Search results for "Fish"

showing 10 items of 3164 documents

Phenotypic and genotypic characterization of a new fish-virulent Vibrio vulnificus serovar that lacks potential to infect humans.

2007

Vibrio vulnificus is a bacterial species that is virulent for humans and fish. Human isolates are classified into biotypes 1 and 3 (BT1 and BT3) and fish isolates into biotype 2 (BT2). However, a few human infections caused by BT2 isolates have been reported worldwide (zoonosis). These BT2 human isolates belong to serovar E (SerE), which is also present in diseased fish. The aim of the present work was to characterize a new BT2 serovar [serovar A (SerA)], which emerged in the European fish-farming industry in 2000, by means of phenotypic, serological and genetic [plasmid profiling, ribotyping and random amplified polymorphic DNA (RAPD)] methodologies. The results confirmed that SerA constit…

SerotypeDNA BacterialLipopolysaccharidesGenotypeVirulenceVibrio vulnificusMicrobiologyRibotypingMicrobiologySerologyRibotypingFish DiseasesMiceGenotypemedicineAnimalsCluster AnalysisHumansSerum Bactericidal TestSerotypingVibrio vulnificusMice Inbred BALB CEelsbiologyVirulenceZoonosisbiology.organism_classificationmedicine.diseaseDNA FingerprintingRAPDRandom Amplified Polymorphic DNA TechniqueDisease Models AnimalPhenotypeVibrio InfectionsPlasmidsMicrobiology (Reading, England)
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The kinetics of antibody production in mucus and serum of European eel (Anguilla anguilla L.) after vaccination against Vibrio vulnificus: developmen…

2003

Abstract Vibrio vulnificus serovar E, a bacterial pathogen for eels cultured in intensive systems, is transmitted through water and enters into new hosts mainly via gills. The main objective of this work was to study the kinetics of antibody production to V. vulnificus in serum and mucus and their relationship with protection after vaccination. To quantify local mucus antibodies, a new ‘in situ’ dot blot immunoassay using image analysis has been developed. This assay was applied to measure antibody production in the skin zone next to the gills. We found that (i) the immune response in mucus was faster (peak at days 3–4) and shorter in duration (titres significantly elevated up to day 5 and …

SerotypeGillanimal structuresImmunoblottingDot blotEnzyme-Linked Immunosorbent AssayVibrio vulnificusAquatic ScienceMicrobiologyFish DiseasesImmune systemImage Processing Computer-AssistedAnimalsEnvironmental ChemistryVibrio vulnificusPathogenSkinbiologyVaccinationGeneral MedicineAnguillabiology.organism_classificationAntibodies BacterialMucusKineticsMucusVibrio InfectionsBacterial Vaccinesbiology.proteinAntibodyFish & Shellfish Immunology
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Microbial and histopathological study of the vibriosis caused by Vibrio vulnificus serovar E in eels: The metalloprotease Vvp is not an essential les…

2008

Vibrio vulnificus biotype 2 serovar E (Bt2-serE) is a zoonotic pathogen that causes a haemorrhagic septicaemia in eels, called warm water vibriosis. The main objective of the present work was to study the onset of the eel vibriosis from the microbiological and histopathological viewpoint, as well as to ascertain the role of the protease Vvp as a lesional factor by comparing the histopathological lesions caused by the wild strain and its vvp deficient derivative. The wild-type strain was observed to attach to the gills, where it multiplied following saturation dynamics, subsequently invading the blood stream and reaching the internal organs. Here it reached population sizes that are notably …

SerotypeGilleducation.field_of_studyEelsHistologyPopulationMetalloendopeptidasesVirulenceVibrio vulnificusBiologyKidneybiology.organism_classificationMicrobiologyMicrobiologyFish DiseasesInfectious DiseasesBacterial ProteinsVibrionaceaeVibrio InfectionsExtracellularAnimalseducationVibrio vulnificusCells CulturedBacteriaMicrobial Pathogenesis
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Comparative study of biological properties and electrophoretic characteristics of lipopolysaccharide from eel-virulent and eel-A virulent Vibrio vuln…

1999

ABSTRACT In Vibrio vulnificus , virulence for eels is associated with serovar E strains. In this study, we investigated some biological properties of purified lipopolysaccharides (LPSs) from serovar E and non-serovar E strains. Purified LPSs retained their O-polysaccharidic side chains and did not show any differences that could be related to host specificity, except for serological differences.

