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Varicella-zoster virus glycoprotein M homolog is glycosylated, is expressed on the viral envelope, and functions in virus cell-to-cell spread.

Varicella-zoster virus glycoprotein M homolog is glycosylated, is expressed on the viral envelope, and functions in virus cell-to-cell spread. Research Abstract Details 

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  • Varicella-zoster virus glycoprotein M homolog is glycosylated, is expressed on the viral envelope, and functions in virus cell-to-cell spread. Abstract Text:

    yoshiaki yamagishiYoshiaki Yamagishi,tomohiko sadaokaTomohiko Sadaoka,hironori yoshiiHironori Yoshii,pranee somboonthumPranee Somboonthum,takayoshi imazawaTakayoshi Imazawa,kazuhiro nagaikeKazuhiro Nagaike,keiichi ozonoKeiichi Ozono,koichi yamanishiKoichi Yamanishi,yasuko moriYasuko Mori,yoshiaki yamagishiYoshiaki Yamagishi,tomohiko sadaokaTomohiko Sadaoka,hironori yoshiiHironori Yoshii,pranee somboonthumPranee Somboonthum,takayoshi imazawaTakayoshi Imazawa,kazuhiro nagaikeKazuhiro Nagaike,keiichi ozonoKeiichi Ozono,koichi yamanishiKoichi Yamanishi,yasuko moriYasuko Mori,

    Although envelope glycoprotein M (gM) is highly conserved among herpesviruses, the varicella-zoster virus (VZV) gM homolog has never been investigated. Here we characterized the VZV gM homolog and analyzed its function in VZV-infected cells. The VZV gM homolog was expressed on virions as a glycoprotein modified with a complex N-linked oligosaccharide and localized mainly to the Golgi apparatus and the trans-Golgi network in infected cells. To analyze its function, a gM deletion mutant was generated using the bacterial artificial chromosome system in Escherichia coli, and the virus was reconstituted in MRC-5 cells. VZV is highly cell associated, and infection proceeds mostly by cell-to-cell spread. Compared with wild-type VZV, the gM deletion mutant showed a 90% reduction in plaque size and 50% of the cell-to-cell spread in MRC-5 cells. The analysis of infected cells by electron microscopy revealed numerous aberrant vacuoles containing electron-dense materials in cells infected with the deletion mutant virus but not in those infected with wild-type virus. However, enveloped immature particles termed L particles were found at the same level on the surfaces of cells infected with either type of virus, indicating that envelopment without a capsid might not be impaired. These results showed that VZV gM is important for efficient cell-to-cell virus spread in cell culture, although it is not essential for virus growth.

    Varicella-zoster virus glycoprotein M homolog is glycosylated, is expressed on the viral envelope, and functions in virus cell-to-cell spread. Publishing Authors By Initials

    y yamagishiY Yamagishi,t sadaokaT Sadaoka,h yoshiiH Yoshii,p somboonthumP Somboonthum,t imazawaT Imazawa,k nagaikeK Nagaike,k ozonoK Ozono,k yamanishiK Yamanishi,y moriY Mori,y yamagishiY Yamagishi,t sadaokaT Sadaoka,h yoshiiH Yoshii,p somboonthumP Somboonthum,t imazawaT Imazawa,k nagaikeK Nagaike,k ozonoK Ozono,k yamanishiK Yamanishi,y moriY Mori,

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    Varicella-zoster virus glycoprotein M homolog is glycosylated, is expressed on the viral envelope, and functions in virus cell-to-cell spread. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Journal of virology

    VOLUME: 82

    Page Numbers: 795-804

    Journal Abbreviation: J. Virol.

    ISSN: 1098-5514

    DAY: 31

    MONTH: 10

    YEAR: 2007

    Varicella-zoster virus glycoprotein M homolog is glycosylated, is expressed on the viral envelope, and functions in virus cell-to-cell spread. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 113724

    Varicella-zoster virus glycoprotein M homolog is glycosylated, is expressed on the viral envelope, and functions in virus cell-to-cell spread. Keywords Mesh Terms:

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    Grant and Affiliation Information for Varicella-zoster virus glycoprotein M homolog is glycosylated, is expressed on the viral envelope, and functions in virus cell-to-cell spread.

    AFFILIATION: Laboratory of Virology and Vaccinology, Division of Biomedical Research, National Institute of Biomedical Innovation, 7-6-8, Saito-Asagi, Ibaraki, Osaka 567-0085, Japan.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: J Virol

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