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青枯雷尔氏菌GMI1000的两种III型分泌系统效应蛋白决定了其在烟草上的寄主范围特异性。

Two type III secretion system effectors from Ralstonia solanacearum GMI1000 determine host-range specificity on tobacco.

作者信息

Poueymiro Marie, Cunnac Sébastien, Barberis Patrick, Deslandes Laurent, Peeters Nemo, Cazale-Noel Anne-Claire, Boucher Christian, Genin Stéphane

机构信息

Laboratoire des Interactions Plantes Micro-organismes, UMR CNRS-INRA 2594/441, Castanet Tolosan, France.

出版信息

Mol Plant Microbe Interact. 2009 May;22(5):538-50. doi: 10.1094/MPMI-22-5-0538.

Abstract

The model pathogen Ralstonia solanacearum GMI1000 is the causal agent of the bacterial wilt disease that attacks many solanaceous plants and other hosts but not tobacco (Nicotiana spp.). We found that two type III secretion system effector genes, avrA and popP1, are limiting the host range of strain GMI1000 on at least three tobacco species (N. tabacum, N. benthamiana, and N. glutinosa). Both effectors elicit the hypersensitive response (HR) on these tobacco species, although in different manners; AvrA is the major determinant recognized by N. tabacum and N. benthamiana, while PopP1 appears to be the major HR elicitor on N. glutinosa. Only the double inactivation of the avrA and popP1 genes allowed GMI1000 to wilt tobacco plants, thus showing that GMI1000 intrinsically possesses the functions necessary to wilt tobacco plants. A focused analysis on AvrA revealed that the first 58 N-terminal amino acids are sufficient to direct its injection into plant cells. We identified a hypervariable region in avrA, which contains variable numbers of tandem repeats (VNTR), each composed of 12 base pairs. We show that an 18-amino acid region in which the VNTR insertion occurs is an important domain involved in HR elicitation on N. benthamiana. avrA appears to be the target of various DNA insertions or mobile elements that probably allow R. solanacearum to evade the recognition and defense responses of tobacco.

摘要

模式病原菌青枯雷尔氏菌GMI1000是细菌性萎蔫病的病原体,该病侵袭许多茄科植物和其他寄主,但不侵染烟草(烟草属植物)。我们发现,两个III型分泌系统效应蛋白基因avrA和popP1限制了菌株GMI1000在至少三种烟草物种(烟草、本氏烟草和黏毛烟草)上的寄主范围。这两种效应蛋白在这些烟草物种上均引发过敏反应(HR),不过方式不同;AvrA是烟草和本氏烟草识别的主要决定因素,而PopP1似乎是黏毛烟草上引发HR的主要因素。只有avrA和popP1基因的双失活才使GMI1000能使烟草植株萎蔫,从而表明GMI1000本身具备使烟草植株萎蔫所需的功能。对AvrA的重点分析表明,N端前58个氨基酸足以将其注入植物细胞。我们在avrA中鉴定出一个高变区,其中包含可变数量的串联重复序列(VNTR),每个由12个碱基对组成。我们表明,VNTR插入的一个18个氨基酸区域是参与本氏烟草HR诱导的重要结构域。avrA似乎是各种DNA插入或移动元件的靶标,这些元件可能使青枯雷尔氏菌逃避烟草的识别和防御反应。

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