Weber Ernst, Koebnik Ralf
Institute of Genetics, Martin-Luther-University, Halle, Germany.
J Bacteriol. 2006 Feb;188(4):1405-10. doi: 10.1128/JB.188.4.1405-1410.2006.
The plant-pathogenic bacterium Xanthomonas campestris pv. vesicatoria possesses a type III secretion (TTS) system which is encoded by the 23-kb hrp (hypersensitive response and pathogenicity) gene cluster. The TTS system is necessary for pathogenicity in susceptible hosts and induction of the hypersensitive response in resistant plants. At the cell surface, the TTS system is associated with an extracellular filamentous structure, the Hrp pilus, which serves as a conduit for the transfer of bacterial proteins into the plant cell cytosol. The major pilus component, the HrpE pilin, is unique to xanthomonads. Previous work showed that HrpE contains two regions: a hypervariable surface-exposed domain, including the N-terminal secretion signal, and a C-terminal polymerization domain. In this study, the evolutionary rate of the hrpE gene was analyzed. Twenty-one alleles were cloned, sequenced, and compared with five known hrpE alleles. The ratio of synonymous (K(s)) and nonsynonymous (K(a)) substitution rates shows that parts of the HrpE N terminus are subjected to positive selection and the C terminus is subjected to purifying selection. The trade-off between positive and purifying selection at the very-N terminus allowed us to ascertain the amphipathic alpha-helical nature of the TTS signal. This is the first report of a surface structure from a plant-pathogenic bacterium that evolved under the constraint of positive selection and hints to the evolutionary adaptation of this extracellular appendage to avoid recognition by the plant defense surveillance system.
植物致病细菌野油菜黄单胞菌辣椒斑点病致病变种拥有一种III型分泌(TTS)系统,该系统由23 kb的hrp(过敏反应和致病性)基因簇编码。TTS系统对于在感病寄主中致病以及在抗病植物中诱导过敏反应是必需的。在细胞表面,TTS系统与一种细胞外丝状结构即Hrp菌毛相关联,Hrp菌毛作为将细菌蛋白转移到植物细胞胞质溶胶中的通道。菌毛的主要成分HrpE菌毛蛋白是黄单胞菌所特有的。先前的研究表明,HrpE包含两个区域:一个高度可变的表面暴露结构域,包括N端分泌信号,以及一个C端聚合结构域。在本研究中,分析了hrpE基因的进化速率。克隆并测序了21个等位基因,并与5个已知的hrpE等位基因进行了比较。同义(K(s))和非同义(K(a))替换率的比值表明,HrpE N端的部分区域受到正选择,而C端受到纯化选择。在最N端正选择和纯化选择之间的权衡使我们能够确定TTS信号两亲性α螺旋的性质。这是关于植物致病细菌表面结构在正选择约束下进化的首次报道,并暗示了这种细胞外附属物为避免被植物防御监测系统识别而发生的进化适应。