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口蹄疫病毒通过靶向 MDA5 的 3C 逃避先天免疫反应。

Foot-and-Mouth Disease Virus Evades Innate Immune Response by 3C-Targeting of MDA5.

机构信息

Animal and Plant Quarantine Agency, Gimcheon-si 39660, Korea.

College of Veterinary Medicine, Animal Disease Intervention Center, Kyungpook National University, Daegu 41566, Korea.

出版信息

Cells. 2021 Jan 29;10(2):271. doi: 10.3390/cells10020271.

Abstract

Foot-and-mouth disease (FMD) is a highly contagious disease caused by FMD virus (FMDV) in cloven-hoofed animals. Retinoic acid-inducible gene I (RIG-I) and melanoma differentiation-associated gene 5 (MDA5) are representative receptors in the cytoplasm for the detection of viral RNA and trigger antiviral responses, leading to the production of type I interferon. Although MDA5 is a crucial receptor for sensing picornavirus RNA, the interplay between MDA5 and FMDV is relatively unknown compared to the interplay between RIG-I and FMDV. Here, we observed that the FMDV infection inhibits MDA5 protein expression. Of the non-structural proteins, the Lb and 3C proteinases (Lb and 3C) were identified to be primarily responsible for this inhibition. However, the inhibition by 3C was independent of proteasome, lysosome and caspase-dependent pathway and was by 3C protease activity. A direct interaction between 3C and MDA5 protein was observed. In conclusion, this is the first report that 3C inhibits MDA5 protein expression as a mechanism to evade the innate immune response during FMDV infection. These results elucidate the pathogenesis of FMDV and provide fundamental insights for the development of a novel vaccine or therapeutic agent.

摘要

口蹄疫(FMD)是一种由口蹄疫病毒(FMDV)引起的偶蹄动物高度传染性疾病。维甲酸诱导基因 I(RIG-I)和黑色素瘤分化相关基因 5(MDA5)是细胞质中用于检测病毒 RNA 并触发抗病毒反应的代表性受体,导致 I 型干扰素的产生。尽管 MDA5 是识别小 RNA 病毒 RNA 的重要受体,但与 RIG-I 和 FMDV 的相互作用相比,MDA5 和 FMDV 之间的相互作用相对未知。在这里,我们观察到 FMDV 感染抑制 MDA5 蛋白表达。在非结构蛋白中,鉴定出 Lb 和 3C 蛋白酶(Lb 和 3C)主要负责这种抑制。然而,3C 的抑制不依赖于蛋白酶体、溶酶体和半胱天冬酶依赖性途径,而是依赖于 3C 蛋白酶活性。观察到 3C 和 MDA5 蛋白之间的直接相互作用。总之,这是第一项报道 3C 通过抑制 MDA5 蛋白表达来逃避 FMDV 感染期间固有免疫反应的机制的报告。这些结果阐明了 FMDV 的发病机制,并为新型疫苗或治疗剂的开发提供了基础见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c61/7912020/44722a21e169/cells-10-00271-g001.jpg

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