Vibrio parahaemolyticus RIMD 2210633


Alias: Vibrio parahaemolyticus str. RIMD 2210633

Top Publications

  1. Ono T, Park K, Ueta M, Iida T, Honda T. Identification of proteins secreted via Vibrio parahaemolyticus type III secretion system 1. Infect Immun. 2006;74:1032-42 pubmed
    ..Adenylate cyclase fusion protein studies proved that the newly identified secreted proteins were translocated into HeLa cells. Thus, these appear to be the TTSS effector proteins in V. parahaemolyticus. ..
  2. Lin Z, Kumagai K, Baba K, Mekalanos J, Nishibuchi M. Vibrio parahaemolyticus has a homolog of the Vibrio cholerae toxRS operon that mediates environmentally induced regulation of the thermostable direct hemolysin gene. J Bacteriol. 1993;175:3844-55 pubmed
    ..These results demonstrate that Vp-ToxR and Vc-ToxR share a strikingly similar function, i.e., direct stimulation at the transcriptional level of the gene encoding a major virulence determinant (enterotoxin) of a Vibrio species. ..
  3. McCarter L. OpaR, a homolog of Vibrio harveyi LuxR, controls opacity of Vibrio parahaemolyticus. J Bacteriol. 1998;180:3166-73 pubmed
    ..The underlying genetic basis for opaque-translucent variation may be the consequence of a genomic alteration detected in the opaR locus of opaque and translucent strains. ..
  4. Trosky J, Mukherjee S, Burdette D, Roberts M, McCarter L, Siegel R, et al. Inhibition of MAPK signaling pathways by VopA from Vibrio parahaemolyticus. J Biol Chem. 2004;279:51953-7 pubmed
  5. Casselli T, Lynch T, Southward C, Jones B, DeVinney R. Vibrio parahaemolyticus inhibition of Rho family GTPase activation requires a functional chromosome I type III secretion system. Infect Immun. 2008;76:2202-11 pubmed publisher
    ..The ability to inhibit Rho family GTPases independently of the CII-T3SS and the hemolytic toxins may provide insight into the mechanisms of virulence used by strains lacking these virulence factors. ..
  6. Funahashi T, Moriya K, Uemura S, Miyoshi S, Shinoda S, Narimatsu S, et al. Identification and characterization of pvuA, a gene encoding the ferric vibrioferrin receptor protein in Vibrio parahaemolyticus. J Bacteriol. 2002;184:936-46 pubmed
    ..A mutant with disruption in the upstream psuA gene also displayed a phenotype impaired in the utilization of ferric vibrioferrin. ..
  7. Funahashi T, Tanabe T, Aso H, Nakao H, Fujii Y, Okamoto K, et al. An iron-regulated gene required for utilization of aerobactin as an exogenous siderophore in Vibrio parahaemolyticus. Microbiology. 2003;149:1217-25 pubmed
    ..parahaemolyticus. However, additional genes required for ferric aerobactin transport across the inner membrane remain to be clarified. ..
  8. Lenz D, Mok K, Lilley B, Kulkarni R, Wingreen N, Bassler B. The small RNA chaperone Hfq and multiple small RNAs control quorum sensing in Vibrio harveyi and Vibrio cholerae. Cell. 2004;118:69-82 pubmed publisher
    ..We propose that Hfq, together with these sRNAs, creates an ultrasensitive regulatory switch that controls the critical transition into the high cell density, quorum-sensing mode...
  9. Miyamoto C, Meighen E. Involvement of LuxR, a quorum sensing regulator in Vibrio harveyi, in the promotion of metabolic genes: argA, purM, lysE and rluA. Biochim Biophys Acta. 2006;1759:296-307 pubmed publisher
    ..Based on analysis of luxR-dependent promoters, particularly that of argA, we describe a LuxR binding site, and implicate the coordination of LuxR with ArgR...

More Information

Publications132 found, 100 shown here

  1. Tanabe T, Funahashi T, Shiuchi K, Okajima N, Nakao H, Miyamoto K, et al. Characterization of Vibrio parahaemolyticus genes encoding the systems for utilization of enterobactin as a xenosiderophore. Microbiology. 2012;158:2039-49 pubmed publisher
  2. Calder T, Kinch L, Fernandez J, Salomon D, Grishin N, Orth K. Vibrio type III effector VPA1380 is related to the cysteine protease domain of large bacterial toxins. PLoS ONE. 2014;9:e104387 pubmed publisher
    ..Furthermore, VPA1380 was not toxic in IP6 deficient yeast cells. Therefore, our findings suggest that VPA1380 is a cysteine protease that requires IP6 as an activator. ..
