Molecular Microbiology · 2010 · 151 citations · 35 references
Life SciencesMicrobiologyMolecular BiologyGene ExpressionGene RegulationMicrobial PathogenesisBacterial BiofilmsBacterial Gene RegulationBacterial PathogenesisBacterial Secretion SystemsBiofilm Formation In InfectionMicrobial BiofilmsBiofilm PhysiologyBiofilm Regulatory NetworksProtein Phosphatase 2CProtein Phosphatases 2CSecretion System RegulationTwo-component Regulatory SystemsTwo-component Signal Transduction SystemsTwo-component Signaling Systems
Bacterial pathogenesis often depends on regulatory networks, two-component systems and small RNAs (sRNAs). In Pseudomonas aeruginosa, the RetS sensor pathway downregulates expression of two sRNAs, rsmY and rsmZ. Consequently, biofilm and the Type Six Secretion System (T6SS) are repressed, whereas the Type III Secretion System (T3SS) is activated. We show that the HptB signalling pathway controls biofilm and T3SS, and fine-tunes P. aeruginosa pathogenesis. We demonstrate that RetS and HptB intersect at the GacA response regulator, which directly controls sRNAs production. Importantly, RetS controls both sRNAs, whereas HptB exclusively regulates rsmY expression. We reveal that HptB signalling is a complex regulatory cascade. This cascade involves a response regulator, with an output domain belonging to the phosphatase 2C family, and likely an anti-anti-sigma factor. This reveals that the initial input in the Gac system comes from several signalling pathways, and the final output is adjusted by a differential control on rsmY and rsmZ. This is exemplified by the RetS-dependent but HptB-independent control on T6SS. We also demonstrate a redundant action of the two sRNAs on T3SS gene expression, while the impact on pel gene expression is additive. These features underpin a novel mechanism in the fine-tuned regulation of gene expression.
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