Ali R W, Johannessen A C, Dahlén G, Socransky S S, Skaug N
Laboratory of Oral Microbiology, University of Bergen, Norway.
J Clin Periodontol. 1997 Nov;24(11):830-5. doi: 10.1111/j.1600-051x.1997.tb01197.x.
Our study is the 1st report on subgingival microbiota in adult Cameronians. The aim was to investigate, using the checkerboard DNA-DNA hybridization technique, the prevalence of 18 oral species in subgingival plaque samples obtained from sex- and age-matched Cameronian adults with and without periodontal destruction. We also compared cultivation and the Affirm DP test with the checkerboard technique in their capability to detect some selected species among the 18. 21 adult periodontitis patients and 21 periodontally healthy subjects were examined and the results were compared statistically. Each periodontitis patient had at least 4 pockets of > or = 6 mm depth, while the healthy subjects had no sites more than 3 mm deep. Results of the checkerboard analysis showed that significantly (p < 0.05) more periodontitis patients tested positive for most of the 18 bacterial species. The Gram-positive species Actinomyces naeslundii, Streptococcus mitis and Streptococcus sanguis, known as microbiota of healthy sites, were detected significantly more frequently in the healthy group. Cultivation demonstrated P. gingivalis, B. forsythus, A. actinomycetemcomitans, P. intermedia and F. nucleatum in significantly lower %s of patients as compared to the checkerboard technique. Furthermore, the Affirm DP test detected P. gingivalis and B. forsythus in significantly fewer patients than did the checkerboard technique. A. actinomycetemcomitans was detected in 52.3% of the patients by the latter technique while the Affirm DP test failed to detect the bacterium in any of the samples. Overall, the results of the present study confirm the importance of the screening method and indicate that the prevalences of the investigated putative periodontal pathogens and beneficial species in the healthy and diseased adult Cameronians were similar to those reported for adults in the West and in some developing countries.
我们的研究是关于喀麦隆成年人龈下微生物群的首份报告。目的是使用棋盘式DNA-DNA杂交技术,调查从年龄和性别匹配的、有或无牙周破坏的喀麦隆成年人口腔中获取的龈下菌斑样本中18种口腔菌种的流行情况。我们还比较了培养法和Affirm DP检测法与棋盘式技术在检测这18种选定菌种中的能力。对21名成年牙周炎患者和21名牙周健康受试者进行了检查,并对结果进行了统计学比较。每位牙周炎患者至少有4个深度≥6 mm的牙周袋,而健康受试者没有深度超过3 mm的部位。棋盘式分析结果显示,18种细菌中的大多数,牙周炎患者检测呈阳性的比例显著更高(p<0.05)。革兰氏阳性菌种内氏放线菌、缓症链球菌和血链球菌,作为健康部位的微生物群,在健康组中检测到的频率显著更高。与棋盘式技术相比,培养法显示牙龈卟啉单胞菌、福赛坦氏菌、伴放线放线杆菌、中间普氏菌和具核梭杆菌在患者中的比例显著更低。此外,Affirm DP检测法检测到的牙龈卟啉单胞菌和福赛坦氏菌患者显著少于棋盘式技术。伴放线放线杆菌通过后一种技术在52.3%的患者中检测到,而Affirm DP检测法在任何样本中均未检测到该细菌。总体而言,本研究结果证实了筛查方法的重要性,并表明在健康和患病的喀麦隆成年人中,所调查的假定牙周病原体和有益菌种的流行情况与西方和一些发展中国家成年人的报告相似。