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A new mouse-adapted strain of SARS-CoV as a lethal model for evaluating antiviral agents in vitro and in vivo

Severe acute respiratory syndrome (SARS) is a highly lethal emerging disease caused by coronavirus SARS-CoV. New lethal animal models for SARS were needed to facilitate antiviral research. We adapted and characterized a new strain of SARS-CoV (strain v2163) that was highly lethal in 5- to 6-week-old...

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Autores principales: Day, Craig W., Baric, Ralph, Cai, Sui Xiong, Frieman, Matt, Kumaki, Yohichi, Morrey, John D., Smee, Donald F., Barnard, Dale L.
Formato: Texto
Lenguaje:English
Publicado: Elsevier Inc. Published by Elsevier Inc. 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2787736/
https://www.ncbi.nlm.nih.gov/pubmed/19853271
http://dx.doi.org/10.1016/j.virol.2009.09.023
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author Day, Craig W.
Baric, Ralph
Cai, Sui Xiong
Frieman, Matt
Kumaki, Yohichi
Morrey, John D.
Smee, Donald F.
Barnard, Dale L.
author_facet Day, Craig W.
Baric, Ralph
Cai, Sui Xiong
Frieman, Matt
Kumaki, Yohichi
Morrey, John D.
Smee, Donald F.
Barnard, Dale L.
author_sort Day, Craig W.
collection PubMed
description Severe acute respiratory syndrome (SARS) is a highly lethal emerging disease caused by coronavirus SARS-CoV. New lethal animal models for SARS were needed to facilitate antiviral research. We adapted and characterized a new strain of SARS-CoV (strain v2163) that was highly lethal in 5- to 6-week-old BALB/c mice. It had nine mutations affecting 10 amino acid residues. Strain v2163 increased IL-1α, IL-6, MIP-1α, MCP-1, and RANTES in mice, and high IL-6 expression correlated with mortality. The infection largely mimicked human disease, but lung pathology lacked hyaline membrane formation. In vitro efficacy against v2163 was shown with known inhibitors of SARS-CoV replication. In v2163-infected mice, Ampligen™ was fully protective, stinging nettle lectin (UDA) was partially protective, ribavirin was disputable and possibly exacerbated disease, and EP128533 was inactive. Ribavirin, UDA, and Ampligen™ decreased IL-6 expression. Strain v2163 provided a valuable model for anti-SARS research.
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spelling pubmed-27877362010-12-20 A new mouse-adapted strain of SARS-CoV as a lethal model for evaluating antiviral agents in vitro and in vivo Day, Craig W. Baric, Ralph Cai, Sui Xiong Frieman, Matt Kumaki, Yohichi Morrey, John D. Smee, Donald F. Barnard, Dale L. Virology Article Severe acute respiratory syndrome (SARS) is a highly lethal emerging disease caused by coronavirus SARS-CoV. New lethal animal models for SARS were needed to facilitate antiviral research. We adapted and characterized a new strain of SARS-CoV (strain v2163) that was highly lethal in 5- to 6-week-old BALB/c mice. It had nine mutations affecting 10 amino acid residues. Strain v2163 increased IL-1α, IL-6, MIP-1α, MCP-1, and RANTES in mice, and high IL-6 expression correlated with mortality. The infection largely mimicked human disease, but lung pathology lacked hyaline membrane formation. In vitro efficacy against v2163 was shown with known inhibitors of SARS-CoV replication. In v2163-infected mice, Ampligen™ was fully protective, stinging nettle lectin (UDA) was partially protective, ribavirin was disputable and possibly exacerbated disease, and EP128533 was inactive. Ribavirin, UDA, and Ampligen™ decreased IL-6 expression. Strain v2163 provided a valuable model for anti-SARS research. Elsevier Inc. Published by Elsevier Inc. 2009-12-20 2009-10-22 /pmc/articles/PMC2787736/ /pubmed/19853271 http://dx.doi.org/10.1016/j.virol.2009.09.023 Text en Copyright © 2009 Elsevier Inc. Published by Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Day, Craig W.
Baric, Ralph
Cai, Sui Xiong
Frieman, Matt
Kumaki, Yohichi
Morrey, John D.
Smee, Donald F.
Barnard, Dale L.
A new mouse-adapted strain of SARS-CoV as a lethal model for evaluating antiviral agents in vitro and in vivo
title A new mouse-adapted strain of SARS-CoV as a lethal model for evaluating antiviral agents in vitro and in vivo
title_full A new mouse-adapted strain of SARS-CoV as a lethal model for evaluating antiviral agents in vitro and in vivo
title_fullStr A new mouse-adapted strain of SARS-CoV as a lethal model for evaluating antiviral agents in vitro and in vivo
title_full_unstemmed A new mouse-adapted strain of SARS-CoV as a lethal model for evaluating antiviral agents in vitro and in vivo
title_short A new mouse-adapted strain of SARS-CoV as a lethal model for evaluating antiviral agents in vitro and in vivo
title_sort new mouse-adapted strain of sars-cov as a lethal model for evaluating antiviral agents in vitro and in vivo
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2787736/
https://www.ncbi.nlm.nih.gov/pubmed/19853271
http://dx.doi.org/10.1016/j.virol.2009.09.023
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