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PEDV结构蛋白颉颃IFN-Ⅰ应答的分子机制研究进展

Advances in molecular mechanisms of PEDV structural protein antagonistic IFN-Ⅰ response

  • 摘要: 猪流行性腹泻(porcine epidemic diarrhea, PED)具有很高的发病率和死亡率,尤其是在猪流行性腹泻病毒(Porcine epidemic diarrhea virus, PEDV)高致病性变异株(GⅡ型毒株)出现以来,更是对全球养猪业构成了巨大威胁。病毒感染宿主之后,宿主会激活抗病毒天然免疫应答机制。干扰素(interferon, IFN)作为一类抵御病毒感染的关键分子,特别是Ⅰ型干扰素(IFN-Ⅰ)可通过激活各种免疫细胞和共刺激分子来颉颃病毒的增殖。与此同时,为实现在宿主内的持续复制,许多病毒建立了颉颃宿主机体IFN-Ⅰ应答的多种分子机制,进而实现免疫逃逸。PEDV编码的多种结构蛋白可以颉颃宿主IFN-Ⅰ免疫应答。文章综述了PEDV结构蛋白颉颃IFN-Ⅰ免疫应答的分子机制,以期为深入阐释PEDV免疫逃逸的分子机制与开发PEDV新型靶向药物和建立防控新策略提供科学参考。

     

    Abstract: Porcine epidemic diarrhea(PED) has high morbidity and mortality, especially since the emergence of highly pathogenic variant of Porcine epidemic diarrhea virus(PEDV)(GⅡ strain). It is a huge threat to the global pig industry. After the virus infects the host, the host will activate the antiviral natural immune response mechanism. Interferon(IFN) is a kind of key molecule to resist virus infection, especially type Ⅰ interferon(IFN-Ⅰ), which can prevent the proliferation of the opponent virus by activating various immune cells and co-stimulating molecules. At the same time, in order to achieve sustained replication in the host, many viruses have established a variety of molecular mechanisms to resist the IFN-Ⅰ response of the opponent host, and thus achieve immune escape. Many structural proteins encoded by PEDV can inhibit the immune response of the opponent host IFN-Ⅰ. In this paper, the molecular mechanism of PEDV structural protein antagonistic IFN-Ⅰ immune response was reviewed, in order to provide scientific reference for further elucidation of the molecular mechanism of PEDV immune escape and development of novel PEDV targeted drugs and new prevention and control strategies.

     

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