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Regmi, A.

Publications and source records attributed to Regmi, A..

2 recordsLinked to original sources

A class IV adenylate cyclase CyaB is required for capsule polysaccharide production and biofilm formation in Vibrio parahaemolyticus

CRP (cyclic AMP receptor protein), encoded by crp, is a global regulator that is activated by cAMP (cyclic AMP), a second messenger synthesized by a class I adenylate cyclase (AC-I) encoded by cyaA in Escherichia coli. cAMP-CRP is required for growth on non-preferred carbon sources and is a global regulator. We constructed in-frame non- polar deletions of the crp and cyaA homologs in Vibrio parahaemolyticus and found that the {Delta}crp mutant did not grow in minimal media supplemented with non-preferred carbon sources, but the {Delta}cyaA mutant grew similar to wild type. Bioinformatics analysis of the V. parahaemolyticus genome identified a 181 amino acid protein annotated as a class IV adenylate cyclase (AC-IV) named CyaB, a member of the CYTH protein superfamily. AC-IV phylogeny showed CyaB was present in Gamma- and Alpha- Proteobacteria as well as Planctomycete and Archaea. Only the bacterial CyaB proteins contained an N-terminal motif HFxxxExExK indicative of adenylyl cyclase activity. Both V. parahaemolyticus cyaA and cyaB genes functionally complemented an E. coli {Delta}cyaA mutant. The {Delta}crp and {Delta}cyaB/{Delta}cyaA mutants showed defects in growth on non- preferred carbon sources, and in swimming and swarming motility, indicating cAMP- CRP is an activator. The {Delta}cyaA and {Delta}cyaB single mutants had no defects in these phenotypes indicating AC-IV complements AC-I. Capsule polysaccharide and biofilm production assays showed significant defects in {Delta}crp, {Delta}cyaB/{Delta}cyaA, and the {Delta}cyaB mutant, whereas {Delta}cyaA behaved similar to wild type. This is consistent with a role of cAMP-CRP as an activator of these phenotypes and establishes a cellular role for AC-IV in capsule and biofilm formation, which to date has been unestablished. IMPORTANCEHere, we characterized the roles of CRP and CyaA in V. parahaemolyticus, showing cAMP-CRP was an activator of metabolism, motility, capsule and biofilm formation. These results are in contrast to cAMP-CRP in V. cholerae, which represses capsule and biofilm formation. Previously, only an AC-I CyaA had been identified in Vibrio species. Our data showed that an AC-IV CyaB homolog is present in V. parahaemolyticus and was required for optimal growth. The data demonstrated that CyaB was essential for capsule production and biofilm formation uncovering a physiological role of AC-IV in bacteria. The data showed that the cyaB gene was widespread among Vibrionaceae species and several other Gamma-Proteobacteria, but in general, its phylogenetic distribution was limited. Our phylogenetic analysis also demonstrated that in some species the cyaB gene was acquired by horizontal gene transfer.

microbiology↗

Fis connects two sensory pathways, quorum sensing and surface sensing, to control motility in Vibrio parahaemolyticus

Fis (Factor for Inversion Stimulation) is a global regulator that is highly expressed during exponential growth and undetectable in stationary growth. Quorum sensing (QS) is a global regulatory mechanism that controls gene expression in response to cell density and growth phase. In V. parahaemolyticus, a marine species and a significant human pathogen, the QS regulatory sRNAs, Qrr1 to Qrr5, negatively regulate the high cell density QS master regulator OpaR. OpaR is a positive regulator of capsule polysaccharide (CPS) formation required for biofilm formation and a repressor of swarming motility. In Vibrio parahaemolyticus, we showed, using genetics and DNA binding assays, that Fis bound directly to the regulatory regions of the qrr genes and was a positive regulator of these genes. In the {Delta}fis mutant, opaR expression was induced and a robust CPS and biofilm was produced, while swarming motility was abolished. Expression analysis and promoter binding assays showed that Fis was a direct activator of both the lateral flagellum laf operon and the surface sensing scrABC operon, both required for swarming motility. In in vitro growth competition assays, {Delta}fis was outcompeted by wild type in minimal media supplemented with intestinal mucus, and we showed that Fis directly modulated catabolism gene expression. In in vivo colonization competition assays, {Delta}fis was outcompeted by wild type, indicating Fis is required for fitness. Overall, these data demonstrate a direct role for Fis in QS, motility, and metabolism in V. parahaemolyticus. IMPORTANCEIn this study, we examined the role of Fis in modulating expression of the five-quorum sensing regulatory sRNAs, qrr1 to qrr5, and showed that Fis is a direct positive regulator of QS, which oppositely controls CPS and swarming motility in V. parahaemolyticus. The {Delta}fis deletion mutant was swarming defective due to a requirement for Fis in lateral flagella and surface sensing gene expression. Thus, Fis links QS and surface sensing to control swarming motility and, indirectly, CPS production. Fis was also required for cell metabolism, acting as a direct regulator of several carbon catabolism loci. Both in vitro and in vivo competition assays showed that the {Delta}fis mutant had a significant defect compared to wild type. Overall, our data demonstrates that Fis plays a critical role in V. parahaemolyticus physiology that was previously unexamined.

microbiology↗