Section of Oral Microbiology and Immunology, Institute of Oral Biology, Center of Dental Medicine, Plattenstrasse 11, 8032, Zürich, Switzerland.
BMC Microbiol. 2012 Oct 5;12:227. doi: 10.1186/1471-2180-12-227.
Periodontitis is caused by a highly complex consortium of bacteria that establishes as biofilms in subgingival pockets. It is a disease that occurs worldwide and its consequences are a major health concern. Investigations in situ are not possible and the bacterial community varies greatly between patients and even within different loci. Due to the high complexity of the consortium and the availability of samples, a clear definition of the pathogenic bacteria and their mechanisms of pathogenicity are still not available. In the current study we addressed the need of a defined model system by advancing our previously described subgingival biofilm model towards a bacterial composition that reflects the one observed in diseased sites of patients and analysed the structure of these biofilms.
We further developed the growth media by systematic variation of key components resulting in improved stability and the firm establishment of spirochetes in the 10-species subgingival Zurich biofilm model. A high concentration of heat-inactivated human serum allowed the best proliferation of the used species. Therefore we further investigated these biofilms by analysing their structure by confocal laser scanning microscopy following fluorescence in situ hybridisation. The species showed mutual interactions as expected from other studies. The abundances of all organisms present in this model were determined by microscopic counting following species-specific identification by both fluorescence in situ hybridisation and immunofluorescence. The newly integrated treponemes were the most abundant organisms.
The use of 50% of heat-inactivated human serum used in the improved growth medium resulted in significantly thicker and more stable biofilms, and the quantitative representation of the used species represents the in vivo community of periodontitis patients much closer than in biofilms grown in the two media with less or no human serum. The appearance of T. denticola, P. gingivalis, and T. forsythia in the top layer of the biofilms, and the high abundance of T. denticola, reflects well the microbial situation observed at diseased sites. The improved model biofilms will allow further investigations of interactions between individual species and of the effects of atmospheric or nutritional changes, as well as interactions with tissue cells.
牙周炎是由高度复杂的细菌联合体引起的,这些细菌在龈下袋中形成生物膜。它是一种全球性疾病,其后果是一个主要的健康问题。原位研究是不可能的,而且细菌群落在患者之间甚至在不同的部位之间差异很大。由于联合体的高度复杂性和样本的可用性,仍然无法明确界定致病菌及其发病机制。在目前的研究中,我们通过进一步发展我们之前描述的龈下生物膜模型,使其细菌组成反映患者患病部位的观察结果,并分析这些生物膜的结构,从而满足了对明确定义模型系统的需求。
我们通过系统地改变关键成分来进一步改进生长培养基,从而提高了稳定性,并在 10 种龈下苏黎世生物膜模型中牢固地建立了螺旋体。高浓度的热灭活人血清允许所用物种的最佳增殖。因此,我们通过分析经荧光原位杂交后的共焦激光扫描显微镜下这些生物膜的结构,进一步研究了这些生物膜。根据其他研究的预期,这些物种表现出相互作用。通过荧光原位杂交和免疫荧光两种方法对每种物种进行特异性鉴定后,通过显微镜计数确定了该模型中所有存在的生物的丰度。新整合的密螺旋体是最丰富的生物体。
在改良生长培养基中使用 50%的热灭活人血清导致生物膜明显变厚且更稳定,并且所用物种的定量表示比在含有较少或不含人血清的两种培养基中生长的生物膜更接近体内牙周炎患者的群落。在生物膜的顶层出现 T. denticola、P. gingivalis 和 T. forsythia,以及 T. denticola 的高丰度,很好地反映了在患病部位观察到的微生物情况。改良后的模型生物膜将允许进一步研究各个物种之间的相互作用以及大气或营养变化的影响,以及与组织细胞的相互作用。