Riggio M P, Lennon A
Infection Research Group, University of Glasgow Dental School, 378 Sauchiehall Street, Glasgow G2 3JZ.
J Med Microbiol. 2002 Dec;51(12):1097-1101. doi: 10.1099/0022-1317-51-12-1097.
Peptostreptococcus anaerobius is a gram-positive anaerobic coccus that is widely distributed in the normal human flora. The organism has also been implicated as a causative agent of several systemic infections, including endocarditis and infections of the genitourinary and gastrointestinal tracts. Its role in oral disease is less well defined, although it has been implicated in periodontal disease, gingivitis and root canal infections. Identification of P. anaerobius in clinical samples is currently reliant upon traditional culture and biochemical methods. The aim of this study was to develop a novel PCR assay for the detection of P. anaerobius and to attempt detection of this organism in oral samples. PCR primers specific for P. anaerobius DNA were developed by alignment of bacterial 16S ribosomal RNA gene sequences and selection of sequences specific at their 3' ends for P. anaerobius. When used in a PCR assay, positivity for P. anaerobius DNA was indicated by the amplification of a 943-bp product. The primers were shown to be specific for P. anaerobius DNA, as no PCR products were obtained when genomic DNA from a wide range of other Peptostreptococcus species and other oral bacteria were used as templates. The PCR assay was then applied to the detection of P. anaerobius DNA in subgingival plaque samples from adult periodontitis patients and pus aspirates from subjects with acute dento-alveolar abscesses. All of 60 subgingival plaque samples from 16 patients were negative for P. anaerobius DNA. None of the 43 pus samples analysed contained P. anaerobius DNA. These results suggest that P. anaerobius is not a major pathogen in adult periodontitis and dento-alveolar abscesses. The PCR assay is a more rapid, sensitive and specific alternative to culture-based methods for identification of P. anaerobius in clinical samples.
厌氧消化链球菌是一种革兰氏阳性厌氧球菌,广泛分布于人体正常菌群中。该菌也被认为是多种全身感染的病原体,包括心内膜炎以及泌尿生殖道和胃肠道感染。尽管它与牙周病、牙龈炎和根管感染有关,但其在口腔疾病中的作用尚不太明确。目前临床样本中厌氧消化链球菌的鉴定依赖于传统的培养和生化方法。本研究的目的是开发一种用于检测厌氧消化链球菌的新型聚合酶链反应(PCR)检测方法,并尝试在口腔样本中检测该菌。通过比对细菌16S核糖体RNA基因序列并选择其3'端对厌氧消化链球菌特异的序列,开发了针对厌氧消化链球菌DNA的PCR引物。当用于PCR检测时,扩增出943 bp的产物表明厌氧消化链球菌DNA呈阳性。这些引物对厌氧消化链球菌DNA具有特异性,因为当使用来自多种其他消化链球菌属物种和其他口腔细菌的基因组DNA作为模板时,未获得PCR产物。然后将该PCR检测方法应用于检测成人牙周炎患者龈下菌斑样本和急性牙槽脓肿患者的脓液抽吸物中的厌氧消化链球菌DNA。来自16名患者的60个龈下菌斑样本中,所有样本的厌氧消化链球菌DNA均为阴性。分析的43份脓液样本中均未含有厌氧消化链球菌DNA。这些结果表明,厌氧消化链球菌不是成人牙周炎和牙槽脓肿的主要病原体。对于临床样本中厌氧消化链球菌的鉴定,PCR检测方法是一种比基于培养的方法更快速、灵敏和特异的替代方法。