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血清型M1 A群链球菌菌株的快速分子遗传分型

Rapid molecular genetic subtyping of serotype M1 group A Streptococcus strains.

作者信息

Hoe N, Nakashima K, Grigsby D, Pan X, Dou S J, Naidich S, Garcia M, Kahn E, Bergmire-Sweat D, Musser J M

机构信息

Baylor College of Medicine, Houston, Texas 77030, USA.

出版信息

Emerg Infect Dis. 1999 Mar-Apr;5(2):254-63. doi: 10.3201/eid0502.990210.

Abstract

Serotype M1 group A Streptococcus, the most common cause of invasive disease in many case series, generally have resisted extensive molecular subtyping by standard techniques (e.g., multilocus enzyme electrophoresis, pulsed-field gel electrophoresis). We used automated sequencing of the sic gene encoding streptococcal inhibitor of complement and of a region of the chromosome with direct repeat sequences to unambiguously differentiate 30 M1 isolates recovered from 28 patients in Texas with invasive disease episodes temporally clustered and thought to represent an outbreak. Sequencing of the emm gene was less useful for M1 strain differentiation, and restriction fragment length polymorphism analysis with IS1548 or IS1562 as Southern hybridization probes did not provide epidemiologically useful subtyping information. Sequence polymorphism in the direct repeat region of the chromosome and IS1548 profiling data support the hypothesis that M1 organisms have two main evolutionary lineages marked by the presence or absence of the speA2 allele encoding streptococcal pyrogenic exotoxin A2.

摘要

血清型M1 A组链球菌是许多病例系列中侵袭性疾病最常见的病因,通常难以通过标准技术(如多位点酶电泳、脉冲场凝胶电泳)进行广泛的分子分型。我们对编码链球菌补体抑制剂的sic基因以及具有直接重复序列的染色体区域进行了自动测序,以明确区分从德克萨斯州28例患者中分离出的30株M1菌株,这些患者的侵袭性疾病发作在时间上聚集,被认为代表一次暴发。emm基因测序对M1菌株的区分作用较小,以IS1548或IS1562作为Southern杂交探针的限制性片段长度多态性分析未提供具有流行病学意义的分型信息。染色体直接重复区域的序列多态性和IS1548谱型分析数据支持以下假说:M1菌株有两个主要的进化谱系,其特征是编码链球菌致热外毒素A2的speA2等位基因的存在或缺失。

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