Search results for "virulence"

showing 10 items of 457 documents

Virulence and Molecular Typing of Vibrio harveyi Strains Isolated from Cultured Dentex, Gilthead Sea Bream and European Sea Bass

2003

Vibrio harveyi was isolated from internal organs or ulcers of diseased and apparently healthy gilthead sea bream (Sparus aurata) and European sea bass (Dicentrarchus labrax) cultured in several fish farms located on the Spanish Mediterranean coast. The prevalence of the bacterium was significantly higher in European sea bass than in gilthead sea bream, and was closely related to the season in both fish species, occurring almost exclusively on warm months (June to November). After phenotypic characterization, a selection of forty five isolates from gilthead sea bream, sea bass, and several isolates previously obtained from common dentex (Dentex dentex) of the same area, were molecularly type…

DNA BacterialFish farmingFisheriesVirulenceZoologyMediterranean aquacultureRibotypingApplied Microbiology and BiotechnologyMicrobiologyFish DiseasesRibotypingRAPDSparus aurataAnimalsDicentrarchus labraxSea bassFish pathogensEcology Evolution Behavior and SystematicsVibrioVirulencebiologyVibrio harveyiLD50Dentex dentexbiology.organism_classificationVibrio harveyiSea BreamBacterial Typing TechniquesPerciformesRandom Amplified Polymorphic DNA TechniqueRAPDFisheryPhenotypeVibrio InfectionsCarrier StateBassDicentrarchussense organsDentex dentexSystematic and Applied Microbiology
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pilF polymorphism-based PCR to distinguish Vibrio vulnificus strains potentially dangerous to public health

2010

ABSTRACT Vibrio vulnificus is a heterogeneous species that comprises strains virulent and avirulent for humans and fish, and it is grouped into three biotypes. In this report, we describe a PCR-based methodology that allows both the species identification and discrimination of those isolates that could be considered dangerous to public health. Discrimination is based on the amplification of a variable region located within the gene pilF , which seems to be associated with potential human pathogenicity, regardless of the biotype of the strain.

DNA BacterialMalemedicine.medical_specialtyVirulence FactorsMolecular Sequence DataVirulenceMicrobiologiaPublic Health MicrobiologyVibrio vulnificusBiologyPolymerase Chain ReactionApplied Microbiology and Biotechnologylaw.inventionMicrobiologyMiceBacterial ProteinslawVibrionaceaeVibrio InfectionsmedicineAnimalsHumansVibrio vulnificusGenePolymerase chain reactionGeneticsBacteriological TechniquesMice Inbred BALB CPolymorphism GeneticBase SequenceVirulenceEcologyPublic healthFishesSequence Analysis DNAbiology.organism_classificationPathogenicityVibrio InfectionsFimbriae ProteinsSequence AlignmentFood ScienceBiotechnology
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Identification of a clone of Escherichia coli O103:H2 as a potential agent of hemolytic-uremic syndrome in France

1993

In a French multicenter study, six verocytotoxin-producing Escherichia coli strains were isolated from the stools of 6 of 69 children suffering from hemolytic-uremic syndrome. All strains belonged to serotype O103:H2, a serotype commonly associated with diarrhea in weaned rabbits in France. To determine whether the strains from humans and rabbits were genetically related, they were compared by analyzing their esterase electropherotypes and the restriction fragment length polymorphisms of the ribosomal DNA regions. A common clonal origin of these pathogenic strains was suggested by their identical esterase electropherotypes and their identical ribotypes, in addition to their identical seroty…

DNA BacterialMicrobiology (medical)SerotypeBacterial ToxinsMolecular Sequence DataClone (cell biology)VirulenceVerocytotoxinShiga Toxin 1medicine.disease_causePolymerase Chain Reactionlaw.inventionMicrobiology03 medical and health scienceschemistry.chemical_compoundlawEscherichia colimedicineHumansSerotyping[SDV.MP] Life Sciences [q-bio]/Microbiology and ParasitologyEscherichia coliEscherichia coli InfectionsComputingMilieux_MISCELLANEOUSPolymerase chain reaction030304 developmental biology0303 health sciencesBase SequenceVirulencebiology030306 microbiologyInfantCorrectionbiology.organism_classificationEnterobacteriaceae3. Good healthBacterial adhesinPOUVOIR PATHOGENE[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologychemistryChild PreschoolHemolytic-Uremic SyndromeFranceResearch ArticleJournal of Clinical Microbiology
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Comparative genomics and proteomics of Helicobacter mustelae, an ulcerogenic and carcinogenic gastric pathogen

2010

Abstract Background Helicobacter mustelae causes gastritis, ulcers and gastric cancer in ferrets and other mustelids. H. mustelae remains the only helicobacter other than H. pylori that causes gastric ulceration and cancer in its natural host. To improve understanding of H. mustelae pathogenesis, and the ulcerogenic and carcinogenic potential of helicobacters in general, we sequenced the H. mustelae genome, and identified 425 expressed proteins in the envelope and cytosolic proteome. Results The H. mustelae genome lacks orthologs of major H. pylori virulence factors including CagA, VacA, BabA, SabA and OipA. However, it encodes ten autotransporter surface proteins, seven of which were detec…

