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Mouse-adapted SARS-CoV-2 protects animals from lethal SARS-CoV challenge.
Muruato, Antonio; Vu, Michelle N; Johnson, Bryan A; Davis-Gardner, Meredith E; Vanderheiden, Abigail; Lokugamage, 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; Shi, Pei-Yong; Xie, Xuping; Menachery, Vineet D.
  • Muruato A; Departments of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, Texas, United States of America.
  • Vu MN; Departments of Microbiology and Immunology, University of Texas Medical Branch, Galveston, Texas, United States of America.
  • Johnson BA; Departments of Microbiology and Immunology, University of Texas Medical Branch, Galveston, Texas, United States of America.
  • Davis-Gardner ME; Departments of Microbiology and Immunology, University of Texas Medical Branch, Galveston, Texas, United States of America.
  • Vanderheiden A; Department of Pediatrics, Emory Vaccine Center, Emory University School of Medicine, Atlanta, Georgia, United States of America.
  • Lokugamage K; Department of Pediatrics, Emory Vaccine Center, Emory University School of Medicine, Atlanta, Georgia, United States of America.
  • Schindewolf C; Departments of Microbiology and Immunology, University of Texas Medical Branch, Galveston, Texas, United States of America.
  • Crocquet-Valdes PA; Departments of Microbiology and Immunology, University of Texas Medical Branch, Galveston, Texas, United States of America.
  • Langsjoen RM; Department of Pathology, University of Texas Medical Branch, Galveston, Texas, United States of America.
  • Plante JA; Departments of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, Texas, United States of America.
  • Plante KS; Departments of Microbiology and Immunology, University of Texas Medical Branch, Galveston, Texas, United States of America.
  • Weaver SC; World Reference Center of Emerging Viruses and Arboviruses, University of Texas Medical Branch, Galveston, Texas, United States of America.
  • Debbink K; Departments of Microbiology and Immunology, University of Texas Medical Branch, Galveston, Texas, United States of America.
  • Routh AL; World Reference Center of Emerging Viruses and Arboviruses, University of Texas Medical Branch, Galveston, Texas, United States of America.
  • Walker D; Departments of Microbiology and Immunology, University of Texas Medical Branch, Galveston, Texas, United States of America.
  • Suthar MS; World Reference Center of Emerging Viruses and Arboviruses, University of Texas Medical Branch, Galveston, Texas, United States of America.
  • Shi PY; Institute for Human Infection and Immunity, University of Texas Medical Branch, Galveston, Texas, United States of America.
  • Xie X; Department of Natural Science, Bowie State University, Bowie, Maryland, United States of America.
  • Menachery VD; Departments of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, Texas, United States of America.
PLoS Biol ; 19(11): e3001284, 2021 11.
Article in English | MEDLINE | ID: covidwho-1502046
Preprint
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ABSTRACT
The emergence of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) has resulted in a pandemic causing significant damage to public health and the economy. Efforts to understand the mechanisms of Coronavirus Disease 2019 (COVID-19) have been hampered by the lack of robust mouse models. To overcome this barrier, we used a reverse genetic system to generate a mouse-adapted strain of SARS-CoV-2. Incorporating key mutations found in SARS-CoV-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. Coupled with the incorporation of mutations found in variants of concern, CMA3p20 offers several advantages over other mouse-adapted SARS-CoV-2 strains. Using this model, we demonstrate that SARS-CoV-2-infected mice are protected from lethal challenge with the original Severe Acute Respiratory Syndrome Coronavirus (SARS-CoV), suggesting immunity from heterologous Coronavirus (CoV) strains. Together, the results highlight the use of this mouse model for further study of SARS-CoV-2 infection and disease.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Vaccines / SARS-CoV-2 / COVID-19 Topics: Vaccines / Variants Limits: Animals / Female / Humans Language: English Journal: PLoS Biol Journal subject: Biology Year: 2021 Document Type: Article Affiliation country: Journal.pbio.3001284

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Vaccines / SARS-CoV-2 / COVID-19 Topics: Vaccines / Variants Limits: Animals / Female / Humans Language: English Journal: PLoS Biol Journal subject: Biology Year: 2021 Document Type: Article Affiliation country: Journal.pbio.3001284