Vibrio

Summary

Alias: Beneckea, Beneckea Campbell 1957, "Microspira" Schroeter 1886, "Pacinia" Trevisan 1885, Microspira, Pacinia, Vibrio Pacini 1854

Top Publications

  1. Bandino J, Hang A, Norton S. The Infectious and Noninfectious Dermatological Consequences of Flooding: A Field Manual for the Responding Provider. Am J Clin Dermatol. 2015;16:399-424 pubmed publisher
    ..b>Vibrio vulnificus is classically associated with exposure to saltwater or brackish water...
  2. Cianciotto N, White R. Expanding Role of Type II Secretion in Bacterial Pathogenesis and Beyond. Infect Immun. 2017;85: pubmed publisher
    ..i>Legionella pneumophila, Pseudomonas aeruginosa, Stenotrophomonas maltophilia, Vibrio cholerae, and Yersinia enterocolitica T2S-expressing plant pathogens include Dickeya dadantii, <..
  3. McDonald N, Lubin J, Chowdhury N, Boyd E. Host-Derived Sialic Acids Are an Important Nutrient Source Required for Optimal Bacterial Fitness In Vivo. MBio. 2016;7:e02237-15 pubmed publisher
    ..A major challenge facing bacterial intestinal pathogens is competition for nutrient sources with the host microbiota.Vibrio cholerae is an intestinal pathogen that causes cholera, which affects millions each year; however, our knowledge ..
  4. Supuran C. Inhibition of bacterial carbonic anhydrases and zinc proteases: from orphan targets to innovative new antibiotic drugs. Curr Med Chem. 2012;19:831-44 pubmed
    ..Streptococcus pneumoniae, Salmonella enterica, Haemophilus influenzae, Listeria spp, Vibrio spp., Pseudomonas aeruginosa, Legionella pneumophila, Streptomyces spp., Clostridium spp., Enterococcus spp., etc...
  5. Zhang D, Lv C, Yu D, Wang Z. Characterization and functional analysis of a tandem-repeat galectin-9 in large yellow croaker Larimichthys crocea. Fish Shellfish Immunol. 2016;52:167-78 pubmed publisher
    ..In contrast, Vibrio parahaemolyticus caused a significant down-regulation in these three tissues, except for in spleen of 48 h and ..
  6. Di Ianni F, Dodi P, Cabassi C, Pelizzone I, Sala A, Cavirani S, et al. Conjunctival flora of clinically normal and diseased turtles and tortoises. BMC Vet Res. 2015;11:91 pubmed publisher
    ..Pseudomonas putida, Salmonella enterica ssp. arizonae, Stenotrophomonas maltophilia and Vibrio parahaemolyticus was evidenced. The presence in 8 animals of Mycoplasma spp...
  7. Wei X, Wang L, Sun W, Zhang M, Ma H, Zhang Y, et al. C-type lectin B (SpCTL-B) regulates the expression of antimicrobial peptides and promotes phagocytosis in mud crab Scylla paramamosain. Dev Comp Immunol. 2018;84:213-229 pubmed publisher
    ..After challenged with Vibrio parahaemolyticus, LPS, polyI:C and white spot syndrome virus (WSSV), the mRNA levels of SpCTL-B in hemocytes and ..
  8. Beaulieu L, Thibodeau J, Desbiens M, Saint Louis R, Zatylny Gaudin C, Thibault S. Evidence of Antibacterial Activities in Peptide Fractions Originating from Snow Crab (Chionoecetes opilio) By-Products. Probiotics Antimicrob Proteins. 2010;2:197-209 pubmed publisher
    ..Aeromonas hydrophila, Campylobacter jejuni, Listonella anguillarum, Morganella morganii, Shewanella putrefasciens, Vibrio parahaemolyticus and Vibrio vulnificus and against a few Gram-positive bacteria such as Listeria monocytogenes, ..
  9. Zhang X, Shi Y, Chen J. Molecular characterization of a transmembrane C-type lectin receptor gene from ayu (Plecoglossus altivelis) and its effect on the recognition of different bacteria by monocytes/macrophages. Mol Immunol. 2015;66:439-50 pubmed publisher
    ..in all tested tissues and cells, with high levels in the liver; and its expression was significantly altered upon Vibrio anguillarum infection...

More Information

Publications324 found, 100 shown here

  1. Lv C, Zhang D, Wang Z. A novel C-type lectin, Nattectin-like protein, with a wide range of bacterial agglutination activity in large yellow croaker Larimichthys crocea. Fish Shellfish Immunol. 2016;50:231-41 pubmed publisher
    ..After challenged with poly I:C and Vibrio parahaemolyticus, the temporal expression of LcNTC was significantly up-regulated in the liver, spleen and head-..
  2. Li L, Heidemann Olsen R, Ye L, Yan H, Nie Q, Meng H, et al. Antimicrobial Resistance and Resistance Genes in Aerobic Bacteria Isolated from Pork at Slaughter. J Food Prot. 2016;79:589-97 pubmed publisher
    ..caseolyticus; sul1 in Vibrio cincinnatiensis; sul2 in Acinetobacter bereziniae, Acinetobacter johnsonii, and V...
  3. Ghosh G, Reddy J, Sambhare S, Sen R. A Bacteriophage Capsid Protein Is an Inhibitor of a Conserved Transcription Terminator of Various Bacterial Pathogens. J Bacteriol. 2018;200: pubmed publisher
    ..tuberculosis, Xanthomonas campestris, Xanthomonas oryzae, Corynebacterium glutamicum, Vibrio cholerae, Salmonella enterica, and Pseudomonas syringae The purified recombinant Rho proteins of ..
