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Cellular Proteostasis During Influenza A Virus Infection—Friend or Foe?

In order to efficiently replicate, viruses require precise interactions with host components and often hijack the host cellular machinery for their own benefit. Several mechanisms involved in protein synthesis and processing are strongly affected and manipulated by viral infections. A better underst...

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Detalles Bibliográficos
Autores principales: Marques, Mariana, Ramos, Bruno, Soares, Ana Raquel, Ribeiro, Daniela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6468813/
https://www.ncbi.nlm.nih.gov/pubmed/30857287
http://dx.doi.org/10.3390/cells8030228
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author Marques, Mariana
Ramos, Bruno
Soares, Ana Raquel
Ribeiro, Daniela
author_facet Marques, Mariana
Ramos, Bruno
Soares, Ana Raquel
Ribeiro, Daniela
author_sort Marques, Mariana
collection PubMed
description In order to efficiently replicate, viruses require precise interactions with host components and often hijack the host cellular machinery for their own benefit. Several mechanisms involved in protein synthesis and processing are strongly affected and manipulated by viral infections. A better understanding of the interplay between viruses and their host-cell machinery will likely contribute to the development of novel antiviral strategies. Here, we discuss the current knowledge on the interactions between influenza A virus (IAV), the causative agent for most of the annual respiratory epidemics in humans, and the host cellular proteostasis machinery during infection. We focus on the manipulative capacity of this virus to usurp the cellular protein processing mechanisms and further review the protein quality control mechanisms in the cytosol and in the endoplasmic reticulum that are affected by this virus.
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spelling pubmed-64688132019-04-23 Cellular Proteostasis During Influenza A Virus Infection—Friend or Foe? Marques, Mariana Ramos, Bruno Soares, Ana Raquel Ribeiro, Daniela Cells Review In order to efficiently replicate, viruses require precise interactions with host components and often hijack the host cellular machinery for their own benefit. Several mechanisms involved in protein synthesis and processing are strongly affected and manipulated by viral infections. A better understanding of the interplay between viruses and their host-cell machinery will likely contribute to the development of novel antiviral strategies. Here, we discuss the current knowledge on the interactions between influenza A virus (IAV), the causative agent for most of the annual respiratory epidemics in humans, and the host cellular proteostasis machinery during infection. We focus on the manipulative capacity of this virus to usurp the cellular protein processing mechanisms and further review the protein quality control mechanisms in the cytosol and in the endoplasmic reticulum that are affected by this virus. MDPI 2019-03-09 /pmc/articles/PMC6468813/ /pubmed/30857287 http://dx.doi.org/10.3390/cells8030228 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
Marques, Mariana
Ramos, Bruno
Soares, Ana Raquel
Ribeiro, Daniela
Cellular Proteostasis During Influenza A Virus Infection—Friend or Foe?
title Cellular Proteostasis During Influenza A Virus Infection—Friend or Foe?
title_full Cellular Proteostasis During Influenza A Virus Infection—Friend or Foe?
title_fullStr Cellular Proteostasis During Influenza A Virus Infection—Friend or Foe?
title_full_unstemmed Cellular Proteostasis During Influenza A Virus Infection—Friend or Foe?
title_short Cellular Proteostasis During Influenza A Virus Infection—Friend or Foe?
title_sort cellular proteostasis during influenza a virus infection—friend or foe?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6468813/
https://www.ncbi.nlm.nih.gov/pubmed/30857287
http://dx.doi.org/10.3390/cells8030228
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