Corby P M, Lyons-Weiler J, Bretz W A, Hart T C, Aas J A, Boumenna T, Goss J, Corby A L, Junior H M, Weyant R J, Paster B J
University of Pittsburgh, School of Dental Medicine, Division of Pediatric and Developmental Dental Sciences, 3501 Terrace St., Room 386, Pittsburgh, PA 15261, USA.
J Clin Microbiol. 2005 Nov;43(11):5753-9. doi: 10.1128/JCM.43.11.5753-5759.2005.
The aim of this study was to use molecular identification methods, such as 16S RNA gene sequence and reverse-capture checkerboard hybridization, for identification of the bacteria associated with dental caries and with dental health in a subset of 204 twins aged 1.5 to 7 years old. A total of 448 plaque samples (118 collected from caries-free subjects and 330 from caries-active subjects) were used for analysis. We compared the bacteria found in biofilms of children exhibiting severe dental caries, with different degrees of lesion severity, with those found in biofilms of caries-free children. A panel of 82 bacterial species was selected, and a PCR-based reverse-capture checkerboard method was used for detection. A simple univariate test was used to determine the overabundance and underabundance of bacterial species in the diseased and in the healthy groups. Features identified with this univariate test were used to construct a probabilistic disease prediction model. Furthermore, a method for the analysis of global patterns of gene expression was performed to permit simultaneous analysis of the abundance of significant species by allowing cross-bacterial comparisons of abundance profiles between caries-active and caries-free subjects. Our results suggested that global patterns of microbial abundance in this population are very distinctive. The top bacterial species found to be overabundant in the caries-active group were Actinomyces sp. strain B19SC, Streptococcus mutans, and Lactobacillus spp., which exhibited an inverse relationship to beneficial bacterial species, such as Streptococcus parasanguinis, Abiotrophia defectiva, Streptococcus mitis, Streptococcus oralis, and Streptococcus sanguinis.
本研究的目的是使用分子鉴定方法,如16S RNA基因序列和反向捕获棋盘杂交技术,对204名年龄在1.5至7岁的双胞胎亚组中与龋齿和牙齿健康相关的细菌进行鉴定。总共448个菌斑样本(118个来自无龋受试者,330个来自患龋受试者)用于分析。我们将患有严重龋齿且病变严重程度不同的儿童生物膜中发现的细菌,与无龋儿童生物膜中发现的细菌进行了比较。选择了一组82种细菌,并使用基于PCR的反向捕获棋盘法进行检测。使用简单的单变量检验来确定患病组和健康组中细菌种类的丰度过高和过低情况。通过该单变量检验确定的特征用于构建概率性疾病预测模型。此外,还进行了一种基因表达全局模式分析方法,通过对患龋和无龋受试者之间的丰度谱进行跨细菌比较,从而能够同时分析重要细菌种类的丰度。我们的结果表明,该人群中微生物丰度的全局模式非常独特。在患龋组中发现丰度过高的主要细菌种类是放线菌属B19SC菌株、变形链球菌和乳酸杆菌属,它们与有益细菌种类,如副血链球菌、缺陷无枝菌属、缓症链球菌、口腔链球菌和血链球菌呈负相关关系。