使用多位点序列分型对铜绿假单胞菌进行群体遗传学分析。

Population genetic analysis of Pseudomonas aeruginosa using multilocus sequence typing.

作者信息

Vernez Isabelle, Hauser Philippe, Bernasconi Marco V, Blanc Dominique S

机构信息

Hospital Preventive Medicine, University Hospital of Lausanne, Bugnon 48, CH-1011 Lausanne, Switzerland.

出版信息

FEMS Immunol Med Microbiol. 2005 Jan 1;43(1):29-35. doi: 10.1016/j.femsim.2004.06.024.

Abstract

To study the population genetic structure of Pseudomonas aeruginosa, we developed a multilocus sequence typing scheme. The sequences of internal fragments of seven housekeeping genes were obtained for 34 P. aeruginosa isolates from patients hospitalized in five different European cities. Twenty-six different allelic profiles were identified. The mean allelic diversity was 0.854 (range: 0.606-0.978), which was about six times greater than the results obtained with the multilocus enzyme electrophoresis method. Linkage disequilibrium was measured with the index of association. An index of 1.95+/-0.24 was calculated when all the strains were considered. This index was 1.76+/-0.27 when only one strain per sequence type was considered. Both results were different from 0, indicating linkage among loci, which means that the population structure of our set of P. aeruginosa isolates is clonal. The clonal structure of the population was also suggested by the congruence of the topology of the different trees obtained from the seven housekeeping genes. These results are in contrast to previous studies, finding a non clonal population structure. Since a small number of isolates was analyzed in this study, there might be a bias of selection which includes the possibility that they belong to widely disseminated epidemic clones. Another possibility is that recombination did not occurred homogeneously throughout the genome of P. aeruginosa, so that part of it has a clonal structure, while the remaining part of the genome is more frequently subject to recombination.

摘要

为研究铜绿假单胞菌的群体遗传结构,我们开发了一种多位点序列分型方案。从欧洲五个不同城市住院患者中分离出34株铜绿假单胞菌,获取了7个管家基因内部片段的序列。鉴定出26种不同的等位基因谱。平均等位基因多样性为0.854(范围:0.606 - 0.978),约为多位点酶电泳法所得结果的6倍。用关联指数测量连锁不平衡。当考虑所有菌株时,计算出的指数为1.95±0.24。当每种序列类型仅考虑一个菌株时,该指数为1.76±0.27。两个结果均不同于0,表明基因座之间存在连锁,这意味着我们所研究的铜绿假单胞菌分离株群体结构是克隆性的。从7个管家基因得到的不同树形拓扑结构的一致性也表明了群体的克隆结构。这些结果与之前发现非克隆群体结构的研究形成对比。由于本研究分析的分离株数量较少,可能存在选择偏差,包括它们属于广泛传播的流行克隆的可能性。另一种可能性是,重组并非在铜绿假单胞菌的整个基因组中均匀发生,因此其一部分具有克隆结构,而基因组的其余部分更频繁地发生重组。

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