  3. Maharaj R, Rumbak E, Jones W, Robb S, Robb F, Woods D. Nucleotide sequence of the Vibrio alginolyticus glnA region. Arch Microbiol. 1989;152:542-9 pubmed
    ..The ntrC gene was located 45 base pairs downstream from the ntrB gene. The V. alginolyticus ntrB and ntrC genes were able to complement ntrB, ntrC deletions in E. coli. ..
  4. Honda T, Abad Lapuebla M, Ni Y, Yamamoto K, Miwatani T. Characterization of a new thermostable direct haemolysin produced by a Kanagawa-phenomenon-negative clinical isolate of Vibrio parahaemolyticus. J Gen Microbiol. 1991;137:253-9 pubmed publisher
    ..We conclude that this clinical isolate produces a new type of Vp-TDH-related haemolysin, which may be involved in the pathogenesis of this organism...
  5. Baba K, Shirai H, Terai A, Kumagai K, Takeda Y, Nishibuchi M. Similarity of the tdh gene-bearing plasmids of Vibrio cholerae non-O1 and Vibrio parahaemolyticus. Microb Pathog. 1991;10:61-70 pubmed
    ..cholerae non-O1 and V. parahaemolyticus by a plasmid, directly or indirectly, and that the nucleotide sequences of the tdh gene-bearing plasmids have undergone minor base changes in the respective genetic backgrounds. ..
  6. Krumholz L, Esser U, Simoni R. Characterization of the H(+)-pumping F1F0 ATPase of Vibrio alginolyticus. J Bacteriol. 1990;172:6809-17 pubmed
    ..4-fold and reconstituted into proteoliposomes. This enzyme catalyzed the pumping of protons coupled to ATP hydrolysis as measured in fluorescence quenching experiments but would not pump Na+ ions under similar conditions. ..
  7. O Boyle N, Houeix B, Kilcoyne M, Joshi L, Boyd A. The MSHA pilus of Vibrio parahaemolyticus has lectin functionality and enables TTSS-mediated pathogenicity. Int J Med Microbiol. 2013;303:563-73 pubmed publisher
    ..We hypothesize that these glycans act as receptors for the MSHA pilus in the gastrointestinal tract, thereby facilitating efficient colonization of the intestinal epithelium by V. parahaemolyticus...
  8. Le T, Mawatari K, Maetani M, Yamamoto T, Hayashida S, Iba H, et al. VP2118 has major roles in Vibrio parahaemolyticus response to oxidative stress. Biochim Biophys Acta. 2012;1820:1686-92 pubmed publisher
    ..parahaemolyticus SOD and is vital for anti-oxidative stress responses. The V. parahaemolyticus FeSOD VP2118 may enhance ROS resistance and could promote its survival in the intestinal tract to facilitate host tissue infection...
  9. McCarter L. MotX, the channel component of the sodium-type flagellar motor. J Bacteriol. 1994;176:5988-98 pubmed
  10. Jaques S, Kim Y, McCarter L. Mutations conferring resistance to phenamil and amiloride, inhibitors of sodium-driven motility of Vibrio parahaemolyticus. Proc Natl Acad Sci U S A. 1999;96:5740-5 pubmed
    ..Thus, evidence supports the existence of more than one class of sodium-interaction site at which inhibitors can interfere with sodium-driven motility. ..
  11. Nishibuchi M, Kaper J. Duplication and variation of the thermostable direct haemolysin (tdh) gene in Vibrio parahaemolyticus. Mol Microbiol. 1990;4:87-99 pubmed
    ..It seems, therefore, that differences in the transcriptional control are primarily responsible for the differences seen in haemolytic phenotype...
  12. Izumoto Y, Mori T, Yamamoto K. Cloning and nucleotide sequence of the gene for NADH:FMN oxidoreductase from Vibrio harveyi. Biochim Biophys Acta. 1994;1185:243-6 pubmed
    ..The deduced amino acid sequence, 237 amino acids long, shows 48% identity with E. coli NAD(P)H:flavin oxidoreductase and 40% identity with Vibrio harveyi luxG gene product. ..
