Back to Search Start Over

The mutation features and geographical distributions of the surface glycoprotein (S gene) in SARS-CoV-2 strains: A comparative analysis of the early and current strains

Authors :
Liu, Rang
Lin, Xinran
Chen, Bing
Hou, Zhenhui
Zhang, Qiuju
Lin, Shouren
Geng, Lan
Sun, Zhongyi
Cao, Canhui
Shi, Yu
Xia, Xi
Liu, Rang
Lin, Xinran
Chen, Bing
Hou, Zhenhui
Zhang, Qiuju
Lin, Shouren
Geng, Lan
Sun, Zhongyi
Cao, Canhui
Shi, Yu
Xia, Xi
Publication Year :
2022

Abstract

The surface glycoprotein (S protein) of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was used to develop coronavirus disease 2019 (COVID-19) vaccines. However, SARS-CoV-2, especially the S protein, has undergone rapid evolution and mutation, which has remained to be determined. Here, we analyzed and compared the early (12 237) and the current (more than 10 million) SARS-CoV-2 strains to identify the mutation features and geographical distribution of the S gene and S protein. Results showed that in the early strains, most of the loci were with relative low mutation frequency except S: 23403 (4486 strains), while in the current strains, there was a surge in the mutation strains and frequency, with S: 23403 constantly being the highest one, but tremendously increased to approximately 1050 times. Furthermore, D614 (S: 23403) was one of the most highly frequent mutations in the S protein of Omicron as of March 2022, and most of the mutant strains were still from the United States, and the United Kingdom. Further analysis demonstrated that in the receptor-binding domain, most of the loci with low mutation frequency in the early strains, while S: 22995 was nowadays the most prevalent loci with 3 122 491 strains in the current strains. Overall, we compare the mutation features of the S region in SARS-CoV-2 strains between the early and the current stains, providing insight into further studies in concert with emerging SARS-CoV-2 variants for COVID-19 vaccines. © 2022 Wiley Periodicals LLC.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1363079160
Document Type :
Electronic Resource