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通过多位点盒 B 序列分型揭示高侵袭性血清型 12F、克隆复合体 218 肺炎链球菌的种群结构。

Population structure of hyperinvasive serotype 12F, clonal complex 218 Streptococcus pneumoniae revealed by multilocus boxB sequence typing.

机构信息

Department of Microbiology, University of Mississippi Medical Center, Jackson, MS, United States.

出版信息

Infect Genet Evol. 2011 Dec;11(8):1929-39. doi: 10.1016/j.meegid.2011.08.016. Epub 2011 Aug 25.

DOI:10.1016/j.meegid.2011.08.016
PMID:21888992
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3230773/
Abstract

At least four outbreaks of invasive disease caused by serotype 12F, clonal complex 218 Streptococcus pneumoniae have occurred in the United States over the past two decades. We studied the population structure of this clonal complex using a sample of 203 outbreak and surveillance isolates that were collected over 22 years from 34 US states and eight other countries. Conventional multilocus sequence typing identified five types and distinguished a single outbreak from the others. To improve typing resolution, multilocus boxB sequence typing (MLBT) was developed from 10 variable boxB minisatellite loci. MLBT identified 86 types and distinguished between each of the four outbreaks. Diversity across boxB loci tended to be positively correlated with repeat array size and, overall, best fit the infinite alleles mutation model. Multilocus linkage disequilibrium was strong, but pairwise disequilibrium decreased with the physical distance between loci and was strongest in one large region of the chromosome, indicating recent recombinations. Two major clusters were identified in the sample, and they were differentiated geographically, as western and more easterly US clusters, and temporally, as clusters that predominated before and after the licensure of pneumococcal conjugate vaccines. The diversity and linkage disequilibrium within these two clusters also differed, suggesting different population dynamics. MLBT revealed hidden aspects of the population structure of these hyperinvasive pneumococci, and it may provide a useful adjunct tool for outbreak investigations, surveillance, and population genetics studies of other pneumococcal clonal complexes.

摘要

在过去的二十年中,美国至少发生了四起由血清型 12F、克隆复合体 218 肺炎链球菌引起的侵袭性疾病暴发。我们使用来自美国 34 个州和其他 8 个国家的 22 年来收集的 203 个暴发和监测分离株样本研究了该克隆复合体的种群结构。传统的多位点序列分型确定了五种类型,并将单一暴发与其他暴发区分开来。为了提高分型分辨率,从 10 个可变的 boxB 微卫星位点开发了 boxB 多位点序列分型(MLBT)。MLBT 确定了 86 种类型,并区分了这四起暴发中的每一起。boxB 基因座的多样性与重复序列大小呈正相关,总体上符合无限等位基因突变模型。多位点连锁不平衡很强,但随着基因座之间的物理距离增加,成对的不平衡减少,在染色体的一个大区域最强,表明存在近期重组。在样本中确定了两个主要的聚类,它们在地理上有所区分,西部和更东部的美国聚类,以及在时间上,在肺炎球菌结合疫苗许可之前和之后占主导地位的聚类。这两个聚类中的多样性和连锁不平衡也有所不同,表明存在不同的种群动态。MLBT 揭示了这些高侵袭性肺炎链球菌种群结构的隐藏方面,它可能为暴发调查、监测和其他肺炎球菌克隆复合体的群体遗传学研究提供有用的辅助工具。