Abstract
We report that severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Delta spike mutation P681R plays a key role in the Alpha-to-Delta variant replacement during the coronavirus disease 2019 (COVID-19) pandemic. Delta SARS-CoV-2 efficiently outcompetes the Alpha variant in human lung epithelial cells and primary human airway tissues. The Delta spike mutation P681R is located at a furin cleavage site that separates the spike 1 (S1) and S2 subunits. Reverting the P681R mutation to wild-type P681 significantly reduces the replication of the Delta variant to a level lower than the Alpha variant. Mechanistically, the Delta P681R mutation enhances the cleavage of the full-length spike to S1 and S2, which could improve cell-surface-mediated virus entry. In contrast, the Alpha spike also has a mutation at the same amino acid (P681H), but the cleavage of the Alpha spike is reduced compared with the Delta spike. Our results suggest P681R as a key mutation in enhancing Delta-variant replication via increased S1/S2 cleavage.
Original language | English (US) |
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Article number | 110829 |
Journal | Cell Reports |
Volume | 39 |
Issue number | 7 |
DOIs | |
State | Published - May 17 2022 |
Keywords
- CP: Microbiology
- Delta variant
- S1/S2 cleavage
- SARS-CoV-2
- fitness
- human airway culture
- spike P681R
- viral entry
ASJC Scopus subject areas
- General Biochemistry, Genetics and Molecular Biology