作者
Jesus A Silvas, Desarey Morales Vasquez, Jun-Gyu Park, Kevin Chiem, Anna Allué-Guardia, Andreu Garcia-Vilanova, Roy Neal Platt, Lisa Miorin, Thomas Kehrer, Anastasija Cupic, Ana S Gonzalez-Reiche, Harm van Bakel, Adolfo García-Sastre, Tim Anderson, Jordi B Torrelles, Chengjin Ye, Luis Martinez-Sobrido
发表日期
2021/8/10
期刊
Journal of Virology
卷号
95
期号
17
页码范围
10.1128/jvi. 00402-21
出版商
American Society for Microbiology
简介
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the viral pathogen responsible for the current coronavirus disease 2019 (COVID-19) pandemic. As of 19 May 2021, John Hopkins University’s COVID-19 tracking platform reported 3.3 million deaths associated with SARS-CoV-2 infection. Currently, the World Health Organization has granted emergency use listing (EUL) to six COVID-19 vaccine candidates. However, much of the pathogenesis observed during SARS-CoV-2 infection remains elusive. To gain insight into the contribution of individual accessory open reading frame (ORF) proteins in SARS-CoV-2 pathogenesis, we used our recently described reverse-genetics system approach to successfully engineer recombinant SARS-CoV-2 (rSARS-CoV-2) constructs; we removed individual viral ORF3a, −6, −7a, −7b, and −8 proteins from them, and we characterized the resulting recombinant …
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