›› 2012, Vol. 3 ›› Issue (4): 201-204.

• 论著 • 上一篇    下一篇

PCR-DGGE检测早期儿童龋治疗前后口腔菌群多样性的初步研究

刘怡然1,王伟健2,沈家平1,沈红1,周红艳3,4,陈霄迟2   

  1. 1. 南京医科大学附属口腔医院
    2. 北京大学口腔医学院
    3. 江苏省儿童预防牙病科
    4.
  • 收稿日期:2012-09-27 修回日期:2012-11-29 出版日期:2012-12-25 发布日期:2013-01-10
  • 通讯作者: 刘怡然 E-mail:riely007@126.com

Preliminary study on oral microbiota associated with early childhood caries by PCR-DGGE method

  • Received:2012-09-27 Revised:2012-11-29 Online:2012-12-25 Published:2013-01-10
  • Contact: Yi-Ran LIU E-mail:riely007@126.com

摘要: 目的 应用PCR-DGGE技术检测早期儿童龋治疗前后唾液中微生物多样性的变化。 方法 选取北京大学燕东幼儿园22名3-5岁儿童进行口腔检查,在龋齿治疗前和治疗后2周分别取样,采用PCR-DGGE技术检测受试儿童唾液样本的微生物多样性,分别分析唾液样本在治疗前后微生物多样性的变化。 结果 治疗前唾液样本DGGE条带数为23±2.9,治疗后唾液样本DGGE条带数为28±4.1,治疗后条带数多于治疗前,差异有显著性(P<0.01);在同一时期内各唾液样本DGGE图谱的相似性高于不同时期样本之间。 结论 PCR-DGGE技术可用于与龋病相关细菌的生物多样性的研究以及监测微生物群落组成的动态变化。

Abstract: Objective To evaluate the difference in microbial diversity between ECC children before treatment and after treatment by means of a cultivation-independent approach called denaturing gradient gel electrophoresis (DGGE). Methods 22 children aged 3-5 years old from Peking University Yandong Kindergarten were selected for this study. Saliva samples were collected before treatment and 2 weeks after treatment. Total microbial genomic DNA was isolated from those subjects, and a portion of the 16S rRNA gene locus was PCR amplified by using universal primers. Then the PCR products were isolated using DGGE method. Results The mean species richness of the bacterial population was greater in the samples collected after treatment (28±4.1) than in those before treatment (23±2.9). The difference was statistically significant (P<0.01). Phylogenetic analysis show similarity within the groups while difference between groups. Conclusions PCR-DGGE method can visualize the diversity and complexity of the microbial biota associated with caries and monitor the dynamic changes of the bacterial compositions.

中图分类号: