Du Heshan, Li Wenhui, Wang Yuqing, Yang Wencai
Beijing Key Laboratory of Growth and Developmental Regulation for Protected Vegetable Crops, Department of Vegetable Science, China Agricultural University, Beijing, China.
PLoS One. 2014 Mar 31;9(3):e93476. doi: 10.1371/journal.pone.0093476. eCollection 2014.
Bacterial spot caused by several Xanthomonas sp. is one of the most devastating diseases in tomato (Solanum lycopersicum L.). The genetics of hypersensitive resistance to X. perforans race T3 has been intensively investigated and regulatory genes during the infection of race T3 have been identified through transcriptional profiling. However, no work on isolating regulatory genes for field resistance has been reported. In this study, cDNA-amplified fragment length polymorphism technique was used to identify differentially expressed transcripts between resistant tomato accession PI 114490 and susceptible variety OH 88119 at 3, 4 and 5 days post-inoculation of the pathogen. Using 256 selective primer combinations, a total of 79 differentially expressed transcript-derived fragments (TDFs) representing 71 genes were obtained. Of which, 60 were up-regulated and 4 were down-regulated in both tomato lines, 4 were uniquely up-regulated and 2 were uniquely down-regulated in PI 114490, and 1 was specifically up-regulated in OH 88119. The expression patterns of 19 representative TDFs were further confirmed by semi-quantitative and/or quantitative real time RT-PCR. These results suggested that the two tomato lines activated partly similar defensive mechanism in response to race T3 infection. The data obtained here will provide some fundamental information for elucidating the molecular mechanism of response to race T3 infection in tomato plants with field resistance.
由多种黄单胞菌引起的细菌性斑点病是番茄(Solanum lycopersicum L.)最具毁灭性的病害之一。对番茄对穿孔黄单胞菌T3小种过敏抗性的遗传学进行了深入研究,并通过转录谱分析鉴定了T3小种感染期间的调控基因。然而,尚未有关于分离田间抗性调控基因的研究报道。在本研究中,利用cDNA扩增片段长度多态性技术,在接种病原菌后3、4和5天,鉴定抗性番茄种质PI 114490和感病品种OH 88119之间差异表达的转录本。使用256种选择性引物组合,共获得79个差异表达的转录本衍生片段(TDF),代表71个基因。其中,60个在两个番茄品系中均上调,4个下调,4个在PI 114490中独特上调,2个在PI 114490中独特下调,1个在OH 88119中特异性上调。通过半定量和/或定量实时RT-PCR进一步证实了19个代表性TDF的表达模式。这些结果表明,两个番茄品系在对T3小种感染的反应中激活了部分相似的防御机制。本研究获得的数据将为阐明具有田间抗性的番茄植株对T3小种感染的反应分子机制提供一些基础信息。