  13. Venkateswaran K, Dohmoto N, Harayama S. Cloning and nucleotide sequence of the gyrB gene of Vibrio parahaemolyticus and its application in detection of this pathogen in shrimp. Appl Environ Microbiol. 1998;64:681-7 pubmed
    ..parahaemolyticus in all of 27 shrimp samples artificially inoculated with this bacterium. We present here a rapid, reliable, and sensitive protocol for the detection of V. parahaemolyticus in shrimp...
  14. Su Z, Nakano M, Koga T, Lian X, Hamamoto A, Shimohata T, et al. Hfq regulates anti-oxidative ability in Vibrio parahaemolyticus. J Gen Appl Microbiol. 2010;56:181-6 pubmed
    ..Genetic experiments indicated that the gene expression of sod and kat was up-regulated in the mutant strain. These results indicate that Hfq down-regulates CAT and SOD activity, and Hfq is associated with the oxidative stress response. ..
  15. Iida T, Yamamoto K. Cloning and expression of two genes encoding highly homologous hemolysins from a Kanagawa phenomenon-positive Vibrio parahaemolyticus T4750 strain. Gene. 1990;93:9-15 pubmed
    ..These data suggest that tdhA is the structural gene for TDH found in the culture supernatant of V. parahaemolyticus T4750, and that there was only partial, if any, tdhS expression in the strain T4750 under the test conditions employed...
  16. Yamamoto S, Funahashi T, Ikai H, Shinoda S. Cloning and sequencing of the Vibrio parahaemolyticus fur gene. Microbiol Immunol. 1997;41:737-40 pubmed
    ..A sequence analysis showed that, at the amino acid level, the V. parahaemolyticus Fur protein is 81% identical with the Fur protein from E. coli and over 90% identical with those of the Vibrio species. ..
  17. Nakamura T, Komano Y, Itaya E, Tsukamoto K, Tsuchiya T, Unemoto T. Cloning and sequencing of an Na+/H+ antiporter gene from the marine bacterium Vibrio alginolyticus. Biochim Biophys Acta. 1994;1190:465-8 pubmed
    ..The hydropathy profile is characteristic of a membrane protein with 11 membrane spanning regions. The deduced amino acid sequence is 58% identical with E. coli NhaA. ..
  18. Asai Y, Kojima S, Kato H, Nishioka N, Kawagishi I, Homma M. Putative channel components for the fast-rotating sodium-driven flagellar motor of a marine bacterium. J Bacteriol. 1997;179:5104-10 pubmed
  19. Nakano H, Yoshida T, Uchiyama S, Kawachi M, Matsuo H, Kato T, et al. Structure and binding mode of a ribosome recycling factor (RRF) from mesophilic bacterium. J Biol Chem. 2003;278:3427-36 pubmed
    ..This is just the reverse of a model that is now widely accepted. However, the new model is in better agreement with published biological findings. ..
  20. Richards G, Hammer C, Garfield M, Parveen S. Characterization of a lysyl aminopeptidase activity associated with phosphoglucose isomerase of Vibrio vulnificus. Biochim Biophys Acta. 2004;1700:219-29 pubmed
    ..The finding of LysAP activity associated with heterodimeric PGI should foster a broad search for putative substrates in an effort to elucidate the role of PGI-LysAP in bacteria and its roles in the pathophysiology of diseases. ..
  21. Nakamura T, Enomoto H, Unemoto T. Cloning and sequencing of nhaB gene encoding an Na+/H+ antiporter from Vibrio alginolyticus. Biochim Biophys Acta. 1996;1275:157-60 pubmed
    ..This gene has 62% identity to nhaB gene at the DNA level from Escherichia coli and the deduced amino acid sequence is 67% identical with E. coli NhaB. This gene is presumably the V. alginolyticus nhaB gene and will be named nhaBv. ..
  22. Lee C, Szittner R, Miyamoto C, Meighen E. The gene convergent to luxG in Vibrio fischeri codes for a protein related in sequence to RibG and deoxycytidylate deaminase. Biochim Biophys Acta. 1993;1143:337-9 pubmed
    ..These results raise the possibility of a linkage between the regulation of the lux genes and riboflavin synthesis in Vibrio fischeri. ..
  23. Tan K, Beattie P, Leach D, Rich P, Coulson A, Ward F. Expression and analysis of the gene for the catalytic beta subunit of the sodium-translocating NADH-ubiquinone oxidoreductase of Vibrio alginolyticus. Biochem Soc Trans. 1996;24:12S pubmed
  24. Stewart B, McCarter L. Vibrio parahaemolyticus FlaJ, a homologue of FliS, is required for production of a flagellin. Mol Microbiol. 1996;20:137-49 pubmed
    ..Therefore the effect of FlaJ was not mediated through flagellar proteins. Nor was it mediated through sigma (54) for enhanced FlaC production was observed in mutants with defects in the gene encoding sigma (54). ..
