Department of Agricultural and Environmental Biology, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Bunkyo-ku, Tokyo 113-8657, Japan.
Mol Plant Microbe Interact. 2011 Apr;24(4):408-20. doi: 10.1094/MPMI-12-10-0279.
Systemic necrosis is the most destructive symptom induced by plant pathogens. We previously identified amino acid 1154, in the polymerase domain (POL) of RNA-dependent RNA polymerase (RdRp) of Plantago asiatica mosaic virus (PlAMV), which affects PlAMV-induced systemic necrosis in Nicotiana benthamiana. By point-mutation analysis, we show that amino acid 1,154 alone is not sufficient for induction of necrotic symptoms. However, PlAMV replicons that can express only RdRp, derived from a necrosis-inducing PlAMV isolate, retain their ability to induce necrosis, and transient expression of PlAMV-encoded proteins indicated that the necrosis-eliciting activity resides in RdRp. Moreover, inducible-overexpression analysis demonstrated that the necrosis was induced in an RdRp dose-dependent manner. In addition, during PlAMV infection, necrotic symptoms are associated with high levels of RdRp accumulation. Surprisingly, necrosis-eliciting activity resides in the helicase domain (HEL), not in the amino acid 1,154-containing POL, of RdRp, and this activity was observed even in HELs of PlAMV isolates of which infection does not cause necrosis. Moreover, HEL-induced necrosis had characteristics similar to those induced by PlAMV infection. Overall, our data suggest that necrotic symptoms induced by PlAMV infection depend on the accumulation of a non-isolate specific elicitor HEL (even from nonnecrosis isolates), whose expression is indirectly regulated by amino acid 1,154 that controls replication.
系统性坏死是植物病原体引起的最具破坏性的症状。我们之前在车前草花叶病毒(PlAMV)的 RNA 依赖性 RNA 聚合酶(RdRp)聚合酶结构域(POL)中鉴定出第 1154 位氨基酸,该氨基酸影响车前草花叶病毒诱导的烟草原生质体系统性坏死。通过定点突变分析,我们表明第 1154 位氨基酸本身不足以诱导坏死症状。然而,只能表达 RdRp 的来自坏死诱导 PlAMV 分离株的 PlAMV 复制子保留了诱导坏死的能力,并且 PlAMV 编码蛋白的瞬时表达表明坏死引发活性存在于 RdRp 中。此外,可诱导的过表达分析表明,坏死是 RdRp 剂量依赖性诱导的。此外,在 PlAMV 感染期间,坏死症状与 RdRp 的高水平积累相关。令人惊讶的是,坏死引发活性存在于 RdRp 的解旋酶结构域(HEL)中,而不是在包含第 1154 位氨基酸的 POL 中,甚至在感染不会引起坏死的 PlAMV 分离株的 HEL 中也观察到了这种活性。此外,HEL 诱导的坏死具有与 PlAMV 感染诱导的坏死相似的特征。总体而言,我们的数据表明,PlAMV 感染诱导的坏死症状取决于非分离特异性引发剂 HEL(甚至来自非坏死分离株)的积累,其表达受控制复制的第 1154 位氨基酸间接调节。