Grapevine downy mildew(DM)is a destructive oomycete disease of viticulture worldwide.MrRPV1 is a typical TIR-NBS-LRR type DM disease resistance gene cloned from the wild North American grapevine species Muscadinia rot...Grapevine downy mildew(DM)is a destructive oomycete disease of viticulture worldwide.MrRPV1 is a typical TIR-NBS-LRR type DM disease resistance gene cloned from the wild North American grapevine species Muscadinia rotundifolia.However,the molecular basis of resistance mediated by MrRPV1 remains poorly understood.Downy mildew-susceptible Vitis vinifera cv.Shiraz was transformed with a genomic fragment containing MrRPV1 to produce DM-resistant transgenic Shiraz lines.Comparative transcriptome analysis was used to compare the transcriptome profiles of the resistant and susceptible genotypes after DM infection.Transcriptome modulation during the response to P.viticola infection was more rapid,and more genes were induced in MrRPV1-transgenic Shiraz than in wild-type plants.In DM-infected MrRPV1-transgenic plants,activation of genes associated with Ca^(2+)release and ROS production was the earliest transcriptional response.Functional analysis of differentially expressed genes revealed that key genes related to multiple phytohormone signaling pathways and secondary metabolism were highly induced during infection.Coexpression network and motif enrichment analysis showed that WRKY and MYB transcription factors strongly coexpress with stilbene synthase(VvSTS)genes during defense against P.viticola in MrRPV1-transgenic plants.Taken together,these findings indicate that multiple pathways play important roles in MrRPV1-mediated resistance to downy mildew.展开更多
基金This research was supported by the National Natural Science Foundation of China(Grant nos.31660567 and 31760505),the Bagui Young Scholars’special fund of Guangxi,the Young Elite Scientists Sponsorship Program by CAST(Project No.2017QNRC001),and the Science and Technology Development Fund of Guangxi(2018GXNSFDA281019,GuikeAD18281056).We also thank Nayana Arunasiri for preparing the P.viticola inoculum and assisting with the time course infection experiment and Angelica Jermakow for preparing the total RNA samples.
文摘Grapevine downy mildew(DM)is a destructive oomycete disease of viticulture worldwide.MrRPV1 is a typical TIR-NBS-LRR type DM disease resistance gene cloned from the wild North American grapevine species Muscadinia rotundifolia.However,the molecular basis of resistance mediated by MrRPV1 remains poorly understood.Downy mildew-susceptible Vitis vinifera cv.Shiraz was transformed with a genomic fragment containing MrRPV1 to produce DM-resistant transgenic Shiraz lines.Comparative transcriptome analysis was used to compare the transcriptome profiles of the resistant and susceptible genotypes after DM infection.Transcriptome modulation during the response to P.viticola infection was more rapid,and more genes were induced in MrRPV1-transgenic Shiraz than in wild-type plants.In DM-infected MrRPV1-transgenic plants,activation of genes associated with Ca^(2+)release and ROS production was the earliest transcriptional response.Functional analysis of differentially expressed genes revealed that key genes related to multiple phytohormone signaling pathways and secondary metabolism were highly induced during infection.Coexpression network and motif enrichment analysis showed that WRKY and MYB transcription factors strongly coexpress with stilbene synthase(VvSTS)genes during defense against P.viticola in MrRPV1-transgenic plants.Taken together,these findings indicate that multiple pathways play important roles in MrRPV1-mediated resistance to downy mildew.
