Yang Yuting, Wang Xuewei, Chen Panpan, Zhou Keke, Xue Wanyu, Abid Kan, Chen Shuxia
College of Horticulture, Northwest A&F University, Shaanxi Engineering Research Center for Vegetables, Yangling, China.
Department of Horticulture, The University of Haripur, Haripur, Pakistan.
Front Plant Sci. 2020 Sep 25;11:559070. doi: 10.3389/fpls.2020.559070. eCollection 2020.
is an important necrotrophic fungal pathogen with a broad host range and the ability to causing great economic losses in cucumber. However, the resistance mechanism against this pathogen in cucumber was not well understood. In this study, the microscopic observation of the spore growth, redox status measurements and transcriptome analysis were carried out after infection in the resistant genotype No.26 and its susceptible mutant 26M. Results revealed shorter hypha, lower rate of spore germination, less acceleration of HO, O , and lower total glutathione content (GSH+GSSG) in No.26 than that in 26M, which were identified by the staining result of DAB and NBT. Transcriptome data showed that after pathogen infection, a total of 3901 and 789 different expression genes (DEGs) were identified in No.26 and 26M respectively. These DEGs were highly enriched in redox regulation pathway, hormone signaling pathway and plant-pathogen interaction pathway. The glutathione S-transferase genes, putative peroxidase gene, and NADPH oxidase were up-regulated in No.26 whereas these genes changed little in 26M after infection. Jasmonic acid and ethylene biosynthesis and signaling pathways were distinctively activated in No.26 comparing with 26M upon infection. Much more plant defense related genes including mitogen-activated protein kinases, calmodulin, calmodulin-like protein, calcium-dependent protein kinase, and WRKY transcription factor were induced in No.26 than 26M after pathogen infection. Finally, a model was established which elucidated the resistance difference between resistant cucumber genotype and susceptible mutant after infection.
是一种重要的坏死营养型真菌病原体,宿主范围广泛,能够在黄瓜上造成巨大经济损失。然而,黄瓜对这种病原体的抗性机制尚不清楚。在本研究中,对接种后抗性基因型26号及其感病突变体26M进行了孢子生长的显微镜观察、氧化还原状态测量和转录组分析。结果显示,通过DAB和NBT染色结果鉴定,26号的菌丝较短,孢子萌发率较低,HO、O的加速较少,总谷胱甘肽含量(GSH+GSSG)低于26M。转录组数据表明,病原体感染后,26号和26M分别鉴定出3901个和789个差异表达基因(DEG)。这些DEG在氧化还原调节途径、激素信号途径和植物-病原体相互作用途径中高度富集。谷胱甘肽S-转移酶基因、假定的过氧化物酶基因和NADPH氧化酶在26号中上调,而感染后这些基因在26M中变化不大。与26M相比,感染后26号中茉莉酸和乙烯生物合成及信号途径被显著激活。病原体感染后,26号中诱导的植物防御相关基因比26M多得多,包括丝裂原活化蛋白激酶、钙调蛋白、类钙调蛋白、钙依赖性蛋白激酶和WRKY转录因子。最后,建立了一个模型,阐明了抗性黄瓜基因型和感病突变体感染后的抗性差异。