Inoculation density and nutrient level determine the formation of mushroom-shaped structures in Pseudomonas

Azadeh Ghanbari1, Jaber Dehghany1, Timo Schwebs2

  • 1Department of Systems Immunology and Braunschweig Integrated Centre of Systems Biology, Helmholtz Centre for Infection Research, Braunschweig, Germany.

Scientific Reports
|September 10, 2016
PubMed

Insights

Pseudomonas aeruginosa biofilms form mushroom shapes when non-motile cells create colonies. Motile cells then migrate to form these structures, offering early intervention possibilities.

Area of Science:

  • Microbiology
  • Computational Biology
  • Biophysics

Background:

  • Pseudomonas aeruginosa frequently colonizes immunocompromised and cystic fibrosis patients.
  • Antibiotic resistance in P. aeruginosa is often due to biofilm formation.
  • Biofilm architecture, including mushroom-shaped structures, influences treatment efficacy.

Purpose of the Study:

  • To develop an agent-based model simulating bacterial dynamics and interactions in P. aeruginosa biofilms.
  • To investigate the influence of cell motility and environmental factors on biofilm morphology.
  • To identify key parameters predicting the formation of mushroom-shaped structures.

Main Methods:

  • Utilized an agent-based modeling approach.
  • Incorporated experimental data on bacterial cell motility.
  • Simulated bacterial growth, motility, and nutrient chemotaxis within a spatial environment.

Main Results:

  • Immotile cells formed initial colonies.
  • Motile cells escaped single colonies via chemotaxis, preventing mushroom formation.
  • High densities of non-motile colonies facilitated motile cell aggregation and mushroom structure development.
  • Mushroom formation was dependent on nutrient levels and initial stalk density.

Conclusions:

  • Mushroom-shaped biofilm structures in P. aeruginosa are predictable based on initial inoculation parameters.
  • Environmental factors and initial cell density critically influence spatial pattern formation.
  • This model provides a framework for early manipulation of biofilm development.