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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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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. |
format | Online Article Text |
id | pubmed-6832212 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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