  4. Halang P, Toulouse C, Geißel B, Michel B, Flauger B, Müller M, et al. Response of Vibrio cholerae to the Catecholamine Hormones Epinephrine and Norepinephrine. J Bacteriol. 2015;197:3769-78 pubmed publisher
    ..Here we show that Vibrio cholerae, the causative agent of cholera, exhibits a specific response to E and NE. These catecholates (0...
  5. Jheng Y, Lee L, Ting C, Pan C, Hui C, Chen J. Zebrafish fed on recombinant Artemia expressing epinecidin-1 exhibit increased survival and altered expression of immunomodulatory genes upon Vibrio vulnificus infection. Fish Shellfish Immunol. 2015;42:1-15 pubmed publisher
    ..bacterial species, including Staphylococcus coagulase, Pseudomonas aeruginosa, Streptococcus pyogenes, and Vibrio vulnificus...
  6. Tanapichatsakul C, Monggoot S, Gentekaki E, Pripdeevech P. Antibacterial and Antioxidant Metabolites of Diaporthe spp. Isolated from Flowers of Melodorum fruticosum. Curr Microbiol. 2018;75:476-483 pubmed publisher
    ..cereus, Klebsiella pneumoniae, Pseudomonas aeruginosa, Escherichia coli, Shigella flexneri, Vibrio cholerae and V. parahaemolyticus...
  7. Tian L, Zhu X, Chen Z, Liu W, Li S, Yu W, et al. Characteristics of bacterial pathogens associated with acute diarrhea in children under 5 years of age: a hospital-based cross-sectional study. BMC Infect Dis. 2016;16:253 pubmed publisher
    ..Shigella spp., Vibrio cholerae, diarrheagenic Escherichia coli (DEC), Aeromonas spp., Plesiomonas spp...
  8. Xiang J, Li X, Chen Y, Lu Y, Yu M, Chen X, et al. Complement factor I from flatfish half-smooth tongue (Cynoglossus semilaevis) exhibited anti-microbial activities. Dev Comp Immunol. 2015;53:199-209 pubmed publisher
    ..Temporal expression levels of CsCfi after challenging with Vibrio anguillarum showed different expression patterns in intestine, spleen, skin, blood, head kidney and liver...
  9. Kostyrko V, Bertsova Y, Serebryakova M, Baykov A, Bogachev A. NqrM (DUF539) Protein Is Required for Maturation of Bacterial Na+-Translocating NADH:Quinone Oxidoreductase. J Bacteriol. 2015;198:655-63 pubmed publisher
    ..Expression of the Vibrio harveyi nqr operon alone or with the associated apbE gene in Escherichia coli, which lacks its own Na(+)-NQR, ..
  10. Obaidat M, Salman A, Roess A. Virulence and Antibiotic Resistance of Vibrio parahaemolyticus Isolates from Seafood from Three Developing Countries and of Worldwide Environmental, Seafood, and Clinical Isolates from 2000 to 2017. J Food Prot. 2017;:2060-2067 pubmed publisher
    b>Vibrio parahaemolyticus is a leading cause of seafood-associated illness. This study investigated the prevalence, virulence, and antibiotic resistance of V. parahaemolyticus in three low- and middle-income countries...
  11. Torrecillas S, Rivero Ramírez F, Izquierdo M, Caballero M, Makol A, Suarez Bregua P, et al. Feeding European sea bass (Dicentrarchus labrax) juveniles with a functional synbiotic additive (mannan oligosaccharides and Pediococcus acidilactici): An effective tool to reduce low fishmeal and fish oil gut health effects?. Fish Shellfish Immunol. 2018;81:10-20 pubmed publisher
    ..After 60 and 90 days of feeding trial, fish were subjected to an experimental infection against Vibrio anguillarum...
  12. Zhang S, Zhou Y, Xu W, Tian L, Chen J, Chen S, et al. Impact of co-infections with enteric pathogens on children suffering from acute diarrhea in southwest China. Infect Dis Poverty. 2016;5:64 pubmed publisher
    ..b>Vibrio cholera; Vibrio parahaemolyticus; Aeromonas spp.; and Plesiomonas spp.), and three protozoan (Cryptosporidium spp...
  13. Weidhaas J, Anderson A, Jamal R. Elucidating Waterborne Pathogen Presence and Aiding Source Apportionment in an Impaired Stream. Appl Environ Microbiol. 2018;84: pubmed publisher
    ..coli, Enterococcus faecalis, Helicobacter spp., Salmonella spp., and Vibrio spp.), and eukaryotes (Acanthamoeba spp...
  14. Cheng C, Huang S, Wu C, Gong H, Ken C, Hu S, et al. Transgenic expression of omega-3 PUFA synthesis genes improves zebrafish survival during Vibrio vulnificus infection. J Biomed Sci. 2015;22:103 pubmed publisher
    ..However, it is unclear how n-3 PUFAs improve immune function in liver. Vibrio vulnificus, a gram-negative bacterial pathogen, causes high mortality of aquaculture fishes upon infection...
  15. Siddiqi K, Husen A, Rao R. A review on biosynthesis of silver nanoparticles and their biocidal properties. J Nanobiotechnology. 2018;16:14 pubmed publisher
    ..aureus, Citrobacter koseri, Salmonella typhii, Pseudomonas aeruginosa, Escherichia coli, Klebsiella pneumonia, Vibrio parahaemolyticus and fungus Candida albicans by binding Ag/Ag+ with the biomolecules present in the ..
  16. Godahewa G, Perera N, Lee S, Kim M, Lee J. A cysteine protease (cathepsin Z) from disk abalone, Haliotis discus discus: Genomic characterization and transcriptional profiling during bacterial infections. Gene. 2017;627:500-507 pubmed publisher
    ..In addition, we found that viable bacteria (Vibrio parahaemolyticus and Listeria monocytogenes) and bacterial lipopolysaccharides significantly modulated AbCTSZ ..
