Rao Weiwei, Ma Tingting, Cao Jiayuan, Zhang Yajun, Chen Sisi, Lin Shu, Liu Xiaoxiao, He Guangcun, Wan Li
Key Laboratory of Plant Design, CAS Center for Excellence in Molecular Plant Sciences, Institute of Plant Physiology and Ecology, Chinese Academy of Sciences, Shanghai, 200032, China.
National Key Laboratory of Hybrid Rice, College of Life Sciences, Wuhan University, Wuhan, 430072, China.
J Integr Plant Biol. 2025 Jan;67(1):150-168. doi: 10.1111/jipb.13800. Epub 2024 Oct 30.
Insects secret chemosensory proteins (CSPs) into plant cells as potential effector proteins during feeding. The molecular mechanisms underlying how CSPs activate plant immunity remain largely unknown. We show that CSPs from six distinct insect orders induce dwarfism when overexpressed in Nicotiana benthamiana. Agrobacterium-mediated transient expression of Nilaparvata lugens CSP11 (NlCSP11) triggered cell death and plant dwarfism, both of which were dependent on ENHANCED DISEASE SUSCEPTIBILITY 1 (EDS1), N requirement gene 1 (NRG1) and SENESCENCE-ASSOCIATED GENE 101 (SAG101), indicating the activation of effector-triggered immunity (ETI) in N. benthamiana. Overexpression of NlCSP11 led to stronger systemic resistance against Pseudomonas syringae DC3000 lacking effector HopQ1-1 and tobacco mosaic virus, and induced higher accumulation of salicylic acid (SA) in uninfiltrated leaves compared to another effector XopQ that is recognized by a Toll-interleukin-1 receptor (TIR) domain nucleotide-binding leucine-rich repeat receptor (TNL) called ROQ1 in N. benthamiana. Consistently, NlCSP11-induced dwarfism and systemic resistance, but not cell death, were abolished in N. benthamiana transgenic line expressing the SA-degrading enzyme NahG. Through large-scale virus-induced gene silencing screening, we identified a TNL protein that mediates the recognition of CSPs (RCSP), including aphid effector MP10 that triggers resistance against aphids in N. benthamiana. Co-immunoprecipitation, bimolecular fluorescence complementation and AlphaFold2 prediction unveiled an interaction between NlCSP11 and RCSP. Interestingly, RCSP does not contain the conserved catalytic glutamic acid in the TIR domain, which is required for TNL function. Our findings point to enhanced ETI and systemic resistance by a TNL protein via hyperactivation of the SA pathway. Moreover, RCSP is the first TNL identified to recognize an insect effector.
昆虫在取食过程中会向植物细胞分泌化学感应蛋白(CSPs)作为潜在的效应蛋白。CSPs激活植物免疫的分子机制在很大程度上仍不清楚。我们发现,来自六个不同昆虫目的CSPs在本氏烟草中过表达时会导致植株矮化。通过农杆菌介导瞬时表达褐飞虱CSP11(NlCSP11)会引发细胞死亡和植株矮化,这两者都依赖于增强的疾病易感性1(EDS1)、N需求基因1(NRG1)和衰老相关基因101(SAG101),表明本氏烟草中效应子触发免疫(ETI)被激活。与另一个效应子XopQ相比,NlCSP11的过表达导致对缺乏效应子HopQ1-1的丁香假单胞菌DC3000和烟草花叶病毒具有更强的系统抗性,并且在未浸润的叶片中诱导水杨酸(SA)积累更高,XopQ在本氏烟草中被一种名为ROQ1的Toll样白细胞介素-1受体(TIR)结构域核苷酸结合富含亮氨酸重复序列受体(TNL)识别。一致地,在表达SA降解酶NahG的本氏烟草转基因系中,NlCSP11诱导的矮化和系统抗性,但不是细胞死亡,被消除。通过大规模病毒诱导的基因沉默筛选,我们鉴定出一种介导对CSPs识别的TNL蛋白(RCSP),包括在本氏烟草中触发对蚜虫抗性的蚜虫效应子MP10。免疫共沉淀、双分子荧光互补和AlphaFold2预测揭示了NlCSP11与RCSP之间的相互作用。有趣的是,RCSP在TIR结构域中不包含TNL功能所需的保守催化谷氨酸。我们的研究结果表明,一种TNL蛋白通过SA途径的过度激活增强了ETI和系统抗性。此外,RCSP是第一个被鉴定出识别昆虫效应子的TNL。