青枯菌
青枯病
效应器
泛素
生物
微生物学
病菌
细胞生物学
基因
遗传学
作者
Peipei Qi,Dan Zhang,Ying Zhang,Wanting Zhu,Xinya Du,Xiaoshuang Ma,Chunfang Xiao,Lin Yang,Jiatao Xie,Jiāsēn Chéng,Yànpíng Fù,Daohong Jiang,Xiao Yu,Bo Li
出处
期刊:Cell Reports
[Elsevier]
日期:2024-08-01
卷期号:43 (8): 114596-114596
标识
DOI:10.1016/j.celrep.2024.114596
摘要
The Ralstonia solanacearum species complex causes bacterial wilt in a variety of crops. Tomato cultivar Hawaii 7996 is a widely used resistance resource; however, the resistance is evaded by virulent strains, with the underlying mechanisms still unknown. Here, we report that the phylotype Ⅱ strain ES5-1 can overcome Hawaii 7996 resistance. RipV2, a type Ⅲ effector specific to phylotype Ⅱ strains, is vital in overcoming tomato resistance. RipV2, which encodes an E3 ubiquitin ligase, suppresses immune responses and Toll/interleukin-1 receptor/resistance nucleotide-binding/leucine-rich repeat (NLR) (TNL)-mediated cell death. Tomato helper NLR N requirement gene 1 (NRG1), enhanced disease susceptibility 1 (EDS1), and senescence-associated gene 101b (SAG101b) are identified as RipV2 target proteins. RipV2 is essential for ES5-1 virulence in Hawaii 7996 but not in SlNRG1-silenced tomato, demonstrating SlNRG1 to be an RipV2 virulence target. Our results dissect the mechanisms of RipV2 in disrupting immunity and highlight the importance of converged immune components in conferring bacterial wilt resistance.
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