4.4 Article

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

Journal

VIROLOGY
Volume 548, Issue -, Pages 39-48

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.virol.2020.05.015

Keywords

Coronavirus; Titration; Plaque assay; Focus-forming assay; Flow cytometry; Virus inactivation; SARS-CoV-2

Categories

Funding

  1. NIH [75N93019C00062, R01 AI127828]
  2. Defense Advanced Research Project Agency [HR001117S0019]
  3. Helen Hay Whitney Foundation postdoctoral fellowship

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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.

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