  25. Furuno M, Sato K, Kawagishi I, Homma M. Characterization of a flagellar sheath component, PF60, and its structural gene in marine Vibrio. J Biochem. 2000;127:29-36 pubmed
    ..The expression of the pfsA gene may be coordinately regulated with flagellar formation and similarly regulated to PF47 flagellin. ..
  26. Kim S, Yang J, Cha J. Cloning and sequence analysis of a novel metalloprotease gene from Vibrio parahaemolyticus 04. Gene. 2002;283:277-86 pubmed
    ..The identification of a new metalloprotease gene expands the role of Vibrio metalloproteases as a virulence factor for host infection. ..
  27. Robinson A, Guilfoyle A, Harrop S, Boucher Y, Stokes H, Curmi P, et al. A putative house-cleaning enzyme encoded within an integron array: 1.8 A crystal structure defines a new MazG subtype. Mol Microbiol. 2007;66:610-21 pubmed publisher
    ..We hypothesize that iMazG acts as a house-cleaning enzyme, preventing the incorporation of damaging non-canonical nucleotides into host-cell DNA...
  28. Yu Y, Zhang Y, Li J, Yang H, Song H, Fang W. [VPA1045 and VPA1049 of Vibrio parahaemolyticus regulate translocation of Hcp2]. Wei Sheng Wu Xue Bao. 2012;52:954-61 pubmed
    ..The two-component regulators VPA1045 and VPA1049 regulate T6SS2 of V. parahaemolyticus post-translationally by up-regulating Hcp2 translocation. ..
  29. Krumholz L, Esser U, Simoni R. Nucleotide sequence of the unc operon of Vibrio alginolyticus. Nucleic Acids Res. 1989;17:7993-4 pubmed
  30. Kuroda T, Shimamoto T, Inaba K, Tsuda M, Tsuchiya T. Properties and sequence of the NhaA Na+/H+ antiporter of Vibrio parahaemolyticus. J Biochem. 1994;116:1030-8 pubmed
    ..parahaemolyticus. We also found that several regions of the NhaA protein showed sequence similarity with transport proteins from some other organisms. Such regions seem to be important for Na+ recognition, transport or amiloride binding...
  31. Shaw J, Chang R, Chuang K, Yen Y, Wang Y, Wang F. Nucleotide sequence of a novel arylesterase gene from Vibro mimicus and characterization of the enzyme expressed in Escherichia coli. Biochem J. 1994;298 Pt 3:675-80 pubmed
    ..1.1.2). N-Terminal analysis showed that Ser-20 was the first amino acid of the mature secreted protein, suggesting that the N-terminal 19 hydrophobic amino acids served as a signal peptide...
  32. Stewart B, Enos Berlage J, McCarter L. The lonS gene regulates swarmer cell differentiation of Vibrio parahaemolyticus. J Bacteriol. 1997;179:107-14 pubmed
    ..Vibrio lonS mutants were UV sensitive. In addition, when grown in liquid and examined in a light microscope, lonS mutant cells were extremely long and thus resembled swarmer cells harvested from a surface. ..
  33. Kawagishi I, Nakada M, Nishioka N, Homma M. Cloning of a Vibrio alginolyticus rpoN gene that is required for polar flagellar formation. J Bacteriol. 1997;179:6851-4 pubmed
    ..The other ORFs are also homologous to the genes adjacent to other rpoN genes. Deletion analysis suggests that ORF2 complements the pof mutation. These results demonstrate that RpoN is involved in the expression of polar flagellar genes. ..
  34. Kodama T, Yamazaki C, Park K, Akeda Y, Iida T, Honda T. Transcription of Vibrio parahaemolyticus T3SS1 genes is regulated by a dual regulation system consisting of the ExsACDE regulatory cascade and H-NS. FEMS Microbiol Lett. 2010;311:10-7 pubmed publisher
    ..These findings indicate that the transcription of V. parahaemolyticus T3SS1 genes is regulated by a dual regulatory system consisting of the ExsACDE regulatory cascade and H-NS...
