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甲型流感病毒核蛋白通过诱导细胞自噬抑制固有免疫反应。

The nucleoprotein of influenza A virus inhibits the innate immune response by inducing mitophagy.

机构信息

State Key Laboratory of Veterinary Etiological Biology, College of Veterinary Medicine, Lanzhou University, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, PR China.

College of Veterinary Medicine, Gansu Agricultural University, Lanzhou, PR China.

出版信息

Autophagy. 2023 Jul;19(7):1916-1933. doi: 10.1080/15548627.2022.2162798. Epub 2023 Jan 1.

Abstract

Mitophagy is a form of autophagy that plays a key role in maintaining the homeostasis of functional mitochondria in the cell. Viruses have evolved various strategies to manipulate mitophagy to escape host immune responses and promote virus replication. In this study, the nucleoprotein (NP) of H1N1 virus (PR8 strain) was identified as a regulator of mitophagy. We revealed that NP-mediated mitophagy leads to the degradation of the mitochondria-anchored protein MAVS, thereby blocking MAVS-mediated antiviral signaling and promoting virus replication. The NP-mediated mitophagy is dependent on the interaction of NP with MAVS and the cargo receptor TOLLIP. Moreover, Y313 of NP is a key residue for the MAVS-NP interaction and NP-mediated mitophagy. The NP mutation significantly attenuates the virus-induced mitophagy and the virus replication and . Taken together, our findings uncover a novel mechanism by which the NP of influenza virus induces mitophagy to attenuate innate immunity. ACTB: actin beta; ATG7: autophagy related 7; ATG12: autophagy related 12; CCCP: carbonyl cyanide 3-chlorophenyl hydrazone; co-IP: co-immunoprecipitation; COX4/COXIV: cytochrome c oxidase subunit 4; DAPI: 4',6-diamidino-2-phenylindole, dihydrochloride; EID: 50% egg infective dose; GAPDH: glyceraldehyde-3-phosphate dehydrogenase; GFP: green fluorescent protein; HEK: human embryonic kidney; hpi: hours post-infection; IAV: influenza A virus; IFN: interferon; IP: immunoprecipitation; LAMP1: lysosomal associated membrane protein 1; MAP1LC3/LC3: microtubule associated protein 1 light chain 3; MAVS: mitochondrial antiviral signaling protein; Mdivi-1: mitochondrial division inhibitor 1; MLD: 50% mouse lethal dose; MOI: multiplicity of infection; NBR1: NBR1 autophagy cargo receptor; NP: nucleoprotein; PB1: basic polymerase 1; RFP: red fluorescent protein; RIGI: RNA sensor RIG-I; RIGI-N: RIGI-CARD; SeV: Sendai virus; SQSTM1/p62: sequestosome 1; TIMM23: translocase of inner mitochondrial membrane 23; TOLLIP: toll interacting protein; TOMM20: translocase of outer mitochondrial membrane 20; TUBA: tubulin alpha; Vec: empty vector; vRNP: viral ribonucleoprotein.

摘要

自噬是一种在细胞内维持功能性线粒体动态平衡的重要过程。病毒已经进化出多种策略来操纵自噬,以逃避宿主的免疫反应并促进病毒复制。在这项研究中,甲型 H1N1 病毒(PR8 株)的核蛋白(NP)被鉴定为自噬的调节剂。我们揭示了 NP 介导的自噬导致线粒体锚定蛋白 MAVS 的降解,从而阻断了 MAVS 介导的抗病毒信号转导并促进了病毒复制。NP 介导的自噬依赖于 NP 与 MAVS 和货物受体 TOLLIP 的相互作用。此外,NP 的 Y313 是 MAVS-NP 相互作用和 NP 介导的自噬的关键残基。NP 突变显著减弱了病毒诱导的自噬和病毒复制。总之,我们的研究结果揭示了流感病毒 NP 通过诱导自噬来减弱先天免疫的新机制。ACTB:肌动蛋白β;ATG7:自噬相关 7;ATG12:自噬相关 12;CCCP:羰基氰化物 3-氯苯腙;co-IP:免疫共沉淀;COX4/COXIV:细胞色素 c 氧化酶亚基 4;DAPI:4',6-二脒基-2-苯基吲哚二盐酸盐;EID:50%鸡胚感染剂量;GAPDH:甘油醛-3-磷酸脱氢酶;GFP:绿色荧光蛋白;HEK:人胚肾;hpi:感染后小时数;IAV:甲型流感病毒;IFN:干扰素;IP:免疫沉淀;LAMP1:溶酶体相关膜蛋白 1;MAP1LC3/LC3:微管相关蛋白 1 轻链 3;MAVS:线粒体抗病毒信号蛋白;Mdivi-1:线粒体分裂抑制剂 1;MLD:50%鼠致死剂量;MOI:感染复数;NBR1:NBR1 自噬货物受体;NP:核蛋白;PB1:基本聚合酶 1;RFP:红色荧光蛋白;RIGI:RNA 传感器 RIG-I;RIGI-N:RIGI-CARD;SeV:仙台病毒;SQSTM1/p62:自噬体相关蛋白 1;TIMM23:线粒体内膜 23 转位酶;TOLLIP: toll 相互作用蛋白;TOMM20:外线粒体膜 20 转位酶;TUB:微管蛋白 α;Vec:空载体;vRNP:病毒核糖核蛋白。

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