Application of stereological principles for quantification of bacteria in intact dental biofilms.

I. Dige, J. Nyengaard, M. Kilian, B. Nyvad
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引用次数: 44

Abstract

INTRODUCTION Quantative confocal laser scanning microscopy (CLSM) in combination with fluorescent in situ hybridization (FISH) may help to increase our knowledge about biofilm formation. The purpose of this study was to develop and evaluate a stereological method for quantification of bacteria in intact biofilm. The method was applied in a quantitative study of the proportion of streptococci relative to other bacteria in initial in-situ-grown dental biofilms as a function of time. METHODS Biofilms were collected on standardized glass slabs mounted in intra-oral appliances and worn by 10 individuals for 6, 12, 24, and 48 h. Biofilms were analysed using CLSM. Quantification of bacteria labelled with 16S ribosomal RNA oligonucleotide probes was performed with stereological tools: the unbiased counting frame and the two-dimensional fractionator. RESULTS Results showed a notable increase in the total number of bacteria and streptococci over time, with a considerable inter-individual variation at each time-point. After 48 h there was a 12.5-fold difference between individuals in the total number of bacteria and a 12.6-fold difference in the number of streptococci. The number of streptococci exceeded that of other bacteria and over the examination period there was a relatively constant relationship between the number of streptococci and other bacteria (streptococci vs. non-streptococci: median 15.2; minimum 1.0; maximum 89.3). CONCLUSION The study demonstrates that the combined use of FISH and stereology is a relevant and reliable tool for obtaining unbiased information about the numerical contributions of specific bacterial populations during early biofilm formation.
体视学原理在完整牙生物膜细菌定量中的应用。
定量共聚焦激光扫描显微镜(CLSM)结合荧光原位杂交(FISH)可能有助于增加我们对生物膜形成的了解。本研究的目的是建立和评估一种体视学方法来定量细菌在完整的生物膜。该方法用于定量研究链球菌相对于其他细菌在初始原位生长的牙生物膜中的比例作为时间的函数。方法10例患者分别于口腔内矫治器固定的标准化玻璃板上采集生物膜,佩戴时间分别为6、12、24和48 h。采用CLSM分析生物膜。用16S核糖体RNA寡核苷酸探针标记的细菌定量用立体学工具进行:无偏计数架和二维分馏仪。结果结果显示,细菌和链球菌的总数随着时间的推移而显著增加,每个时间点的个体间差异很大。48小时后,个体之间的细菌总数差异为12.5倍,链球菌数量差异为12.6倍。链球菌的数量超过其他细菌的数量,并且在检查期间,链球菌与其他细菌的数量之间存在相对恒定的关系(链球菌与非链球菌:中位数为15.2;最低1.0;最大89.3)。结论该研究表明,FISH和立体学的结合使用是获得早期生物膜形成过程中特定细菌群体的数值贡献的公正信息的相关和可靠的工具。
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