青枯病
基因
生物
乙烯利
基因表达
栽培
转录组
WRKY蛋白质结构域
转录因子
植物抗病性
抄写(语言学)
乙烯
基因表达调控
细胞生物学
细菌
青枯菌
遗传学
微生物学
植物
抗性(生态学)
发起人
转录调控
作者
Weiwei Cai,Qikai Li,Feina Liu,Yilin Tao,Zhen Xu,Zhujun Zhu,Yuan Chen,Tian Li
标识
DOI:10.3389/fpls.2025.1753391
摘要
Bacterial wilt that caused by Ralstonia solanacearum poses a major threat to tomatoes. Some disease-resistant cultivars have been shown to significantly improve tomato resistance to bacterial wilt. Analyzing and harnessing the resistance mechanism of bacterial wilt-resistant cultivars is therefore of considerable importance for tomato resistance breeding. In this study, we have confirmed that the tomato disease-resistant cultivars “ZJ-7” and “04056” were more resistant to bacterial wilt than the susceptible cultivar Ailsa Craig cv. (AC), and then transcriptome sequencing analysis of roots from “ZJ-7” and “04056” revealed extensive changes in gene expression at 3 and 6 hours post-inoculation (hpi) with R. solanacearum . In both disease-resistant cultivars, the transcriptional expression levels of genes encoding pathogenesis-related (PR) proteins and transcription factors were markedly elevated in response to R. solanacearum infection at both time points. In contrast, the susceptible cultivar AC exhibited a considerably lower number of transcription factors responding to the infection, with up-regulated occuring only at 6 hpi, while the up-regulation of PR gene expression was observed only at 3 hpi. Although the specific up-regulated genes differed between “ZJ-7” and “04056”, both showed activation of ethylene biosynthesis-related genes. Ethephon application in AC promoted the expression of transcription factors at 3 hpi and restore PR gene expression at 6 hpi. These results indicate that sustained defense against bacterial wilt in tomato is closely assocated with ethylene synthesis, providing a theoretical basis for elucidating the resistance mechanism and enhancing disease resistance in tomato.
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