Journal of Integrative Agriculture ›› 2021, Vol. 20 ›› Issue (5): 1314-1326.DOI: 10.1016/S2095-3119(20)63267-1

所属专题: 动物科学合辑Animal Science 植物抗病遗传合辑Plant Disease-resistance Genetics

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  • 收稿日期:2020-02-08 出版日期:2021-05-01 发布日期:2021-04-12

Jasmonic acid and ethylene signaling pathways participate in the defense response of Chinese cabbage to Pectobacterium carotovorum infection

CHEN Chang-long1, 2, YUAN Fang1, LI Xiao-ying1, 2, MA Rong-cai1, 2, XIE Hua1, 2 
  

  1. 1 Beijing Agro-Biotechnology Research Center, Beijing Academy of Agriculture and Forestry Sciences, Beijing 100097, P.R.China
    2 Beijing Key Laboratory of Agricultural Genetic Resources and Biotechnology, Beijing 100097, P.R.China
  • Received:2020-02-08 Online:2021-05-01 Published:2021-04-12
  • Contact: Correspondence XIE Hua, Tel: +86-10-51503832, E-mail: xiehua@baafs.net.cn
  • About author:CHEN Chang-long, E-mail: chenchanglong@baafs.net.cn;
  • Supported by:
    This research was funded by the Beijing Leafy Vegetables Innovation Team of Modern Agro-industry Technology Research System, China (BAIC07), and the Beijing Natural Science Foundation, China (5051002).

摘要:

胡萝卜果胶杆菌Pectobacterium carotovorum (Pc)引发的软腐病对大白菜(Brassica rapa subsp. pekinensis)危害严重。为探索大白菜响应胡萝卜果胶杆菌侵染的防御反应机制,本研究构建了Pc侵染大白菜的抑制消减(SSH)文库,共获得1,919个非冗余表达序列标签(ESTs)。采用ESTs进行cDNA芯片杂交,与接种无菌水的对照大白菜相比,在接种Pc后不同时间点的大白菜中共检测到800个差异表达基因(DEGs),通过实时荧光定量PCR和半定量PCR对部分差异表达基因进行表达检测,结果与芯片杂交结果基本一致,验证了芯片杂交结果的可靠性。通过MapMan软件进行可视化分析发现,1/4的差异表达基因可能参与植物的生物胁迫通路。其中,分别有8、8、1、3和2个差异表达基因与茉莉酸(JA)、乙烯(ET)、茉莉酸&乙烯、生长素和脱落酸(ABA)信号通路有关,然而并未检测到与水杨酸(SA)信号通路相关的差异表达基因。对胡萝卜果胶杆菌侵染大白菜叶片中产生的激素水平进行检测,发现茉莉酸和乙烯水平增加,而水杨酸水平降低。对大白菜进行激素处理后接种胡萝卜果胶杆菌,发现茉莉酸(JA)、茉莉酸甲酯(MeJA)、乙烯前体1-氨基环丙烷-1-羧酸(ACC)或它们的组合(MeJA+ACC、JA+ACC)的处理,相比于对照(无菌水处理),可以减轻软腐病的发病严重程度,其中JA和JA+ACC的处理效果最为明显且其效果相当。这些研究表明茉莉酸和乙烯信号通路可能在Pc侵染大白菜过程中协同作用以抵御Pc,且茉莉酸介导的信号通路作用可能更加强烈。本研究对大白菜响应软腐病的防御反应机制进行了初步解析,对大白菜抗病分子育种和软腐病防治策略的开发具有重要理论价值。


Abstract:

Chinese cabbage (Brassica rapa subsp. pekinensis) suffers from soft rot disease caused by Pectobacterium carotovorum (Pc).  To uncover the mechanisms underlying the defense response of Chinese cabbage to Pc, we constructed a suppression subtractive hybridization (SSH) library from Pc-infected cabbage and obtained 1 919 non-redundant expressed sequence tags (ESTs), which were used for cDNA microarray.  We detected 800 differentially expressed genes (DEGs) in cabbage at different time points post-Pc inoculation, which were further confirmed by quantitative real-time PCR.  One quarter of these DEGs were involved in the biotic stress pathways visualized by MapMan.  Among them, 8, 8, 1, 3, and 2 DEGs were related to jasmonic acid (JA), ethylene (ET), JA+ET, auxin, and abscisic acid (ABA) signaling pathways, respectively, while no DEG was detected for salicylic acid (SA) signaling.  Assessment of phytohormone production in the Pc-infected leaves showed that JA and ET production was increased, while SA production was decreased.  Treatment with JA, methyl jasmonate (MeJA), the ET precursor 1-aminocyclopropane-1-carboxylate (ACC), or combinations thereof, reduced the disease severity, and the JA and JA+ACC treatments were superior and performed equally well.  Our findings suggest that JA and ET may act synergistically against Pc infection in Chinese cabbage, and JA-mediated signaling might be the most significant. 

Key words: Brassica rapa ,  Pectobacterium carotovorum ,  gene expression ,  defense response ,  hormone signaling