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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

This protocol describes a robust method for developing pellicle biofilm. The method is scalable to different culture volumes, allowing easy adoption for various experimental objectives. The method's design enables qualitative or quantitative assessment of the biofilm-forming potential of several mycobacterial species.

Abstract

Many bacteria thrive in intricate natural communities, exhibiting key attributes of multicellularity such as communication, cooperation, and competition. The most prevalent manifestation of bacterial multicellular behavior is the formation of biofilms, often linked to pathogenicity. Biofilms offer a haven against antimicrobial agents, fostering the emergence of antimicrobial resistance. The conventional practice of cultivating bacteria in shake flask liquid cultures fails to represent their proper physiological growth in nature, consequently limiting our comprehension of their intricate dynamics. Notably, the metabolic and transcriptional profiles of bacteria residing in biofilms closely resemble those of naturally growing cells. This parallelism underscores the significance of biofilms as an ideal model for foundational and translational research. This article focuses on utilizing Mycobacterium smegmatis as a model organism to illustrate a technique for cultivating pellicle biofilms. The approach is adaptable to various culture volumes, facilitating its implementation for diverse experimental objectives such as antimicrobial studies. Moreover, the method's design enables the qualitative or quantitative evaluation of the biofilm-forming capabilities of different mycobacterial species with minor adjustments.

Introduction

Bacteria are able to survive as single-celled entities; however, in most physiologically relevant conditions, they organize into community mimetics. Biofilm is a widely recognized community organization of bacteria formed by aggregated cells encased in a self-produced matrix1. Such assembly possesses signatures of early multicellularity and provides higher stress resilience to bacterial systems. Biofilms are often tolerant to antimicrobials and are estimated to be responsible for almost 80% of microbial infections2,3.

Shake flask and plate-based cultures have....

Protocol

The details of all the reagents and equipment used for the study are listed in the Table of Materials.

1. Sauton's media preparation

  1. Prepare 50 mL of 2.5% potassium dihydrogen phosphate solution by carefully weighing 1.25 g of potassium dihydrogen phosphate and dissolving it in 50 mL of deionized water.
  2. Prepare 50 mL of 2.5% magnesium sulfate solution by weighing 2.56 g of magnesium sulfate and dissolving it in 50 mL of deionized wate.......

Representative Results

Biofilm pellicles become visible to the naked eye from the third day onwards. Although biofilm grows on Sauton's media without 2% glucose, an improvement was observed in the reticulation when it was added. We obtained 10.48 mg ± 3.13 mg (n = 4) of biofilm dry weight from each well of a 24-well plate with 1.5 mL of Sauton's media (supplemented with 2% glucose) grown for four days. In Figure 2, biofilm development was visible from day 3 to day 6. It starts forming a film with slig.......

Discussion

The multicellular lifestyle of microbes was described almost a century ago; however, clinical studies remain sparse, mostly due to the lack of robust methods14. Methods described in works on biofilm biology are often difficult to adapt. Here, the detailed methodology, aided by demonstrations of critical steps, is expected to improve the reproducibility of the protocols.

The method of biofilm production described in this article is scalable, requiring a proportional incr.......

Acknowledgements

This work was supported by the DBT-Ramalingaswami Fellowship awarded to Amitesh Anand.

....

Materials

NameCompanyCatalog NumberComments
0.2 µM PVDF syringe filterAxivaSFNY04 R
1 mL tipsGenetixGXM-611000 C
10 µL tipsGenetixGXM-6110 C
200 µL tipsGenetixGXM-61200C
6-well polypropylene platesTarsons980010
Amber tubesTarsons546051
AutoclaveHospharma
Biosafety Cabinet A IIMSET
Blotting paperAny suitable vendor
CentrifugeEppendorf
Citric acidSigma251275
CuvettesBio-Rad2239955
Ferric ammonium citrateSigmaF5879
Gel documentation systemBio-Rad
Glass BeadsSigmaG8772
GlucoseSigma49139
GlycerolSigmaG5516
Inoculation loopsGenaxyHS81121C
L-AspargineSigmaA0884
LB-agarHimediaM1151
LB-mediaHimediaM575
M. smegmatis mc2155 cryo-stockATCC700084
Magnesium sulfateSigmaM2643
MicropipettesGilson
ParafilmTarsons
Petri DishTarsons460020
pH meterLabman Scientific Instruments
Plate ReaderTecan
Polypropylene test tubesGenaxyGEN-14100-PS
Potassium phosphate monobasicSigmaP5379
RifampicinMedchemExpressHY-B0272
Serological pipetteSPL Life Sciences95210
Shaker IncubatorEppendorf
Spatula
SpectrophotometerThermo Scientific
Static IncubatorCARON
Sterile 10 mL syringeBecton Dickinson309642
Sterile 50 mL syringeBecton Dickinson309653
Tween-80SigmaP1754
Weighing balanceSartorius
Zinc sulfateSigmaZ0251

References

  1. Davey, M. E., O'toole, G. A. Microbial biofilms: From ecology to molecular genetics. Microbiol Mol Biol Rev. 64 (4), 847-867 (2000).
  2. Rumbaugh, K. P., Sauer, K. Biofilm dispersion. Nat Rev Microbiol. 18 (10), 571-586 (2020).
  3. ....

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Mycobacterial BiofilmAntimicrobial ResistanceBacterial MetabolismEnergy MetabolismBiofilm FormationPlanktonic MethodsModel OrganismMycobacterium SmegmatisPhysiological RelevanceMulticellularityCommunicationCooperationCompetitionScreening SystemCultivation TechniqueExperimental Objectives

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