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A severe acute respiratory syndrome-associated coronavirus-specific protein enhances virulence of an attenuated murine coronavirus
Journal article   Open access   Peer reviewed

A severe acute respiratory syndrome-associated coronavirus-specific protein enhances virulence of an attenuated murine coronavirus

Lecia Pewe, Haixia Zhou, Jason Netland, Chandra Tangudu, Heidi Olivares, Lei Shi, Dwight Look, Thomas Gallagher and Stanley Perlman
Journal of virology, Vol.79(17), pp.11335-11342
09/2005
DOI: 10.1128/JVI.79.17.11335-11342.2005
PMCID: PMC1193615
PMID: 16103185
url
https://europepmc.org/articles/pmc1193615View
Published (Version of record) Open Access

Abstract

Most animal species that can be infected with the severe acute respiratory syndrome-associated coronavirus (SARS-CoV) do not reproducibly develop clinical disease, hindering studies of pathogenesis. To develop an alternative system for the study of SARS-CoV, we introduced individual SARS-CoV genes (open reading frames [ORFs]) into the genome of an attenuated murine coronavirus. One protein, the product of SARS-CoV ORF6, converted a sublethal infection to a uniformly lethal encephalitis and enhanced virus growth in tissue culture cells, indicating that SARS-CoV proteins function in the context of a heterologous coronavirus infection. Furthermore, these results suggest that the attenuated murine coronavirus lacks a virulence gene residing in SARS-CoV. Recombinant murine coronaviruses cause a reproducible and well-characterized clinical disease, offer virtually no risk to laboratory personnel, and should be useful for elucidating the role of SARS-CoV nonstructural proteins in viral replication and pathogenesis.
Cell Line Reassortant Viruses - pathogenicity Encephalitis - virology Humans Mice, Inbred C57BL Virulence Viral Nonstructural Proteins - genetics Murine hepatitis virus - pathogenicity Open Reading Frames - genetics SARS Virus - chemistry SARS Virus - pathogenicity Animals Coronavirus Infections - virology Virus Replication Viral Nonstructural Proteins - metabolism Mice SARS Virus - physiology Murine hepatitis virus - genetics Disease Models, Animal

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