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Delta spike P681R mutation enhances SARS-CoV-2 fitness over Alpha variant
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 epitheli...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Authors.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050581/ https://www.ncbi.nlm.nih.gov/pubmed/35550680 http://dx.doi.org/10.1016/j.celrep.2022.110829 |
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author | Liu, Yang Liu, Jianying Johnson, Bryan A. Xia, Hongjie Ku, Zhiqiang Schindewolf, Craig Widen, Steven G. An, Zhiqiang Weaver, Scott C. Menachery, Vineet D. Xie, Xuping Shi, Pei-Yong |
author_facet | Liu, Yang Liu, Jianying Johnson, Bryan A. Xia, Hongjie Ku, Zhiqiang Schindewolf, Craig Widen, Steven G. An, Zhiqiang Weaver, Scott C. Menachery, Vineet D. Xie, Xuping Shi, Pei-Yong |
author_sort | Liu, Yang |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-9050581 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Authors. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90505812022-04-29 Delta spike P681R mutation enhances SARS-CoV-2 fitness over Alpha variant Liu, Yang Liu, Jianying Johnson, Bryan A. Xia, Hongjie Ku, Zhiqiang Schindewolf, Craig Widen, Steven G. An, Zhiqiang Weaver, Scott C. Menachery, Vineet D. Xie, Xuping Shi, Pei-Yong Cell Rep Report 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. The Authors. 2022-05-17 2022-04-29 /pmc/articles/PMC9050581/ /pubmed/35550680 http://dx.doi.org/10.1016/j.celrep.2022.110829 Text en © 2022 The Authors Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Report Liu, Yang Liu, Jianying Johnson, Bryan A. Xia, Hongjie Ku, Zhiqiang Schindewolf, Craig Widen, Steven G. An, Zhiqiang Weaver, Scott C. Menachery, Vineet D. Xie, Xuping Shi, Pei-Yong Delta spike P681R mutation enhances SARS-CoV-2 fitness over Alpha variant |
title | Delta spike P681R mutation enhances SARS-CoV-2 fitness over Alpha variant |
title_full | Delta spike P681R mutation enhances SARS-CoV-2 fitness over Alpha variant |
title_fullStr | Delta spike P681R mutation enhances SARS-CoV-2 fitness over Alpha variant |
title_full_unstemmed | Delta spike P681R mutation enhances SARS-CoV-2 fitness over Alpha variant |
title_short | Delta spike P681R mutation enhances SARS-CoV-2 fitness over Alpha variant |
title_sort | delta spike p681r mutation enhances sars-cov-2 fitness over alpha variant |
topic | Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050581/ https://www.ncbi.nlm.nih.gov/pubmed/35550680 http://dx.doi.org/10.1016/j.celrep.2022.110829 |
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