Walker C, Sedlacek M J
Department of Oral Biology, University of Florida, Gainesville, FL 32610, USA.
Oral Microbiol Immunol. 2007 Jun;22(3):152-61. doi: 10.1111/j.1399-302X.2007.00336.x.
Numerous biofilm models have been described for the study of bacteria associated with the supragingival plaque. However, there are fewer models available for the study of subgingival plaque. The purpose of this study was to develop and validate a model that closely mimicked the composition of the subgingival flora.
The model was developed as follows: calcium hydroxyapatite disks were coated overnight with 10% sterile saliva, placed in flat-bottomed tissue culture plates containing trypticase-soy broth, directly inoculated with a small aliquot of dispersed subgingival plaque, incubated anaerobically, and transferred to fresh medium at 48-h intervals until climax (steady-state) biofilms were formed ( approximately 10 days).
The model, based on samples from eight periodontitis patients and eight healthy subjects, yielded a multi-species, heterogeneous biofilm, consisting of both gram-positive and gram-negative species, and comprising 15-20 cultivable species associated with the subgingival flora. The species present and their proportions were reflective of the initial cultivable subgingival flora. Comparisons of the initial plaque samples from healthy subjects and the mature biofilms showed 81% similarity in species and 70% similarity in the proportions present. Biofilms formed from samples obtained from periodontally diseased subjects were 69% similar in species and 57% similar in the proportions present.
The biofilm model described here closely reproduces the composition of the cultivable subgingival plaque both in the species present and in their relative proportions. Differences existed between biofilms grown from diseased and non-diseased sites with the former being characterized by the presence of periodontal pathogens at microbially significant levels.
已描述了多种用于研究与龈上菌斑相关细菌的生物膜模型。然而,用于研究龈下菌斑的模型较少。本研究的目的是开发并验证一种能紧密模拟龈下菌群组成的模型。
该模型的构建如下:将羟基磷灰石圆盘用10%无菌唾液包被过夜,置于含有胰蛋白酶大豆肉汤的平底组织培养板中,直接接种一小份分散的龈下菌斑,厌氧培养,并每隔48小时转移至新鲜培养基中,直至形成成熟(稳态)生物膜(约10天)。
基于来自8名牙周炎患者和8名健康受试者的样本构建的该模型,产生了一种多物种、异质性的生物膜,由革兰氏阳性菌和革兰氏阴性菌组成,包含15 - 20种与龈下菌群相关的可培养物种。所存在的物种及其比例反映了初始可培养的龈下菌群。健康受试者的初始菌斑样本与成熟生物膜的比较显示,物种相似度为81%,比例相似度为70%。由牙周病患者样本形成的生物膜在物种上相似度为69%,比例相似度为57%。
此处描述的生物膜模型在存在的物种及其相对比例方面都能紧密再现可培养龈下菌斑的组成。患病部位和未患病部位形成的生物膜之间存在差异,前者的特征是存在具有微生物学显著水平的牙周病原体。