Singla Divya, Sharma Arun, Sachdev Vinod, Chopra Radhika
Senior Resident, Department of Dental Surgery, Dr. Ram Manohar Lohia Hospital , New Delhi, India .
Professor and Head, Department of Pedodontics and Preventive Dentistry, People's College of Dental Sciences and Research Centre , Bhopal, Madhya Pradesh, India .
J Clin Diagn Res. 2016 Nov;10(11):ZC60-ZC63. doi: 10.7860/JCDR/2016/19256.8909. Epub 2016 Nov 1.
Dental caries is one of the most common infectious diseases affecting the oral cavity. Among the oral bacteria, mutans streptococci have been implicated as major cariogenic bacteria as they can produce high levels of dental caries causing substances such as lactic acid and extracellular polysaccharides.
The aim of the study was to detect the presence of and in dental plaque by using Polymerase Chain Reaction (PCR) method, quantification of these micro-organisms using Modified Sucrose-Bacitracin (SB-20M) agar medium and to correlate their presence in Caries Active (CA) and Caries Free (CF) pre-school children.
Sixty-eight pre-school children, in the age group of 3-5 years were divided equally into 34 CA and 34 CF children. Dental plaque samples were obtained for detection of these microorganisms by PCR method and quantification was done using SB-20M culture medium. The data was analyzed using statistical software SPSS version 16. For statistical analysis, the frequencies and means of Colony Forming Units (CFU) were used with CI = 95%. For bivariate analysis, Fisher exact test was used at 5% level of significance. The comparison of mean of number of CFU of and was made by Mann Whitney U test and Spearman's Rho test at 1% level of significance was used for correlation between dmft and CFU in CA group.
The results showed that was significantly higher in CA group as compared to CF group whereas showed no significant difference. On quantification of these micro-organisms, was present in significantly higher numbers in CA group as compared to CF group. On correlating the CFU/ml of the micro-organisms with the dmft index, both the micro-organisms showed a positive correlation.
We conclude that and were detected in higher numbers in CA children as compared to CF children. PCR is a sensitive, specific, rapid and an effective method for the detection of oral microorganisms.
龋齿是影响口腔的最常见传染病之一。在口腔细菌中,变形链球菌被认为是主要的致龋菌,因为它们能产生大量导致龋齿的物质,如乳酸和细胞外多糖。
本研究的目的是通过聚合酶链反应(PCR)方法检测牙菌斑中[具体微生物名称未给出]的存在,使用改良蔗糖-杆菌肽(SB-20M)琼脂培养基对这些微生物进行定量,并将它们在患龋活跃(CA)和无龋(CF)学龄前儿童中的存在情况进行关联分析。
68名3至5岁的学龄前儿童被平均分为34名患龋活跃儿童和34名无龋儿童。采集牙菌斑样本,通过PCR方法检测这些微生物,并使用SB-20M培养基进行定量。数据使用统计软件SPSS 16版进行分析。对于统计分析,使用菌落形成单位(CFU)的频率和均值,置信区间为95%。对于双变量分析,在5%的显著性水平下使用Fisher精确检验。通过Mann Whitney U检验比较[具体微生物名称未给出]和[具体微生物名称未给出]的CFU数量均值,并在1%的显著性水平下使用Spearman秩相关检验分析患龋活跃组中乳牙龋失补牙面数(dmft)与CFU之间的相关性。
结果显示,与无龋组相比,患龋活跃组中[具体微生物名称未给出]显著更高,而[具体微生物名称未给出]无显著差异。对这些微生物进行定量时,与无龋组相比,患龋活跃组中[具体微生物名称未给出]的数量显著更高。将微生物的CFU/ml与dmft指数进行关联分析时,两种微生物均显示出正相关。
我们得出结论,与无龋儿童相比,患龋活跃儿童中[具体微生物名称未给出]和[具体微生物名称未给出]的数量更高。PCR是一种检测口腔微生物的灵敏、特异、快速且有效的方法。