State Key Laboratory of Rice Biology, Institute of Biotechnology, Zhejiang University, Hangzhou, China.
State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, China.
Mol Plant Pathol. 2018 Oct;19(10):2288-2301. doi: 10.1111/mpp.12699. Epub 2018 Aug 7.
Nucleorhabdoviruses such as Sonchus yellow net virus (SYNV) replicate in the nuclei and undergo morphogenesis at the inner nuclear membrane (IM) in plant cells. Mature particles are presumed to form by budding of the Matrix (M) protein-nucleocapsid complexes through host IMs to acquire host phospholipids and the surface glycoproteins (G). To address mechanisms underlying nucleorhabdovirus budding, we generated recombinant SYNV G mutants containing a truncated amino-terminal (NT) or carboxyl-terminal (CT) domain. Electron microscopy and sucrose gradient centrifugation analyses showed that the CT domain is essential for virion morphogenesis whereas the NT domain is also required for efficient budding. SYNV infection induces IM invaginations that are thought to provide membrane sites for virus budding. We found that in the context of viral infections, interactions of the M protein with the CT domain of the membrane-anchored G protein mediate M protein translocation and IM invagination. Interestingly, tethering the M protein to endomembranes, either by co-expression with a transmembrane G protein CT domain or by artificial fusion with the G protein membrane targeting sequence, induces IM invagination in uninfected cells. Further evidence to support functions of G-M interactions in virus budding came from dominant negative effects on SYNV-induced IM invagination and viral infections that were elicited by expression of a soluble version of the G protein CT domain. Based on these data, we propose that cooperative G-M interactions promote efficient SYNV budding.
核型多角体病毒(如向日葵黄网病毒,SYNV)在植物细胞核内复制,并在内核膜(IM)处进行形态发生。成熟颗粒被认为是通过基质(M)蛋白-核衣壳复合物通过宿主 IM 出芽形成的,以获得宿主磷脂和表面糖蛋白(G)。为了解核型多角体病毒出芽的机制,我们生成了含有截短的氨基末端(NT)或羧基末端(CT)结构域的重组 SYNV G 突变体。电子显微镜和蔗糖梯度离心分析表明,CT 结构域对于病毒形态发生至关重要,而 NT 结构域对于有效的出芽也是必需的。SYNV 感染诱导内体凹陷,这些凹陷被认为是病毒出芽的膜位点。我们发现,在病毒感染的情况下,M 蛋白与膜锚定 G 蛋白的 CT 结构域的相互作用介导 M 蛋白易位和内体凹陷。有趣的是,通过与跨膜 G 蛋白 CT 结构域共表达或与 G 蛋白膜靶向序列的人工融合将 M 蛋白固定在内质网上,会在未感染的细胞中诱导内体凹陷。支持 G-M 相互作用在病毒出芽中的功能的进一步证据来自于通过表达可溶性 G 蛋白 CT 结构域表达对 SYNV 诱导的内体凹陷和病毒感染的显性负效应。基于这些数据,我们提出协同的 G-M 相互作用促进了 SYNV 的有效出芽。