Search results for "VIRULENCE FACTORS"

showing 10 items of 67 documents

The Fish Pathogen Vibrio vulnificus Biotype 2: Epidemiology, Phylogeny, and Virulence Factors Involved in Warm-Water Vibriosis

2015

ABSTRACT Vibrio vulnificus biotype 2 is the etiological agent of warm-water vibriosis, a disease that affects eels and other teleosts, especially in fish farms. Biotype 2 is polyphyletic and probably emerged from aquatic bacteria by acquisition of a transferable virulence plasmid that encodes resistance to innate immunity of eels and other teleosts. Interestingly, biotype 2 comprises a zoonotic clonal complex designated as serovar E that has extended worldwide. One of the most interesting virulence factors produced by serovar E is RtxA1 3 , a multifunctional protein that acts as a lethal factor for fish, an invasion factor for mice, and a survival factor outside the host. Two practically id…

Microbiology (medical)Gene Transfer HorizontalVirulence FactorsPhysiologyFish farmingBacterial ToxinsVirulenceVibrio vulnificusMicrobiologyFish DiseasesMicePlasmidReceptors TransferrinGeneticsAnimalsHumansVibrio vulnificusGenePathogenPhylogenyEelsGeneral Immunology and MicrobiologyEcologybiologyCell Biologybiology.organism_classificationImmunity InnateInfectious DiseasesVibrio InfectionsHorizontal gene transferWater MicrobiologyBacterial outer membranePlasmidsMicrobiology Spectrum
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Characterization of Listeria monocytogenes isolates from human listeriosis cases in Italy.

2009

ABSTRACT The objective of this study was to characterize by serotyping, pulsed-field gel electrophoresis (PFGE), and PCR amplification of virulence genes and markers of epidemic clones I, II, and III (ECI, ECII, and ECIII) 54 human isolates from apparently sporadic cases of infection occurring in the Lombardy region and in the province of Florence, Tuscany, Italy, in the years 1996 to 2007. Listeria monocytogenes isolates were provided by the clinical microbiology laboratories of the Lombardy region and the “Careggi” Hospital of Florence, Tuscany, Italy. Serotyping, PFGE after digestion with the AscI and ApaI enzymes, and PCR amplification for the inlA , inlC , and inlJ genes and ECI, ECII,…

Microbiology (medical)SerotypeGenotypeVirulence FactorsEpidemiologyepidemic clonesBiologySettore MED/42 - Igiene Generale E Applicatamedicine.disease_causePolymerase Chain Reactionlaw.inventionMicrobiologyListeria monocytogeneslawPregnancyGenotypehuman casemedicinePulsed-field gel electrophoresisCluster AnalysisHumansListeriosisSerotypingPolymerase chain reactionListeria monocytogeneAgedMolecular EpidemiologyMolecular epidemiologyInfant NewbornPFGEVirologyDNA FingerprintingListeria monocytogenesSubtypingBacterial Typing TechniquesElectrophoresis Gel Pulsed-FieldDNA profilingItalyFemaleJournal of clinical microbiology
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Resistance to clarithromycin and genotypes in Helicobacter pylori strains isolated in Sicily

2015

The resistance of Helicobacter pylori strains to clarithromycin is increasing in several developed countries and their association with a genetic pattern circulation has been variously explained as related to different geographical areas. In this study we have reported: the prevalence of the resistance of H. pylori, isolated in Sicily, to clarithromycin; the principal point of mutation associated with this resistance; and the more frequent association between resistance to clarithromycin and cagA, the EPIYA motif, and the vacA and oipA genes. Resistance to clarithromycin was detected in 25 % of cases, the main genetic mutation involved being A2143G. The cagA gene was present in 48 % of case…

Microbiology (medical)Settore MED/07 - Microbiologia E Microbiologia ClinicaVirulence FactorsMolecular Sequence Datamedicine.disease_causeMicrobiologyMicrobiology (medical); MicrobiologyMicrobiologyHelicobacter InfectionsBacterial ProteinsClarithromycinClarithromycinGenotypeDrug Resistance BacterialmedicinePrevalenceCagAHumansAlleleGeneSicilyMutationbiologyHelicobacter pyloriPrincipal pointGeneral MedicineHelicobacter pyloribacterial infections and mycosesbiology.organism_classificationVirologyAnti-Bacterial Agentsmedicine.drug
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Staphylococcus aureus α-Toxin’s Close Contacts Ensure the Kill

2018

The membrane pore-forming α-toxin is an important virulence factor of Staphylococcus aureus. Target cells can remove pores from their surface, but recent work shows that α-toxin may undermine this self-defense by clinging to epithelial cell junctions. The findings could lead to the development of novel remedies against S. aureus infections.

