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Expression Profiling of Cucumis sativus in Response to Infection by Pseudoperonospora cubensis

机译:黄瓜对黄瓜假单胞菌感染的表达谱分析

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摘要

The oomycete pathogen, Pseudoperonospora cubensis, is the causal agent of downy mildew on cucurbits, and at present, no effective resistance to this pathogen is available in cultivated cucumber (Cucumis sativus). To better understand the host response to a virulent pathogen, we performed expression profiling throughout a time course of a compatible interaction using whole transcriptome sequencing. As described herein, we were able to detect the expression of 15,286 cucumber genes, of which 14,476 were expressed throughout the infection process from 1 day post-inoculation (dpi) to 8 dpi. A large number of genes, 1,612 to 3,286, were differentially expressed in pair-wise comparisons between time points. We observed the rapid induction of key defense related genes, including catalases, chitinases, lipoxygenases, peroxidases, and protease inhibitors within 1 dpi, suggesting detection of the pathogen by the host. Co-expression network analyses revealed transcriptional networks with distinct patterns of expression including down-regulation at 2 dpi of known defense response genes suggesting coordinated suppression of host responses by the pathogen. Comparative analyses of cucumber gene expression patterns with that of orthologous Arabidopsis thaliana genes following challenge with Hyaloperonospora arabidopsidis revealed correlated expression patterns of single copy orthologs suggesting that these two dicot hosts have similar transcriptional responses to related pathogens. In total, the work described herein presents an in-depth analysis of the interplay between host susceptibility and pathogen virulence in an agriculturally important pathosystem.
机译:卵菌病原体Pseudoperonospora cubensis是葫芦科的霜霉病的病原体,目前,在栽培黄瓜(Cucumis sativus)中没有对该病原体的有效抗性。为了更好地了解宿主对强毒病原体的反应,我们使用完整的转录组测序在兼容相互作用的整个时间过程中进行了表达谱分析。如本文所述,我们能够检测到15,286个黄瓜基因的表达,其中从接种后1天(dpi)到8 dpi,整个感染过程中表达了14,476个。在时间点之间的成对比较中,差异表达了大量的基因(1,612至3,286)。我们观察到关键防御相关基因的快速诱导,包括1 dpi内的过氧化氢酶,几丁质酶,脂氧合酶,过氧化物酶和蛋白酶抑制剂,提示宿主已检测到病原体。共表达网络分析揭示了具有不同表达模式的转录网络,包括已知防御反应基因在2 dpi下调,提示病原体协同抑制宿主反应。黄瓜基因表达模式与拟南芥拟南芥透明质子菌攻击后的直系同源拟南芥基因表达模式的比较分析显示,单拷贝直系同源物的相关表达模式表明这两个双子叶植物宿主对相关病原体的转录反应相似。总的来说,本文所述的工作提出了对在农业上重要的病理系统中宿主易感性和病原体毒力之间相互作用的深入分析。

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