  17. Yi Y, Zhang Z, Zhao F, Liu H, Yu L, Zha J, et al. Probiotic potential of Bacillus velezensis JW: Antimicrobial activity against fish pathogenic bacteria and immune enhancement effects on Carassius auratus. Fish Shellfish Immunol. 2018;78:322-330 pubmed publisher
    ..including Aeromonas hydrophila, Aeromonas salmonicida, Lactococcus garvieae, Streptococcus agalactiae, and Vibrio Parahemolyticus...
  18. Naik O, Shashidhar R, Rath D, Bandekar J, Rath A. Characterization of multiple antibiotic resistance of culturable microorganisms and metagenomic analysis of total microbial diversity of marine fish sold in retail shops in Mumbai, India. Environ Sci Pollut Res Int. 2018;25:6228-6239 pubmed publisher
    ..Photobacterium and Vibrio were two major fish and human pathogens which were identified in the fish metagenome...
  19. Xiang Z, Qu F, Wang F, Li J, Zhang Y, Yu Z. Characteristic and functional analysis of a ficolin-like protein from the oyster Crassostrea hongkongensis. Fish Shellfish Immunol. 2014;40:514-23 pubmed publisher
    ..50 kD bind Saccharomyces cerevisiae, Staphylococcus haemolyticus or Escherichia coli K-12, but not those from Vibrio alginolyticus. Furthermore, the rChFCN protein could agglutinate Gram-negative bacteria E...
  20. Sabbatani S. [The experiments conducted by Japanese on human guinea pigs, and the use of biological weapons during the Sino-Japanese war (1937-1945)]. Infez Med. 2014;22:255-66 pubmed
    ..and bone fractures, were performed, as well as the inoculation of microorganisms (including Yersinia pestis, Vibrio cholerae, Richettsia typhi, and Salmonella typhi), and spores of Bacillus anthracis...
  21. Vidya R, Makesh M, Purushothaman C, Chaudhari A, Gireesh Babu P, Rajendran K. Report of leucine-rich repeats (LRRs) from Scylla serrata: Ontogeny, molecular cloning, characterization and expression analysis following ligand stimulation, and upon bacterial and viral infections. Gene. 2016;590:159-68 pubmed publisher
    ..However, a delayed 5-fold up-regulation was observed in vivo against Vibrio parahaemolyticus infection at 72hpi...
  22. Wang Z, Sun B, Zhu F. The shrimp hormone receptor acts as an anti-apoptosis and anti-inflammatory factor in innate immunity. Fish Shellfish Immunol. 2018;72:581-592 pubmed publisher
    ..WSSV infection could cause the down-regulation of mjHR, while infection with Vibrio alginolyticus could cause significant up-regulation of mjHR...
  23. Singh P, Singh H, Kim Y, Mathiyalagan R, Wang C, Yang D. Extracellular synthesis of silver and gold nanoparticles by Sporosarcina koreensis DC4 and their biological applications. Enzyme Microb Technol. 2016;86:75-83 pubmed publisher
    ..the silver nanoparticles have been explored in terms of MIC and MBC against pathogenic microorganisms such as Vibrio parahaemolyticus, Escherichia coli, Salmonella enterica, Bacillus anthracis, Bacillus cereus and Staphylococcus ..
  24. Gladney L, Tarr C. Molecular and phenotypic characterization of Vibrio navarrensis isolates associated with human illness. J Clin Microbiol. 2014;52:4070-4 pubmed publisher
    We characterized 18 Vibrio isolates, including 15 recovered from human clinical specimens, and found that they clustered with two previously characterized Vibrio navarrensis isolates in a phylogenetic analysis...
  25. Salem W, Leitner D, Zingl F, Schratter G, Prassl R, Goessler W, et al. Antibacterial activity of silver and zinc nanoparticles against Vibrio cholerae and enterotoxic Escherichia coli. Int J Med Microbiol. 2015;305:85-95 pubmed publisher
    b>Vibrio cholerae and enterotoxic Escherichia coli (ETEC) remain two dominant bacterial causes of severe secretory diarrhea and still a significant cause of death, especially in developing countries...
  26. Erler R, Wichels A, Heinemeyer E, Hauk G, Hippelein M, Reyes N, et al. VibrioBase: A MALDI-TOF MS database for fast identification of Vibrio spp. that are potentially pathogenic in humans. Syst Appl Microbiol. 2015;38:16-25 pubmed publisher
    ..Due to climate-change-driven temperature increases, higher Vibrio abundances and infections are predicted for Northern Europe, which in turn necessitates environmental surveillance ..
  27. Richards G, Bono J, Watson M, Needleman D. Complete Genome Sequence for the Shellfish Pathogen Vibrio coralliilyticus RE98 Isolated from a Shellfish Hatchery. Genome Announc. 2014;2: pubmed publisher
    b>Vibrio coralliilyticus is a pathogen of corals and larval shellfish. Publications on strain RE98 list it as a Vibrio tubiashii; however, whole genome sequencing confirms RE98 as V...
  28. Liu L, Liu S, Yu M, Chen F. Application of the combination index integrated with confidence intervals to study the toxicological interactions of antibiotics and pesticides in Vibrio qinghaiensis sp.-Q67. Environ Toxicol Pharmacol. 2015;39:447-56 pubmed publisher
    ..three chemicals (imidacloprid (IMI), pirimicarb (PIR) and streptomycin sulfate (STR)) and their binary mixtures on Vibrio qinghaiensis sp.-Q67 were determined by the microplate toxicity analysis (MTA)...
