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Evasion of I Interferon-Mediated Innate Immunity by Pseudorabies Virus

Type I interferon (IFN-I) mediated innate immunity serves as the first line of host defense against viral infection, ranging from IFN-I production upon viral detection, IFN-I triggered signaling pathway that induces antiviral gene transcription the antiviral effects of IFN-I induced gene products. D...

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Detalles Bibliográficos
Autores principales: Zhang, Rui, Tang, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8712723/
https://www.ncbi.nlm.nih.gov/pubmed/34970252
http://dx.doi.org/10.3389/fmicb.2021.801257
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author Zhang, Rui
Tang, Jun
author_facet Zhang, Rui
Tang, Jun
author_sort Zhang, Rui
collection PubMed
description Type I interferon (IFN-I) mediated innate immunity serves as the first line of host defense against viral infection, ranging from IFN-I production upon viral detection, IFN-I triggered signaling pathway that induces antiviral gene transcription the antiviral effects of IFN-I induced gene products. During coevolution, herpesviruses have developed multiple countermeasures to inhibit the various steps involved to evade the IFN response. This mini-review focuses on the strategies used by the alphaherpesvirus Pseudorabies virus (PRV) to antagonize IFN-I mediated innate immunity, with a particular emphasis on the mechanisms inhibiting IFN-I induced gene transcription through the JAK-STAT pathway. The knowledge obtained from PRV enriches the current understanding of the alphaherpesviral immune evasion mechanisms and provides insight into the vaccine development for PRV control.
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spelling pubmed-87127232021-12-29 Evasion of I Interferon-Mediated Innate Immunity by Pseudorabies Virus Zhang, Rui Tang, Jun Front Microbiol Microbiology Type I interferon (IFN-I) mediated innate immunity serves as the first line of host defense against viral infection, ranging from IFN-I production upon viral detection, IFN-I triggered signaling pathway that induces antiviral gene transcription the antiviral effects of IFN-I induced gene products. During coevolution, herpesviruses have developed multiple countermeasures to inhibit the various steps involved to evade the IFN response. This mini-review focuses on the strategies used by the alphaherpesvirus Pseudorabies virus (PRV) to antagonize IFN-I mediated innate immunity, with a particular emphasis on the mechanisms inhibiting IFN-I induced gene transcription through the JAK-STAT pathway. The knowledge obtained from PRV enriches the current understanding of the alphaherpesviral immune evasion mechanisms and provides insight into the vaccine development for PRV control. Frontiers Media S.A. 2021-12-14 /pmc/articles/PMC8712723/ /pubmed/34970252 http://dx.doi.org/10.3389/fmicb.2021.801257 Text en Copyright © 2021 Zhang and Tang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Zhang, Rui
Tang, Jun
Evasion of I Interferon-Mediated Innate Immunity by Pseudorabies Virus
title Evasion of I Interferon-Mediated Innate Immunity by Pseudorabies Virus
title_full Evasion of I Interferon-Mediated Innate Immunity by Pseudorabies Virus
title_fullStr Evasion of I Interferon-Mediated Innate Immunity by Pseudorabies Virus
title_full_unstemmed Evasion of I Interferon-Mediated Innate Immunity by Pseudorabies Virus
title_short Evasion of I Interferon-Mediated Innate Immunity by Pseudorabies Virus
title_sort evasion of i interferon-mediated innate immunity by pseudorabies virus
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8712723/
https://www.ncbi.nlm.nih.gov/pubmed/34970252
http://dx.doi.org/10.3389/fmicb.2021.801257
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