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口蹄疫病毒靶向宿主抗病毒反应的分子机制

Molecular Mechanisms of Foot-and-Mouth Disease Virus Targeting the Host Antiviral Response.

作者信息

Rodríguez Pulido Miguel, Sáiz Margarita

机构信息

Centro de Biología Molecular Severo Ochoa (Consejo Superior de Investigaciones Científicas-UAM)Madrid, Spain.

出版信息

Front Cell Infect Microbiol. 2017 Jun 13;7:252. doi: 10.3389/fcimb.2017.00252. eCollection 2017.

Abstract

Foot-and-mouth disease virus (FMDV) is the causative agent of an acute vesicular disease affecting pigs, cattle and other domestic, and wild animals worldwide. The aim of the host interferon (IFN) response is to limit viral replication and spread. Detection of the viral genome and products by specialized cellular sensors initiates a signaling cascade that leads to a rapid antiviral response involving the secretion of type I- and type III-IFNs and other antiviral cytokines with antiproliferative and immunomodulatory functions. During co-evolution with their hosts, viruses have acquired strategies to actively counteract host antiviral responses and the balance between innate response and viral antagonism may determine the outcome of disease and pathogenesis. FMDV proteases Lpro and 3C have been found to antagonize the host IFN response by a repertoire of mechanisms. Moreover, the putative role of other viral proteins in IFN antagonism is being recently unveiled, uncovering sophisticated immune evasion strategies different to those reported to date for other members of the family. Here, we review the interplay between antiviral responses induced by FMDV infection and viral countermeasures to block them. Research on strategies used by viruses to modulate immunity will provide insights into the function of host pathways involved in defense against pathogens and will also lead to development of new therapeutic strategies to fight virus infections.

摘要

口蹄疫病毒(FMDV)是一种急性水疱性疾病的病原体,可感染全球范围内的猪、牛及其他家养和野生动物。宿主干扰素(IFN)反应的目的是限制病毒的复制和传播。专门的细胞传感器对病毒基因组和产物的检测启动了一个信号级联反应,导致快速的抗病毒反应,包括分泌I型和III型干扰素以及其他具有抗增殖和免疫调节功能的抗病毒细胞因子。在与宿主共同进化的过程中,病毒获得了主动对抗宿主抗病毒反应的策略,先天反应与病毒拮抗作用之间的平衡可能决定疾病的结果和发病机制。已发现FMDV蛋白酶Lpro和3C通过一系列机制拮抗宿主IFN反应。此外,最近还揭示了其他病毒蛋白在IFN拮抗作用中的假定作用,发现了与该病毒家族其他成员迄今报道的不同的复杂免疫逃避策略。在此,我们综述了FMDV感染诱导的抗病毒反应与病毒阻断这些反应的对策之间的相互作用。对病毒用于调节免疫的策略的研究将为参与抵御病原体的宿主途径的功能提供见解,也将导致开发对抗病毒感染的新治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/223b/5468379/913eedf185ee/fcimb-07-00252-g0001.jpg

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