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黄瓜绿斑驳花叶病毒外壳蛋白劫持线粒体 ATPδ 促进病毒感染。

Cucumber Green Mottle Mosaic Virus Coat Protein Hijacks Mitochondrial ATPδ to Promote Viral Infection.

机构信息

College of Plant Protection, Henan Agricultural University, Zhengzhou, China.

State Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-Products, Institute of Plant Virology, Ningbo University, Ningbo, China.

出版信息

Mol Plant Pathol. 2024 Nov;25(11):e70034. doi: 10.1111/mpp.70034.

Abstract

The production and scavenging of reactive oxygen species (ROS) are critical for plants to adapt to biotic and abiotic stresses. In this study, we investigated the interaction between the coat protein (CP) of cucumber green mottle mosaic virus (CGMMV) and ATP synthase subunit δ (ATPδ) in mitochondria. Silencing of ATPδ by tobacco rattle virus-based virus-induced gene silencing impeded CGMMV accumulation in Nicotiana benthamiana leaves. Both the overexpression of ATPδ in transgenic plants and transient expression promoted CGMMV infection. Nitro blue tetrazolium (NBT) and 3,3'-diaminobenzidine (DAB) staining revealed that ATPδ inhibited O production but not HO production. The treatment of CGMMV-infected leaves with the ROS inhibitor diphenylene iodonium (DPI) induced a ROS burst that inhibited CGMMV infection. Reverse transcription-quantitative PCR and superoxide dismutase (SOD) activity assays showed that ATPδ, CGMMV infection, and CP expression specifically induced NbFeSOD3/4 expression and SOD activity, and silencing NbFeSOD3/4 inhibited CGMMV infection. We speculate that CGMMV CP interacts with ATPδ and hijacks it, thereby enhancing O quenching by upregulating NbFeSOD expression and, in turn, SOD activity.

摘要

活性氧(ROS)的产生和清除对于植物适应生物和非生物胁迫至关重要。在本研究中,我们研究了黄瓜绿斑驳花叶病毒(CGMMV)衣壳蛋白(CP)与线粒体中 ATP 合酶亚基 δ(ATPδ)之间的相互作用。基于烟草脆裂病毒的病毒诱导基因沉默使 ATPδ 沉默,从而阻碍了 CGMMV 在烟草原生质体叶片中的积累。在转基因植物中过表达 ATPδ 和瞬时表达均促进了 CGMMV 的感染。氮蓝四唑(NBT)和 3,3'-二氨基联苯胺(DAB)染色表明,ATPδ 抑制了 O2 的产生但不抑制 HO 的产生。用 ROS 抑制剂二苯基碘鎓(DPI)处理感染 CGMMV 的叶片会引发 ROS 爆发,从而抑制 CGMMV 的感染。逆转录定量 PCR 和超氧化物歧化酶(SOD)活性测定表明,ATPδ、CGMMV 感染和 CP 表达特异性诱导了 NbFeSOD3/4 的表达和 SOD 活性,而沉默 NbFeSOD3/4 则抑制了 CGMMV 的感染。我们推测 CGMMV CP 与 ATPδ 相互作用并劫持它,从而通过上调 NbFeSOD 的表达增强 O2 的猝灭作用,并由此增强 SOD 活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15e2/11588859/5d3ebc26d176/MPP-25-e70034-g004.jpg

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