  29. Lin L, Lin G, Tseng Y, Yu M. Draft Genome Sequence of Vibrio owensii GRA50-12, Isolated from Green Algae in the Intertidal Zone of Eastern Taiwan. Genome Announc. 2015;3: pubmed publisher
    b>Vibrio owensii GRA50-12 was isolated from symbiotic green algae of coral...
  30. Zhou S, Li M, Yang N, Liu S, Yuan X, Tao Z, et al. First description and expression analysis of tumor necrosis factor receptor-associated factor 6 (TRAF6) from the swimming crab, Portunus trituberculatus. Fish Shellfish Immunol. 2015;45:205-10 pubmed publisher
    ..Interestingly, the level of Pt-TRAF6 transcript differed between male and female crabs. After Vibrio alginolyticus or lipopolysaccharide (LPS) challenge, the Pt-TRAF6 transcript was down-regulated in hemocytes and ..
  31. Osorio C, Rivas A, Balado M, Fuentes Monteverde J, Rodríguez J, Jiménez C, et al. A Transmissible Plasmid-Borne Pathogenicity Island Confers Piscibactin Biosynthesis in the Fish Pathogen Photobacterium damselae subsp. piscicida. Appl Environ Microbiol. 2015;81:5867-79 pubmed publisher
    ..damselae subsp. piscicida to a mollusk pathogenic Vibrio alginolyticus strain and to other Gram-negative bacteria, likely dependent on the conjugative functions of the ..
  32. Kinsey T, Lydon K, Bowers J, Jones J. Effects of Dry Storage and Resubmersion of Oysters on Total Vibrio vulnificus and Total and Pathogenic (tdh+/trh+) Vibrio parahaemolyticus Levels. J Food Prot. 2015;78:1574-80 pubmed publisher
    b>Vibrio vulnificus (Vv) and Vibrio parahaemolyticus (Vp) are the two leading causes of bacterial illnesses associated with raw shellfish consumption...
  33. Xuan G, Jia J, Chen Y, Wang J, Tang J, Jiang Y, et al. Strain-level visualized analysis of cold-stressed Vibrio parahaemolyticus based on MALDI-TOF mass fingerprinting. Microb Pathog. 2015;88:16-21 pubmed publisher
    In this study, strain-level visualized analysis of cold-stressed Vibrio parahaemolyticus based on matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF) mass fingerprinting was investigated...
  34. Ali M, You Y, Sur D, Kanungo S, Kim D, Deen J, et al. Validity of the estimates of oral cholera vaccine effectiveness derived from the test-negative design. Vaccine. 2016;34:479-485 pubmed publisher
    ..studies, VE using the TND was estimated from the odds ratio (OR) relating vaccination status to fecal test status (Vibrio cholerae O1 positive or negative) among diarrheal patients enrolled during surveillance (VE= (1-OR)×100%)...
  35. Wu C, Chen C, Morales C, Kiang D. Draft Genome Sequence of an ortho-Nitrophenyl-?-d-Galactoside (ONPG)-Negative Strain of Vibrio cholerae, Isolated from Drakes Bay, California. Genome Announc. 2016;4: pubmed publisher
    We present the draft whole-genome sequence of a Vibrio cholerae strain (Vc25-3) isolated from Drakes Bay, California. This environmental isolate has an atypical morphology and is ortho-nitrophenyl-?-d-galactoside (ONPG)-negative.
  36. Wen Y, Kim I, Kim K. Iron- and Quorum-sensing Signals Converge on Small Quorum-regulatory RNAs for Coordinated Regulation of Virulence Factors in Vibrio vulnificus. J Biol Chem. 2016;291:14213-30 pubmed publisher
    b>Vibrio vulnificus is a marine bacterium that causes human infections resulting in high mortality...
  37. Deng Y, Chen C, Zhao Z, Huang X, Yang Y, Ding X. Complete Genome Sequence of Vibrio alginolyticus ZJ-T. Genome Announc. 2016;4: pubmed publisher
    b>Vibrio alginolyticus is a ubiquitous Gram-negative bacterium which is normally distributed in the coastal and estuarine environments...
  38. Melin F, Xie H, Meyer T, Ahn Y, Gennis R, Michel H, et al. The unusual redox properties of C-type oxidases. Biochim Biophys Acta. 2016;1857:1892-1899 pubmed publisher
    ..We address here the redox properties of cbb3 oxidases from three organisms, Rhodobacter sphaeroides, Vibrio cholerae and Pseudomonas stutzeri by means of electrochemical and spectroscopic techniques...
  39. Pretzer C, Druzhinina I, Amaro C, Benediktsdóttir E, Hedenström I, Hervio Heath D, et al. High genetic diversity of Vibrio cholerae in the European lake Neusiedler See is associated with intensive recombination in the reed habitat and the long-distance transfer of strains. Environ Microbiol. 2017;19:328-344 pubmed publisher
    Coastal marine Vibrio cholerae populations usually exhibit high genetic diversity. To assess the genetic diversity of abundant V...
  40. Park B, Choi S. Sensitive immunoassay-based detection of Vibrio parahaemolyticus using capture and labeling particles in a stationary liquid phase lab-on-a-chip. Biosens Bioelectron. 2017;90:269-275 pubmed publisher
    In the present study, a method was developed for detection of Vibrio parahaemolyticus based on a stationary liquid phase lab-on-a-chip (SLP LOC)...
  41. Lee S, Katya K, Park Y, Won S, Seong M, Hamidoghli A, et al. Comparative evaluation of dietary probiotics Bacillus subtilis WB60 and Lactobacillus plantarum KCTC3928 on the growth performance, immunological parameters, gut morphology and disease resistance in Japanese eel, Anguilla japonica. Fish Shellfish Immunol. 2017;61:201-210 pubmed publisher
    ..Whereas, results from the disease challenge test with bacteria Vibrio angulillarum showed significantly lower survival rate for fish fed CON diet than those of fish fed other ..
