Literature DB >> 14982727

A combination of mutations in the S1 part of the spike glycoprotein gene of coronavirus MHV-A59 abolishes demyelination.

Li Fu1, Donna M Gonzales, Jayasri Das Sarma, Ehud Lavi.   

Abstract

The A59 strain of coronavirus, mouse hepatitis virus (MHV), produces acute hepatitis, meningoencephalitis, and chronic demyelination. The authors have previously shown that the spike (S) glycoprotein gene of MHV contains determinants of virulence, hepatitis, and demyelination. They then identified viruses containing mutations in the S gene that exhibit alterations in viral pathogenesis. In the present study, the authors produced new recombinant viruses with each one of these S gene mutations by site-directed mutagenesis and targeted recombination and studied the effect of each individual mutation on the pathogenesis of the virus. They identified a combination of mutations in the S1 gene (I375M and L652I) that abolishes demyelination. Individual mutation and other combinations of mutations in the S gene only interfere with virulence and hepatitis and only reduce demyelination (I375M), but do not abolish demyelination completely. Thus, demyelination determinants exist within genomic regions on both sides of the hypervariable region, downstream from the receptor-binding domain in the S1 part of the MHV spike glycoprotein gene. The structure and precise function of these regions awaits further investigation.

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Year:  2004        PMID: 14982727      PMCID: PMC7095319          DOI: 10.1080/13550280490262229

Source DB:  PubMed          Journal:  J Neurovirol        ISSN: 1355-0284            Impact factor:   2.643


  40 in total

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Journal:  Curr Top Microbiol Immunol       Date:  1982       Impact factor: 4.291

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Journal:  J Virol       Date:  1999-09       Impact factor: 5.103

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Journal:  Neurology       Date:  1984-05       Impact factor: 9.910

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Journal:  J Gen Virol       Date:  1981-05       Impact factor: 3.891

8.  RNA recombination of murine coronaviruses: recombination between fusion-positive mouse hepatitis virus A59 and fusion-negative mouse hepatitis virus 2.

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Journal:  J Virol       Date:  1988-06       Impact factor: 5.103

9.  Quaternary structure of coronavirus spikes in complex with carcinoembryonic antigen-related cell adhesion molecule cellular receptors.

Authors:  Daniel N Lewicki; Thomas M Gallagher
Journal:  J Biol Chem       Date:  2002-03-23       Impact factor: 5.157

10.  Targeted recombination within the spike gene of murine coronavirus mouse hepatitis virus-A59: Q159 is a determinant of hepatotropism.

Authors:  I Leparc-Goffart; S T Hingley; M M Chua; J Phillips; E Lavi; S R Weiss
Journal:  J Virol       Date:  1998-12       Impact factor: 5.103

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  2 in total

1.  Coronaviruses: propagation, quantification, storage, and construction of recombinant mouse hepatitis virus.

Authors:  Julian Leibowitz; Gili Kaufman; Pinghua Liu
Journal:  Curr Protoc Microbiol       Date:  2011-05

2.  Recombinant mouse hepatitis virus strain A59 from cloned, full-length cDNA replicates to high titers in vitro and is fully pathogenic in vivo.

Authors:  Scott E Coley; Ehud Lavi; Stanley G Sawicki; Li Fu; Barbara Schelle; Nadja Karl; Stuart G Siddell; Volker Thiel
Journal:  J Virol       Date:  2005-03       Impact factor: 5.103

  2 in total

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