Zhang Wen-Kang, Yan Jia-Min, Chu Min, Li Bang, Gu Xiao-Lan, Jiang Ze-Zheng, Li Ze-Min, Liu Pan-Pan, Yu Tian-Mei, Zhou Chuan-Min, Yu Xue-Jie
State Key Laboratory of Virology, School of Public Health, Wuhan University, Wuhan, China.
Department of Laboratory Medicine, Wuhan Children's Hospital (Wuhan Maternal and Child Healthcare Hospital), Tongji Medical College, Huazhong University of Science and Technology, Wuhan, P. R. China.
Autophagy. 2025 Jan;21(1):102-119. doi: 10.1080/15548627.2024.2393067. Epub 2024 Sep 12.
Severe fever with thrombocytopenia syndrome is an emerging viral hemorrhagic fever caused by a tick-borne bunyavirus, severe fever with thrombocytopenia syndrome virus (SFTSV), with a high case fatality. We previously found that SFTSV nucleoprotein (NP) induces macroautophagy/autophagy to facilitate virus replication. However, the role of NP in antagonizing host innate immunity remains unclear. Mitophagy, a selected form of autophagy, eliminates damaged mitochondria to maintain mitochondrial homeostasis. Here, we demonstrate that SFTSV NP triggers mitophagy to degrade MAVS (mitochondrial antiviral signaling protein), thereby blocking MAVS-mediated antiviral signaling to escape the host immune response. Mechanistically, SFTSV NP translocates to mitochondria by interacting with TUFM (Tu translation elongation factor, mitochondrial), and mediates mitochondrial sequestration into phagophores through interacting with LC3, thus inducing mitophagy. Notably, the N-terminal LC3-interacting region (LIR) motif of NP is essential for mitophagy induction. Collectively, our results demonstrated that SFTSV NP serves as a novel virulence factor, inducing TUFM-mediated mitophagy to degrade MAVS and evade the host immune response. 3-MA: 3-methyladenine; ACTB: actin beta; co-IP: co-immunoprecipitation; CQ: chloroquine; DAPI: 4',6-diamidino-2-phenylindole, dihydrochloride; DMSO: dimethyl sulfoxide; FCCP: carbonyl cyanide 4-(trifluoromethoxy)phenylhydrazone; GFP: green fluorescent protein; HTNV: Hantan virus; IAV: influenza A virus; IFN: interferon; LAMP1: lysosomal associated membraneprotein 1; LIR: LC3-interacting region; MAP1LC3B/LC3B: microtubule associatedprotein 1 light chain 3 beta; MAVS: mitochondrial antiviral signaling protein; Mdivi-1: mitochondrial division inhibitor 1; MOI: multiplicity of infection; MT-CO2/COXII: mitochondrially encoded cytochrome C oxidase II; NP: nucleoprotein; NSs: nonstructural proteins; poly(I:C): polyinosinic:polycytidylic acid; RIGI: RNA sensor RIG-I; RLR: RIGI-like receptor; SFTSV: severe fever withthrombocytopenia syndrome virus; TCID50: 50% tissue culture infectiousdose; TIMM23: translocase of inner mitochondrial membrane 23; TOMM20:translocase of outer mitochondrial membrane 20; TUFM: Tu translation elongationfactor, mitochondrial.
发热伴血小板减少综合征是一种由蜱传布尼亚病毒——发热伴血小板减少综合征病毒(SFTSV)引起的新型病毒性出血热,病死率高。我们先前发现,SFTSV核蛋白(NP)可诱导巨自噬/自噬以促进病毒复制。然而,NP在拮抗宿主天然免疫中的作用仍不清楚。线粒体自噬是一种特定形式的自噬,可清除受损线粒体以维持线粒体稳态。在此,我们证明SFTSV NP触发线粒体自噬以降解线粒体抗病毒信号蛋白(MAVS),从而阻断MAVS介导的抗病毒信号传导以逃避宿主免疫反应。机制上,SFTSV NP通过与线粒体Tu翻译延伸因子(TUFM)相互作用转位至线粒体,并通过与微管相关蛋白1轻链3β(MAP1LC3B/LC3B)相互作用介导线粒体被隔离至吞噬体中,从而诱导线粒体自噬。值得注意的是,NP的N端LC3相互作用区域(LIR)基序对于诱导线粒体自噬至关重要。总体而言,我们的结果表明,SFTSV NP作为一种新型毒力因子,诱导TUFM介导的线粒体自噬以降解MAVS并逃避宿主免疫反应。3-MA:3-甲基腺嘌呤;ACTB:肌动蛋白β;免疫共沉淀:co-免疫沉淀;CQ:氯喹;DAPI:4′,6-二脒基-2-苯基吲哚二盐酸盐;DMSO:二甲基亚砜;FCCP:羰基氰化物4-(三氟甲氧基)苯腙;GFP:绿色荧光蛋白;汉坦病毒:HTNV;甲型流感病毒:IAV;干扰素:IFN;溶酶体相关膜蛋白1:LAMP1;LIR:LC3相互作用区域;微管相关蛋白1轻链3β:MAP1LC3B/LC3B;线粒体抗病毒信号蛋白:MAVS;线粒体分裂抑制剂1:Mdivi-1;感染复数:MOI;线粒体编码的细胞色素C氧化酶II:MT-CO2/COXII;核蛋白:NP;非结构蛋白:NSs;聚肌苷酸:聚胞苷酸:poly(I:C);RNA传感器视黄酸诱导基因I:RIGI;RIGI样受体:RLR;发热伴血小板减少综合征病毒:SFTSV;50%组织培养感染剂量:TCID50;线粒体内膜转位酶23:TIMM23;线粒体外膜转位酶20:TOMM20;线粒体Tu翻译延伸因子:TUFM