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SV40 Hijacks Cellular Transport, Membrane Penetration, and Disassembly Machineries to Promote Infection

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 cellula...

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Detalles Bibliográficos
Autores principales: Chen, Yu-Jie, Liu, Xiaofang, Tsai, Billy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6832212/
https://www.ncbi.nlm.nih.gov/pubmed/31590347
http://dx.doi.org/10.3390/v11100917
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author Chen, Yu-Jie
Liu, Xiaofang
Tsai, Billy
author_facet Chen, Yu-Jie
Liu, Xiaofang
Tsai, Billy
author_sort Chen, Yu-Jie
collection PubMed
description 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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spelling pubmed-68322122019-11-21 SV40 Hijacks Cellular Transport, Membrane Penetration, and Disassembly Machineries to Promote Infection Chen, Yu-Jie Liu, Xiaofang Tsai, Billy Viruses Review 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. MDPI 2019-10-05 /pmc/articles/PMC6832212/ /pubmed/31590347 http://dx.doi.org/10.3390/v11100917 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Chen, Yu-Jie
Liu, Xiaofang
Tsai, Billy
SV40 Hijacks Cellular Transport, Membrane Penetration, and Disassembly Machineries to Promote Infection
title SV40 Hijacks Cellular Transport, Membrane Penetration, and Disassembly Machineries to Promote Infection
title_full SV40 Hijacks Cellular Transport, Membrane Penetration, and Disassembly Machineries to Promote Infection
title_fullStr SV40 Hijacks Cellular Transport, Membrane Penetration, and Disassembly Machineries to Promote Infection
title_full_unstemmed SV40 Hijacks Cellular Transport, Membrane Penetration, and Disassembly Machineries to Promote Infection
title_short SV40 Hijacks Cellular Transport, Membrane Penetration, and Disassembly Machineries to Promote Infection
title_sort sv40 hijacks cellular transport, membrane penetration, and disassembly machineries to promote infection
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6832212/
https://www.ncbi.nlm.nih.gov/pubmed/31590347
http://dx.doi.org/10.3390/v11100917
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