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通过rRNA基因的限制性片段多态性分析对口腔甲型溶血性链球菌进行菌种鉴定。

Species identification of oral viridans streptococci by restriction fragment polymorphism analysis of rRNA genes.

作者信息

Rudney J D, Larson C J

机构信息

Department of Oral Science, School of Dentistry, University of Minnesota, Minneapolis 55455.

出版信息

J Clin Microbiol. 1993 Sep;31(9):2467-73. doi: 10.1128/jcm.31.9.2467-2473.1993.

Abstract

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.

摘要

以前归类为血链球菌的口腔链球菌已被分为六个基因群。需要通过基因型鉴定这些菌种的方法。本研究比较了先前DNA杂交研究中分类的7株戈登链球菌、3株血链球菌、4株口腔链球菌、3株缓症链球菌、1株嵴链球菌和7株副血链球菌菌株以及1株临床分离株的rRNA基因限制性片段多态性(核糖型)。用HindIII、PvuII、HindIII和PvuII联合酶、EcoRI、BamHI、AatII、AlwNI和DraII消化DNA。DNA片段与通过大肠杆菌16S和23S rRNA逆转录获得的地高辛标记的cDNA探针杂交。口腔链球菌、缓症链球菌和副血链球菌在AatII核糖型中均显示出一条孤立的2290bp条带,而戈登链球菌、血链球菌和嵴链球菌中没有。后三组在AatII以及PvuII核糖型中显示出物种特异性条带。在AlwNI和DraII核糖型中,口腔链球菌可与缓症链球菌和副血链球菌区分开来。缓症链球菌和副血链球菌无法区分,因为它们在PvuII、AlwNI和EcoRI模式中共有多条条带。该组中的临床分离株在用所有酶检测时都与血链球菌非常相似。我们的研究结果表明,核糖分型可能有助于口腔草绿色链球菌的基因型鉴定。临床分离株的初步消化可以先用AatII,然后用PvuII或AlwNI。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分离株。这种方法可以促进对这些新定义物种的临床研究。

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