Ohara-Nemoto Y, Tajika S, Sasaki M, Kaneko M
Department of Microbiology, School of Dentistry, Iwate Medical University, Morioka, Japan.
J Clin Microbiol. 1997 Oct;35(10):2458-63. doi: 10.1128/jcm.35.10.2458-2463.1997.
Abiotrophia adiacens and Abiotrophia defectiva, previously referred to as nutritionally variant streptococci, Streptococcus adjacens and Streptococcus defectivus, respectively, are causes of infective endocarditis. We describe a method of identifying these two species and also of distinguishing them from 15 other major etiological pathogens of infective endocarditis by means of 16S rRNA gene PCR amplification followed by restriction fragment length polymorphism analysis (PCR-RFLP). The 16S rRNA genes were successfully amplified with a set of universal primers from all 17 species of bacteria examined, including viridans group streptococci. The RFLP patterns of A. adiacens and A. defectiva obtained by HaeIII or MspI digestion were readily distinguished from each other and from those of other bacteria. When PCR analysis was performed with the supernatant of a suspension of a boiled colony, the 16S rRNA genes of 80 of 82 isolates (97%) of A. adiacens and all isolates (11 of 11) of A. defectiva were amplified. The HaeIII RFLP patterns of the isolates were the same as those of the corresponding type strains, although 28% of A. adiacens isolates revealed intraspecies polymorphism. The detection limit of this method was 0.1 pg of genomic DNA, as assessed by using the digoxigenin-labeling DNA detection system. Thus, the PCR-RFLP analysis that we developed is applicable for the routine detection of Abiotrophia from clinical specimens.
毗邻贫养菌和缺陷贫养菌,以前分别称为营养变异链球菌、毗邻链球菌和缺陷链球菌,是感染性心内膜炎的病因。我们描述了一种鉴定这两个菌种的方法,并且通过16S rRNA基因PCR扩增,随后进行限制性片段长度多态性分析(PCR-RFLP),将它们与感染性心内膜炎的其他15种主要病原体区分开来。使用一组通用引物成功地从所有17种检测的细菌中扩增出16S rRNA基因,包括草绿色链球菌。通过HaeIII或MspI消化获得的毗邻贫养菌和缺陷贫养菌的RFLP模式很容易相互区分,也能与其他细菌的模式区分开来。当用煮沸菌落悬液的上清液进行PCR分析时,82株毗邻贫养菌分离株中的80株(97%)和所有缺陷贫养菌分离株(11株中的11株)的16S rRNA基因被扩增。分离株的HaeIII RFLP模式与相应模式菌株的相同,尽管28%的毗邻贫养菌分离株显示种内多态性。使用地高辛标记DNA检测系统评估,该方法的检测限为0.1 pg基因组DNA。因此,我们开发的PCR-RFLP分析适用于从临床标本中常规检测贫养菌。