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植物病原体丁香假单胞菌番茄致病变种ES4326五质粒互补体的核苷酸序列与进化

Nucleotide sequence and evolution of the five-plasmid complement of the phytopathogen Pseudomonas syringae pv. maculicola ES4326.

作者信息

Stavrinides John, Guttman David S

机构信息

Department of Botany, University of Toronto, 25 Willcocks St., Toronto, ON M5S 3B2, Canada.

出版信息

J Bacteriol. 2004 Aug;186(15):5101-15. doi: 10.1128/JB.186.15.5101-5115.2004.

Abstract

Plasmids are transmissible, extrachromosomal genetic elements that are often responsible for environmental or host-specific adaptations. In order to identify the forces driving the evolution of these important molecules, we determined the complete nucleotide sequence of the five-plasmid complement of the radish and Arabidopsis pathogen Pseudomonas syringae pv. maculicola ES4326 and conducted an intraspecific comparative genomic analysis. To date, this is the most complex fully sequenced plasmid complement of any gram-negative bacterium. The plasmid complement comprises two pPT23A-like replicons, pPMA4326A (46,697 bp) and pPMA4326B (40,110 bp); a pPS10-like replicon, pPMA4326C (8,244 bp); and two atypical, replicase-deficient replicons, pPMA4326D (4,833 bp) and pPMA4326E (4,217 bp). A complete type IV secretion system is found on pPMA4326A, while the type III secreted effector hopPmaA is present on pPMA4326B. The region around hopPmaA includes a shorter hopPmaA homolog, insertion sequence (IS) elements, and a three-element cassette composed of a resolvase, an integrase, and an exeA gene that is also present in several human pathogens. We have also identified a novel genetic element (E622) that is present on all but the smallest plasmid (pPMA4326E) that has features of an IS element but lacks an identifiable transposase. This element is associated with virulence-related genes found in a wide range of P. syringae strains. Comparative genomic analyses of these and other P. syringae plasmids suggest a role for recombination and integrative elements in driving plasmid evolution.

摘要

质粒是可传播的染色体外遗传元件,通常负责环境适应或宿主特异性适应。为了确定驱动这些重要分子进化的因素,我们测定了萝卜和拟南芥病原体丁香假单胞菌番茄致病变种ES4326的五质粒互补体的完整核苷酸序列,并进行了种内比较基因组分析。迄今为止,这是任何革兰氏阴性细菌中最复杂的完全测序的质粒互补体。该质粒互补体包括两个pPT23A样复制子,pPMA4326A(46,697 bp)和pPMA4326B(40,110 bp);一个pPS10样复制子,pPMA4326C(8,244 bp);以及两个非典型的、缺乏复制酶的复制子,pPMA4326D(4,833 bp)和pPMA4326E(4,217 bp)。在pPMA4326A上发现了一个完整的IV型分泌系统,而III型分泌效应蛋白hopPmaA存在于pPMA4326B上。hopPmaA周围的区域包括一个较短的hopPmaA同源物、插入序列(IS)元件,以及一个由解离酶、整合酶和exeA基因组成的三元件盒,该盒也存在于几种人类病原体中。我们还鉴定了一种新型遗传元件(E622),除了最小的质粒(pPMA4326E)外,它存在于所有质粒上,该元件具有IS元件的特征,但缺乏可识别的转座酶。该元件与广泛存在于丁香假单胞菌菌株中的毒力相关基因有关。对这些以及其他丁香假单胞菌质粒的比较基因组分析表明,重组和整合元件在驱动质粒进化中起作用。

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