Pseudomonas aeruginosa is a versatile Gram-negative pathogen that causes various infections in humans. The bacterium possesses a type III secretion system (T3SS) to deliver cytotoxic effector proteins into host cells, which plays an important role in bacterial pathogenesis. The T3SS is regulated by the master regulator ExsA, whose expression is controlled by multiple pathways. Here, we demonstrate that the catabolite repression control protein Crc controls T3SS activity by modulating exsA expression. We find that mutation of crc reduces the intracellular cAMP level by 1.76-fold under T3SS-inducing conditions, leading to approximately 2-fold reduction of the exsA expression. Further investigation reveals that Crc affects the mRNA stability of cyaB, which encodes an adenylate cyclase involved in cAMP synthesis. The cyaB 5'-UTR is identified as a key region through which Crc affects its mRNA stability. Our study elucidates a novel regulatory mechanism by which Crc controls the T3SS through modulating cyaB mRNA stability and subsequent cAMP synthesis under T3SS-inducing conditions.
Keywords: Crc; CyaB; P. aeruginosa; type III secretion system.