4.4 Article

Methodologies for Studying B-subtilis Biofilms as a Model for Characterizing Small Molecule Biofilm Inhibitors

Journal

JOVE-JOURNAL OF VISUALIZED EXPERIMENTS
Volume -, Issue 116, Pages -

Publisher

JOURNAL OF VISUALIZED EXPERIMENTS
DOI: 10.3791/54612

Keywords

Infection; Issue 116; Bacillus subtilis; Biofilms; D-amino acids; Antibacterial agents; Stress resistance; Scanning Electron Microscopy

Funding

  1. Irving and Cherna Moskowitz Center
  2. ISF I-CORE [152/1]
  3. Yeda-Sela
  4. Larson Charitable Foundation
  5. Ilse Katz Institute for Materials Sciences and Magnetic Resonance Research
  6. Ministry of Health
  7. France-Israel Cooperation

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This work assesses different methodologies to study the impact of small molecule biofilm inhibitors, such as D-amino acids, on the development and resilience of Bacillus subtilis biofilms. First, methods are presented that select for small molecule inhibitors with biofilm-specific targets in order to separate the effect of the small molecule inhibitors on planktonic growth from their effect on biofilm formation. Next, we focus on how inoculation conditions affect the sensitivity of multicellular, floating B. subtilis cultures to small molecule inhibitors. The results suggest that discrepancies in the reported effects of such inhibitors such as D-amino acids are due to inconsistent pre-culture conditions. Furthermore, a recently developed protocol is described for evaluating the contribution of small molecule treatments towards biofilm resistance to antibacterial substances. Lastly, scanning electron microscopy (SEM) techniques are presented to analyze the three-dimensional spatial arrangement of cells and their surrounding extracellular matrix in a B. subtilis biofilm. SEM facilitates insight into the three-dimensional biofilm architecture and the matrix texture. A combination of the methods described here can greatly assist the study of biofilm development in the presence and absence of biofilm inhibitors, and shed light on the mechanism of action of these inhibitors.

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