Many coronaviruses including MERS have a furin cleavage site and they're common and likely evolved independently multiple times, showing that this acquisition of an FCS is common:
https://www.sciencedirect.com/science/article/pii/S187350612...
The FCS in SARS-CoV-2 is NSPRRAR, we now know of sarbecoviruses like like the BANAL viruses in Laos which have NSPAAR, some other viruses like RmYN02 have NSPAAR or NSPVAR. If you insert an R into the BANAL spike protein you get the SARS-CoV-2 FCS.
https://www.nature.com/articles/d41586-021-02596-2
https://www.biorxiv.org/content/10.1101/2021.01.26.428212v1
Finding bat sarbecoviruses which are one insertion away from having the original FCS really blows a gaping hole in this whole idea that the FCS is some kind of smoking gun.
Delta has P681R and Omicron has P681H mutations in the FCS region which may be behind why they're more infectious/transmissible. So the FCS is also still evolving and adapting to humans.
It's if you line up the related bat coronaviruses sequences they are all much the same in that region apart from Sars-Cov-2 which seems to have a clean insert of a PRRA sequence.
Hence the "bothered by the furin site and has a hard time (to) explain that as an event outside the lab, though there are possible ways in nature but highly unlikely." in the article. If it had got there through evolution you'd expect the adjacent sequences to vary more.
This kind of thing https://media.springernature.com/lw685/springer-static/image...
That is from:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7211627/#mmc1
Specifically the lower bit of figure 2:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7211627/figure/...
If RmYN02 picks up the QTQT sequence from recombination with other bat coronaviruses (or RmYN02 is a deletion away from a common progenitor we haven't found yet -- and the QTQT deletion is seen in SARS-CoV-2 variants in humans) then it is one insertion away from PRAAR which would be an active FCS, which is then one substitution away from the PRRAR SARS-CoV-2.
There is this very hilarious paper where they talk about this, but also rejigger the phylogenetic trees without describing how they pick what to put in and hide from the trees, e.g. they overload "trivially similar" sequences that happen to have furin cleavage sites, and then there are diagrams where they omit entire huge families of coronaviruses that don't contain the furin cleavage site to "lie to you with pictures" that the furin cleavage site is more common than it actually is.
Currently, it seems most helpful in aggregating some of the arguments folks put forth in examining claims, including describing the basic issues and linking some references. Plus it seems to offer some insight into what folks are thinking.
Then from an academic perspective, I really like the sort of approach that they're trying to use. A well-developed implementation of that general approach would seem like it could be awesome.
That said, dunno if I find their current methodology or numbers too convincing, as far as actual conclusions go.
https://virological.org/t/tackling-rumors-of-a-suspicious-or...