  42. Lopez Perez M, Ramon Marco N, Rodriguez Valera F. Networking in microbes: conjugative elements and plasmids in the genus Alteromonas. BMC Genomics. 2017;18:36 pubmed publisher
    ..A nearly identical ICE was found in A. mediterranea MED64 and Vibrio cholera AHV1003 isolated from a human pathogen, indicating the potential exchange of these genes across ..
  43. da C Leite D, Barbosa L, Mantuano N, Goulart C, Veríssimo da Costa G, Bisch P, et al. Transcriptional and post-transcriptional regulation of pst2 operon expression in Vibrio cholerae O1. Infect Genet Evol. 2017;51:10-16 pubmed publisher
    ..The relatively higher stability of pstS and pstB transcripts seems to rely on the secondary structures at their 3' untranslated regions that are known to block 3'-5' exonucleolytic attacks. ..
  44. Yu W, Shen X, Pan H, Xiao T, Shen P, Xiao Y. Clinical features and treatment of patients with Vibrio vulnificus infection. Int J Infect Dis. 2017;59:1-6 pubmed publisher
    Infections with Vibrio vulnificus are commonly fatal, and the speed and accuracy of diagnosis and treatment is directly linked to mortality...
  45. Li A, Wu P, Law J, Chow C, Postigo C, Guo Y, et al. Transformation of acesulfame in chlorination: Kinetics study, identification of byproducts, and toxicity assessment. Water Res. 2017;117:157-166 pubmed publisher
    ..A preliminary assessment of chlorinated mixtures by luminescence inhibition of Vibrio fischeri showed that these by-products were up to 1.8-fold more toxic than the parent compound...
  46. Zhang J, Ito H, Hino M, Kimura M. A RelE/ParE superfamily toxin in Vibrio parahaemolyticus has DNA nicking endonuclease activity. Biochem Biophys Res Commun. 2017;489:29-34 pubmed publisher
    ..Previously, we found a TA system, vp1842/vp1843, on the Vibrio parahaemolyticus genome whose toxin Vp1843 belongs to the RelE/ParE toxin superfamily...
  47. Gargano J, Adam E, Collier S, Fullerton K, Feinman S, Beach M. Mortality from selected diseases that can be transmitted by water - United States, 2003-2009. J Water Health. 2017;15:438-450 pubmed publisher
    ..nontuberculous mycobacteria (NTM), Pseudomonas-related pneumonia or septicemia, Salmonella, Shigella, and Vibrio)...
  48. Izumiya H, Furukawa M, Ogata K, Isobe J, Watanabe S, Sasaki M, et al. A double-quadratic model for predicting Vibrio species in water environments of Japan. Arch Microbiol. 2017;199:1293-1302 pubmed publisher
    b>Vibrio spp. are natural inhabitants of marine and estuarine environments. Vibrio cholerae, Vibrio parahaemolyticus, and Vibrio vulnificus are the major infectious agents for humans...
  49. Mao F, Li J, Zhang Y, Xiang Z, Zhang Y, Yu Z. Molecular cloning and functional analysis of tumor necrosis factor receptor-associated factor 6 (TRAF6) in Crossastrea gigas. Fish Shellfish Immunol. 2017;68:37-45 pubmed publisher
    ..Immune challenge with Vibrio alginolyticus and poly I:C resulted in significant up-regulation of CgTRAF6 expression...
  50. Fakhry C, Kulkarni P, Chen P, Kulkarni R, Zarringhalam K. Prediction of bacterial small RNAs in the RsmA (CsrA) and ToxT pathways: a machine learning approach. BMC Genomics. 2017;18:645 pubmed publisher
    ..RsmA/CsrA in diverse bacterial species and 2) sRNAs regulated by the master regulator of virulence, ToxT, in Vibrio cholerae...
  51. Yan J, Nadell C, Stone H, Wingreen N, Bassler B. Extracellular-matrix-mediated osmotic pressure drives Vibrio cholerae biofilm expansion and cheater exclusion. Nat Commun. 2017;8:327 pubmed publisher
    ..Here, using Vibrio cholerae as our model organism, we show that during active cell growth, matrix production enables biofilm-dwelling ..
  52. Simner P, Oethinger M, Stellrecht K, Pillai D, Yogev R, Leblond H, et al. Multisite Evaluation of the BD Max Extended Enteric Bacterial Panel for Detection of Yersinia enterocolitica, Enterotoxigenic Escherichia coli, Vibrio, and Plesiomonas shigelloides from Stool Specimens. J Clin Microbiol. 2017;55:3258-3266 pubmed publisher
    ..specimens for the detection of Yersinia enterocolitica, enterotoxigenic Escherichia coli (ETEC), Vibrio, and Plesiomonas shigelloides The study included prospective, retrospective, and prepared contrived ..
  53. Sarwar S, Ali A, Pal M, Chakrabarti P. Zinc oxide nanoparticles provide anti-cholera activity by disrupting the interaction of cholera toxin with the human GM1 receptor. J Biol Chem. 2017;292:18303-18311 pubmed publisher
    i>Vibrio cholerae causes cholera and is the leading cause of diarrhea in developing countries, highlighting the need for the development of new treatment strategies to combat this disease agent...
  54. Fri J, Ndip R, Njom H, Clarke A. Occurrence of Virulence Genes Associated with Human Pathogenic Vibrios Isolated from Two Commercial Dusky Kob (Argyrosmus japonicus) Farms and Kareiga Estuary in the Eastern Cape Province, South Africa. Int J Environ Res Public Health. 2017;14: pubmed publisher
    i>Background: Seafood-borne Vibrio infections, often linked to contaminated seafood and water, are of increasing global public health concern...
