Dickson E M, Riggio M P, Macpherson L
Infection and Immunity Research Section, University of Glasgow Dental School, 378 Sauchiehall Street, Glasgow G2 3JZ, UK.
J Med Microbiol. 2005 Mar;54(Pt 3):299-303. doi: 10.1099/jmm.0.45770-0.
Lactobacillus fermentum is a Gram-positive bacterium that is associated with active caries lesions. Methods for identifying Lactobacillus species traditionally have been based upon culture methods coupled with biochemical tests, which are generally unreliable. The aim of this study was to develop a species-specific PCR assay for the direct detection of L. fermentum in oral clinical samples. PCR primers specific for L. fermentum were identified by alignment of bacterial 16S rRNA genes and selection of sequences specific for L. fermentum at their 3' ends. PCR positivity for L. fermentum DNA was indicated by amplification of a 337 bp product. The primers were shown to be specific for L. fermentum DNA, since no PCR product was obtained when genomic DNA from a wide range of other oral bacteria, including closely related Lactobacillus species, were used as test species. The PCR assay was then used in an attempt to identify L. fermentum DNA in supragingival plaque samples and in pus aspirates from subjects with acute dento-alveolar abscesses. Four out of 70 (5.7 %) supragingival plaque samples analysed were positive for the presence of L. fermentum DNA while none of the 19 pus samples analysed was positive for L. fermentum DNA. This PCR assay provides a more rapid, specific and sensitive alternative to conventional culture methods for the identification of L. fermentum in clinical specimens.
发酵乳杆菌是一种与活动性龋损相关的革兰氏阳性菌。传统上,鉴定乳杆菌属菌种的方法是基于培养方法结合生化试验,但这些方法通常不可靠。本研究的目的是开发一种种特异性PCR检测方法,用于直接检测口腔临床样本中的发酵乳杆菌。通过比对细菌16S rRNA基因并选择其3'端对发酵乳杆菌特异的序列,鉴定出了对发酵乳杆菌特异的PCR引物。发酵乳杆菌DNA的PCR阳性通过扩增出一条337 bp的产物来指示。这些引物对发酵乳杆菌DNA具有特异性,因为当使用来自多种其他口腔细菌(包括密切相关的乳杆菌属菌种)的基因组DNA作为测试菌种时,未获得PCR产物。然后将该PCR检测方法用于尝试鉴定龈上菌斑样本和急性牙源性牙槽脓肿患者的脓液抽吸物中的发酵乳杆菌DNA。在分析的70份龈上菌斑样本中,有4份(5.7%)发酵乳杆菌DNA检测呈阳性,而在分析的19份脓液样本中,没有一份发酵乳杆菌DNA检测呈阳性。这种PCR检测方法为临床标本中发酵乳杆菌的鉴定提供了一种比传统培养方法更快速、特异和灵敏的替代方法。