Hoshino Tomonori, Kawaguchi Mamoru, Shimizu Noriko, Hoshino Naoko, Ooshima Takashi, Fujiwara Taku
Department of Pediatric Dentistry, Osaka University Graduate School of Dentistry, Suita-shi Osaka 565-0871, Japan.
Diagn Microbiol Infect Dis. 2004 Mar;48(3):195-9. doi: 10.1016/j.diagmicrobio.2003.10.002.
Oral streptococci are major constituents of dental plaque, and their prevalence is implicated in various pathologies. Therefore, accurate identification of oral streptococci would be valuable for studies of cariogenic plaque and for diagnostic use in infective endocarditis. Many oral streptococci possess glucosyltransferase enzymes that synthesize glucan, which is an obligate component of dental plaque. We established a rapid and precise method to identify oral streptococci by PCR using the species-specific region from the glucosyltransferase gene. With the species-specific primers, Streptococcus mutans, S. sobrinus, S. salivarius, S. sanguinis, S. oralis, and S. gordonii could be successfully distinguished. Further, we developed a simple method to extract the bacterial DNA from saliva. Using the resultant DNA as a template, the proposed PCR detection was performed. Their distribution was in accord with results of conventional biochemical tests. These findings indicate that the present PCR method is useful for the analysis of oral streptococci and can be successfully used in clinical applications to identify pathogenic bacteria associated with oral infectious disease and/or endocarditis.
口腔链球菌是牙菌斑的主要成分,其流行与多种病理状况有关。因此,准确鉴定口腔链球菌对于致龋菌斑的研究以及感染性心内膜炎的诊断具有重要价值。许多口腔链球菌拥有合成葡聚糖的葡糖基转移酶,葡聚糖是牙菌斑的必需成分。我们建立了一种快速精确的方法,通过使用葡糖基转移酶基因的种属特异性区域进行PCR来鉴定口腔链球菌。使用种属特异性引物,可以成功区分变形链球菌、远缘链球菌、唾液链球菌、血链球菌、口腔链球菌和戈登链球菌。此外,我们开发了一种从唾液中提取细菌DNA的简单方法。以所得DNA为模板,进行了所提出的PCR检测。它们的分布与传统生化试验结果一致。这些发现表明,目前的PCR方法可用于口腔链球菌的分析,并可成功应用于临床,以鉴定与口腔传染病和/或心内膜炎相关的病原菌。