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Role of spike in the pathogenic and antigenic behavior of SARS-CoV-2 BA.1 Omicron.

Da-Yuan ChenDevin KenneyChue Vin ChinAlexander H TavaresNazimuddin KhanHasahn L ConwayGuanQun LiuManish C ChoudharyHans P GertjeAoife K O'ConnellDarrell N KottonAlexandra HerrmannEnsser ArminJohn H ConnorMarkus BosmannJonathan Z LiMichaela U GackSusan C BakerRobert N KirchdoerferYachana KatariaNicholas A CrosslandFlorian DouamMohsan Saeed
Published in: bioRxiv : the preprint server for biology (2022)
The recently identified, globally predominant SARS-CoV-2 Omicron variant (BA.1) is highly transmissible, even in fully vaccinated individuals, and causes attenuated disease compared with other major viral variants recognized to date 1-7 . The Omicron spike (S) protein, with an unusually large number of mutations, is considered the major driver of these phenotypes 3,8 . We generated chimeric recombinant SARS-CoV-2 encoding the S gene of Omicron in the backbone of an ancestral SARS-CoV-2 isolate and compared this virus with the naturally circulating Omicron variant. The Omicron S-bearing virus robustly escapes vaccine-induced humoral immunity, mainly due to mutations in the receptor-binding motif (RBM), yet unlike naturally occurring Omicron, efficiently replicates in cell lines and primary-like distal lung cells. In K18-hACE2 mice, while Omicron causes mild, non-fatal infection, the Omicron S-carrying virus inflicts severe disease with a mortality rate of 80%. This indicates that while the vaccine escape of Omicron is defined by mutations in S, major determinants of viral pathogenicity reside outside of S.
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