  55. Białk Bielińska A, Mulkiewicz E, Stokowski M, Stolte S, Stepnowski P. Acute aquatic toxicity assessment of six anti-cancer drugs and one metabolite using biotest battery - Biological effects and stability under test conditions. Chemosphere. 2017;189:689-698 pubmed publisher
    ..MET) and its metabolite - 7-hydroxymethotrexate (7-OH-MET), towards selected aquatic organisms, namely bacteria Vibrio fischeri, algae Raphidocelis subcapitata, crustaceans Daphnia magna and duckweed Lemna minor...
  56. Bourque D, Bhuiyan T, Genereux D, Rashu R, Ellis C, Chowdhury F, et al. Analysis of the Human Mucosal Response to Cholera Reveals Sustained Activation of Innate Immune Signaling Pathways. Infect Immun. 2018;86: pubmed publisher
    To better understand the innate immune response to Vibrio cholerae infection, we tracked gene expression in the duodenal mucosa of 11 Bangladeshi adults with cholera, using biopsy specimens obtained immediately after rehydration ..
  57. Montalbán M, Villora G, Licence P. Ecotoxicity assessment of dicationic versus monocationic ionic liquids as a more environmentally friendly alternative. Ecotoxicol Environ Saf. 2018;150:129-135 pubmed publisher
    ..were synthesized, characterized and tested for their toxicity, which was assessed using the luminescent bacterium Vibrio fischeri...
  58. Yu Z, Zhu B, Wang W, Tan H, Yin H. Characterization of a new oligoalginate lyase from marine bacterium Vibrio sp. Int J Biol Macromol. 2018;112:937-942 pubmed publisher
    A new oligoalginate lyase encoding gene, designed oal17A, was cloned from marine bacterium Vibrio sp. W13, and then expressed in Escherichia coli. The recombinant Oal17A was purified by NTA-Ni resin with maximal activity at 30°C and pH7...
  59. Su B, Lin W, Chen J. Recombinant Epinephelus lanceolatus serum amyloid A as a feed additive: Effects on immune gene expression and resistance to Vibrio alginolyticus infection in Epinephelus lanceolatus. Fish Shellfish Immunol. 2018;76:233-239 pubmed publisher
    ..88, 4.4 or 22?mg/kg rElSAA-containing diet for 3, 7, 14, 21 or 28 days, followed by challenge with Vibrio alginolyticus. Survival was then monitored for 4 days...
  60. Wang F, Yu Z, Wang W, Li Y, Lu G, Qu C, et al. A novel caspase-associated recruitment domain (CARD) containing protein (CgCARDCP-1) involved in LPS recognition and NF-?B activation in oyster (Crassostrea gigas). Fish Shellfish Immunol. 2018;79:120-129 pubmed publisher
    ..CgCARDCP-1 mRNA expression level in hemocytes was significantly up-regulated after lipopolysaccharide (LPS) and Vibrio splendidus stimulations. The recombinant CgCARDCP-1 displayed strong binding activity with LPS in vitro...
  61. Xue D, Guang Hua W, Yan Li S, Min Z, Yong Hua H. Black rockfish C-type lectin, SsCTL4: A pattern recognition receptor that promotes bactericidal activity and virus escape from host immune defense. Fish Shellfish Immunol. 2018;79:340-350 pubmed publisher
    ..Recombinant SsCTL4 (rSsCTL4) exhibited apparent binding activities against bacteria (Edwardsiella tarda and Vibrio anguillarum) and virus (infectious spleen and kidney necrosis virus, ISKNV)...
  62. Tandel G, Hipolito S, Kondo H, Hirono I. Comparative sequence analysis of crustin isoform MjCRS7 and MjWFDC-like gene from kuruma shrimp Marsupenaeus japonicus shows variant of the WFDC domain. Infect Genet Evol. 2018;64:139-148 pubmed publisher
    ..Neither of the genes was responsive to Vibrio parahaemolyticus, Vibrio penaeicida or white spot syndrome virus (WSSV) either by immersion or injection challenge ..
  63. Diaz E, Monsalvo V, Lopez J, Mena I, Palomar J, Rodriguez J, et al. Assessment the ecotoxicity and inhibition of imidazolium ionic liquids by respiration inhibition assays. Ecotoxicol Environ Saf. 2018;162:29-34 pubmed publisher
    ..For comparison purposes, the EC50 values were also determined by the Microtox test (Vibrio fischeri)...
  64. Yin B, Liu H, Tan B, Dong X, Chi S, Yang Q, et al. Cottonseed protein concentrate (CPC) suppresses immune function in different intestinal segments of hybrid grouper ?Epinephelus fuscoguttatus×?Epinephelus lanceolatu via TLR-2/MyD88 signaling pathways. Fish Shellfish Immunol. 2018;81:318-328 pubmed publisher
    ..23?g) for 8 weeks. Thena challenge test with injection of Vibrio parahaemolyticus was conducted for 7 days until the fish stabilized...
  65. Hu B, Pan Y, Li Z, Yuan W, Deng L. EmPis-1L, an Effective Antimicrobial Peptide Against the Antibiotic-Resistant VBNC State Cells of Pathogenic Bacteria. Probiotics Antimicrob Proteins. 2018;: pubmed publisher
    ..AMP piscidin killing the VBNC state cells of pathogenic bacteria Escherichia coli O157, Staphylococcus aureus, and Vibrio parahaemolyticus OS4 was studied. After entering the VBNC state, cells of E. coli O157, S. aureus, and V...
  66. Weber G, Kortmann J, Narberhaus F, Klose K. RNA thermometer controls temperature-dependent virulence factor expression in Vibrio cholerae. Proc Natl Acad Sci U S A. 2014;111:14241-6 pubmed publisher
    b>Vibrio cholerae is the bacterium that causes the diarrheal disease cholera. The bacteria experience a temperature shift as V. cholerae transition from contaminated water at lower temperatures into the 37 °C human intestine...
