College of Medical Laboratory, Dalian Medical University, Dalian, China.
Dr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, Pakistan.
Microb Pathog. 2018 Oct;123:473-477. doi: 10.1016/j.micpath.2018.08.011. Epub 2018 Aug 8.
Orthodontic treatments often include dental displacement using a fixed retainer such as braces, which may result in the accumulation of plaque that provides a suitable environment for microorganisms to cause oral infection. So, this study was designed to investigate the microbial diversity among orthodontic patients and healthy individuals.
Fifty individuals i.e. 30 orthodontic patients and 20 normal individuals were included in this study. Samples were collected during the midterm of orthodontic treatment (10-12 months). Saliva samples were collected and total DNA was isolated. Polymerase chain reaction denaturing gradient gel electrophoresis (PCR-DGGE) with universal primers targeting the V3 region of 16s rRNA was used to study the bacterial diversity among different orthodontic and control groups. After DGGE profile analysis, the predominant product bands from the gel were excised, cloned, and sequenced to confirm the taxonomic identity followed by its quantification by using real-time PCR with gene-specific primers.
Both orthodontic treatment and control groups formed two distinct clustering profiles, but the Shannon-Weaver index (H') indicated greater microbial diversity in the orthodontic group (P = 0.08). Sequence analysis and real-time PCR revealed a greater number of Pseudomonas spp. in the orthodontic group, while there was no significant difference in Streptococcal spp.
This study suggested alterations in the oral microbiota following orthodontic treatment would provide diagnostic tools to identify prevalent microbes associated with oral infections that may prove useful for developing future therapies.
正畸治疗通常包括使用固定保持器(如牙套)来移动牙齿,这可能导致菌斑的积累,为微生物提供适宜的环境,从而引起口腔感染。因此,本研究旨在调查正畸患者和健康个体之间的微生物多样性。
本研究纳入了 50 名个体,即 30 名正畸患者和 20 名正常个体。在正畸治疗中期(10-12 个月)收集样本。收集唾液样本并提取总 DNA。使用针对 16s rRNA V3 区的通用引物进行聚合酶链反应变性梯度凝胶电泳(PCR-DGGE),以研究不同正畸组和对照组之间的细菌多样性。在 DGGE 图谱分析后,从凝胶中切下优势产物条带,进行克隆和测序以确认分类学身份,然后使用针对基因的实时 PCR 定量。
正畸治疗组和对照组均形成了两个不同的聚类图谱,但正畸组的 Shannon-Weaver 指数(H')表明微生物多样性更大(P=0.08)。序列分析和实时 PCR 显示正畸组中假单胞菌属的数量较多,而链球菌属的数量则没有显著差异。
本研究表明正畸治疗后口腔微生物群的改变将为识别与口腔感染相关的常见微生物提供诊断工具,这可能有助于开发未来的治疗方法。