Periasamy Saravanan, Chalmers Natalia I, Du-Thumm Laurence, Kolenbrander Paul E
National Institute of Dental and Craniofacial Research, National Institutes of Health, Building 30, Room 310, Bethesda, MD 20892-4350, USA.
Appl Environ Microbiol. 2009 May;75(10):3250-7. doi: 10.1128/AEM.02901-08. Epub 2009 Mar 13.
Formation of dental plaque is a developmental process involving initial and late colonizing species that form polymicrobial communities. Fusobacteria are the most numerous gram-negative bacteria in dental plaque, but they become prevalent after the initial commensal colonizers, such as streptococci and actinomyces, have established communities. The unusual ability of these bacteria to coaggregate with commensals, as well as pathogenic late colonizers, has been proposed to facilitate colonization by the latter organisms. We investigated the integration of Fusobacterium nucleatum into multispecies communities by employing two in vitro models with saliva as the sole nutritional source. In flow cell biofilms, numbers of cells were quantified using fluorescently conjugated antibodies against each species, and static biofilms were analyzed by quantitative real-time PCR (q-PCR) using species-specific primers. Unable to grow as single-species biofilms, F. nucleatum grew in two-species biofilms with Actinomyces naeslundii but not with Streptococcus oralis. However, enhanced growth of fusobacteria was observed in three-species biofilms, indicating that there was multispecies cooperation. Importantly, these community dynamics yielded an 18-fold increase in the F. nucleatum biomass between 4 h and 18 h in the flow cell inoculated with three species. q-PCR analysis of static biofilms revealed that maximum growth of the three species occurred at 24 h to 36 h. Lower numbers of cells were observed at 48 h, suggesting that saliva could not support higher cell densities as the sole nutrient. Integration of F. nucleatum into multispecies commensal communities was evident from the interdigitation of fusobacteria in coaggregates with A. naeslundii and S. oralis and from the improved growth of fusobacteria, which was dependent on the presence of A. naeslundii.
牙菌斑的形成是一个发育过程,涉及形成多微生物群落的早期和晚期定植物种。梭杆菌是牙菌斑中数量最多的革兰氏阴性菌,但在诸如链球菌和放线菌等早期共生定植菌建立群落之后,它们才变得普遍。这些细菌与共生菌以及致病性晚期定植菌共聚集的特殊能力,被认为有助于后者的定植。我们通过使用两种以唾液作为唯一营养源的体外模型,研究了具核梭杆菌融入多物种群落的情况。在流动细胞生物膜中,使用针对每种物种的荧光共轭抗体对细胞数量进行定量,而静态生物膜则使用物种特异性引物通过定量实时PCR(q-PCR)进行分析。具核梭杆菌无法形成单物种生物膜,但能与内氏放线菌形成双物种生物膜生长,而与口腔链球菌则不能。然而,在三物种生物膜中观察到梭杆菌的生长增强,表明存在多物种间的协作。重要的是,在接种了三种物种的流动细胞中,这些群落动态使具核梭杆菌的生物量在4小时至18小时之间增加了18倍。对静态生物膜的q-PCR分析表明,这三种物种的最大生长发生在24小时至36小时。在48小时时观察到细胞数量减少,这表明唾液作为唯一营养源无法支持更高的细胞密度。具核梭杆菌融入多物种共生群落从具核梭杆菌与内氏放线菌和口腔链球菌在共聚集体中的相互交错以及具核梭杆菌生长的改善中明显可见,而具核梭杆菌的生长改善依赖于内氏放线菌的存在。