Author: Deigin, Yuri; Segreto, Rossana
Title: SARSâ€CoVâ€2′s claimed natural origin is undermined by issues with genome sequences of its relative strains: Coronavirus sequences RaTG13, MP789 and RmYN02 raise multiple questions to be critically addressed by the scientific community Cord-id: dudzx2hh Document date: 2021_5_27
ID: dudzx2hh
Snippet: RaTG13, MP789, and RmYN02 are the strains closest to SARSâ€CoVâ€2, and their existence came to light only after the start of the pandemic. Their genomes have been used to support a natural origin of SARSâ€CoVâ€2 but after a close examination all of them exhibit several issues. We specifically address the presence in RmYN02 and closely related RacCSxxx strains of a claimed natural PAA/PVA amino acid insertion at the S1/S2 junction of their spike protein at the same position where the PRRA ins
Document: RaTG13, MP789, and RmYN02 are the strains closest to SARSâ€CoVâ€2, and their existence came to light only after the start of the pandemic. Their genomes have been used to support a natural origin of SARSâ€CoVâ€2 but after a close examination all of them exhibit several issues. We specifically address the presence in RmYN02 and closely related RacCSxxx strains of a claimed natural PAA/PVA amino acid insertion at the S1/S2 junction of their spike protein at the same position where the PRRA insertion in SARSâ€CoVâ€2 has created a polybasic furin cleavage site. We show that RmYN02/RacCSxxx instead of the claimed insertion carry a 6â€nucleotide deletion in the region and that the 12â€nucleotide insertion in SARSâ€CoVâ€2 remains unique among Sarbecoviruses. Also, our analysis of RaTG13 and RmYN02's metagenomic datasets found unexpected reads which could indicate possible contamination. Because of their importance to inferring SARSâ€CoVâ€2′s origin, we call for a careful reevaluation of RaTG13, MP789 and RmYN02 sequencing records and assembly methods.
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