Rhabdovirus encoded glycoprotein induces and harnesses host antiviral autophagy for maintaining its compatible infection.

IF 14.6 1区 生物学 Q1 CELL BIOLOGY
Autophagy Pub Date : 2024-02-01 Epub Date: 2023-09-01 DOI:10.1080/15548627.2023.2252273
Xiuqin Huang, Junkai Wang, Siping Chen, Siying Liu, Zhanbiao Li, Zhiyi Wang, Biao Chen, Chong Zhang, Yifei Zhang, Jinhui Wu, Xiaorong Yang, Qingjun Xie, Faqiang Li, Hong An, Jilei Huang, Huali Li, Chuanhe Liu, Xiaoxian Wu, Ding Xiang Liu, Xin Yang, Guohui Zhou, Tong Zhang
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引用次数: 0

Abstract

Macroautophagy/autophagy has been recognized as a central antiviral defense mechanism in plant, which involves complex interactions between viral proteins and host factors. Rhabdoviruses are single-stranded RNA viruses, and the infection causes serious harm to public health, livestock, and crop production. However, little is known about the role of autophagy in the defense against rhabdovirus infection by plant. In this work, we showed that Rice stripe mosaic cytorhabdovirus(RSMV) activated autophagy in plants and that autophagy served as an indispensable defense mechanism during RSMV infection. We identified RSMV glycoprotein as an autophagy inducer that interacted with OsSnRK1B and promoted the kinase activity of OsSnRK1B on OsATG6b. RSMV glycoprotein was toxic to rice cells and its targeted degradation by OsATG6b-mediated autophagy was essential to restrict the viral titer in plants. Importantly, SnRK1-glycoprotein and ATG6-glycoprotein interactions were well-conserved between several other rhabdoviruses and plants. Together, our data support a model that SnRK1 senses rhabdovirus glycoprotein for autophagy initiation, while ATG6 mediates targeted degradation of viral glycoprotein. This conserved mechanism ensures compatible infection by limiting the toxicity of viral glycoprotein and restricting the infection of rhabdoviruses.Abbreviations: AMPK: adenosine 5'-monophosphate (AMP)-activated protein kinase; ANOVA: analysis of variance; ATG: autophagy related; AZD: AZD8055; BiFC: bimolecular fluorescence complementation; BYSMV: barley yellow striate mosaic virus; Co-IP: co-immunoprecipitation; ConA: concanamycin A; CTD: C-terminal domain; DEX: dexamethasone; DMSO: dimethyl sulfoxide; G: glycoprotein; GFP: green fluorescent protein; MD: middle domain; MDC: monodansylcadaverine; NTD: N-terminal domain; OE: over expression; Os: Oryza sativa; PBS: phosphate-buffered saline; PtdIns3K: class III phosphatidylinositol-3-kinase; qRT-PCR: quantitative real-time reverse-transcription PCR; RFP: red fluorescent protein; RSMV: rice stripe mosaic virus; RSV: rice stripe virus; SGS3: suppressor of gene silencing 3; SnRK1: sucrose nonfermenting1-related protein kinase1; SYNV: sonchus yellow net virus; TEM: transmission electron microscopy; TM: transmembrane region; TOR: target of rapamycin; TRV: tobacco rattle virus; TYMaV: tomato yellow mottle-associated virus; VSV: vesicular stomatitis virus; WT: wild type; Y2H: yeast two-hybrid; YFP: yellow fluorescent protein.

横纹肌病毒编码的糖蛋白诱导并利用宿主的抗病毒自噬作用来维持其兼容感染。
大自噬/自噬被认为是植物的一种核心抗病毒防御机制,它涉及病毒蛋白与宿主因子之间复杂的相互作用。横纹肌病毒是单链 RNA 病毒,感染后会对公共卫生、牲畜和作物生产造成严重危害。然而,人们对自噬在植物防御横纹肌病毒感染中的作用知之甚少。在这项研究中,我们发现水稻条纹花叶病毒(RSMV)能激活植物的自噬,自噬是RSMV感染过程中不可或缺的防御机制。我们发现RSMV糖蛋白是一种自噬诱导物,它能与OsSnRK1B相互作用并促进OsSnRK1B对OsATG6b的激酶活性。RSMV 糖蛋白对水稻细胞有毒性,OsATG6b 介导的自噬作用对其定向降解是限制植物体内病毒滴度的关键。重要的是,SnRK1-糖蛋白和ATG6-糖蛋白之间的相互作用在其他几种横纹肌病毒和植物之间保存良好。总之,我们的数据支持这样一个模型,即 SnRK1 感知横纹肌病毒糖蛋白以启动自噬,而 ATG6 则介导病毒糖蛋白的定向降解。这种保守的机制通过限制病毒糖蛋白的毒性和限制横纹肌病毒的感染来确保兼容感染:缩写:AMPK:5'-单磷酸腺苷(AMP)激活的蛋白激酶;ANOVA:方差分析;ATG:自噬相关;AZD:AZD8055;BiFC:双分子荧光互补;BYSMV:大麦黄条纹花叶病毒;Co-IP:共免疫沉淀;BYSMV:大麦黄条纹花叶病毒:CTD:C-末端结构域;DEX:地塞米松;DMSO:二甲基亚砜;G:糖蛋白;GFP:绿色荧光蛋白;MD:中间结构域;MDC:单丹参素;NTD:N-末端结构域;OE:过度表达;Os:PBS:磷酸盐缓冲盐水;PtdIns3K:第三类磷脂酰肌醇-3-激酶;qRT-PCR:定量实时反转录 PCR;RFP:红色荧光蛋白;RSMV:水稻条纹花叶病毒;RSV:水稻条纹病毒;SGS3:基因沉默抑制因子 3;SnRK1:蔗糖不发酵 1 相关蛋白激酶 1;SYNV:TEM:透射电子显微镜;TM:跨膜区;TOR:雷帕霉素靶标;TRV:烟草纹枯病病毒;TYMaV:番茄黄斑相关病毒;VSV:水泡性口炎病毒;WT:野生型;Y2H:酵母双杂交;YFP:黄色荧光蛋白。
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来源期刊
Autophagy
Autophagy 生物-细胞生物学
CiteScore
21.30
自引率
2.30%
发文量
277
审稿时长
1 months
期刊介绍: Autophagy is a peer-reviewed journal that publishes research on autophagic processes, including the lysosome/vacuole dependent degradation of intracellular material. It aims to be the premier journal in the field and covers various connections between autophagy and human health and disease, such as cancer, neurodegeneration, aging, diabetes, myopathies, and heart disease. Autophagy is interested in all experimental systems, from yeast to human. Suggestions for specialized topics are welcome. The journal accepts the following types of articles: Original research, Reviews, Technical papers, Brief Reports, Addenda, Letters to the Editor, Commentaries and Views, and Articles on science and art. Autophagy is abstracted/indexed in Adis International Ltd (Reactions Weekly), EBSCOhost (Biological Abstracts), Elsevier BV (EMBASE and Scopus), PubMed, Biological Abstracts, Science Citation Index Expanded, Web of Science, and MEDLINE.
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