摘要
目的 使用聚合酶链反应 (polymerasechainreaction ,PCR)检测龈下菌斑的牙龈卟啉菌 ,并与常规的培养法和间接免疫荧光法相比较。方法 设计纤毛亚单位蛋白基因内的一对引物 ,用PCR对 92个龈下菌斑标本进行扩增 ,与其他两种方法的检出率进行比较。结果 相同的菌斑标本 ,PCR的检出率为 94 6 % ,培养法为 48 9% ,间接免疫荧光法为 6 8 5 % ,前者明显高于后两者 (P <0 0 0 1)。结论 对牙周病致病菌的检测 ,PCR较培养法和间接免疫荧光法具有较高的敏感性。
Objective To compare the efficiency of polymerase chain reaction (PCR) with cultural method and indirect immunofluorescence(IF) in detection of Porphyromonas gingivalis (P g) in oral plaque samples Methods 92 subgingival plaque samples were collected from patients of three kinds of periodontal disease A program using PCR to detect Fimbrilin gene (Fim A) was designed to detect P g The efficiency of this PCR method was compared with cultural method and IF Results The positive rate of PCR was 94 6%, while that of cultural method and IF was only 48 9% and 68 5% respectively The difference was significant in statistical analysis ( P <0 001) Conclusion PCR is more sensitive than culture method and IF in detecting pathogens of periodontal diseases The study provides a simplified and efficient method for oral clinical use
出处
《中华口腔医学杂志》
CAS
CSCD
北大核心
2000年第1期38-40,共3页
Chinese Journal of Stomatology
