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首页> 外文期刊>Journal of Clinical Microbiology >Species identification of oral viridans streptococci by restriction fragment polymorphism analysis of rRNA genes.
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Species identification of oral viridans streptococci by restriction fragment polymorphism analysis of rRNA genes.

机译:通过rRNA基因的限制性片段多态性分析,鉴定口腔翠绿链球菌。

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Oral streptococci formerly classified as Streptococcus sanguis have been divided into six genetic groups. Methods to identify those species by genotype are needed. This study compared restriction fragment polymorphisms of rRNA genes (ribotypes) for seven S. gordonii, three S. sanguis, four S. oralis, three S. mitis, one S. crista, and seven S. parasanguis strains classified in previous DNA hybridization studies, as well as one clinical isolate. DNA was digested with HindIII, PvuII, HindIII and PvuII combined, EcoRI, BamHI, AatII, AlwNI, and DraII. DNA fragments were hybridized with a digoxigenin-labeled cDNA probe obtained by reverse transcription of Escherichia coli 16S and 23S rRNA. S. oralis, S. mitis, and S. parasanguis all showed an isolated 2,290-bp band in AatII ribotypes that was absent from S. gordonii, S. sanguis, and S. crista. The last three groups showed species-specific bands with AatII and also with PvuII. S. oralis could be distinguished from S. mitis and S. parasanguis in AlwNI and DraII ribotypes. S. mitis and S. parasanguis could not be distinguished, since they shared multiple bands in PvuII, AlwNI, and EcoRI patterns. The clinical isolate in the panel was very similar to S. sanguis by all enzymes used. Our findings suggest that ribotyping may be useful for genotypic identification of oral viridans streptococci. Initial digests of clinical isolates might be made with AatII, followed by PvuII or AlwNI. Isolates then could be identified by comparing ribotype patterns with those of reference strains. This approach could facilitate clinical studies of these newly defined species.
机译:以前被归类为血链球菌的口腔链球菌已被分为六个基因组。需要通过基因型鉴定那些物种的方法。这项研究比较了先前DNA杂交研究中归类的七个S. gordonii,三个S. sanguis,四个S. oralis,三个S. mitis,一个S. crista和七个S. parasanguis菌株的rRNA基因(核糖体)的限制性片段多态性。 ,以及一种临床隔离株。用HindIII,PvuII,HindIII和PvuII组合,EcoRI,BamHI,AatII,AlwNI和DraII消化DNA。将DNA片段与洋地黄毒苷标记的cDNA探针杂交,该探针通过大肠杆菌16S和23S rRNA的反转录获得。口头链球菌,链霉菌和副链球菌均在AatII核型中均显示出一条孤立的2290 bp的条带,而戈氏链球菌,桑氏链球菌和crista链球菌则不存在。后三组显示AatII和PvuII的物种特异性条带。在AlwNI和DraII核糖型中,口头链球菌可与链球菌和副链球菌区分开。由于它们以PvuII,AlwNI和EcoRI模式共享多个条带,因此无法区分S. mitis和parasanguis。小组中使用的所有酶与临床分离株都非常相似。我们的发现表明,核糖分型可能对口腔绿色链球菌的基因型鉴定有用。临床分离株的初步消化物可能由AatII制成,然后由PvuII或AlwNI制成。然后可以通过将核糖型模式与参考菌株的模式进行比较来鉴定出分离株。这种方法可以促进这些新定义物种的临床研究。

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