> To investigate the importance of the spike polybasic CS of SARS-CoV-2 (PRRAR), a number of spike mutants predicted to modulate the efficiency of furin cleavage were generated (Fig. 1a), including: substituting two upstream arginines to produce a monobasic CS similar to SARS-CoV spike (monoCS), replacing the tribasic CS with the furin CS of a highly pathogenic H5N1 avian influenza haemagglutinin containing seven basic amino acids (H5CS) and two naturally occurring deletions seen following passage in Vero E6 cells and/or in clinical isolates21,26. The first deletion removes eight amino acids including all three arginines of the PRRAR site (ΔCS), while the other removes five flanking amino acids but retains the tribasic CS (Δflank). The mutations were engineered into a spike expression plasmid to enable cell surface expression and generation of coronavirus lentiviral PVs. In addition, to study the importance of the PRRAR motif in the context of live virus, we used a naturally occurring Vero-cell-adapted mutant SARS-CoV-2, ΔCS26. This variant and the wild-type (WT) virus from which it was derived were cloned by limiting dilution to enable studies using individual genotypes.
This is the horror of in vitro and in vivo viral lab research and the result is a magnificent advancement of our understanding of SARS-CoV-2, the furin cleavage site, and its role in TMPRSS2 assisted membrane entry. This research follows the equally eye-opening paper covered in TWiV 715 that explained why hydroxychloroquine (HCQ) failed; Vero E6 cells lack TMPRRS2 so HCQ fully blocks entry via endocytosis. It should be noted that this study includes MERS-CoV which also has a furin cleavage site; falsifying one of the claims of Wade's article.
Regardless, lab experiments begin with one or more viral isolates and molecular clock techniques should show that the original Wuhan variant has almost identical non-coding genome segments compared to existing lab isolates. The RaTG13 sequence is a very distant relative using this measure. Also, RaTG13 is not an isolate, only an RNA sample collected in wild bat anal swabs. Conflating viral isolates with RNA samples seems to be a common error; an entry in a genetic database does not imply that a viable viral line exists in a lab. A RaTG13 lab isolate would have been an important achievement to further our scientific understanding.
I'm confused by the dismissals of the natural origins hypothesis. The horseshoe bat roosts, that are studied, are mostly found in or near Kunming, Yunnan. This lush wild area is part of the Lancang/Mekong River watershed/ecosystem shared by nocturnal bats and nocturnal arboreal mammals like palm civets, pangolins, and raccoon dogs. The nearby villages contain people engaged in guano collection, the wildlife trade, and domestic livestock farming.
The average incubation time of COVID-19 is 4.5 days. Armed with Google maps and a basic understanding of planes, trains, and automobiles we can gauge travel time from Kunming Airport to either Wuhan Tianhe International Airport (2 hr 5 min) or Guangzhou Baiyun International Airport (2 hrs). In 2003, SARS-1 emerged in Guangzhou (near Hong Kong) and the now demonized Dr. Zheng-li Shi and her team traced the origins to palm civets (the intermediate host). Why is this so hard? Why do we not ridicule the assumption that travel between major Chinese transportation hubs must leave a wake of infections along the path?
Finally, Wade's article mentions a U.S. State Department claim [2]:
> The U.S. government has reason to believe that several researchers inside the WIV became sick in autumn 2019, before the first identified case of the outbreak, with symptoms consistent with both COVID-19 and common seasonal illnesses.
If true, this is an important early super-spreader event but the remainder of the release consists of a facile analysis performed by people more knowledgeable in geopolitics than science.
[1] https://www.nature.com/articles/s41564-021-00908-w
[2] https://2017-2021.state.gov/fact-sheet-activity-at-the-wuhan...