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Updated: Nov 19, 2025

Establishment of a High-throughput Setup for Screening Small Molecules That Modulate c-di-GMP Signaling in Pseudomonas aeruginosa
Published on: June 30, 2016
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.
Abstract:
While the early stages of biofilm formation have been well characterized, less is known about the requirements for Pseudomonas aeruginosa to maintain a mature biofilm. We utilized a P. aeruginosa-phage interaction to identify rmcA and morA, two genes which encode bis-(3',5')-cyclic dimeric GMP (c-di-GMP)-degrading phosphodiesterases (PDEs) and are important for the regulation of biofilm maintenance. Deletion of these genes initially results in an elevated biofilm phenotype characterized by increased production of c-di-GMP, Pel polysaccharide, and/or biofilm biomass. In contrast to the wild-type strain, these mutants were unable to maintain the biofilm when exposed to carbon-limited conditions. The susceptibility to nutrient limitation, as well as subsequent loss of biofilm viability of these mutants, was phenotypically reproduced with a stringent response mutant (ΔrelA ΔspoT), indicating that the ΔrmcA and ΔmorA mutants may be unable to appropriately respond to nutrient limitation. Genetic and biochemical data indicate that RmcA and MorA physically interact with the Pel biosynthesis machinery, supporting a model whereby unregulated Pel biosynthesis contributes to the death of the ΔrmcA and ΔmorA mutant strains in an established biofilm under nutrient limitation. These findings provide evidence that c-di-GMP-mediated regulation is required for mature biofilms of P. aeruginosa to effectively respond to changing availability of nutrients. Furthermore, the PDEs involved in biofilm maintenance are distinct from those required for establishing a biofilm, suggesting that a wide variety of c-di-GMP metabolizing enzymes in organisms such as P. aeruginosa allows for discrete control over the formation, maintenance or dispersion of biofilms.IMPORTANCE Recent advances in our understanding of c-di-GMP signaling have provided key insights into the regulation of biofilms. Despite an improved understanding of how biofilms initially form, the processes that facilitate the long-term maintenance of these multicellular communities remain opaque. We found that P. aeruginosa requires two phosphodiesterases, RmcA and MorA, to maintain a mature biofilm and that biofilms lacking these PDEs succumb to nutrient limitation and die. The biofilm maintenance deficiency observed in ΔrmcA and ΔmorA mutants was also found in the stringent response-defective ΔrelA ΔspoT strain, suggesting that a regulatory intersection between c-di-GMP signaling, extracellular polysaccharide biosynthesis, and the nutrient limitation response is important for biofilm persistence. We uncover components of an important regulatory system needed for P. aeruginosa biofilms to persist in nutrient-poor conditions and provide some of the first evidence that maintaining a mature biofilm is an active process.
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.
Related Concept Videos
Gene Regulation in Microbial Communities: Quorum Sensing
Biofilms
Global Regulatory Systems
Stringent Response in E. coli

