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从识别中剖析毒力功能:XopQ/HopQ1家族效应子对本氏烟草细胞死亡的抑制依赖于EDS1介导的免疫反应

Dissecting virulence function from recognition: cell death suppression in Nicotiana benthamiana by XopQ/HopQ1-family effectors relies on EDS1-dependent immunity.

作者信息

Adlung Norman, Bonas Ulla

机构信息

Institute for Biology, Department of Genetics, Martin Luther University Halle-Wittenberg, 06099, Halle (Saale), Germany.

出版信息

Plant J. 2017 Aug;91(3):430-442. doi: 10.1111/tpj.13578. Epub 2017 Jun 1.

DOI:10.1111/tpj.13578
PMID:28423458
Abstract

Many Gram-negative plant pathogenic bacteria express effector proteins of the XopQ/HopQ1 family which are translocated into plant cells via the type III secretion system during infection. In Nicotiana benthamiana, recognition of XopQ/HopQ1 proteins induces an effector-triggered immunity (ETI) reaction which is not associated with strong cell death but renders plants immune against Pseudomonas syringae and Xanthomonas campestris pv. vesicatoria strains. Additionally, XopQ suppresses cell death in N. benthamiana when transiently co-expressed with cell death inducers. Here, we show that representative XopQ/HopQ1 proteins are recognized similarly, likely by a single resistance protein of the TIR-NB-LRR class. Extensive analysis of XopQ derivatives indicates the recognition of structural features. We performed Agrobacterium-mediated protein expression experiments in wild-type and EDS1-deficient (eds1) N. benthamiana leaves, not recognizing XopQ/HopQ1. XopQ recognition limits multiplication of Agrobacterium and attenuates levels of transiently expressed proteins. Remarkably, XopQ fails to suppress cell death reactions induced by different effectors in eds1 plants. We conclude that XopQ-mediated cell death suppression in N. benthamiana is due to the attenuation of Agrobacterium-mediated protein expression rather than the cause of the genuine XopQ virulence activity. Thus, our study expands our understanding of XopQ recognition and function, and also challenges the commonly used co-expression assays for elucidation of in planta effector activities, at least under conditions of ETI induction.

摘要

许多革兰氏阴性植物病原细菌表达XopQ/HopQ1家族的效应蛋白,在感染过程中这些蛋白通过III型分泌系统转运到植物细胞中。在本氏烟草中,对XopQ/HopQ1蛋白的识别会诱导效应子触发的免疫(ETI)反应,该反应与强烈的细胞死亡无关,但能使植物对丁香假单胞菌和野油菜黄单胞菌疮痂致病变种菌株产生免疫。此外,当XopQ与细胞死亡诱导剂瞬时共表达时,它能抑制本氏烟草中的细胞死亡。在这里,我们表明代表性的XopQ/HopQ1蛋白以类似的方式被识别,可能是由TIR-NB-LRR类的单个抗性蛋白识别。对XopQ衍生物的广泛分析表明了对其结构特征的识别。我们在野生型和EDS1缺陷型(eds1)本氏烟草叶片中进行了农杆菌介导的蛋白表达实验,eds1不识别XopQ/HopQ1。XopQ的识别限制了农杆菌的增殖,并降低了瞬时表达蛋白的水平。值得注意的是,XopQ无法抑制eds1植物中由不同效应子诱导的细胞死亡反应。我们得出结论,本氏烟草中XopQ介导的细胞死亡抑制是由于农杆菌介导的蛋白表达减弱,而不是XopQ真正毒力活性的原因。因此,我们的研究扩展了我们对XopQ识别和功能的理解,也对常用于阐明植物效应子活性的共表达分析提出了挑战,至少在ETI诱导的条件下是这样。

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