  35. Tanabe T, Miyamoto K, Tsujibo H, Yamamoto S, Funahashi T. The small RNA Spot 42 regulates the expression of the type III secretion system 1 (T3SS1) chaperone protein VP1682 in Vibrio parahaemolyticus. FEMS Microbiol Lett. 2015;362: pubmed publisher
    ..These results indicate that Spot 42 post-transcriptionally regulates the expression of VP1682 in V. parahaemolyticus, which contributes to cytotoxicity in vivo. ..
  36. Giladi H, Wang W, Oppenheim A. Isolation and characterization of the hupA gene coding for HU of Aeromonas proteolytica. Nucleic Acids Res. 1992;20:4092 pubmed
  37. Kim Y, McCarter L. ScrG, a GGDEF-EAL protein, participates in regulating swarming and sticking in Vibrio parahaemolyticus. J Bacteriol. 2007;189:4094-107 pubmed publisher
  38. Shimohata T, Nakano M, Lian X, Shigeyama T, Iba H, Hamamoto A, et al. Vibrio parahaemolyticus infection induces modulation of IL-8 secretion through dual pathway via VP1680 in Caco-2 cells. J Infect Dis. 2011;203:537-44 pubmed publisher
    ..We showed that V. parahaemolyticus infection of Caco-2 cells results in the secretion of IL-8, and that VP1680 plays a pivotal role in manipulating host cell signaling and is responsible for triggering IL-8 secretion...
  39. Shyu Y, Lin F. Cloning and characterization of manganese superoxide dismutase gene from Vibrio parahaemolyticus and application to preliminary identification of Vibrio strains. IUBMB Life. 1999;48:345-52 pubmed
    ..The specificity of V. parahaemolyticus Mn-SOD gene probe was analyzed by cross-species polymerase chain reaction to provide information for Vibrio strain identification. ..
  40. Morita Y, Kataoka A, Shiota S, Mizushima T, Tsuchiya T. NorM of vibrio parahaemolyticus is an Na(+)-driven multidrug efflux pump. J Bacteriol. 2000;182:6694-7 pubmed
    ..Judging from the similarity of the NorM sequence to those of putative proteins in sequence databases, it seems that Na(+)/drug antiporters are present not only in V. parahaemolyticus but also in a wide range of other organisms...
  41. Maeda T, Furushita M, Hamamura K, Shiba T. Structures of ribonuclease P RNAs of Vibrio core species. FEMS Microbiol Lett. 2001;198:141-6 pubmed
    ..The genes for the RNase P RNAs of all species were located between two open reading frames, the amino acid sequences of which were similar to the hypothetical proteins located at 70.92 and 1.94 min in the Escherichia coli chromosome. ..
  42. Ohishi K, Murase K, Ohta T, Etoh H. Cloning and sequencing of a chitinase gene from Vibrio alginolyticus H-8. J Biosci Bioeng. 2000;89:501-5 pubmed
    ..harveyi (24.4%), and the chitodextrinase from V. furnissii (23.9%). Chitinase E found in cell extract is considered an intracellular chitinase which is different from chitodextrinases. ..
  43. Nagayama K, Yamamoto K, Mitawani T, Honda T. Characterisation of a haemolysin related to Vp-TDH produced by a Kanagawa phenomenon-negative clinical isolate of Vibrio parahaemolyticus. J Med Microbiol. 1995;42:83-90 pubmed
    ..The plasmid-determined structural gene for Vp-TDH/II was cloned and the nucleotide sequence determined. The deduced amino acid sequence of Vp-TDH/II differed from those of Vp-TDH, Vp-TRH and Vp-TDH/I. ..
  44. Skorupski K, Taylor R. Sequence and functional analysis of the gene encoding Vibrio cholerae cAMP receptor protein. Gene. 1997;198:297-303 pubmed
    ..In the Vc crp mutant, the cloned crp gene also restored the normal repression of ToxR-regulated virulence genes which occurs under certain environmental conditions. ..
  45. Tanaka Y, Kimura B, Takahashi H, Watanabe T, Obata H, Kai A, et al. Lysine decarboxylase of Vibrio parahaemolyticus: kinetics of transcription and role in acid resistance. J Appl Microbiol. 2008;104:1283-93 pubmed publisher
    ..The cadA-mutated strain constructed in this study showed weaker tolerance to acidic conditions than the wild-type strain. Vibrio parahaemolyticus utilizes the lysine decarboxylation pathway for survival in acidic conditions...
