Abstract:We showed that
Vibrio parahaemolyticus
was able to naturally and reversibly switch between wrinkly and smooth phenotypes and disclosed the gene expression profiles related to wrinkly-smooth switching, showing that the significantly differentially expressed genes between the two colony morphology phenotypes were involved in various biological behaviors, including virulence factor production, biofilm formation, metabolism, adaptation, and colonization.
“…The data presented here showed that Mg 2+ not only affected the swimming and swarming motility but also the gene expression of both two flagellar systems. Flagellar gene expression in V. parahaemolyticus is strictly regulated by various factors, including regulators such as ToxR [ 54 ], LafK [ 55 ], H-NS [ 56 ] and CalR [ 57 ], chemicals such as chloramphenicol [ 44 ] and l -arabinose [ 44 ], and different biological behavior processes such as biofilm formation [ 36 ] and EPS phase variation [ 44 ]. The resented data further enriched the regulatory networks of flagellar genes in V. parahaemolyticus .…”
Section: Resultsmentioning
confidence: 99%
“…In this work, the data showed that all the cps genes ( cpsA-K ) and four scv genes were significantly downregulated by Mg 2+ ( Table 1 ). Although both the cps and scv gene loci are involved in the synthesis of EPS and biofilm formation, but only the cps gene cluster affects the switching between wrinkled and smooth colony phenotype of V. parahaemolyticus [ 16 , 36 ], indicating that the cps gene cluster may contribute more to EPS synthesis.…”
Section: Resultsmentioning
confidence: 99%
“…7 ), suggesting that Mg 2+ had no regulatory effect on the production of CPS. V. parahaemolyticus undergoes phase variation between wrinkled and smooth colony phenotypes, and the wrinkled strain has stronger biofilm capacity than the smooth strain [ 36 ]. Chloramphenicol also has a negative effect on biofilm formation by V. parahaemolyticus [ 44 ].…”
Section: Resultsmentioning
confidence: 99%
“…cDNA sequencing was performed on an Illumina Hiseq platform [ 36 ]. Raw reads filtration and clean reads alignment were performed as previously described [ 37 ].…”
“…The data presented here showed that Mg 2+ not only affected the swimming and swarming motility but also the gene expression of both two flagellar systems. Flagellar gene expression in V. parahaemolyticus is strictly regulated by various factors, including regulators such as ToxR [ 54 ], LafK [ 55 ], H-NS [ 56 ] and CalR [ 57 ], chemicals such as chloramphenicol [ 44 ] and l -arabinose [ 44 ], and different biological behavior processes such as biofilm formation [ 36 ] and EPS phase variation [ 44 ]. The resented data further enriched the regulatory networks of flagellar genes in V. parahaemolyticus .…”
Section: Resultsmentioning
confidence: 99%
“…In this work, the data showed that all the cps genes ( cpsA-K ) and four scv genes were significantly downregulated by Mg 2+ ( Table 1 ). Although both the cps and scv gene loci are involved in the synthesis of EPS and biofilm formation, but only the cps gene cluster affects the switching between wrinkled and smooth colony phenotype of V. parahaemolyticus [ 16 , 36 ], indicating that the cps gene cluster may contribute more to EPS synthesis.…”
Section: Resultsmentioning
confidence: 99%
“…7 ), suggesting that Mg 2+ had no regulatory effect on the production of CPS. V. parahaemolyticus undergoes phase variation between wrinkled and smooth colony phenotypes, and the wrinkled strain has stronger biofilm capacity than the smooth strain [ 36 ]. Chloramphenicol also has a negative effect on biofilm formation by V. parahaemolyticus [ 44 ].…”
Section: Resultsmentioning
confidence: 99%
“…cDNA sequencing was performed on an Illumina Hiseq platform [ 36 ]. Raw reads filtration and clean reads alignment were performed as previously described [ 37 ].…”
“…The intracellular c‐di‐GMP concentration was measured as reported previously (Liu et al, 2022; Wu, Li, et al, 2022), with some modifications. Briefly, the overnight V. parahaemolyticus cultures were subcultured into a fresh MLB medium or on a swarming plate at 37°C for 8 h. When required, the strains in the MLB medium were incubated for 3 (low cell density, OD 600 ≈ 0.1) or 9 h (high cell density, OD 600 ≈ 1.0).…”
Vibrio parahaemolyticus is a significant food‐borne pathogen that is found in diverse aquatic habitats. Quorum sensing (QS), a signaling system for cell–cell communication, plays an important role in V. parahaemolyticus persistence. We characterized the function of three V. parahaemolyticus QS signal synthases, CqsAvp, LuxMvp, and LuxSvp, and show that they are essential to activate QS and regulate swarming. We found that CqsAvp, LuxMvp, and LuxSvp activate a QS bioluminescence reporter through OpaR. However, V. parahaemolyticus exhibits swarming defects in the absence of CqsAvp, LuxMvp, and LuxSvp, but not OpaR. The swarming defect of this synthase mutant (termed Δ3AI) was recovered by overexpressing either LuxOvpD47A, a mimic of dephosphorylated LuxOvp mutant, or the scrABC operon. CqsAvp, LuxMvp, and LuxSvp inhibit lateral flagellar (laf) gene expression by inhibiting the phosphorylation of LuxOvp and the expression of scrABC. Phosphorylated LuxOvp enhances laf gene expression in a mechanism that involves modulating c‐di‐GMP levels. However, enhancing swarming requires phosphorylated and dephosphorylated LuxOvp which is regulated by the QS signals that are synthesized by CqsAvp, LuxMvp, and LuxSvp. The data presented here suggest an important strategy of swarming regulation by the integration of QS and c‐di‐GMP signaling pathways in V. parahaemolyticus.
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