COVID-19 Records

Slack / Private Message Drop — page 1015

of 1123 pages · Bates SLACK_001229

← p.1014 p.1016 → · this page in the original PDF · package

[2021-10-04 13:29:05] [Kristian Andersen] His "About" page is undoubtedly quite helpful to get the health and safety exemption: https://disinformationchronicle.substack.com/about?utm_source=menu-dropdown [shared file(s): Screen Shot 2021-10-04 at 13.28.06.png] [2021-10-04 13:31:13] [Eddie Holmes] Yes, he's already accused me of conflicts. He's an arse [2021-10-04 13:34:43] [Kristian Andersen] Arse, yes - and exceptionally dumb. [2021-10-05 14:59:37] [Robert Garry] So, I'm taking another look at the BANAL-20-50 virus. To be honest I'm starting to think that this is even more than a smoking gun. The BANAL-20-50 nucleoprotein is *99.3%* similar to SARS2 Wu-1 at the amino acid level - that 's 3 amino acids in an approximately 400 amino acid protein. The BANAL-20-50 spike is *98.4%* similar to SARS2 Wu-1 at the amino acid level, including the PRRA insert. The long 1ab and 1a polyproteins are pretty much the same story ~98% identical [there is a 9 amino acid insertion in nsp3 - don't hold me to that] in SC2 relative to BANAL-20-50. At least at the amino acid level BANAL-20-50 is SARS-CoV-1.98. [2021-10-05 15:03:48] [Eddie Holmes] Thanks Bob. So where does BANAL-20-50 differ most from SC2? [2021-10-05 15:09:10] [Kristian Andersen] Yes. These viruses are about as far from banal as can be... [2021-10-05 15:18:20] [Robert Garry] Not anywhere that I can see at least at the amino acid level. All of the proteins I've looked at so far are very very similar. Just looking at the proteins, you would really be hard pressed to call this a different virus species IMO. I'm guessing that most of the nt changes are third base changes (codon usage). [2021-10-05 15:37:56] [Robert Garry] From the paper - I think most of that minor orf3a difference is the 9 aa indel. [shared file(s): image.png] [2021-10-05 16:09:26] [Robert Garry] https://www.science.org/doi/10.1126/science.1092002?url_ver=Z39.88-2003&rfr_id=ori:rid:crossref.org&rf r_dat=cr_pub%20%200pubmed Between the coronavirus sequences of the palm civets (SZ3 or SZ16) and each of the human SARS-CoV sequences, the ratios of the rates of nonsynonymous to synonymous changes (Ka/Ks) for the S gene sequences were always greater than 1, indicating an overall positive selection pressure. However, pairwise analysis of the Ka/Ks for the genotypes in each epidemic group (fig. S6) (_14_) shows that the average Ka/Ks for the early phase was significantly larger than that for the middle phase, which in turn was significantly larger than the ratio for the late phase, which in fact was significantly less than 1 (table S3). These data indicate that the S gene showed the strongest positive selection pressures initially, with subsequent purifying selections and eventual stabilization. For Orf1a, we observed a pattern similar to that for the S gene (table S3). In contrast, Orf1b (nt coordinate: 13,398 to 21,485) seems to be undergoing purifying selection during the whole course of the epidemic. Indeed, it is the most conserved genomic region of SARS-CoV (_7_). [2021-10-05 16:11:36] [Robert Garry]

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Records on this page

RecordDateTypePages
slack_pm:msg:10595 2021-10-04 chat message 1015
slack_pm:msg:10596 2021-10-04 chat message 1015
slack_pm:msg:10597 2021-10-04 chat message 1015
slack_pm:msg:10598 2021-10-05 chat message 1015
slack_pm:msg:10599 2021-10-05 chat message 1015
slack_pm:msg:10600 2021-10-05 chat message 1015
slack_pm:msg:10601 2021-10-05 chat message 1015
slack_pm:msg:10602 2021-10-05 chat message 1015
slack_pm:msg:10603 2021-10-05 chat message 1015
slack_pm:msg:10604 2021-10-05 chat message 1015–1016