  46. Zhou X, Konkel M, Call D. Vp1659 is a Vibrio parahaemolyticus type III secretion system 1 protein that contributes to translocation of effector proteins needed to induce cytolysis, autophagy, and disruption of actin structure in HeLa cells. J Bacteriol. 2010;192:3491-502 pubmed publisher
    ..On the basis of these data, we conclude that Vp1659 is a T3SS1-associated protein that is a component of the secretion apparatus and that it is necessary for the efficient translocation of effector proteins into epithelial cells...
  47. Hu X, Zhang Y, Huang Q, Wang L, Yang R, Li X, et al. [Purification and DNA-binding of ToxR truncated protein of Vibrio parahaemolyticus]. Wei Sheng Wu Xue Bao. 2014;54:956-61 pubmed
    ..parahaemolyticus. ToxR fulfills a mechanism of negative regulation of T3SS1 genes by activating the expression of calR through protein-proximal promoter DNA association. ..
  48. Zhang Y, Osei Adjei G, Ni B, Fang H, Zhang L, Zhao X, et al. Transcription of exsD is repressed directly by H-NS in Vibrio parahaemolyticus. Microb Pathog. 2016;97:221-5 pubmed publisher
    ..Therefore, a single H-NS-dependent promoter was transcribed for exsD in V. parahaemolyticus. Thus, all three genes in the ExsA-ExsC-ExsD regulatory system of T3SS1 are directly repressed by H-NS in V. parahaemolyticus. ..
  49. Boles B, McCarter L. Insertional inactivation of genes encoding components of the sodium-type flagellar motor and switch of Vibrio parahaemolyticus. J Bacteriol. 2000;182:1035-45 pubmed
    ..Thus, although central chemotaxis genes are shared by the polar and lateral systems, genes encoding the switch components, as well as the motor genes, are distinct for each motility system. ..
  50. Tsunasawa S, Sugihara A, Masaki T, Sakiyama F, Takeda Y, Miwatani T, et al. Amino acid sequence of thermostable direct hemolysin produced by Vibrio parahaemolyticus. J Biochem. 1987;101:111-21 pubmed
  51. Taniguchi H, Hirano H, Kubomura S, Higashi K, Mizuguchi Y. Comparison of the nucleotide sequences of the genes for the thermostable direct hemolysin and the thermolabile hemolysin from Vibrio parahaemolyticus. Microb Pathog. 1986;1:425-32 pubmed
    ..0 and 19.5 kDa, and that of the protein encoded by the TL hemolysin gene was 45.5 kDa, and that the promoters of these two hemolysin genes of V. parahaemolyticus were functional in Escherichia coli...
  52. Otsuka M, Yasuda M, Morita Y, Otsuka C, Tsuchiya T, Omote H, et al. Identification of essential amino acid residues of the NorM Na+/multidrug antiporter in Vibrio parahaemolyticus. J Bacteriol. 2005;187:1552-8 pubmed publisher
    ..In contrast, D367E caused increased transport of ethidium ions and Na+. These results suggest that Asp32, Glu251, and Asp367 are involved in the Na+-dependent drug transport process...
  53. Wang H, Wong M, O Toole D, Mak M, Wu R, Kong R. Identification of a DNA methyltransferase gene carried on a pathogenicity island-like element (VPAI) in Vibrio parahaemolyticus and its prevalence among clinical and environmental isolates. Appl Environ Microbiol. 2006;72:4455-60 pubmed publisher
    ..parahaemolyticus MTase gene was shown by PCR to be prevalent (>98%) in pandemic thermostable direct hemolysin gene-positive isolates, which suggests that VPAI may confer unique virulence traits to pandemic strains of V. parahaemolyticus...
  54. Yarbrough M, Li Y, Kinch L, Grishin N, Ball H, Orth K. AMPylation of Rho GTPases by Vibrio VopS disrupts effector binding and downstream signaling. Science. 2009;323:269-72 pubmed publisher
    ..Eukaryotic proteins were also directly modified with AMP, potentially expanding the repertoire of posttranslational modifications for molecular signaling...
  55. Terai A, Baba K, Shirai H, Yoshida O, Takeda Y, Nishibuchi M. Evidence for insertion sequence-mediated spread of the thermostable direct hemolysin gene among Vibrio species. J Bacteriol. 1991;173:5036-46 pubmed
    ..The possible mode of ISV-mediated spread of the tdh gene is discussed from an evolutionary standpoint...
