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Published on: June 30, 2016
Functional Characterization of Pseudomonas Contact Dependent Growth Inhibition (CDI) Systems
Chryslène Mercy1,2, Bérengère Ize1, Suzana P Salcedo2
1Laboratoire d'Ingénierie des Systèmes Macromoléculaires, CNRS UMR7255, Université Aix Marseille, Marseille, France.
Abstract:
Contact-dependent inhibition (CDI) toxins, delivered into the cytoplasm of target bacterial cells, confer to host strain a significant competitive advantage. Upon cell contact, the toxic C-terminal region of surface-exposed CdiA protein (CdiA-CT) inhibits the growth of CDI- bacteria. CDI+ cells express a specific immunity protein, CdiI, which protects from autoinhibition by blocking the activity of cognate CdiA-CT. CdiA-CT are separated from the rest of the protein by conserved peptide motifs falling into two distinct classes, the "E. coli"- and "Burkholderia-type". CDI systems have been described in numerous species except in Pseudomonadaceae. In this study, we identified functional toxin/immunity genes linked to CDI systems in the Pseudomonas genus, which extend beyond the conventional CDI classes by the variability of the peptide motif that delimits the polymorphic CdiA-CT domain. Using P. aeruginosa PAO1 as a model, we identified the translational repressor RsmA as a negative regulator of CDI systems. Our data further suggest that under conditions of expression, P. aeruginosa CDI systems are implicated in adhesion and biofilm formation and provide an advantage in competition assays. All together our data imply that CDI systems could play an important role in niche adaptation of Pseudomonadaceae.
Insights
Contact-dependent inhibition (CDI) systems in Pseudomonas offer competitive advantages. These bacterial toxin-delivery systems are implicated in adhesion, biofilm formation, and niche adaptation.
Area of Science:
- Microbiology
- Bacterial Genetics
- Molecular Biology
Background:
- Contact-dependent inhibition (CDI) is a bacterial mechanism for inter-bacterial competition.
- CDI systems involve toxins (CdiA-CT) and immunity proteins (CdiI).
- CDI systems are widespread but previously undescribed in Pseudomonadaceae.
Purpose of the Study:
- To identify and characterize functional CDI systems in the Pseudomonas genus.
- To investigate the regulation and ecological role of CDI systems in Pseudomonas aeruginosa.
Main Methods:
- Bioinformatic analysis to identify CDI toxin/immunity genes.
- Experimental validation in Pseudomonas aeruginosa PAO1.
- Identification of regulatory elements using genetic approaches.
Main Results:
- Functional CDI toxin/immunity genes were identified in Pseudomonas.
- Variability in peptide motifs delimiting CdiA-CT domains was observed.
- The translational repressor RsmA was identified as a negative regulator of CDI systems.
- CDI systems in P. aeruginosa are linked to adhesion, biofilm formation, and competitive fitness.
Conclusions:
- CDI systems are present and functional in Pseudomonas, exhibiting novel variations.
- RsmA plays a crucial role in regulating CDI system expression.
- CDI systems likely contribute to niche adaptation and ecological success in Pseudomonadaceae.
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