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Published on: February 19, 2019
Two-Component Signaling Systems Regulate Diverse Virulence-Associated Traits in Pseudomonas aeruginosa
Benjamin X Wang1,2, Kyle C Cady1,3, Gerardo C Oyarce2
1Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
Abstract:
Pseudomonas aeruginosa is an opportunistic pathogen that can cause problematic infections at different sites throughout the human body. P. aeruginosa encodes a large suite of over 60 two-component signaling systems that enable cells to rapidly sense and respond to external signals. Previous work has shown that some of these sensory systems contribute to P. aeruginosa pathogenesis, but the virulence-associated processes and phenotypic traits that each of these systems controls are still largely unclear. To aid investigations of these sensory systems, we have generated deletion strains for each of 64 genes encoding histidine kinases and one histidine phosphotransferase in P. aeruginosa PA14. We carried out initial phenotypic characterizations of this collection by assaying these mutants for over a dozen virulence-associated traits, and we found that each of these phenotypes is regulated by multiple sensory systems. Our work highlights the usefulness of this collection for further studies of P. aeruginosa two-component signaling systems and provides insight into how these systems may contribute to P. aeruginosa infection.IMPORTANCEPseudomonas aeruginosa can grow and survive under a wide range of conditions, including as a human pathogen. As such, P. aeruginosa must be able to sense and respond to diverse signals and cues in its environment. This sensory capability is endowed in part by the hundreds of two-component signaling proteins encoded in the P. aeruginosa genome, but the precise roles of each remain poorly defined. To facilitate systematic study of the signaling repertoire of P. aeruginosa PA14, we generated a library of deletion strains, each lacking one of the 64 histidine kinases. By subjecting these strains to a battery of phenotypic assays, we confirmed the functions of many and unveiled roles for dozens of previously uncharacterized histidine kinases in controlling various traits, many of which are associated with P. aeruginosa virulence. Thus, this work provides new insight into the functions of two-component signaling proteins and provides a resource for future investigations.
Insights
Pseudomonas aeruginosa uses over 60 two-component systems to sense its environment. Researchers created deletion strains to study these systems, revealing new insights into Pseudomonas aeruginosa virulence.
Area of Science:
- Microbiology
- Bacterial Pathogenesis
- Molecular Biology
Background:
- Pseudomonas aeruginosa is an opportunistic pathogen causing diverse human infections.
- Two-component signaling systems (TCS) are crucial for P. aeruginosa to adapt to various environments.
- The specific roles of most P. aeruginosa TCS in virulence remain largely uncharacterized.
Purpose of the Study:
- To systematically investigate the roles of histidine kinases (HKs) in P. aeruginosa PA14.
- To generate a comprehensive library of P. aeruginosa deletion mutants for TCS research.
- To identify virulence-associated traits regulated by specific TCS.
Main Methods:
- Generated deletion strains for 64 histidine kinase genes and 1 histidine phosphotransferase gene in P. aeruginosa PA14.
- Performed phenotypic characterization of these mutants using over a dozen virulence-associated assays.
- Analyzed the regulation of virulence traits by multiple TCS.
Main Results:
- Confirmed known functions and identified novel roles for numerous histidine kinases.
- Demonstrated that multiple TCS regulate each tested virulence-associated phenotype.
- Unveiled previously uncharacterized roles for dozens of HKs in controlling P. aeruginosa traits.
Conclusions:
- The generated mutant library is a valuable resource for studying P. aeruginosa TCS.
- This work provides new insights into the complex regulatory network controlling P. aeruginosa virulence.
- Multiple TCS collectively contribute to P. aeruginosa pathogenesis and adaptation.
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