Byun Roy, Nadkarni Mangala A, Chhour Kim-Ly, Martin F Elizabeth, Jacques Nicholas A, Hunter Neil
Institute of Dental Research, Westmead Centre for Oral Health, P.O. Box 533, Wentworthville, NSW 2145, Australia.
J Clin Microbiol. 2004 Jul;42(7):3128-36. doi: 10.1128/JCM.42.7.3128-3136.2004.
Our previous analysis of 65 advanced dental caries lesions by traditional culture techniques indicated that lactobacilli were numerous in the advancing front of the progressive lesion. Production of organic acids by lactobacilli is considered to be important in causing decalcification of the dentinal matrix. The present study was undertaken to define more precisely the diversity of lactobacilli found in this environment and to quantify the major species and phylotypes relative to total load of lactobacilli by real-time PCR. Pooled DNA was amplified by PCR with Lactobacillus genus-specific primers for subsequent cloning, sequencing, and phylogenetic analysis. Based on 16S ribosomal DNA sequence comparisons, 18 different phylotypes of lactobacilli were detected, including strong representation of both novel and gastrointestinal phylotypes. Specific PCR primers were designed for nine prominent species, including Lactobacillus gasseri, L. ultunensis, L. salivarius, L. rhamnosus, L. casei, L. crispatus, L. delbrueckii, L. fermentum, and L. gallinarum. More than three different species were identified as being present in most of the dentine samples, confirming the widespread distribution and numerical importance of various Lactobacillus spp. in carious dentine. Quantification by real-time PCR revealed various proportions of the nine species colonizing carious dentine, with higher mean loads of L. gasseri and L. ultunensis than of the other prevalent species. The findings provide a basis for further characterization of the pathogenicity of Lactobacillus spp. in the context of extension of the carious lesion.
我们之前通过传统培养技术对65个晚期龋齿病变进行分析,结果表明在进行性病变的进展前沿存在大量乳酸杆菌。乳酸杆菌产生有机酸被认为在导致牙本质基质脱矿方面很重要。本研究旨在更精确地确定在这种环境中发现的乳酸杆菌的多样性,并通过实时PCR对主要菌种和系统型相对于乳酸杆菌总负荷进行定量。通过使用乳酸杆菌属特异性引物进行PCR扩增混合DNA,用于后续的克隆、测序和系统发育分析。基于16S核糖体DNA序列比较,检测到18种不同的乳酸杆菌系统型,包括新的和胃肠道系统型的大量代表。针对9种主要菌种设计了特异性PCR引物,包括加氏乳酸杆菌、乌尔图乳酸杆菌、唾液乳酸杆菌、鼠李糖乳酸杆菌、干酪乳杆菌、卷曲乳酸杆菌、德氏乳酸杆菌、发酵乳酸杆菌和鸡乳酸杆菌。在大多数牙本质样本中鉴定出存在三种以上不同的菌种,证实了各种乳酸杆菌在龋坏牙本质中的广泛分布和数量重要性。通过实时PCR定量显示,9种菌种在龋坏牙本质中的定殖比例各不相同,加氏乳酸杆菌和乌尔图乳酸杆菌的平均负荷高于其他常见菌种。这些发现为进一步表征乳酸杆菌在龋损扩展背景下的致病性提供了基础。