DNA BacterialProteomicslcsh:QH426-470Proteomelcsh:BiotechnologyMolecular Sequence DataVirulenceCarcinogenicHelicobacter mustelaeProteomicsFN555004MicrobiologyUlcerogenic03 medical and health sciencesBacterial ProteinsHelicobacterlcsh:TP248.13-248.65medicineGeneticsCagAHelicobacterAmino Acid SequencePhylogeny030304 developmental biology0303 health sciencesComparative Genomic HybridizationbiologyHelicobacter pyloriVirulence030306 microbiologyCancerGene Expression Regulation BacterialGenomicsSequence Analysis DNAHelicobacter pylorimedicine.diseasebiology.organism_classificationdigestive system diseases3. Good healthlcsh:GeneticsProteomeGastritismedicine.symptomSequence AlignmentH. pyloriGenome BacterialBiotechnologyResearch ArticleBMC Genomics
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R plasmids in environmental Vibrio cholerae non-O1 strains.

1988

The occurrence of drug resistance and its plasmid-mediated transferability was investigated in 140 environmental strains of Vibrio cholerae non-O1 and 6 strains of Vibrio cholerae, both O1 and non-O1, of clinical origin. Of the 146 strains tested, 93% were resistant to at least one drug and 74% were resistant to two or more antibiotics. The O1 strains were susceptible to all antibiotics used. A total of 26 of 28 selected resistant wild strains carried R plasmids that were transferable by intraspecific and intergeneric matings. The most common transmissible R factor determined resistance to ampicillin, amoxicillin, and sulfanilamide (30%), followed by resistance to ampicillin and amoxicillin…

DNA BacterialR FactorsFresh WaterDrug resistancemedicine.disease_causeApplied Microbiology and BiotechnologyMicrobiologyPlasmidVibrio cholerae non-O1VibrionaceaeAmpicillinmedicineSeawaterVibrio choleraeElectrophoresis Agar GelEcologybiologyVirulenceGenetic transferDrug Resistance MicrobialSulfanilamidebiology.organism_classificationAnti-Bacterial AgentsVibrio choleraeConjugation GeneticWater MicrobiologyFood ScienceBiotechnologymedicine.drugResearch Article
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Molecular relationship among Salmonella dublin isolates identified at the Center for Enterobacteriaceae of Palermo during the years 1971-85.

1987

SUMMARYA molecular epidemiological study was carried out on 60Salmonella dublinisolates identified at the Southern Italy Enterobacteriaceae Center between 1971 and 1985. These included 23 isolates from children with diarrhoea in Palermo obtained during 1984.All isolates from the outbreak of gastroenteritis in children were resistant to chloramphenicol and streptomycin and harboured two plasmids of 50 MDa and 3 MDa molecular weight, whereas the majority of the isolates identified before 1984 were susceptible to these antibiotics and carried only a 50 MDa molecular weight plasmid. FourS. dublinstrains successively identified from cattle (Palermo, Foggia, Portici) and from a child (Palermo) we…

DNA BacterialSalmonellaEpidemiologyVirulenceChloramphenicol ResistanceBiologymedicine.disease_causeMicrobiologyDisease OutbreaksMicePlasmidAntibiotic resistanceAmp resistanceSalmonellamedicineAnimalsHumansChildMice Inbred BALB CSalmonella Infections AnimalMolecular epidemiologyVirulenceTetracycline ResistanceOutbreakDrug Resistance MicrobialVirologyGastroenteritisInfectious DiseasesItalyStreptomycinMetalsSalmonella InfectionsStreptomycinCattleFemaleAmpicillin Resistancemedicine.drugPlasmidsResearch ArticleEpidemiology and infection
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Definition of the single integration site of the pathogenicity locus in Clostridium difficile.

1996

We determined the nucleotide sequence 3.8 kb upstream and 5.2 kb downstream of the toxin genes A and B of Clostridium difficile. Nine ORFs were discovered. Based on PCR-directed approaches, two were attributed to the pathogenicity locus (PaLoc). The other seven were found in every C. difficile isolate obtained from the human gastrointestinal tract, respectless of their toxinogenicity. The ORFs cdu1 and cdu2/2' upstream of the PaLoc displayed similarity to repressors of Gram-positive bacteria (cdu1), and to an Na+/H+ antiporter described for Enterococcus hirae (cdu2/2'). Downstream of the locus a putative ABC transporter (cdd2-4) was identified. With a set of three paired primers used in pol…

