Growth, detection, quantification, and inactivation of SARS-CoV-2

被引:161
作者
Case, James Brett [1 ]
Bailey, Adam L. [2 ]
Kim, Arthur S. [1 ,2 ]
Chen, Rita E. [1 ,2 ]
Diamond, Michael S. [1 ,2 ,3 ,4 ]
机构
[1] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA
[3] Washington Univ, Sch Med, Dept Mol Microbiol, St Louis, MO 63110 USA
[4] Washington Univ, Andrew M & Jane M Bursky Ctr Human Immunol & Immu, Sch Med, St Louis, MO USA
关键词
Coronavirus; Titration; Plaque assay; Focus-forming assay; Flow cytometry; Virus inactivation; SARS-CoV-2; ACUTE RESPIRATORY SYNDROME; SARS CORONAVIRUS; SPIKE; RECEPTOR; BINDING; PROTEIN;
D O I
10.1016/j.virol.2020.05.015
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Severe acute respiratory syndrome coronavirus (SARS-CoV)-2 is the agent responsible for the coronavirus disease 2019 (COVID-19) global pandemic. SARS-CoV-2 is closely related to SARS-CoV, which caused the 2003 SARS outbreak. Although numerous reagents were developed to study SARS-CoV infections, few have been applicable to evaluating SARS-CoV-2 infection and immunity. Current limitations in studying SARS-CoV-2 include few validated assays with fully replication-competent wild-type virus. We have developed protocols to propagate, quantify, and work with infectious SARS-CoV-2. Here, we describe: (1) virus stock generation, (2) RTqPCR quantification of SARS-CoV-2 RNA; (3) detection of SARS-CoV-2 antigen by flow cytometry, (4) quantification of infectious SARS-CoV-2 by focus-forming and plaque assays; and (5) validated protocols for virus inactivation. Collectively, these methods can be adapted to a variety of experimental designs, which should accelerate our understanding of SARS-CoV-2 biology and the development of effective countermeasures against COVID-19.
引用
收藏
页码:39 / 48
页数:10
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