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Impacts of virus-mediated manipulation of host Dynein

In general viruses' modus operandi to propagate is achieved by the co-opting host cell components, membranes, proteins, and machineries to their advantage. This is true for virtually every aspect of a virus' replication cycle from virus entry to the budding or release of progeny virus part...

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Autores principales: Milev, Miroslav P., Yao, Xaojian, Berthoux, Lionel, Mouland, Andrew J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7150161/
http://dx.doi.org/10.1016/B978-0-12-809470-9.00010-2
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author Milev, Miroslav P.
Yao, Xaojian
Berthoux, Lionel
Mouland, Andrew J.
author_facet Milev, Miroslav P.
Yao, Xaojian
Berthoux, Lionel
Mouland, Andrew J.
author_sort Milev, Miroslav P.
collection PubMed
description In general viruses' modus operandi to propagate is achieved by the co-opting host cell components, membranes, proteins, and machineries to their advantage. This is true for virtually every aspect of a virus' replication cycle from virus entry to the budding or release of progeny virus particles. In this chapter, we will discuss new information on the impacts of virus-mediated manipulation of Dynein motor complexes and associated machineries and factors. We will highlight how these host cell components impact on pathogenicity and immune responses, as many of the virus-mediated hijacked components also play pivotal roles in immune responses to pathogen insult. There are several comprehensive reviews that define virus–Dynein interactions including the first edition of this book that describes how viruses manipulate the host cell machineries their advantage. An updated table is included to summarize these virus–host interactions. Notably, barriers to intracellular translocation represent major hurdles to viral components during de novo infection and during active replication and the generation of progeny virus particles. Clearly, the subversion of host cell molecular motor protein activities takes advantage of constitutive and regulated membrane trafficking events and will target virus components to intracytoplasmic locales and membrane assembly. Broadening our understanding of the interplay between viruses, Dynein and the cytoskeleton will likely inform on new types of therapies. Continual enhancement of the breadth of new information on how viruses manipulate host cell biology will inevitably aid in the identification of new targets that can be poisoned to block old, new, and emerging viruses alike in their tracks.
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spelling pubmed-71501612020-04-13 Impacts of virus-mediated manipulation of host Dynein Milev, Miroslav P. Yao, Xaojian Berthoux, Lionel Mouland, Andrew J. Dyneins Article In general viruses' modus operandi to propagate is achieved by the co-opting host cell components, membranes, proteins, and machineries to their advantage. This is true for virtually every aspect of a virus' replication cycle from virus entry to the budding or release of progeny virus particles. In this chapter, we will discuss new information on the impacts of virus-mediated manipulation of Dynein motor complexes and associated machineries and factors. We will highlight how these host cell components impact on pathogenicity and immune responses, as many of the virus-mediated hijacked components also play pivotal roles in immune responses to pathogen insult. There are several comprehensive reviews that define virus–Dynein interactions including the first edition of this book that describes how viruses manipulate the host cell machineries their advantage. An updated table is included to summarize these virus–host interactions. Notably, barriers to intracellular translocation represent major hurdles to viral components during de novo infection and during active replication and the generation of progeny virus particles. Clearly, the subversion of host cell molecular motor protein activities takes advantage of constitutive and regulated membrane trafficking events and will target virus components to intracytoplasmic locales and membrane assembly. Broadening our understanding of the interplay between viruses, Dynein and the cytoskeleton will likely inform on new types of therapies. Continual enhancement of the breadth of new information on how viruses manipulate host cell biology will inevitably aid in the identification of new targets that can be poisoned to block old, new, and emerging viruses alike in their tracks. 2018 2017-12-01 /pmc/articles/PMC7150161/ http://dx.doi.org/10.1016/B978-0-12-809470-9.00010-2 Text en Copyright © 2018 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Milev, Miroslav P.
Yao, Xaojian
Berthoux, Lionel
Mouland, Andrew J.
Impacts of virus-mediated manipulation of host Dynein
title Impacts of virus-mediated manipulation of host Dynein
title_full Impacts of virus-mediated manipulation of host Dynein
title_fullStr Impacts of virus-mediated manipulation of host Dynein
title_full_unstemmed Impacts of virus-mediated manipulation of host Dynein
title_short Impacts of virus-mediated manipulation of host Dynein
title_sort impacts of virus-mediated manipulation of host dynein
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7150161/
http://dx.doi.org/10.1016/B978-0-12-809470-9.00010-2
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