De Gheldre Y, Vandamme P, Goossens H, Struelens M J
Department of Microbiology, Hôpital Erasme, Université Libre de Bruxelles, Belgium.
Int J Syst Bacteriol. 1999 Oct;49 Pt 4:1591-8. doi: 10.1099/00207713-49-4-1591.
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.
运用转移DNA基因间隔区长度多态性(tDNA - ILP)的聚合酶链反应(PCR)分析来鉴定临床相关草绿色链球菌至种水平的效用,通过收集唾液链球菌、咽峡炎链球菌、缓症链球菌和变形链球菌rRNA同源组15个种的参考菌株进行了评估。使用荧光、向外定向的共有tDNA引物产生的PCR产物,通过在变性聚丙烯酰胺凝胶上电泳和激光荧光扫描进行分析。11个种显示出特异且不同的tDNA图谱:克里斯塔斯链球菌、戈登链球菌、口腔链球菌、缓症链球菌、肺炎链球菌、血链球菌、副血链球菌、咽峡炎链球菌、变形链球菌、仓鼠链球菌和鼠链球菌。在两组种之间获得了难以区分的图谱:一方面是前庭链球菌和唾液链球菌,另一方面是星座链球菌和中间链球菌。缓症链球菌菌株产生了异质图谱,可分为三组:一组包含缓症链球菌生物变种1和两个缓症链球菌生物变种2组,其中一组与副血链球菌菌株聚类,而另一组显示出与其他种无关的图谱。这些结果部分与蛋白质电泳分析一致,表明缓症链球菌生物变种2菌株属于几个链球菌分类群。总之,tDNA - ILP的PCR分析有望快速鉴定通过表型试验难以鉴定的草绿色链球菌。