DNA BacterialSequence analysisBacterial ToxinsMolecular Sequence DataVirulenceLocus (genetics)BiologyEnterotoxinsOpen Reading FramesBacterial ProteinsSpecies SpecificityGeneticsHumansAmino Acid SequenceORFSGeneGeneticsBase SequenceSequence Homology Amino AcidVirulenceClostridioides difficileNucleic acid sequenceGeneral MedicineMolecular biologyIntestinesTerminator (genetics)DNA Transposable ElementsATP-Binding Cassette TransportersMobile genetic elementsGene
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pilF polymorphism-based real-time PCR to distinguish Vibrio vulnificus strains of human health relevance

2012

The Gram-negative bacterium Vibrio vulnificus is a common inhabitant of estuarine environments. Globally, V. vulnificus is a significant foodborne pathogen capable of causing necrotizing wound infections and primary septicemia, and is a leading cause of seafood-related mortality. Unfortunately, molecular methods for the detection and enumeration of pathogenic V. vulnificus are hampered by the genetically diverse nature of this pathogen, the range of different biotypes capable of infecting humans and aquatic animals, and the fact that V. vulnificus contains pathogenic as well as non-pathogenic variants. Here we report an alternative approach utilizing the development of a real-time PCR assay…

DNA BacterialSequence analysisMolecular Sequence DataColony Count MicrobialVirulenceMicrobiologiaFood ContaminationVibrio vulnificusReal-Time Polymerase Chain ReactionMicrobiologyBacterial geneticsMicrobiologyBacterial ProteinsGenePathogenVibrio vulnificusPolymorphism GeneticbiologyBase SequenceVirulenceintegumentary systemfungiSequence Analysis DNAbiology.organism_classificationbacterial infections and mycosesVirologyReal-time polymerase chain reactionSeafoodFood MicrobiologybacteriaBacteriaFood Science
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Transcription analysis of the genes tcdA-E of the pathogenicity locus of Clostridium difficile.

1997

To analyse the transcription pattern of the five tcdA-E genes of the pathogenicity locus (PaLoc) of Clostridium difficile a protocol was established to purify RNA from strain VPI10463. Transcription analysis of the five tcdA-E genes showed that they were all transcribed. In the early exponential phase, a high level of tcdC and low levels of tcdA,B,D,E transcripts were detectable; this was inverted in the stationary phase, suggesting that TcdC might have a negative influence on transcription of the other genes. Three transcription initiation sites, one for tcdA and two for tcdB were determined by primer extension analysis. Readthrough transcripts from outside the locus were not obtainable, s…

DNA BacterialTranscription GeneticBacterial ToxinsMolecular Sequence DataLocus (genetics)Helix-turn-helixBiologymedicine.disease_causeBiochemistryPolymerase Chain ReactionPrimer extensionchemistry.chemical_compoundEnterotoxinsBacterial ProteinsTranscription (biology)medicineAmino Acid SequencePromoter Regions GeneticGeneDNA PrimersRegulation of gene expressionGeneticsBase SequenceSequence Homology Amino AcidVirulenceClostridioides difficileClostridium perfringensMolecular biologyDNA-Binding ProteinsRepressor ProteinschemistryGenes BacterialDNAEuropean journal of biochemistry
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Pseudomonas corrugata crpCDE is part of the cyclic lipopeptide corpeptin biosynthetic gene cluster and is involved in bacterial virulence in tomato a…

2014

Summary: Pseudomonas corrugataCFBP 5454 produces two kinds of cyclic lipopeptides (CLPs), cormycin A and corpeptins, both of which possess surfactant, antimicrobial and phytotoxic activities. In this study, we identified genes coding for a putative non-ribosomal peptide synthetase and an ABC-type transport system involved in corpeptin production. These genes belong to the same transcriptional unit, designated crpCDE. The genetic organization of this locus is highly similar to other PseudomonasCLP biosynthetic clusters. Matrix-assisted laser desorption ionization-time of flight-mass spectrometry (MALDI-TOF-MS) analysis revealed that transporter and synthetase genomic knock-out mutants were u…

DNA BacteriallipodepsipeptidesABC transporters corpeptins Lux R transcriptional regulators non-ribosomal peptide synthetase Pseudomonas.chromobacterium-violaceumcloningPeptides CyclicLipopeptidesSolanum lycopersicumPseudomonasABC transporters Lux R transcriptional regulators non-ribosomal peptide synthetaseTobaccoPeptide SynthasesLux R transcriptional regulatorsnon-ribosomal peptide synthetasePhylogenyVLAGPlant DiseasesCell-Free SystemVirulenceputisolvin-iisyringae pv.-syringaeSettore AGR/12 - Patologia VegetaleOriginal Articlesgram-negative bacteriapeptideBiosynthetic PathwayssyringomycinRepressor ProteinssyringopeptinFood Quality and DesignABC transportersGenesGenes BacterialMultigene FamilyHost-Pathogen InteractionsMutationTrans-ActivatorsATP-Binding Cassette Transportersquorum-sensing system
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