SerotypeLipopolysaccharidesErythrocytesLipopolysaccharideVirulenceVibrio vulnificusApplied Microbiology and BiotechnologyHemolysisMicrobiologychemistry.chemical_compoundFish DiseasesMiceVibrionaceaeVibrio InfectionsAnimalsVibrioEelsEcologybiologyVirulenceO Antigensbiology.organism_classificationVibrioRatscarbohydrates (lipids)Environmental and Public Health MicrobiologychemistryVibrio Infectionslipids (amino acids peptides and proteins)BacteriaFood ScienceBiotechnologyApplied and environmental microbiology
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First description of non-motile Yersinia ruckeri serovar I strains causing disease in rainbow trout, Oncorhynchus mykiss (Walbaum), cultured in Spain.

2006

Yersinia ruckeri, the causal agent of enteric redmouth (ERM) disease, was isolated from epizootics that occurred in different Spanish rainbow trout, Oncorhynchus mykiss (Walbaum), farms in which vaccination against ERM had been performed. In all episodes, the most pronounced clinical signs exhibited by affected fish were severe haemorrhages in the mouth, eyes and around the vent. The isolates were identified as Y. ruckeri serovar I by 16S rRNA sequencing together with serological tests. They lacked motility and lipase activity and thus belonged to biotype 2, and were highly virulent for juvenile rainbow trout, both by intraperitoneal injection (from 3.1 x 10(2) to 6.3 x 10(3) cfu per fish) …

SerotypeLipopolysaccharidesYersinia InfectionsVeterinary (miscellaneous)FisheriesVirulenceAquatic ScienceCommunicable Diseases EmergingPolymerase Chain ReactionMicrobiologyFish DiseasesAquacultureAgglutination TestsRNA Ribosomal 16SAnimalsSerologic TestsPathogenDNA PrimersbiologyVirulencebusiness.industryEnteric redmouth diseaseO Antigensbiology.organism_classificationAntibodies BacterialYersiniaTroutSpainOncorhynchus mykissRainbow troutYersinia ruckeribusinessJournal of fish diseases
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Effectiveness of different vaccine formulations against vibriosis caused by Vibrio vulnificus serovar E (biotype 2) in European eels Anguilla anguilla

2001

Vibriosis due to Vibrio vulnificus serovar E (biotype 2) is one of the main causes of mortality in European eels cultured in Europe. The main objective of this study was to develop a vaccine and a vaccination procedure against this pathogen. With this aim, we tested several vaccine formulations (inactivated whole-cells with and without toxoids‹inactivated extracellular products‹from capsulated and uncapsulated strains, attenuated live vaccines and purified lipopolysaccharide [LPS]) on eels maintained under controlled laboratory conditions using different delivery routes (injection and immersion). To study the immune response we estimated antibody titers and bactericidal/bacteriostatic activ…

SerotypeQuality ControlVibrio vulnificus serovar E ; Vibrio vulnificus biotype 2 ; Eel vaccines ; Vibrio vaccines ; Vaccination by injection ; Vaccination by prolonged immersionImmunization SecondaryVibrio vulnificus biotype 2Eel vaccinesVibrio vulnificusAquacultureAquatic ScienceBiologyAntibodies Viral:CIENCIAS DE LA VIDA [UNESCO]MicrobiologyFish DiseasesVaccination by injectionAntigenVibrionaceaeImmunityAntibody SpecificityUNESCO::CIENCIAS DE LA VIDAAnimalsUNESCO::CIENCIAS DE LA VIDA::Biología animal (Zoología)Vibrio vaccinesPathogenEcology Evolution Behavior and SystematicsVaccination by prolonged immersionSkinVibrio:CIENCIAS DE LA VIDA::Biología animal (Zoología) [UNESCO]VaccinationAntibody titerbiology.organism_classificationAnguillaVirologyVaccinationEuropeVibrio vulnificus serovar EVibrio InfectionsBacterial Vaccines
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An indirect immunofluorescent antibody technique for detection and enumeration of Vibrio vulnificus serovar E (biotype 2): delevopment and applicatio…

2000

The applications of an indirect fluorescent antibody technique (IFAT), developed to detect and enumerate the pathogenic bacterium Vibrio vulnificus serovar E from water and clinical samples, are described. This technique proved accurate for detecting V. vulnificus, even under starvation conditions and in the non-culturable state, and could differentiate this species from other bacteria which share the same habitats. The IFAT was successfully used to diagnose vibriosis from naturally- and artificially-infected eels. The overall data suggest that applying this technique properly in environmental and epidemiological/epizootiological studies could significantly increase our knowledge of this ba…