  67. Li B, Tan H, Wang D, Ke B, Chen J, He D, et al. [Etiologic characteristics of Vibrio cholerae in Guangdong province in 2009-2013]. Zhonghua Liu Xing Bing Xue Za Zhi. 2014;35:825-31 pubmed
    To analyze the etiologic characteristics of O1/O139 Vibrio cholerae in Guangdong province in 2009-2013...
  68. Oyarbide U, Iturria I, Rainieri S, Pardo M. Use of gnotobiotic zebrafish to study Vibrio anguillarum pathogenicity. Zebrafish. 2015;12:71-80 pubmed publisher
    ..Using a GFP-labeled strain of Vibrio anguillarum, we fluorescently monitored colonization of the zebrafish intestinal tract and used gene expression ..
  69. Fillion K, Mileno M. Cholera in travelers: shifting tides in epidemiology, management, and prevention. Curr Infect Dis Rep. 2015;17:455 pubmed publisher
    ..Hopeful news reported the containment of an outbreak through the use of a Vibrio cholera vaccine...
  70. Yang J, Kim H, Kang S, Kim K, Kim D, Yun C, et al. TLR2, but not TLR4, plays a predominant role in the immune responses to cholera vaccines. J Leukoc Biol. 2015;98:661-9 pubmed publisher
    b>Vibrio cholerae can cause severe diarrhea and dehydration leading to high mortality and morbidity. Current cholera vaccines are formulated with KVC...
  71. Wang C, Alpatova A, McPhedran K, Gamal El Din M. Coagulation/flocculation process with polyaluminum chloride for the remediation of oil sands process-affected water: Performance and mechanism study. J Environ Manage. 2015;160:254-62 pubmed publisher
    ..At the highest applied coagulant dose of 3.0 mM Al, the synthetic PACl reduced Vibrio fischeri inhibition effect to 43.3 ± 3.0% from 49.5 ± 0.4% in raw OSPW...
  72. Richards G, Fay J, Uknalis J, Olanya O, Watson M. Purification and Host Specificity of Predatory Halobacteriovorax Isolates from Seawater. Appl Environ Microbiol. 2016;82:922-7 pubmed publisher
    ..Four strains of Halobacteriovorax originally isolated in Vibrio parahaemolyticus O3:K6 host cells were separated from their prey by an enrichment-filtration-dilution technique ..
  73. Shanthi S, Jayaseelan B, Velusamy P, Vijayakumar S, Chih C, Vaseeharan B. Biosynthesis of silver nanoparticles using a probiotic Bacillus licheniformis Dahb1 and their antibiofilm activity and toxicity effects in Ceriodaphnia cornuta. Microb Pathog. 2016;93:70-7 pubmed publisher
    ..Confocal Laser Scanning Microscope (CLSM) images showed a weak adherence and disintegrated biofilm formation of Vibrio parahaemolyticus Dav1 treated with BLCFE-AgNPs compared to control...
  74. Richard G, Guérard F, Corporeau C, Lambert C, Paillard C, Pernet F. Metabolic responses of clam Ruditapes philippinarum exposed to its pathogen Vibrio tapetis in relation to diet. Dev Comp Immunol. 2016;60:96-107 pubmed publisher
    ..We found that algal diet did not impact the metabolic response of clams exposed to Vibrio tapetis...
  75. Heath Heckman E, FOSTER J, Apicella M, Goldman W, McFall Ngai M. Environmental cues and symbiont microbe-associated molecular patterns function in concert to drive the daily remodelling of the crypt-cell brush border of the Euprymna scolopes light organ. Cell Microbiol. 2016;18:1642-1652 pubmed publisher
    ..The squid-vibrio system exhibits two modifications of the brush border that supports the symbionts: effacement and repolarization...
  76. Zuo H, Gao J, Yuan J, Deng H, Yang L, Weng S, et al. Fatty acid synthase plays a positive role in shrimp immune responses against Vibrio parahaemolyticus infection. Fish Shellfish Immunol. 2017;60:282-288 pubmed publisher
    ..study, the role of the FAS gene from pacific white shrimp Litopenaeus vannamei (LvFAS) in immune responses against Vibrio parahaemolyticus infection was studied. The expression of LvFAS could be up-regulated upon infection of V...
  77. Walker L, Tfaily M, Shaw J, Hess N, Paša Tolić L, Koppenaal D. Unambiguous identification and discovery of bacterial siderophores by direct injection 21 Tesla Fourier transform ion cyclotron resonance mass spectrometry. Metallomics. 2017;9:82-92 pubmed publisher
    ..In this study, the type of siderophores produced by two marine bacterial species, Synechococcus sp. PCC 7002 and Vibrio cyclitrophicus 1F53, were characterized by use of a newly developed 21 T Fourier Transform Ion Cyclotron Resonance ..
  78. Taheri R, Rezayan A, Rahimi F, Mohammadnejad J, Kamali M. Comparison of antibody immobilization strategies in detection of Vibrio cholerae by surface plasmon resonance. Biointerphases. 2016;11:041006 pubmed
    ..using protein G-mediated immobilization and using mixed SAM of alkane thiols on signal strength of detection of Vibrio cholerae using these modified surfaces...
  79. Moonens K, Remaut H. Evolution and structural dynamics of bacterial glycan binding adhesins. Curr Opin Struct Biol. 2017;44:48-58 pubmed publisher
    ..human pathogens like uropathogenic and enteropathogenic Escherichia coli, Helicobacter pylori, Yersinia pestis or Vibrio cholerae...
