Identification of clinically relevant viridans streptococci by analysis of transfer DNA intergenic spacer length polymorphism.

Y De Gheldre, P Vandamme, H Goossens, M J Struelens
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引用次数: 51

Abstract

The utility of PCR analysis of transfer DNA intergenic spacer length polymorphism (tDNA-ILP) for the identification to the species level of clinically relevant viridans streptococci was evaluated with a collection of reference strains of 15 species of the salivarius, anginosus, mitis and mutans rRNA homology groups. PCR products generated by using fluorescent, outwardly directed, consensus tDNA primers were analysed by electrophoresis on denaturating polyacrylamide gels and by laser fluorescence scanning. Eleven species showed specific and distinct tDNA patterns: Streptococcus cristatus, Streptococcus gordonii, Streptococcus oralis, Streptococcus mitis, Streptococcus pneumoniae, Streptococcus sanguinis, Streptococcus parasanguinis, Streptococcus anginosus, Streptococcus mutans, Streptococcus criceti and Streptococcus ratti. Indistinguishable patterns were obtained among two groups of species: Streptococcus vestibularis and Streptococcus salivarius on the one hand and Streptococcus constellatus and Streptococcus intermedius on the other. S. mitis strains produced heterogeneous patterns that could be separated into three groups: a group containing S. mitis biovar 1 and two S. mitis biovar 2 groups, one of which clustered with S. parasanguinis strains while the other showed patterns unrelated to other species. These results agree in part with protein electrophoretic analysis showing that S. mitis biovar 2 strains belong to several streptococcal taxa. In conclusion, PCR analysis of tDNA-ILP holds promise for rapid identification of viridans streptococci that are difficult to identify by phenotypic tests.

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通过分析转移DNA基因间隔段长度多态性鉴定临床相关的绿绿链球菌。
以唾液、血管、炎、突变等15种链球菌的rRNA同源群为参考菌株,评价了PCR转移DNA基因间隔长度多态性(tDNA-ILP)在临床相关绿链球菌鉴定中的应用价值。通过变性聚丙烯酰胺凝胶电泳和激光荧光扫描对荧光外定向一致tDNA引物产生的PCR产物进行分析。11种链球菌的tDNA图谱表现出特异性和明显的差异,分别为:猪链球菌、哥donii链球菌、口腔链球菌、mitis链球菌、肺炎链球菌、血链球菌、副血链球菌、血管链球菌、变形链球菌、蟋蟀链球菌和ratti链球菌。前庭链球菌和唾液链球菌以及星座链球菌和中间链球菌这两组物种之间存在难以区分的模式。S. mitis菌株产生异质模式,可分为三组:一个包含S. mitis生物变种1的组和两个S. mitis生物变种2的组,其中一个与S. paranguinis菌株聚集在一起,而另一个与其他物种无关。这些结果与蛋白质电泳分析结果部分一致,表明S. mitis生物变种2菌株属于几个链球菌分类群。总之,tDNA-ILP的PCR分析有望快速鉴定难以通过表型试验鉴定的翠绿链球菌。
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