Munson M A, Banerjee A, Watson T F, Wade W G
Infection Research Group, The Dental Institute, King's College London, United Kingdom.
J Clin Microbiol. 2004 Jul;42(7):3023-9. doi: 10.1128/JCM.42.7.3023-3029.2004.
Molecular techniques have revealed many novel, presumed unculturable, taxa in oral infections. The aim of this study was to characterize the bacterial community of the middle and advancing front of carious dental lesions by cultural and molecular analyses. Samples were collected with a hand excavator from five teeth with carious lesions involving dentine. Samples were cultured on blood agar and Rogosa agar incubated in air plus 5% CO(2) and on fastidious anaerobe agar anaerobically. DNA was also extracted directly from the samples and 16S rRNA genes were amplified by PCR with universal primers. PCR products were singularized by cloning, and the cloned inserts and cultured isolates were identified by 16S rRNA gene sequence analysis. We identified 95 taxa among the 496 isolates and 1,577 clones sequenced; 44 taxa were detected by the molecular method alone; 31 taxa were previously undescribed. Only three taxa, Streptococcus mutans, Rothia dentocariosa, and an unnamed Propionibacterium sp., were found in all five samples. The predominant taxa by anaerobic cultivation were the novel Propionibacterium sp. (18%), Olsenella profusa (14%), and Lactobacillus rhamnosus (8%). The predominant taxa in the molecular analysis were Streptococcus mutans (16%), Lactobacillus gasseri/johnsonii (13%), and Lactobacillus rhamnosus (8%). There was no significant difference between the compositions of the microflora in the middle and advancing front samples (P < 0.05, Wilcoxon matched pairs, signed ranks test). In conclusion, combined cultural and molecular analyses have shown that a diverse bacterial community is found in dentinal caries and that numerous novel taxa are present.
分子技术已揭示出许多存在于口腔感染中、推测为不可培养的新分类单元。本研究的目的是通过培养和分子分析来表征龋损牙本质中层及进展前沿的细菌群落。用手用挖匙从5颗累及牙本质的龋损牙齿采集样本。样本接种于血琼脂和罗戈萨琼脂上,分别在空气加5%二氧化碳环境中培养以及在厌氧条件下接种于苛求厌氧菌琼脂上培养。还直接从样本中提取DNA,用通用引物通过PCR扩增16S rRNA基因。PCR产物通过克隆进行单一化处理,克隆插入片段和培养分离株通过16S rRNA基因序列分析进行鉴定。在测序的496株分离株和1577个克隆中,我们鉴定出95个分类单元;仅通过分子方法检测到44个分类单元;31个分类单元此前未被描述。在所有5个样本中仅发现3个分类单元,即变形链球菌、龋齿罗氏菌和一种未命名的丙酸杆菌属细菌。厌氧培养的主要分类单元是新的丙酸杆菌属细菌(18%)、丰富奥尔森菌(14%)和鼠李糖乳杆菌(8%)。分子分析中的主要分类单元是变形链球菌(16%)、加氏乳杆菌/约翰逊乳杆菌(13%)和鼠李糖乳杆菌(8%)。中层和进展前沿样本中的微生物群落组成之间无显著差异(P<0.05,威尔科克森配对符号秩检验)。总之,培养分析和分子分析相结合表明,在牙本质龋中发现了多样化的细菌群落,并且存在许多新的分类单元。