Background: Burkholderia cenocepacia belongs to a group of closely related organisms called the B. cepacia complex (Bcc) which are important opportunistic human pathogens. B. cenocepacia utilizes a mechanism of cell-cell communication called quorum sensing to control gene expression including genes involved in virulence. The B. cenocepacia quorum sensing network includes the CepIR and CciIR regulatory systems.

The ability of Pseudomonas aeruginosa to cause a broad range of infections in humans is due, at least in part, to its adaptability and its capacity to regulate the expression of key virulence genes in response to specific environmental conditions. Multiple two-component response regulators have been shown to facilitate rapid responses to these environmental conditions, including the coordinated expression of specific virulence determinants. RsmA is a posttranscriptional regulatory protein which controls the expression of a number of virulence-related genes with relevance for acute and chronic infections. Many membrane-bound sensors, including RetS, LadS, and GacS, are responsible for the reciprocal regulation of genes associated with acute infection and chronic persistence. In P. aeruginosa this is due to sensors influencing the expression of the regulatory RNA RsmZ, with subsequent effects on the level of free RsmA. While interactions between an rsmA mutant and human airway epithelial cells have been examined in vitro, the role of RsmA during infection in vivo has not been determined yet. Here the function of RsmA in both acute and chronic models of infection was examined. The results demonstrate that RsmA is involved in initial colonization and dissemination in a mouse model of acute pneumonia. Furthermore, while loss of RsmA results in reduced colonization during the initial stages of acute infection, the data show that mutation of rsmA ultimately favors chronic persistence and results in increased inflammation in the lungs of infected mice.Pseudomomas aeruginosa is a metabolically versatile gramnegative bacterium that is capable of causing opportunistic infections in plants, animals, and humans. In humans, P. aeruginosa infections occur in the gastrointestinal tract and respiratory system and in patients with ocular infections, burn wounds, and cystic fibrosis (CF). The characteristics of acute and chronic infections caused by P. aeruginosa are quite distinct and are associated with selected expression of a certain subset of virulence factors. The pathogenesis of acute infections, such as ventilator-associated pneumonia, is thought to require the expression of a functional type III secretion system (T3SS), along with other toxins and proteases (37). These infections typically result in systemic infections and ultimately mortality. On the other hand, individuals with CF are usually colonized with P. aeruginosa early in life (1), and while P. aeruginosa can reach densities of 10 9 CFU/ml of sputum (33), P. aeruginosa infections in the lungs of CF patients are minimally invasive and rarely progress to septicemia. Rather, it is the inflammation and deterioration of pulmonary function resulting from chronic P. aeruginosa infection that is the main cause of mortality in CF patients. Therefore, investigating the mechanism(s) by which P. aeruginosa colonizes and becomes firmly established is critical for understanding the nature of life-long infections in CF patients.The substantial proportion of the P. aeruginosa g...

Burkholderia cenocepacia utilizes quorum sensing to control gene expression, including the expression of genes involved in virulence. In addition to CepR and CciR, a third LuxR homolog, CepR2, was found to regulate gene expression and virulence factor production. All B. cenocepacia strains examined contained this orphan LuxR homolog, which was not associated with an adjacent N-acyl-homoserine lactone synthase gene. Expression of cepR2 was negatively autoregulated and was negatively regulated by CciR in strain K56-2. Microarray analysis and quantitative reverse transcription-PCR determined that CepR2 did not influence expression of cepIR or cciIR. However, in strain K56-2, CepR2 negatively regulated expression of several known quorum-sensing-controlled genes, including genes encoding zinc metalloproteases. CepR2 exerted positive and negative regulation on genes on three chromosomes, including strong negative regulation of a gene cluster located adjacent to cepR2. In strain H111, which lacks the CciIR quorum-sensing system, CepR2 positively regulated pyochelin production by controlling transcription of one of the operons required for the biosynthesis of the siderophore in an N-acyl-homoserine lactone-independent manner. CepR2 activation of a luxI promoter was demonstrated in a heterologous Escherichia coli host, providing further evidence that CepR2 can function in the absence of signaling molecules. This study demonstrates that the orphan LuxR homolog CepR2 contributes to the quorum-sensing regulatory network in two distinct strains of B. cenocepacia.

Posttranscriptional regulation of certain virulence-related genes inPseudomonas aeruginosa is an opportunistic gram-negative bacillus that causes a variety of serious infections in immunocompromised patients and cystic fibrosis sufferers. Colonization is brought about by the production of virulence factors, including structural and extracellular proteins, secondary metabolites, and the type III secretion system (TTSS). P. aeruginosa tightly regulates the production of virulence determinants through numerous interlinked systems, including quorum sensing, alternative sigma factors, the GacS/GacA/RsmZ regulatory network and the posttranscriptional regulator RsmA. RsmA is a small RNA-binding protein that plays an important role in the posttranscriptional regulation of a number of virulence-related genes in P. aeruginosa (4,17,27). Because of the impact that RsmA has on virulence factor production, we sought to investigate the consequences of RsmA mutation for the interaction between P. aeruginosa and human airway epithelial cells in a cell culture model.

Burkholderia cenocepacia is a significant opportunistic pathogen in individuals with cystic fibrosis. ShvR, a LysR-type transcriptional regulator, has previously been shown to influence colony morphology, biofilm formation, virulence in plant and animal infection models, and some quorum-sensing-dependent phenotypes. In the present study, it was shown that ShvR negatively regulates its own expression, as is typical for LysR-type regulators. The production of quorum-sensing signal molecules was detected earlier in growth in the shvR mutant than in the wild type, and ShvR repressed expression of the quorum-sensing regulatory genes cepIR and cciIR. Microarray analysis and transcriptional fusions revealed that ShvR regulated over 1,000 genes, including the zinc metalloproteases zmpA and zmpB. The shvR mutant displayed increased gene expression of the type II secretion system and significantly increased protease and lipase activities. Both ShvR and CepR influence expression of a 24-kb genomic region adjacent to shvR that includes the afcA and afcC operons, required for the production of an antifungal agent; however, the reduction in expression was substantially greater in the shvR mutant than in the cepR mutant. Only the shvR mutation resulted in reduced antifungal activity against Rhizoctonia solani. ShvR, but not CepR, was shown to directly regulate expression of the afcA and afcC promoters. In summary, ShvR was determined to have a significant influence on the expression of quorum-sensing, protease, lipase, type II secretion, and afc genes.