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Decoding type I and III interferon signalling during viral infection

Interferon (IFN)-mediated antiviral responses are central to host defence against viral infection. Despite the existence of at least 20 IFNs, there are only three known cell surface receptors. IFN signalling and viral evasion mechanisms form an immensely complex network that differs across species....

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Detalles Bibliográficos
Autores principales: Mesev, Emily V., LeDesma, Robert A., Ploss, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6554024/
https://www.ncbi.nlm.nih.gov/pubmed/30936491
http://dx.doi.org/10.1038/s41564-019-0421-x
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author Mesev, Emily V.
LeDesma, Robert A.
Ploss, Alexander
author_facet Mesev, Emily V.
LeDesma, Robert A.
Ploss, Alexander
author_sort Mesev, Emily V.
collection PubMed
description Interferon (IFN)-mediated antiviral responses are central to host defence against viral infection. Despite the existence of at least 20 IFNs, there are only three known cell surface receptors. IFN signalling and viral evasion mechanisms form an immensely complex network that differs across species. In this Review, we begin by highlighting some of the advances that have been made towards understanding the complexity of differential IFN signalling inputs and outputs that contribute to antiviral defences. Next, we explore some of the ways viruses can interfere with, or circumvent, these defences. Lastly, we address the largely under-reviewed impact of IFN signalling on host tropism, and we offer perspectives on the future of research into IFN signalling complexity and viral evasion across species.
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spelling pubmed-65540242019-06-06 Decoding type I and III interferon signalling during viral infection Mesev, Emily V. LeDesma, Robert A. Ploss, Alexander Nat Microbiol Review Article Interferon (IFN)-mediated antiviral responses are central to host defence against viral infection. Despite the existence of at least 20 IFNs, there are only three known cell surface receptors. IFN signalling and viral evasion mechanisms form an immensely complex network that differs across species. In this Review, we begin by highlighting some of the advances that have been made towards understanding the complexity of differential IFN signalling inputs and outputs that contribute to antiviral defences. Next, we explore some of the ways viruses can interfere with, or circumvent, these defences. Lastly, we address the largely under-reviewed impact of IFN signalling on host tropism, and we offer perspectives on the future of research into IFN signalling complexity and viral evasion across species. Nature Publishing Group UK 2019-04-01 2019 /pmc/articles/PMC6554024/ /pubmed/30936491 http://dx.doi.org/10.1038/s41564-019-0421-x Text en © The Author(s), under exclusive licence to Springer Nature Limited 2019 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Review Article
Mesev, Emily V.
LeDesma, Robert A.
Ploss, Alexander
Decoding type I and III interferon signalling during viral infection
title Decoding type I and III interferon signalling during viral infection
title_full Decoding type I and III interferon signalling during viral infection
title_fullStr Decoding type I and III interferon signalling during viral infection
title_full_unstemmed Decoding type I and III interferon signalling during viral infection
title_short Decoding type I and III interferon signalling during viral infection
title_sort decoding type i and iii interferon signalling during viral infection
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6554024/
https://www.ncbi.nlm.nih.gov/pubmed/30936491
http://dx.doi.org/10.1038/s41564-019-0421-x
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