  80. Garcia Carmona M, Romero Freire A, Sierra Aragón M, Martínez Garzón F, Martín Peinado F. Evaluation of remediation techniques in soils affected by residual contamination with heavy metals and arsenic. J Environ Manage. 2017;191:228-236 pubmed publisher
    ..The effectiveness of these techniques was assessed by toxicity bioassays: Lactuca sativa L. root elongation test, Vibrio fischeri bioluminescence reduction test, soil induced respiration test, and Eisenia andrei survival and metal ..
  81. Liang S, Luo X, You W, Ke C. Hybridization improved bacteria resistance in abalone: Evidence from physiological and molecular responses. Fish Shellfish Immunol. 2018;72:679-689 pubmed publisher
    ..discus hannai ? × H. gigantea ? (DG), H. gigantea ? × H. discus hannai ? (GD) challenged with a mixture of Vibrio harveyi, V. alginolyticus and V. parahaemolyticus (which have been demonstrated to be pathogenic to abalone)...
  82. Hennebert P. Proposal of concentration limits for determining the hazard property HP 14 for waste using ecotoxicological tests. Waste Manag. 2018;74:74-85 pubmed publisher
    ..the culture/dilution medium producing 50% of biological effect relative to the control EC50-30?min of Vibrio fischeri (EN ISO 11348-3) is lower than 15...
  83. Bao M, Huo L, Wu J, Ge D, Lv Z, Chi C, et al. A novel biomarker for marine environmental pollution of CAT from Mytilus coruscus. Mar Pollut Bull. 2018;127:717-725 pubmed publisher
    ..The maximum expression appeared at 8h after pathogenic bacteria injecting, with 15-fold in Vibrio parahemolyticus and 60-fold in Aeromonas hydrophila than that of 0h...
  84. Rezaei M, Karimi F, Shariatifar N, Mohammadpourfard I, Shiri Malekabad E. Antimicrobial Activity of the Essential Oil from the Leaves and Seeds of Coriandrum sativum toward Food-borne Pathogens. West Indian Med J. 2015;65:8-12 pubmed publisher
    ..comprising Escherichia coli, Staphylococcus aureus, Yersinia enterocolitica, Salmonella enterica and Vibrio cholerae were used for the antibacterial tests...
  85. Chakraborty K, Thilakan B, Raola V. Previously Undescribed Antibacterial Polyketides from Heterotrophic Bacillus amyloliquefaciens Associated with Seaweed Padina gymnospora. Appl Biochem Biotechnol. 2018;184:716-732 pubmed publisher
    ..gymnospora exhibited broad spectra of antibacterial activities against pathogenic bacteria Aeromonas hydrophila, Vibrio harveyi, Vibrio vulnificus, and Vibrio parahaemolyticus. The seaweed-associated B...
  86. Martín Rodríguez A, Ticona J, Jiménez I, Flores N, Fernández J, Bazzocchi I. Flavonoids from Piper delineatum modulate quorum-sensing-regulated phenotypes in Vibrio harveyi. Phytochemistry. 2015;117:98-106 pubmed publisher
    ..The compounds were screened for their ability to interfere with QS signaling in the bacterial model Vibrio harveyi...
  87. von Hoven G, Neukirch C, Meyenburg M, Füser S, Petrivna M, Rivas A, et al. eIF2α Confers Cellular Tolerance to S. aureus α-Toxin. Front Immunol. 2015;6:383 pubmed publisher
    ..MEFs was toxin-selective, as wild-type MEFs and eIF2α (S51A/S51A) MEFs exhibited virtually equal sensitivity to Vibrio cholerae cytolysin. Binding of S...
  88. Peng E, Wyckoff E, Mey A, Fisher C, Payne S. Nonredundant Roles of Iron Acquisition Systems in Vibrio cholerae. Infect Immun. 2016;84:511-23 pubmed publisher
    b>Vibrio cholerae, the causative agent of the severe diarrheal disease cholera, thrives in both marine environments and the human host...
  89. Graziano M, Rizzo C, Michaud L, Porporato E, De Domenico E, Spanò N, et al. Biosurfactant production by hydrocarbon-degrading Brevibacterium and Vibrio isolates from the sea pen Pteroeides spinosum (Ellis, 1764). J Basic Microbiol. 2016;56:963-74 pubmed publisher
    ..16S rRNA gene sequencing revealed the affiliation of the most promising isolates to the genera Brevibacterium and Vibrio. Biosurfactant production resulted strongly affected by salinity and temperature conditions, and occurred in the ..
  90. Jang H, Kim Y, Choi S, Lee Y, Shin S, Unno T, et al. Prevalence of antibiotic resistance genes from effluent of coastal aquaculture, South Korea. Environ Pollut. 2018;233:1049-1057 pubmed publisher
    ..Microbial community analysis revealed potential host bacteria for ARGs and intI1. Two genera, Vibrio and Marinomonas belonging to Gammaproteobacteria, showed significant correlation with tetB and tetD, the most ..
  91. Wildschutte H, Preheim S, Hernandez Y, Polz M. O-antigen diversity and lateral transfer of the wbe region among Vibrio splendidus isolates. Environ Microbiol. 2010;12:2977-87 pubmed publisher
    ..While heterogeneous O-antigens are observed within Vibrio species, characterization of these structures has been devoted almost exclusively to pathogens...
  92. Phiwsaiya K, Charoensapsri W, Taengphu S, Dong H, Sangsuriya P, Nguyen G, et al. A natural Vibrio parahaemolyticus PirvpA-B+ mutant kills shrimp but produces no Pirvp toxins or AHPND lesions. Appl Environ Microbiol. 2017;: pubmed publisher
    Acute hepatopancreatic necrosis disease (AHPND) of shrimp is caused by Vibrio parahaemolyticus (VP) isolates that harbor a pVA plasmid encoding toxins PirvpA and PirvpB (VPAHPND)...