Pseudomonas aeruginosa Uses c-di-GMP Phosphodiesterases RmcA and MorA To Regulate Biofilm Maintenance

S Katharios-Lanwermeyer1, G B Whitfield2,3,4, P L Howell2,3

  • 1Department of Microbiology and Immunology, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire, USA.

Mbio
|February 3, 2021
PubMed

Insights

Pseudomonas aeruginosa requires two phosphodiesterases, RmcA and MorA, to maintain mature biofilms. Without these enzymes, biofilms fail under nutrient limitation, highlighting the importance of cyclic-di-GMP signaling for biofilm persistence.

Area of Science:

  • Microbiology
  • Molecular Biology
  • Biochemistry

Background:

  • Biofilm formation is crucial for bacterial survival, but mechanisms for maintaining mature biofilms are less understood.
  • Pseudomonas aeruginosa biofilms are significant in clinical and environmental settings.
  • Cyclic-di-GMP (c-di-GMP) signaling regulates various bacterial processes, including biofilm development.

Purpose of the Study:

  • To identify genes essential for maintaining mature Pseudomonas aeruginosa biofilms.
  • To investigate the role of cyclic-di-GMP (c-di-GMP) degrading phosphodiesterases (PDEs) in biofilm maintenance.
  • To elucidate the regulatory mechanisms underlying biofilm persistence under nutrient limitation.

Main Methods:

  • Utilized a P. aeruginosa-phage interaction screen to identify relevant genes.
  • Generated deletion mutants for rmcA and morA genes.
  • Assessed biofilm phenotypes under varying nutrient conditions (carbon limitation).
  • Analyzed c-di-GMP levels, Pel polysaccharide production, and biofilm biomass.
  • Investigated interactions between PDEs and Pel biosynthesis machinery.
  • Compared mutant phenotypes with stringent response mutants (ΔrelA ΔspoT).

Main Results:

  • Deletion of rmcA and morA initially led to increased biofilm formation, c-di-GMP, Pel polysaccharide, and biomass.
  • These mutants failed to maintain biofilms under carbon-limited conditions, exhibiting reduced viability.
  • The biofilm maintenance defect phenocopied stringent response mutants (ΔrelA ΔspoT), suggesting impaired nutrient limitation response.
  • RmcA and MorA were found to interact with the Pel biosynthesis machinery.
  • Unregulated Pel biosynthesis likely contributes to mutant cell death under nutrient stress.

Conclusions:

  • RmcA and MorA, c-di-GMP degrading phosphodiesterases, are critical for maintaining mature P. aeruginosa biofilms.
  • Effective response to nutrient limitation is essential for biofilm persistence and requires functional c-di-GMP regulation.
  • Distinct PDEs regulate biofilm formation versus maintenance, allowing for complex control over biofilm lifecycle.
  • This study reveals key regulatory components enabling P. aeruginosa biofilms to survive nutrient-poor environments.

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