  56. Shinoda S, Matsuoka H, Tsuchie T, Miyoshi S, Yamamoto S, Taniguchi H, et al. Purification and characterization of a lecithin-dependent haemolysin from Escherichia coli transformed by a Vibrio parahaemolyticus gene. J Gen Microbiol. 1991;137:2705-11 pubmed publisher
    ..This is the reason that LDH shows haemolytic activity. Therefore, LDH of V. parahaemolyticus is an atypical phospholipase to be designated as phospholipase A2/lysophospholipase...
  57. Matsumoto C, Okuda J, Ishibashi M, Iwanaga M, Garg P, Rammamurthy T, et al. Pandemic spread of an O3:K6 clone of Vibrio parahaemolyticus and emergence of related strains evidenced by arbitrarily primed PCR and toxRS sequence analyses. J Clin Microbiol. 2000;38:578-85 pubmed
    ..parahaemolyticus and reports a novel toxRS-targeted PCR method that will be useful in epidemiological investigation of the cases associated with the current pandemic spread...
  58. Kim Y, McCarter L. Analysis of the polar flagellar gene system of Vibrio parahaemolyticus. J Bacteriol. 2000;182:3693-704 pubmed
  59. Parvathi A, Kumar H, Bhanumathi A, Ishibashi M, Nishibuchi M, Karunasagar I, et al. Molecular characterization of thermostable direct haemolysin-related haemolysin (TRH)-positive Vibrio parahaemolyticus from oysters in Mangalore, India. Environ Microbiol. 2006;8:997-1004 pubmed publisher
    ..The results suggest that genetically diverse V. parahaemolyticus carrying virulence genes are associated with the aquatic environment in this region...
  60. Kamruzzaman M, Nishibuchi M. Detection and characterization of a functional insertion sequence, ISVpa2, in Vibrio parahaemolyticus. Gene. 2008;409:92-9 pubmed publisher
    ..The data demonstrate that ISVpa2 is a transpositionally active IS discovered for the first time in V. parahaemolyticus and suggest that ISVpa2 may be transferred among the species of the genus Vibrio...
  61. Kodama T, Hiyoshi H, Gotoh K, Akeda Y, Matsuda S, Park K, et al. Identification of two translocon proteins of Vibrio parahaemolyticus type III secretion system 2. Infect Immun. 2008;76:4282-9 pubmed publisher
    ..These results indicate that VopB2 and VopD2 act as translocon proteins of V. parahaemolyticus T3SS2 and hence have a critical role in the T3SS2-dependent enterotoxicity of this bacterium...
  62. Ma L, Zhang Y, Yan X, Guo L, Wang L, Qiu J, et al. Expression of the type VI secretion system 1 component Hcp1 is indirectly repressed by OpaR in Vibrio parahaemolyticus. ScientificWorldJournal. 2012;2012:982140 pubmed publisher
    ..parahaemolyticus, and its activity was repressed by the OpaR regulator. Since the OpaR protein could not bind to the upstream region of hcp1, OpaR would repress the transcription of hcp1 in an indirect manner...
  63. Okada R, Zhou X, Hiyoshi H, Matsuda S, Chen X, Akeda Y, et al. The Vibrio parahaemolyticus effector VopC mediates Cdc42-dependent invasion of cultured cells but is not required for pathogenicity in an animal model of infection. Cell Microbiol. 2014;16:938-47 pubmed publisher
    ..Thus, although VopC can promote host cell invasion, such internalization is not a critical step of the disease process, consistent with the traditional view of V.?parahaemolyticus as an extracellular pathogen...
  64. Ringgaard S, Zepeda Rivera M, Wu X, Schirner K, Davis B, Waldor M. ParP prevents dissociation of CheA from chemotactic signaling arrays and tethers them to a polar anchor. Proc Natl Acad Sci U S A. 2014;111:E255-64 pubmed publisher
    ..Localization and sequestration of chemotaxis clusters adjacent to the flagella--to which the chemotactic signal is transmitted--facilitates proper chemotaxis as well as accurate inheritance of these macromolecular machines...
  65. Miller V, Taylor R, Mekalanos J. Cholera toxin transcriptional activator toxR is a transmembrane DNA binding protein. Cell. 1987;48:271-9 pubmed
  66. Xu M, Iida T, Yamamoto K, Takarada Y, Miwatani T, Honda T. Demonstration and characterization of simultaneous production of a thermostable direct hemolysin (TDH/I) and a TDH-related hemolysin (TRHx) by a clinically isolated Vibrio parahaemolyticus strain, TH3766. Infect Immun. 1994;62:166-71 pubmed
    ..Thus, these findings suggest that the TH3766 strain produces two types of hemolysins simultaneously. This is the first evidence that a strain of V. parahaemolyticus produces two types of toxins of the TDH-TRH family at the same time...
