Author:
Muruato Antonio,Vu Michelle N.,Johnson Bryan A.,Davis-Gardner Meredith E.,Vanderheiden Abigail,Lokugmage Kumari,Schindewolf Craig,Crocquet-Valdes Patricia A.,Langsjoen Rose M.,Plante Jessica A.,Plante Kenneth S.,Weaver Scott C.,Debbink Kari,Routh Andrew L.,Walker David,Suthar Mehul S.,Xie Xuping,Shi Pei-Yong,Menachery Vineet D.
Abstract
AbstractThe emergence of SARS-CoV-2 has resulted in a worldwide pandemic causing significant damage to public health and the economy. Efforts to understand the mechanisms of COVID-19 disease have been hampered by the lack of robust mouse models. To overcome this barrier, we utilized a reverse genetic system to generate a mouse-adapted strain of SARS-CoV-2. Incorporating key mutations found in SARSCoV-2 variants, this model recapitulates critical elements of human infection including viral replication in the lung, immune cell infiltration, and significant in vivo disease. Importantly, mouse-adaptation of SARS-CoV-2 does not impair replication in human airway cells and maintains antigenicity similar to human SARS-CoV-2 strains. Utilizing this model, we demonstrate that SARS-CoV-2 infected mice are protected from lethal challenge with the original SARS-CoV, suggesting immunity from heterologous CoV strains. Together, the results highlight the utility of this mouse model for further study of SARS-CoV-2 infection and disease.
Publisher
Cold Spring Harbor Laboratory
Cited by
14 articles.
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