Stacking potato NLR genes activates a calcium‐dependent protein kinase and confers broad‐spectrum disease resistance to late blight

疫病疫霉菌 生物 卵菌 枯萎病 基因 R基因 植物抗病性 转基因 遗传学 转录组 基因表达 植物
作者
Xiao‐Qiang Zhao,Fan Zhang,Xiaoqing Chen,Chongyuan Zhang,Haoyi Zhang,Tian Wang,Jinzhe Zhang,Cheng He,Shuo Wang,X. Zhang,Xi Meng,Vladimir Nekrasov,Liang Kong,Suomeng Dong
出处
期刊:Journal of Integrative Plant Biology [Wiley]
标识
DOI:10.1111/jipb.13892
摘要

Late blight, caused by the oomycete plant pathogen Phytophthora infestans, is a destructive disease that leads to significant yield loss in potatoes and tomatoes. The introgression of disease resistance (R) genes, which encode nucleotide-binding domain leucine-rich repeat-containing receptors (NLRs), into cultivated potatoes, is highly effective in controlling late blight. Here, we generated transgenic 2R and 3R potato lines by stacking R genes Rpi-blb2/Rpi-vnt1.1 and Rpi-vnt1.1/RB/R8, respectively, in the susceptible cv. Desiree background. The resulting 2R and 3R transgenic potato plants showed resistance to highly virulent P. infestans field isolates. We hypothesized that stacking R genes either resulted in up-regulation of a broader range of immune-related genes, or, more importantly, increase in the fold change of gene expression. To test our hypotheses, we performed transcriptome analysis and identified a subset of core immune-related genes that are induced in response to P. infestans in transgenic lines carrying single R genes versus lines carrying stacks of multiple R genes. In our analysis, stacking R genes resulted not only in the induction of a broader range of defense-associated genes but also a global increase in gene expression fold change, caused by the pathogen. We further demonstrated that the calcium-dependent protein kinase 16 (StCDPK16) gene significantly contributed to resistance to a virulent P. infestans strain, in the R gene background, in a kinase activity-dependent manner. Thus, our data suggest that stacking the R genes enhances late blight resistance through modulating the expression of a broader range of defense-related genes and highlights CDPK16 as a novel player in potato R gene-mediated resistance.
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