Ghazala Walid, Varrelmann Mark
University of Göttingen, Department of Crop Sciences, Section Plant Virology, Grisebachstr. 6, 37077 Göttingen, Germany.
Mol Plant Microbe Interact. 2007 Nov;20(11):1396-405. doi: 10.1094/MPMI-20-11-1396.
Leaf infection experiments were used to analyze the host responses of Solanum tuberosum cultivars known to be resistant or susceptible to natural, nematode-mediated infection of tubers and necrosis induction ("spraing") by Tobacco rattle virus (TRV) isolate PpK20 (TRV-PpK20). Extreme and hypersensitive-like resistance (ER and HR-like, respectively) as well as spreading veinal necrosis and systemic infection were observed. Agroinfection of leaves with a DsRed-expressing TRV cDNA clone revealed ER to function on the single-cell level, inhibiting virus replication and possessing the potential to initiate a cell death response. HR-like necrosis was characterized by initial virus replication and cell-to-cell movement before the onset of necrosis. Transient agroexpression and Potato virus X (PVX)-mediated expression assays demonstrated that the 29K-PpK20 movement protein (MP) can elicit ER and HR-like cell-death. A TRV isolate, PpO85M, known to overcome the resistance to spraing in plants that are resistant to TRV-PpK20 encoded a variant 29K protein which did not elicit HR in PpK20-HR plants. Our results show that the TRV MP is the elicitor of both ER and HR-like cell-death, that no other TRV-encoded proteins or RNA replication are required for its elicitor activity, and that the host reactions are likely to be controlled by single dominant resistance genes.
通过叶片感染实验分析了马铃薯(Solanum tuberosum)品种对烟草脆裂病毒(TRV)分离株PpK20(TRV-PpK20)介导的块茎自然感染和坏死诱导(“块茎畸形”)的抗性或敏感性的宿主反应。观察到了极端抗性和类过敏抗性(分别为ER和HR样)以及脉间坏死扩展和系统感染。用表达DsRed的TRV cDNA克隆对叶片进行农杆菌感染,结果显示ER在单细胞水平上起作用,抑制病毒复制并具有引发细胞死亡反应的潜力。类过敏坏死的特征是在坏死发生之前病毒先进行复制并在细胞间移动。瞬时农杆菌表达和马铃薯X病毒(PVX)介导的表达分析表明,29K-PpK20运动蛋白(MP)可引发ER和类过敏细胞死亡。已知TRV分离株PpO85M能克服对TRV-PpK20具有抗性的植物对块茎畸形的抗性,它编码一种变体29K蛋白,在PpK20-HR植物中不会引发HR。我们的结果表明,TRV MP是ER和类过敏细胞死亡的激发子,其激发子活性不需要其他TRV编码的蛋白或RNA复制,并且宿主反应可能由单个显性抗性基因控制。