SerotypeVibrio vulnificusImmunofluorescenceSensitivity and SpecificityApplied Microbiology and BiotechnologyMicrobiologyFish DiseasesVibrionaceaeVibrio InfectionsEnumerationmedicineAnimalsSeawaterFluorescent Antibody Technique IndirectVibrioEelsbiologymedicine.diagnostic_testfungiGeneral Medicinebacterial infections and mycosesbiology.organism_classificationAntibodies BacterialVibrioVibrio InfectionsWater MicrobiologyBacteriaBiotechnologyJournal of Applied Microbiology
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Protocol for Specific Isolation of Virulent Strains of Vibrio vulnificus Serovar E (Biotype 2) from Environmental Samples

2004

ABSTRACT The eel pathogen Vibrio vulnificus biotype 2 comprises at least three serovars, with serovar E being the only one involved in both epizootics of eel vibriosis and sporadic cases of human infections. The virulent strains of this serovar (VSE) have only been recovered from clinical (mainly eel tissue) sources. The main objective of this work was to design and validate a new protocol for VSE-specific isolation from environmental samples. The key element of the new protocol is the broth used for the first step (saline eel serum broth [SEB]), which contains eel serum as a nutritive and selective component. This approach takes advantage of the ability of VSE cells to grow in eel serum an…

Serotypeanimal structuresPlating efficiencyfood.ingredientVirulenceFresh WaterPublic Health MicrobiologyVibrio vulnificusApplied Microbiology and BiotechnologyMicrobiologyFish DiseasesMicefoodVibrionaceaeAnimalsHumansAgarSeawaterSerotypingVibrio vulnificusPathogenBacteriological TechniquesMice Inbred BALB CEelsVirulenceEcologybiologybiology.organism_classificationCulture MediaVibrio InfectionsWater MicrobiologyBacteriaFood ScienceBiotechnologyApplied and Environmental Microbiology
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Efficacy of a bivalent vaccine against eel diseases caused by Vibrio vulnificus after its administration by four different routes

2003

Vulnivaccine, a vaccine against vibriosis caused by Vibrio vulnificus serovar E (formerly biotype 2), confers acceptable levels of protection to eels after its administration by prolonged immersion in three doses. Recently, a new pathogenic serovar, named serovar A, has been isolated from vaccinated eels in a Spanish freshwater eel farm. The main objective of this work was to design a bivalent vaccine, and to study its effectiveness against the two pathogenic serovars. With this aim, eels weighing around 20 g were immunised with the bivalent vaccine by oral and anal intubation, intraperitoneal injection (i.p.) and prolonged immersion. The overall results indicated that: (i) the new vaccine …

Serotypeanimal structuresmedicine.medical_treatmentIntraperitoneal injectionVibrio vulnificusAquatic ScienceMicrobiologyFish DiseasesImmune systemImmersionmedicineAnimalsEnvironmental ChemistryIntubation GastrointestinalVibrio vulnificusbiologyGeneral MedicineAnguillabiology.organism_classificationAntibodies BacterialMucusVirologyVaccinationKineticsSpainVibrio InfectionsBacterial VaccinesHumoral immunitybiology.proteinAntibodyInjections IntraperitonealFish & Shellfish Immunology
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Field testing of a vaccine against eel diseases caused by Vibrio vulnificus

2001

The field results of a vaccination programme against Vibrio vulnificus serovar E (biotype 2) in a Spanish eel farm are reported. A total of 9.5 million glass eels were vaccinated from January 1998 to March 2000 by prolonged immersion followed by 2 subsequent reimmunisations after 12 to 14 and 24 to 28 d, respectively. The acquired protection and the immune response against serovar E were estimated over a period of 6 mo after vaccination. A similar vaccination schedule was conducted with elvers in a Danish eel farm. In this case, the acquired protection and the immune response against serovar E and the new eel-pathogenic serovars, recently described in Denmark, were evaluated over a short te…

Serotypeendocrine systemTime Factorsanimal structuresVaccination scheduleField vaccination. vibriosisVibrio vulnificus biotype 2Eel vaccinesVibrio vulnificusAquatic Science:CIENCIAS DE LA VIDA [UNESCO]MicrobiologyFish DiseasesImmune systemVibrionaceaeAnguillidaeUNESCO::CIENCIAS DE LA VIDAAnimalsUNESCO::CIENCIAS DE LA VIDA::Biología animal (Zoología)Vibrio vaccinesEcology Evolution Behavior and SystematicsVaccination by prolonged immersionVibrioEels:CIENCIAS DE LA VIDA::Biología animal (Zoología) [UNESCO]biologyVibrio vulnificus serovar E ; Vibrio vulnificus biotype 2 ; Eel vaccines ; Vibrio vaccines ; Vaccination by prolonged immersion ; Field vaccination. vibriosisBody WeightVaccinationbiology.organism_classificationAntibodies BacterialVaccinationVibrio vulnificus serovar EVibrio InfectionsHumoral immunityBacterial Vaccines
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