Journal of Oral Microbiology (Apr 2016)

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

  • Catherine M.C. Volgenant,
  • Michel A. Hoogenkamp,
  • Mark J. Buijs,
  • Egija Zaura,
  • Jacob (Bob) M. ten Cate,
  • Monique H. van der Veen

DOI
https://doi.org/10.3402/jom.v8.30346
Journal volume & issue
Vol. 8, no. 0
pp. 1 – 9

Abstract

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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 (λexc405 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.

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