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SV40 Hijacks Cellular Transport, Membrane Penetration, and Disassembly Machineries to Promote Infection.
Chen, Yu-Jie; Liu, Xiaofang; Tsai, Billy.
Afiliação
  • Chen YJ; Department of Cell and Developmental Biology, University of Michigan Medical School, 109 Zina Pitcher Place, BSRB 3043, Ann Arbor, MI 48109, USA. chenyuj@med.umich.edu.
  • Liu X; Department of Cell and Developmental Biology, University of Michigan Medical School, 109 Zina Pitcher Place, BSRB 3043, Ann Arbor, MI 48109, USA. xiaofanl@med.umich.edu.
  • Tsai B; Department of Cell and Developmental Biology, University of Michigan Medical School, 109 Zina Pitcher Place, BSRB 3043, Ann Arbor, MI 48109, USA. btsai@umich.edu.
Viruses ; 11(10)2019 10 05.
Article em En | MEDLINE | ID: mdl-31590347
ABSTRACT
During entry, a virus must be transported through the endomembrane system of the host cell, penetrate a cellular membrane, and undergo capsid disassembly, to reach the cytosol and often the nucleus in order to cause infection. To do so requires the virus to coordinately exploit the action of cellular membrane transport, penetration, and disassembly machineries. How this is accomplished remains enigmatic for many viruses, especially for viruses belonging to the nonenveloped virus family. In this review, we present the current model describing infectious entry of the nonenveloped polyomavirus (PyV) SV40. Insights from SV40 entry are likely to provide strategies to combat PyV-induced diseases, and to illuminate cellular trafficking, membrane transport, and disassembly mechanisms.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transporte Biológico / Vírus 40 dos Símios / Infecções por Polyomavirus / Membranas Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transporte Biológico / Vírus 40 dos Símios / Infecções por Polyomavirus / Membranas Idioma: En Ano de publicação: 2019 Tipo de documento: Article