Lemée Ludovic, Bourgeois Ingrid, Ruffin Elodie, Collignon Anne, Lemeland Jean-François, Pons Jean-Louis
Groupe de Recherche sur les Antimicrobiens et les Micro-organismes (GRAM EA 2656, IFR 23), Université de Rouen, Faculté de Médecine-Pharmacie, 22 Boulevard Gambetta, F-76183 Rouen Cedex, France.
Département de Microbiologie-Immunologie, Faculté de Pharmacie Paris XI, Châtenay-Malabry, France.
Microbiology (Reading). 2005 Oct;151(Pt 10):3171-3180. doi: 10.1099/mic.0.28155-0.
A multilocus sequence analysis of ten virulence-associated genes was performed to study the genetic relationships between 29 Clostridium difficile isolates of various origins, hosts and clinical presentations, and selected from the main lineages previously defined by multilocus sequence typing (MLST) of housekeeping genes. Colonization-factor-encoding genes (cwp66, cwp84, fbp68, fliC, fliD, groEL and slpA), toxin A and B genes (tcdA and tcdB), and the toxin A and B positive regulator gene (tcdD) were investigated. Binary toxin genes (cdtA and cdtB) were also detected, and internal fragments were sequenced for positive isolates. Virulence-associated genes exhibited a moderate polymorphism, comparable to the polymorphism of housekeeping genes, whereas cwp66 and slpA genes appeared highly polymorphic. Isolates recovered from human pseudomembranous colitis cases did not define a specific lineage. The presence of binary toxin genes, detected in five of the 29 isolates (17 %), was also not linked to clinical presentation. Conversely, toxigenic A-B+ isolates defined a very homogeneous lineage, which is distantly related to other isolates. By clustering analysis, animal isolates were intermixed with human isolates. Multilocus sequence analysis of virulence-associated genes is consistent with a clonal population structure for C. difficile and with the lack of host specificity. The data suggest a co-evolution of several of the virulence-associated genes studied (including toxins A and B and the binary toxin genes) with housekeeping genes, reflecting the genetic background of C. difficile, whereas flagellin, cwp66 and slpA genes may undergo recombination events and/or environmental selective pressure.
对十个与毒力相关的基因进行多位点序列分析,以研究29株艰难梭菌分离株之间的遗传关系,这些分离株来自不同的来源、宿主和临床表现,且选自先前通过管家基因多位点序列分型(MLST)定义的主要谱系。对编码定植因子的基因(cwp66、cwp84、fbp68、fliC、fliD、groEL和slpA)、毒素A和B基因(tcdA和tcdB)以及毒素A和B阳性调节基因(tcdD)进行了研究。还检测了二元毒素基因(cdtA和cdtB),并对阳性分离株的内部片段进行了测序。与毒力相关的基因表现出中等程度的多态性,与管家基因的多态性相当,而cwp66和slpA基因似乎具有高度多态性。从人类假膜性结肠炎病例中分离出的菌株并未定义出特定的谱系。在29株分离株中的5株(17%)中检测到二元毒素基因的存在,这也与临床表现无关。相反,产毒A-B+分离株定义了一个非常同质的谱系,与其他分离株关系较远。通过聚类分析,动物分离株与人类分离株混合在一起。与毒力相关基因的多位点序列分析与艰难梭菌的克隆群体结构以及缺乏宿主特异性一致。数据表明,所研究的几种与毒力相关的基因(包括毒素A和B以及二元毒素基因)与管家基因共同进化,反映了艰难梭菌的遗传背景,而鞭毛蛋白、cwp66和slpA基因可能经历重组事件和/或环境选择压力。