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副猪嗜血杆菌的三聚体自转运蛋白:针对致病菌株产生广泛的乘客结构域库

Trimeric autotransporters of Haemophilus parasuis: generation of an extensive passenger domain repertoire specific for pathogenic strains.

作者信息

Pina Sonia, Olvera Alex, Barceló Anna, Bensaid Albert

机构信息

Centre de Recerca en Sanitat Animal, UAB-IRTA, Campus de la Universitat Autònoma de Barcelona, 08193 Bellaterra, Barcelona, Spain.

出版信息

J Bacteriol. 2009 Jan;191(2):576-87. doi: 10.1128/JB.00703-08. Epub 2008 Nov 14.

Abstract

Haemophilus parasuis is the agent responsible for causing Glässer's disease, but little is known about the pathogenic determinants of this major pig disease. Here we describe, for the pathogenic strain Nagasaki, the molecular characterization of 13 trimeric autotransporters as assessed by the presence of YadA C-terminal translocator domains which were classified into three groups. All passenger domains possess motifs and repeats characteristic of adhesins, hemagglutinins, and invasins with various centrally located copies of collagen-like repeats. This domain architecture is shared with two trimeric autotransporter proteins of H. somnus 129Pt. Genomic comparison by microarray hybridization demonstrated homologies among H. parasuis virulent strains and high divergence with respect to nonvirulent strains. Therefore, these genes were named vtaA (virulence-associated trimeric autotransporters). The sequencing of 17 homologous vtaA genes of different invasive strains highlighted an extensive mosaic structure. Based also on the presence of DNA uptake signal sequences within the vtaA genes, we propose a mechanism of evolution by which gene duplication and the accumulation of mutations and recombinations, plus the lateral gene transfer of the passenger domain, led to the diversity of this multigene family. This study provides insights to help understand the tissue colonization and invasiveness characteristic of H. parasuis pathogenic strains.

摘要

副猪嗜血杆菌是引起格拉泽氏病的病原体,但对于这种主要猪病的致病决定因素知之甚少。在此,我们描述了致病性菌株长崎株的13种三聚体自转运蛋白的分子特征,通过存在YadA C末端转运结构域进行评估,这些结构域被分为三组。所有乘客结构域都具有粘附素、血凝素和侵袭素的特征基序和重复序列,中间有各种胶原样重复序列的拷贝。这种结构域结构与睡眠嗜血杆菌129Pt的两种三聚体自转运蛋白相同。通过微阵列杂交进行的基因组比较表明,副猪嗜血杆菌致病菌株之间存在同源性,与非致病菌株有很大差异。因此,这些基因被命名为vtaA(毒力相关三聚体自转运蛋白)。对不同侵袭性菌株的17个同源vtaA基因进行测序,突出了广泛的镶嵌结构。同样基于vtaA基因内DNA摄取信号序列的存在,我们提出了一种进化机制,即基因复制、突变和重组的积累,加上乘客结构域的横向基因转移,导致了这个多基因家族的多样性。这项研究为理解副猪嗜血杆菌致病菌株的组织定植和侵袭特性提供了见解。

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