Alphavirus Infection: Host Cell Shut-Off and Inhibition of Antiviral Responses

Alphaviruses cause debilitating disease in humans and animals and are transmitted by blood-feeding arthropods, typically mosquitoes. With a traditional focus on two models, Sindbis virus and Semliki Forest virus, alphavirus research has significantly intensified in the last decade partly due to the...

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Main Authors: Jelke J. Fros, Gorben P. Pijlman
Format: Article
Language:English
Published: MDPI AG 2016-06-01
Series:Viruses
Subjects:
Online Access:http://www.mdpi.com/1999-4915/8/6/166
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spelling doaj-f8ae777f432c482a929390c45bc1e8ac2020-11-24T23:00:00ZengMDPI AGViruses1999-49152016-06-018616610.3390/v8060166v8060166Alphavirus Infection: Host Cell Shut-Off and Inhibition of Antiviral ResponsesJelke J. Fros0Gorben P. Pijlman1Nuffield Department of Medicine, Peter Medawar Building for Pathogen Research, University of Oxford, Oxford OX1 3SY, England, UKLaboratory of Virology, Wageningen University, Droevendaalsesteeg 1, 6708 PB, Wageningen 6700 AB, The NetherlandsAlphaviruses cause debilitating disease in humans and animals and are transmitted by blood-feeding arthropods, typically mosquitoes. With a traditional focus on two models, Sindbis virus and Semliki Forest virus, alphavirus research has significantly intensified in the last decade partly due to the re-emergence and dramatic expansion of chikungunya virus in Asia, Europe, and the Americas. As a consequence, alphavirus–host interactions are now understood in much more molecular detail, and important novel mechanisms have been elucidated. It has become clear that alphaviruses not only cause a general host shut-off in infected vertebrate cells, but also specifically suppress different host antiviral pathways using their viral nonstructural proteins, nsP2 and nsP3. Here we review the current state of the art of alphavirus host cell shut-off of viral transcription and translation, and describe recent insights in viral subversion of interferon induction and signaling, the unfolded protein response, and stress granule assembly.http://www.mdpi.com/1999-4915/8/6/166alphaviruschikungunyaSindbisSemliki Foresthost shut-offtranscriptiontranslationantiviral responsestress granulesinterferonunfolded protein response
collection DOAJ
language English
format Article
sources DOAJ
author Jelke J. Fros
Gorben P. Pijlman
spellingShingle Jelke J. Fros
Gorben P. Pijlman
Alphavirus Infection: Host Cell Shut-Off and Inhibition of Antiviral Responses
Viruses
alphavirus
chikungunya
Sindbis
Semliki Forest
host shut-off
transcription
translation
antiviral response
stress granules
interferon
unfolded protein response
author_facet Jelke J. Fros
Gorben P. Pijlman
author_sort Jelke J. Fros
title Alphavirus Infection: Host Cell Shut-Off and Inhibition of Antiviral Responses
title_short Alphavirus Infection: Host Cell Shut-Off and Inhibition of Antiviral Responses
title_full Alphavirus Infection: Host Cell Shut-Off and Inhibition of Antiviral Responses
title_fullStr Alphavirus Infection: Host Cell Shut-Off and Inhibition of Antiviral Responses
title_full_unstemmed Alphavirus Infection: Host Cell Shut-Off and Inhibition of Antiviral Responses
title_sort alphavirus infection: host cell shut-off and inhibition of antiviral responses
publisher MDPI AG
series Viruses
issn 1999-4915
publishDate 2016-06-01
description Alphaviruses cause debilitating disease in humans and animals and are transmitted by blood-feeding arthropods, typically mosquitoes. With a traditional focus on two models, Sindbis virus and Semliki Forest virus, alphavirus research has significantly intensified in the last decade partly due to the re-emergence and dramatic expansion of chikungunya virus in Asia, Europe, and the Americas. As a consequence, alphavirus–host interactions are now understood in much more molecular detail, and important novel mechanisms have been elucidated. It has become clear that alphaviruses not only cause a general host shut-off in infected vertebrate cells, but also specifically suppress different host antiviral pathways using their viral nonstructural proteins, nsP2 and nsP3. Here we review the current state of the art of alphavirus host cell shut-off of viral transcription and translation, and describe recent insights in viral subversion of interferon induction and signaling, the unfolded protein response, and stress granule assembly.
topic alphavirus
chikungunya
Sindbis
Semliki Forest
host shut-off
transcription
translation
antiviral response
stress granules
interferon
unfolded protein response
url http://www.mdpi.com/1999-4915/8/6/166
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