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Time-lapse confocal microscopy to study in vitro Streptococcus mutans surface colonization

  • Jason T.F. Wing
  • , Michael A.L. Hayashi
  • , Aneesa F. Redissi
  • , M. Margaret Vickerman
  • , Livia M.A. Tenuta
  • , J. Christopher Fenno
  • , Alexander H. Rickard
  • University of Michigan, Ann Arbor

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

The cariogenicity of Streptococcus mutans relates to its ability to form biofilms on dental surfaces. The aim of this work was to develop a flowcell system compatible with time-lapse confocal microscopy to compare the adhesion and accumulation of S. mutans cells on surfaces in unsupplemented media against media containing sucrose or sucralose (a non-metabolized sweetener) over a short period of time. Fluorescent S. mutans 3209/pVMCherry was suspended in unsupplemented media or media supplemented with 1% sucrose or 1% sucralose and passed through a 3D-printed flowcell system. Flowcells were imaged over 60 minutes using a confocal microscope. Image analysis was performed, including a newly developed object-movement-based method to measure biomass adhesion. Streptococcus mutans 3209/pVMCherry grown in 1% sucrose-supplemented media formed small, dense, relatively immobile clumps in the flowcell system measured by biovolume, surface area, and median object centroid movement. Sucralose-supplemented and un-supplemented media yielded large, loose, mobile aggregates. Architectural metrics and per-object movement were significantly different (P < 0.05) when comparing sucrose-supplemented media to either unsupplemented or sucralose-supplemented media. These results demonstrate the utility of a flowcell system compatible with time-lapse confocal microscopy and image analysis when studying initial biofilm formation and adhesion under different nutritional conditions.

Original languageEnglish
Article numberovae012
JournalLetters in Applied Microbiology
Volume77
Issue number2
DOIs
StatePublished - Feb 2024

Keywords

  • biofilms
  • in vitro models
  • method development
  • microbial-cell interaction
  • streptococci

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