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Characterization of SARS-CoV-2 Variants N501Y.V1 and N501Y.V2 Spike on Viral Infectivity

SARS-coronavirus 2 (SARS-CoV-2), pathogen of coronavirus disease 2019 (COVID-19), is constantly evolving to adapt to the host and evade antiviral immunity. The newly emerging variants N501Y.V1 (B.1.1.7) and N501Y.V2 (B.1.351), first reported in the United Kingdom and South Africa respectively, raise...

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Autores principales: Tang, Haijun, Gao, Long, Wu, Zhao, Meng, Fang, Zhao, Xin, Shao, Yun, Shi, Xiaohua, Qiao, Shigang, An, Jianzhong, Du, Xiaohong, Qin, F. Xiao-Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8549493/
https://www.ncbi.nlm.nih.gov/pubmed/34722330
http://dx.doi.org/10.3389/fcimb.2021.720357
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author Tang, Haijun
Gao, Long
Wu, Zhao
Meng, Fang
Zhao, Xin
Shao, Yun
Shi, Xiaohua
Qiao, Shigang
An, Jianzhong
Du, Xiaohong
Qin, F. Xiao-Feng
author_facet Tang, Haijun
Gao, Long
Wu, Zhao
Meng, Fang
Zhao, Xin
Shao, Yun
Shi, Xiaohua
Qiao, Shigang
An, Jianzhong
Du, Xiaohong
Qin, F. Xiao-Feng
author_sort Tang, Haijun
collection PubMed
description SARS-coronavirus 2 (SARS-CoV-2), pathogen of coronavirus disease 2019 (COVID-19), is constantly evolving to adapt to the host and evade antiviral immunity. The newly emerging variants N501Y.V1 (B.1.1.7) and N501Y.V2 (B.1.351), first reported in the United Kingdom and South Africa respectively, raised concerns due to the unusually rapid global spread. The mutations in spike (S) protein may contribute to the rapid spread of these variants. Here, with a vesicular stomatitis virus (VSV)-based pseudotype system, we demonstrated that the pseudovirus bearing N501Y.V2 S protein has higher infection efficiency than pseudovirus with wildtype (WT) and D614G S protein. Moreover, pseudovirus with N501Y.V1 or N501Y.V2 S protein has better thermal stability than WT and D614G, suggesting these mutations of variants may increase the stability of SARS-CoV-2 S protein and virion. However, the pseudovirus bearing N501Y.V1 or N501Y.V2 S protein has similar sensitivity to inhibitors of protease and endocytosis with WT and D614G. These findings could be of value in preventing the spread of virus and developing drugs for emerging SARS-CoV-2 variants.
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spelling pubmed-85494932021-10-28 Characterization of SARS-CoV-2 Variants N501Y.V1 and N501Y.V2 Spike on Viral Infectivity Tang, Haijun Gao, Long Wu, Zhao Meng, Fang Zhao, Xin Shao, Yun Shi, Xiaohua Qiao, Shigang An, Jianzhong Du, Xiaohong Qin, F. Xiao-Feng Front Cell Infect Microbiol Cellular and Infection Microbiology SARS-coronavirus 2 (SARS-CoV-2), pathogen of coronavirus disease 2019 (COVID-19), is constantly evolving to adapt to the host and evade antiviral immunity. The newly emerging variants N501Y.V1 (B.1.1.7) and N501Y.V2 (B.1.351), first reported in the United Kingdom and South Africa respectively, raised concerns due to the unusually rapid global spread. The mutations in spike (S) protein may contribute to the rapid spread of these variants. Here, with a vesicular stomatitis virus (VSV)-based pseudotype system, we demonstrated that the pseudovirus bearing N501Y.V2 S protein has higher infection efficiency than pseudovirus with wildtype (WT) and D614G S protein. Moreover, pseudovirus with N501Y.V1 or N501Y.V2 S protein has better thermal stability than WT and D614G, suggesting these mutations of variants may increase the stability of SARS-CoV-2 S protein and virion. However, the pseudovirus bearing N501Y.V1 or N501Y.V2 S protein has similar sensitivity to inhibitors of protease and endocytosis with WT and D614G. These findings could be of value in preventing the spread of virus and developing drugs for emerging SARS-CoV-2 variants. Frontiers Media S.A. 2021-10-13 /pmc/articles/PMC8549493/ /pubmed/34722330 http://dx.doi.org/10.3389/fcimb.2021.720357 Text en Copyright © 2021 Tang, Gao, Wu, Meng, Zhao, Shao, Shi, Qiao, An, Du and Qin https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular and Infection Microbiology
Tang, Haijun
Gao, Long
Wu, Zhao
Meng, Fang
Zhao, Xin
Shao, Yun
Shi, Xiaohua
Qiao, Shigang
An, Jianzhong
Du, Xiaohong
Qin, F. Xiao-Feng
Characterization of SARS-CoV-2 Variants N501Y.V1 and N501Y.V2 Spike on Viral Infectivity
title Characterization of SARS-CoV-2 Variants N501Y.V1 and N501Y.V2 Spike on Viral Infectivity
title_full Characterization of SARS-CoV-2 Variants N501Y.V1 and N501Y.V2 Spike on Viral Infectivity
title_fullStr Characterization of SARS-CoV-2 Variants N501Y.V1 and N501Y.V2 Spike on Viral Infectivity
title_full_unstemmed Characterization of SARS-CoV-2 Variants N501Y.V1 and N501Y.V2 Spike on Viral Infectivity
title_short Characterization of SARS-CoV-2 Variants N501Y.V1 and N501Y.V2 Spike on Viral Infectivity
title_sort characterization of sars-cov-2 variants n501y.v1 and n501y.v2 spike on viral infectivity
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8549493/
https://www.ncbi.nlm.nih.gov/pubmed/34722330
http://dx.doi.org/10.3389/fcimb.2021.720357
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