Moreover, the tight colocalization might indicate necessary symbiotic relationships that could help to explain the fastidiousness of Filifactor. Just like group I treponemes [31], F. alocis predominantly colonizes the apical
and middle third of the carriers and could only casually be detected in the cervical third. Most interestingly, the organism preferably settles on the side of the carrier facing the soft tissues and is thus in immediate contact to the host’s immune defence. All these observations point to a causal involvement of F. alocis in the formation and maintenance of the analysed biofilms. However, one might question whether these carrier-borne biofilms accurately model the unperturbed biofilms in periodontitis patients. Wecke et al. [31] compared the bacterial BAY 80-6946 purchase load after 3 and 6 days and showed that the biofilm mass covering the carriers increases with time. The presence of F. alocis on only one side of the membranes is further evidence that these samples are not simply fragments of biofilm torn out of the pocket during the removal of the Selleckchem Anlotinib carriers, but in fact newly grown biofilms that form while the carriers are in situ. Although FISH reveals structural elements specific to periodontal
biofilms, one cannot deny that the introduction of the carrier into the check details periodontal pocket creates an artificial environment. The barrier between root surface and pocket epithelium might hamper access of the immune system to the bacteria on the tooth side, while only the biofilm growing on the soft tissue side actually faces the host. Moreover, these biofilms do not form on natural substrate but instead on ePTFE membranes. However, it seems likely that the substrate is of minor importance to the biofilm development. Wecke et al. [31] did not observe differences between biofilms grown on different carrier materials, and it is likely that the
acquired pellicle, which covers both the root and the membrane, renders colonization conditions on a broad range of materials alike. This claim is supported by microscopic examination of the biopsy submitted to FISH. F. alocis could be visualized GNA12 in high numbers and detected in arrangements similar to those seen in carrier-borne biofilms. Thus, a contribution of Filifactor to the structural organisation of ‘naturally’ grown biofilms seems highly probable. The applied carrier system proves to be a valuable tool for the exploration of periodontal biofilms as it allows to investigate topographic relations within the pocket without invasive treatment. Subsequent FISH permits to analyse the distribution and colocalization of potential pathogens within the biofilm and can thus contribute to a better understanding of the complex host-microbe interactions that lead to periodontal destruction.