Abstract

Oral bacteria possess the ability to form biofilms on solid surfaces. After the penetration of oral bacteria into the pulp, the contact between biofilms and pulp tissue may result in pulpitis, pulp necrosis and/or periapical lesion. Depending on the environmental conditions and the availability of nutrients in the pulp chamber and root canals, mainly Gram-negative anaerobic microorganisms predominate and form the intracanal endodontic biofilm. The objective of the present study was to investigate the role of different substrates on biofilm formation as well as the separate and collective incorporation of six endodontic pathogens, namely Enterococcus faecalis, Staphylococcus aureus, Prevotella nigrescens, Selenomonas sputigena, Parvimonas micra and Treponema denticola into a nine-species “basic biofilm”. This biofilm was formed in vitro as a standard subgingival biofilm, comprising Actinomyces oris, Veillonella dispar, Fusobacterium nucleatum, Streptococcus anginosus, Streptococcus oralis, Prevotella intermedia, Campylobacter rectus, Porphyromonas gingivalis, and Tannerella forsythia. The resulting endodontic-like biofilms were grown 64 h under the same conditions on hydroxyapatite and dentin discs. After harvesting the endodontic-like biofilms, the bacterial growth was determined using quantitative real-time PCR, were labeled using fluorescence in situ hybridization (FISH) and analyzed by confocal laser scanning microscopy (CLSM). The addition of six endodontic pathogens to the “basic biofilm” induced a decrease in the cell number of the “basic” species. Interestingly, C. rectus counts increased in biofilms containing E. faecalis, S. aureus, P. nigrescens and S. sputigena, respectively, both on hydroxyapatite and on dentin discs, whereas P. intermedia counts increased only on dentin discs by addition of E. faecalis. The growth of E. faecalis on hydroxyapatite discs and of E. faecalis and S. aureus on dentin discs were significantly higher in the biofilm containing all species than in the “basic biofilm”. Contrarily, the counts of P. nigrescens, S. sputigena and P. micra on hydroxyapatite discs as well as counts of P. micra and T. denticola on dentin discs decreased in the all-species biofilm. Overall, all bacterial species associated with endodontic infections were successfully incorporated into the standard multispecies biofilm model both on hydroxyapatite and dentin discs. Thus, future investigations on endodontic infections can rely on this newly established endodontic-like multispecies biofilm model.

Highlights

  • Most oral bacteria are commensal [1], but depending on host immune response and dysbiotic microbial interactions rather than on specific pathogens [2], they contribute to oral diseases [3]

  • This “basic” subgingival biofilm consisted of Actinomyces oris, Veillonella dispar, Fusobacterium nucleatum, Streptococcus anginosus, Streptococcus oralis, Prevotella intermedia, Campylobacter rectus, Porphyromonas gingivalis, and Tannerella forsythia

  • To form endodontic-like multispecies biofilms, a total of six endodontic pathogens were separately added to a “basic” nine-species subgingival biofilm

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Summary

Introduction

Most oral bacteria are commensal [1], but depending on host immune response and dysbiotic microbial interactions rather than on specific pathogens [2], they contribute to oral diseases [3]. Like bacterial species in general, oral bacteria possess the ability to form biofilms on solid surfaces in the presence of nutrient-containing fluids [4]. Biofilms were described decades ago as communities of bacterial cells that are embedded in a polymeric matrix that contains polysaccharides, DNA, RNA, proteins, lipids and other components, adhering to various surfaces and showing different phenotypical and biochemical characteristics compared to their planktonic counterparts [5,6,7,8]. Biofilms protect bacterial cells from host defense mechanisms and antibiotics; likewise, they disseminate planktonic bacterial cells that can cause acute disease. Studies have shown that bacterial signal molecules and positioning mechanisms predetermine the position and spatial relationships of biofilms. The biofilm demonstrates a level of differentiation that requires a sophisticated network of cell–cell signals and a high degree of cellular specialization [9,10]

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