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Red fluorescent biofilm: the thick, the old, and the cariogenic

BACKGROUND: Some dental plaque fluoresces red. The factors involved in this fluorescence are yet unknown. OBJECTIVE: The aim of this study was to assess systematically the effect of age, thickness, and cariogenicity on the extent of red fluorescence produced by in vitro microcosm biofilms. DESIGN: T...

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Detalles Bibliográficos
Autores principales: Volgenant, Catherine M.C., Hoogenkamp, Michel A., Buijs, Mark J., Zaura, Egija, ten Cate, Jacob (Bob) M., van der Veen, Monique H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Co-Action Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4826460/
https://www.ncbi.nlm.nih.gov/pubmed/27060056
http://dx.doi.org/10.3402/jom.v8.30346
Descripción
Sumario:BACKGROUND: Some dental plaque fluoresces red. The factors involved in this fluorescence are yet unknown. OBJECTIVE: The aim of this study was to assess systematically the effect of age, thickness, and cariogenicity on the extent of red fluorescence produced by in vitro microcosm biofilms. DESIGN: The effects of biofilm age and thickness on red fluorescence were tested in a constant depth film fermentor (CDFF) by growing biofilms of variable thicknesses that received a constant supply of defined mucin medium (DMM) and eight pulses of sucrose/day. The influence of cariogenicity on red fluorescence was tested by growing biofilm on dentin disks receiving DMM, supplemented with three or eight pulses of sucrose/day. The biofilms were analyzed at different time points after inoculation, up to 24 days. Emission spectra were measured using a fluorescence spectrophotometer (λ(exc)405 nm) and the biofilms were photographed with a fluorescence camera. The composition of the biofilms was assessed using 454-pyrosequecing of the 16S rDNA gene. RESULTS: From day 7 onward, the biofilms emitted increasing intensities of red fluorescence as evidenced by the combined red fluorescence peaks. The red fluorescence intensity correlated with biofilm thickness but not in a linear way. Biofilm fluorescence also correlated with the imposed cariogenicity, evidenced by the induced dentin mineral loss. Increasing the biofilm age or increasing the sucrose pulsing frequency led to a shift in the microbial composition. These shifts in composition were accompanied by an increase in red fluorescence. CONCLUSIONS: The current study shows that a thicker, older, or more cariogenic biofilm results in a higher intensity of red fluorescence.