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一种在体内绘制牙菌斑中致龋性链球菌分布模式的方法。

A method for mapping the distribution pattern of cariogenic streptococci within dental plaque in vivo.

作者信息

Kato K, Sato T, Takahashi N, Fukui K, Yamamoto K, Nakagaki H

机构信息

Department of Preventive Dentistry and Dental Public Health, School of Dentistry, Aichi-Gakuin University, Chikusa-ku, Nagoya 464-8650, Japan.

出版信息

Caries Res. 2004 Sep-Oct;38(5):448-53. doi: 10.1159/000079626.

Abstract

This study was carried out to develop a method for mapping the distribution of cariogenic oral streptococci, Streptococcus mutans and Streptococcus sobrinus, from the outermost to the innermost plaque. Ten consenting subjects were asked to form plaque by abstaining from tooth brushing over 3 days within in situ plaque-generating devices, which were placed on the upper molars. The plaque formed in the devices was separated into 8-10 layered fractions (100 microm thick). Genomic DNA was extracted from each plaque fraction by a commercial DNA purification kit and used for the amplification of the 16S ribosomal RNA gene sequences by polymerase chain reaction (PCR) with universal primers. The products were then amplified by PCR with S. mutans- or S. sobrinus-specific nested primers. The final products were separated on agarose gels, stained and photographed to confirm the existence of S. mutans and S. sobrinus. The results showed that S. mutans was detected in the plaque obtained from all of the 10 subjects and S. sobrinus in the plaque of 7 subjects. However, the distribution patterns of fractions positive for S. mutans and S. sobrinus varied among the subjects, with a tendency for frequent detection of both species in the outer to middle layers of dental plaque. There were no plaque fractions in which only S. sobrinus was found. This method could be useful to map the distribution of cariogenic microorganisms and to estimate the bacterial ecology for oral biofilm.

摘要

本研究旨在开发一种方法,用于绘制致龋口腔链球菌——变形链球菌和远缘链球菌从菌斑最外层到最内层的分布情况。10名受试者同意在置于上颌磨牙的原位菌斑生成装置内3天不刷牙以形成菌斑。将装置中形成的菌斑分离成8 - 10个分层部分(100微米厚)。使用商业DNA纯化试剂盒从每个菌斑部分提取基因组DNA,并用于通过聚合酶链反应(PCR)用通用引物扩增16S核糖体RNA基因序列。然后用变形链球菌或远缘链球菌特异性巢式引物通过PCR扩增产物。将最终产物在琼脂糖凝胶上分离、染色并拍照以确认变形链球菌和远缘链球菌的存在。结果显示,在10名受试者获取的菌斑中均检测到变形链球菌,7名受试者的菌斑中检测到远缘链球菌。然而,变形链球菌和远缘链球菌阳性部分的分布模式在受试者之间有所不同,在牙菌斑的外层到中层有同时频繁检测到这两种菌的趋势。未发现仅含有远缘链球菌的菌斑部分。该方法可能有助于绘制致龋微生物的分布图谱并评估口腔生物膜中的细菌生态学。

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