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Rhabdovirus 编码的糖蛋白诱导并利用宿主抗病毒自噬来维持其兼容感染。

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

机构信息

National Key Laboratory of Green Pesticide, South China Agricultural University, Guangzhou, Guangdong, China.

Guangdong Province Key Laboratory of Microbial Signals and Disease Control, College of Plant Protection, South China Agricultural University, Guangzhou, Guangdong, China.

出版信息

Autophagy. 2024 Feb;20(2):275-294. doi: 10.1080/15548627.2023.2252273. Epub 2023 Sep 1.

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 (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. 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: ; 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.

摘要

自噬/自噬已被确认为植物中的一种重要的抗病毒防御机制,其中涉及病毒蛋白与宿主因子之间的复杂相互作用。弹状病毒是单链 RNA 病毒,其感染对公共卫生、畜牧业和作物生产造成严重危害。然而,对于自噬在植物抵抗弹状病毒感染中的作用知之甚少。在这项工作中,我们表明(RSMV)在植物中激活了自噬,并且自噬是 RSMV 感染过程中不可或缺的防御机制。我们鉴定出 RSMV 糖蛋白是一种自噬诱导物,它与 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,其通过 OsATG6b 介导的自噬靶向降解对于限制植物中的病毒滴度至关重要。重要的是,SnRK1-糖蛋白和 ATG6-糖蛋白之间的相互作用在几种其他弹状病毒和植物之间很好地保守。总之,我们的数据支持这样一种模型,即 SnRK1 感应弹状病毒糖蛋白以启动自噬,而 ATG6 介导病毒糖蛋白的靶向降解。这种保守的机制通过限制病毒糖蛋白的毒性并限制弹状病毒的感染,确保了兼容感染。AMPK:腺苷 5'-单磷酸(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:大麦黄花条纹花叶病毒;Co-IP:免疫共沉淀;ConA:康纳霉素 A;CTD:C 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:中域;MDC:单丹磺酰尸胺;NTD:N 端结构域;OE:过表达;Os:;PBS:磷酸盐缓冲盐水;PtdIns3K:III 类磷酸肌醇 3-激酶;qRT-PCR:实时定量 RT-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:基因沉默抑制物 3 抑制物;SnRK1:蔗糖非发酵 1 相关蛋白激酶 1;SYNV:丝瓜黄网病毒;TEM:透射电子显微镜;TM:跨膜区;TOR:雷帕霉素靶蛋白;TRV:烟草脆裂病毒;TYMaV:番茄黄斑驳相关病毒;VSV:水疱性口炎病毒;WT:野生型;Y2H:酵母双杂交;YFP:黄色荧光蛋白。

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