  67. Nozaki K, Inaba K, Kuroda T, Tsuda M, Tsuchiya T. Cloning and sequencing of the gene for Na+/H+ antiporter of Vibrio parahaemolyticus. Biochem Biophys Res Commun. 1996;222:774-9 pubmed publisher
    ..We detected Na+/H+ antiporter activity due to the gene in membrane vesicles. The gene was sequenced and the deduced amino acid sequence was found to be 72% identical to the NhaB Na+/H+ antiporter of E. coli...
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    ..Except for D(155), C(196), and Y(384), all of these residues are located in periplasmic loops...
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    ..Our results suggest an important role for Vibrio effector protein VP1686 that activate a conserved apoptotic pathway in macrophages through suppression of NF-kappaB activation independent of Toll-like receptor signaling...
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    ..This provides evidence for functional association of the VP1686 in triggering an eat-me-and-die signal to the host...
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    ..HAP mutants displayed new phenotypes, which were different from those of Salmonella typhimurium and most probably were the result of the filament being sheathed...
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    ..Our findings suggest that enhanced adherence and cytotoxicity may contribute to the apparent unique pathogenic potential of V. parahaemolyticus O3:K6 strains...
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    ..Primer extension analysis of the promoter region revealed three transcription initiation sites used by E. coli cells harboring the chb gene, two of which were also evident in V. harveyi cells...
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    ..alginolyticus. These results indicate that quite similar to the salt-loving marine bacteria, the blood-loving H. influenzae has a redox-driven Na+ pump and utilizes Na+ circulation for energy coupling...
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    ..The increase in fluorescence intensity correlated with the loss of enzyme activity. Gel filtration of the Ag+-treated Na+-NQR confirmed that FAD had been displaced from the holo-enzyme...
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    ..Measurements of net K(+)-uptake rates indicated that the presence of these genes in E. coli renders the Trk systems independent of products from the E. coli sapABCDF (trkE) operon...
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    ..varA represents an additional modulating factor in the coordinate expression of virulence factors in V. cholerae...
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    ..cholerae is similar to that of the ompB operon of E. coli, S. typhimurium and X. nematophilus, the Vibrio operon exhibits a number of novel features. The structural organisation and features of the V. cholerae ompB operon are described...
  84. Hayashi M, Nakayama Y, Yasui M, Maeda M, Furuishi K, Unemoto T. FMN is covalently attached to a threonine residue in the NqrB and NqrC subunits of Na(+)-translocating NADH-quinone reductase from Vibrio alginolyticus. FEBS Lett. 2001;488:5-8 pubmed
    ..The phosphoester binding of FMN to a threonine residue reported here is a new type of flavin attachment to a polypeptide...
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    ..Cells challenged with NaCl and various hyperosmotic stresses accumulated higher levels of glutamate than control cells, indicating that glutamate is a compatible solute in V. vulnificus...
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    ..We also demonstrate that the fabB gene of Vibrio cholerae El Tor N16961 does not contain a frameshift mutation as was previously reported...
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    ..nov. (type strain LMG 22228(T)=CBMAI 623(T)=CC17(T)) are proposed to accommodate these new isolates. The G+C contents of the DNA of the two type strains are respectively 47.6 and 48.2 mol%...
  89. Kundu N, Tichkule S, Pandit S, Chattopadhyay K. Disulphide bond restrains the C-terminal region of thermostable direct hemolysin during folding to promote oligomerization. Biochem J. 2017;474:317-331 pubmed publisher
    ..Our study provides critical insights regarding the regulation of the oligomerization mechanism of TDH, which has not been previously documented in the PFT family. ..
  90. Zhang L, Osei Adjei G, Zhang Y, Gao H, Yang W, Zhou D, et al. CalR is required for the expression of T6SS2 and the adhesion of Vibrio parahaemolyticus to HeLa cells. Arch Microbiol. 2017;199:931-938 pubmed publisher
    ..parahaemolyticus to HeLa cells. In addition, competitive EMSAs demonstrated that CalR acts as an antagonist of H-NS in V. parahaemolyticus. Collectively, these studies confirmed a new physiological role for CalR in V. parahaemolyticus. ..
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    ..Among the subclones selected by probe C, the expression of the beta-subunit as a gene product was detected in Escherichia coli membranes by activity staining and Western blotting...