Phytophthora infestans RXLR effector Pi23014 targets host RNA-binding protein NbRBP3a to suppress plant immunity

被引:3
|
作者
Li, Wanyue [1 ,2 ]
Liu, Zeming [1 ,2 ]
Huang, Yuli [1 ,2 ]
Zheng, Jie [1 ,2 ]
Yang, Yang [1 ,2 ,3 ,4 ]
Cao, Yimeng [1 ,2 ]
Ding, Liwen [1 ,2 ]
Meng, Yuling [1 ,2 ]
Shan, Weixing [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Northwest A&F Univ, State Key Lab Crop Stress Resistance & High Effic, Yangling, Shaanxi, Peoples R China
[2] Northwest A&F Univ, Coll Agron, Yangling, Shaanxi, Peoples R China
[3] Northwest A&F Univ, State Key Lab Crop Stress Resistance & High Effic, Yangling, Shaanxi, Peoples R China
[4] Northwest A&F Univ, Coll Plant Protect, Yangling, Shaanxi, Peoples R China
[5] Northwest A&F Univ, State Key Lab Crop Stress Resistance & High Effic, Coll Agron, Yangling 712100, Shaanxi, Peoples R China
[6] Northwest A&F Univ, Coll Plant Protect, Yangling 712100, Shaanxi, Peoples R China
关键词
glycine-rich RNA-binding protein; Phytophthora infestans; Pi23014; PSII activity; PTI; RXLR effectors; SINGLET OXYGEN; CELL-DEATH; CHLOROPLASTS; RESPONSES; DISEASE;
D O I
10.1111/mpp.13416
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Phytophthora infestans is a destructive oomycete that causes the late blight of potato and tomato worldwide. It secretes numerous small proteins called effectors in order to manipulate host cell components and suppress plant immunity. Identifying the targets of these effectors is crucial for understanding P. infestans pathogenesis and host plant immunity. In this study, we show that the virulence RXLR effector Pi23014 of P. infestans targets the host nucleus and chloroplasts. By using a liquid chromatogrpahy-tandem mass spectrometry assay and co-immunoprecipitation assasys, we show that it interacts with NbRBP3a, a putative glycine-rich RNA-binding protein. We confirmed the co-localization of Pi23014 and NbRBP3a within the nucleus, by using bimolecular fluorescence complementation. Reverse transcription-quantitative PCR assays showed that the expression of NbRBP3a was induced in Nicotiana benthamiana during P. infestans infection and the expression of marker genes for multiple defence pathways were significantly down-regulated in NbRBP3-silenced plants compared with GFP-silenced plants. Agrobacterium tumefaciens-mediated transient overexpression of NbRBP3a significantly enhanced plant resistance to P. infestans. Mutations in the N-terminus RNA recognition motif (RRM) of NbRBP3a abolished its interaction with Pi23014 and eliminated its capability to enhance plant resistance to leaf colonization by P. infestans. We further showed that silencing NbRBP3 reduced photosystem II activity, reduced host photosynthetic efficiency, attenuated Pi23014-mediated suppression of cell death triggered by P. infestans pathogen-associated molecular pattern elicitor INF1, and suppressed plant immunity.
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页数:15
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