Host-Selective Toxins of Pyrenophora tritici-repentis Induce Common Responses Associated with Host Susceptibility

被引:32
|
作者
Pandelova, Iovanna [1 ,2 ]
Figueroa, Melania [1 ,2 ,3 ]
Wilhelm, Larry J. [1 ,2 ]
Manning, Viola A. [1 ,2 ]
Mankaney, Aakash N. [1 ,2 ]
Mockler, Todd C. [1 ,2 ,4 ]
Ciuffetti, Lynda M. [1 ,2 ]
机构
[1] Oregon State Univ, Dept Bot & Plant Pathol, Corvallis, OR 97331 USA
[2] Oregon State Univ, Ctr Genome Res & Biocomp, Corvallis, OR 97331 USA
[3] Oregon State Univ, USDA, ARS, Forage Seed & Cereal Res Unit, Corvallis, OR 97331 USA
[4] Donald Danforth Plant Sci Ctr, St Louis, MO USA
来源
PLOS ONE | 2012年 / 7卷 / 07期
基金
美国食品与农业研究所; 美国农业部;
关键词
PROGRAMMED CELL-DEATH; TAN SPOT; PTR TOXA; GENE-EXPRESSION; MICROARRAY ANALYSIS; CHLOROSIS TOXIN; POWDERY MILDEW; JASMONIC ACID; CAUSAL AGENT; WHEAT;
D O I
10.1371/journal.pone.0040240
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Pyrenophora tritici-repentis (Ptr), a necrotrophic fungus and the causal agent of tan spot of wheat, produces one or a combination of host-selective toxins (HSTs) necessary for disease development. The two most studied toxins produced by Ptr, Ptr ToxA (ToxA) and Ptr ToxB (ToxB), are proteins that cause necrotic or chlorotic symptoms respectively. Investigation of host responses induced by HSTs provides better insight into the nature of the host susceptibility. Microarray analysis of ToxA has provided evidence that it can elicit responses similar to those associated with defense. In order to evaluate whether there are consistent host responses associated with susceptibility, a similar analysis of ToxB-induced changes in the same sensitive cultivar was conducted. Comparative analysis of ToxA-and ToxB-induced transcriptional changes showed that similar groups of genes encoding WRKY transcription factors, RLKs, PRs, components of the phenylpropanoid and jasmonic acid pathways are activated. ROS accumulation and photosystem dysfunction proved to be common mechanism-of-action for these toxins. Despite similarities in defense responses, transcriptional and biochemical responses as well as symptom development occur more rapidly for ToxA compared to ToxB, which could be explained by differences in perception as well as by differences in activation of a specific process, for example, ethylene biosynthesis in ToxA treatment. Results of this study suggest that perception of HSTs will result in activation of defense responses as part of a susceptible interaction and further supports the hypothesis that necrotrophic fungi exploit defense responses in order to induce cell death.
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页数:16
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