology.
6. The special RBD of SARS2 was claimed to be natural in The Proximal paper because present in 2 pangolin CoV samples. Now we know we can’t trust those samples
https://t.co/U2qvG3tXBG
7. The new Cambodian CoV shows now a similar RBD claimed to possibly be able to bind to human ACE2, but not yet verified. It should be also demonstrated that this RBD is not the product of cell passage, as supposed to be for pangolin CoV.
https://t.co/cNEwlgtnBb
8. Important to notice that the presence of the QTQTNS motif might be the result of cell passage in presence of TMPRSS2 and Cathepsin
https://t.co/1D7iVZc8Md
9. This motif is often deleted together with the FCS or alone in cell cultures without selection pressure:
https://t.co/GFrrxzCvbq
10. “Notably, the QTQTNS motif near the S1/S2 cleavage site is present in Cambodian bat coronavirus, RaTG13, GD Pangolin coronavirus and SARS-CoV-2. None of these sequences were determined until after the COVID-19 pandemic began.” Exactly, this is very weird.
11. I find alarming that “experts” are retweeting false information from another “expert” to support their conclusions, for example that the QTQTNS motif arose multiple times as proof that SARS2 is natural:
https://t.co/pBF4ZDqNat
12. And even if the Cambodian and the pangolin CoV are natural, what do they show? RaTG13 is still much closer to SARS2. But the cave where it has been collected is not accessible to independently collect and analyse the samples there.
https://t.co/DjbJm40hni
13. Another faulty observation: “On the contrary, SARS-CoV-2 binds efficiently to ACE2 of several animal species thereby invalidating claims that the SARS-CoV-2 RBD was either selected or specifically optimized for human ACE2 binding”.
14. But the binding of SARS2 is still best for human ACE2!
https://t.co/lp9C8vtBWg
https://t.co/viqvfzv1Xa
And of course, after millions of passages in humans the virus can mutate to bind even better than possibly obtained in cell culture or humanized mouse.
15. The best is their conclusion:” Newly sequenced sarbecoviruses from bats captured in Cambodia, Thailand and Japan possess different combinations of spike motifs in the RBD and the S1/S2 junction that were first described in SARS-CoV-2...
16. ..These observations are consistent with the natural origin of SARS-CoV-2 and strongly inconsistent with a laboratory origin.” Not at all, it is still very possible that the FCS of SARS2 has been artificially inserted and the RBD optimized by passage to strongly bind to hACE2
17. I hope to be proven wrong, but I fear to see this shameful preprint published in Nature again. Honestly, these authors should be interrogated. Why are they trying to push so hard a natural origin of SARS2 using faulty arguments?
18. Is this because of the fear of losing grants for their research?:” In this regard there have been suggestions that scientists should stop investigating the diversity of coronaviruses in bats and other animals (Baker, 2021)...
19. ...We contend that the world should do the opposite if we are to be better prepared to prevent the next pandemic of an emergent coronavirus.” Or do they have other reasons?

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Keep dwelling on this:
Further Examination of the Motif near PRRA Reveals Close Structural Similarity to the SEB Superantigen as well as Sequence Similarities to Neurotoxins and a Viral SAg.

The insertion PRRA together with 7 sequentially preceding residues & succeeding R685 (conserved in β-CoVs) form a motif, Y674QTQTNSPRRAR685, homologous to those of neurotoxins from Ophiophagus (cobra) and Bungarus genera, as well as neurotoxin-like regions from three RABV strains

(20) (Fig. 2D). We further noticed that the same segment bears close similarity to the HIV-1 glycoprotein gp120 SAg motif F164 to V174.
https://t.co/EwwJOSa8RK


In (B), the segment S680PPRAR685 including the PRRA insert and highly conserved cleavage site *R685* is shown in van der Waals representation (black labels) and nearby CDR residues of the TCRVβ domain are labeled in blue/white
https://t.co/BsY8BAIzDa


Sequence Identity %
https://t.co/BsY8BAIzDa
Y674 - QTQTNSPRRA - R685
Similar to neurotoxins from Ophiophagus (cobra) & Bungarus genera & neurotoxin-like regions from three RABV strains
T678 - NSPRRA- R685
Superantigenic core, consistently aligned against bacterial or viral SAgs
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2) If you want to study real history contd...

then study Islamic& European history.
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4) He says you hindu people don't have any history coz you people were busy writing about your imaginary Gods.

5 ) He says us to read history books of Romilla Thapar ( hindu hater)

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Students of JNU and overall all the student community. He says Lala Lajpat Rai & all the nationalist politicians of that time were casteist including former President of India Mr Rajendra Prasad.

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a long time. Now what should I do ? Should I stand against them. Should I oppose them ? My inner Hindu does not allow me to tolerate anymore.
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@VIBHU_Tweet
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Scientists of the modern world credit an English scientist John Dalton (1766 CE -1844 CE) for the Atomic Theory.


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First up: JavaScript flavors. There's TypeScript at 47% adoption, a tad higher than npm's own survey results (which said 46%). npm's survey is coming up again soon and will ask about TypeScript in a lot more detail.


I really, *really* like SoJ's "would not use again" question, which lets people who've abandoned a tech self-identify. This is noticeable in the graph above with Flow users -- 41% of people who've used Flow say they wouldn't use it again.

Now JavaScript frameworks. It's been a full year since npm's survey, so these numbers differ from ours in the directions I expected:
React 65% (vs. 60%)
Vue 29% (vs. 24%)
Ember 5% (vs 4%, I was expecting a bigger rise)

But there's a shocker in here: Angular.


npm's survey had Angular at 40% last year and SoJ has it at either:
- 58% (if you include those who don't want to use it again)
- 24% (if you count only those who like it)
Since npm's question didn't ask if they intend to *continue* using it I think that might explain this.
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