Microbiology (medical)Staphylococcus aureusVirulence FactorsBacterial ToxinsBiologymedicine.disease_causeMicrobiologyVirulence factorCell LineMicrobiologyAdherens junctionADAM10 ProteinHemolysin Proteins03 medical and health sciencesVirologymedicineAnimalsHumans030304 developmental biology0303 health sciencesPore-forming toxin030306 microbiologyMembrane ProteinsEpithelial CellsAdherens JunctionsStaphylococcal InfectionsEpitheliumInfectious Diseasesmedicine.anatomical_structureStaphylococcus aureusPinocytosisCarrier ProteinsTrends in Microbiology
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Comparing the different morphotypes of a fish pathogen - implications for key virulence factors in Flavobacterium columnare

2014

Background: Flavobacterium columnare (Bacteroidetes) is the causative agent of columnaris disease in farmed freshwater fish around the world. The bacterium forms three colony morphotypes (Rhizoid, Rough and Soft), but the differences of the morphotypes are poorly known. We studied the virulence of the morphotypes produced by F. columnare strain B067 in rainbow trout ( Onconrhynchus mykiss ) and used high-resolution scanning electron microscopy to identify the fine structures of the cells grown in liquid and on agar. We also analysed the proteins secreted extracellularly and in membrane vesicles to identify possible virulence factors. Results: Only the Rhizoid morphotype was virulent in rain…

Microbiology (medical)Virulence FactorsGliding motilityVirulenceFlavobacteriumMicrobiologyBacterial AdhesionVirulence factorMicrobiologyFish Diseases03 medical and health sciencesBacterial ProteinsFlavobacteriaceae InfectionsAnimals14. Life underwaterPathogen030304 developmental biologydisease0303 health sciencesVirulencebiology030306 microbiologySecretory VesiclesBiofilmbacteriumbiology.organism_classificationRhizoidfreshwater fishOncorhynchus mykissFlavobacterium columnareMicroscopy Electron ScanningLocomotionFlavobacteriumResearch ArticleBMC Microbiology
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Crystal structure of the N-terminal domain of the major virulence factor BB0323 from the Lyme disease agent Borrelia burgdorferi.

2019

Lyme disease is an infection caused by the spirochete Borrelia burgdorferi after it is transmitted to a mammalian organism during a tick blood meal. B. burgdorferi encodes at least 140 lipoproteins located on the outer or inner membrane, thus facing the surroundings or the periplasmic space, respectively. However, most of the predicted lipoproteins are of unknown function, and only a few proteins are known to be essential for the persistence and virulence of the pathogen. One such protein is the periplasmic BB0323, which is indispensable for B. burgdorferi to cause Lyme disease and the function of which is associated with cell fission and outer membrane integrity. After expression and trans…

Models MolecularLyme DiseaseVirulence FactorsLipoproteinsVirulencePeriplasmic spaceBiologybiology.organism_classificationVirulence factorCell biologyBacterial ProteinsStructural BiologyBorrelia burgdorferiInner membraneSpectrinAmino Acid SequenceBorrelia burgdorferiBacterial outer membranePathogenActa crystallographica. Section D, Structural biology
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The structure of Yersinia pestis Caf1 polymer in free and adjuvant bound states

2010

Caf1 of the plague bacterium, Yersinia pestis is a polymeric virulence factor and vaccine component, formed from monomers by a donor strand exchange (DSE) mechanism. Here, EM images of Caf1 reveal flexible polymers up to 1.5 microm long (4MDa). The bead-like structures along the polymer are 5.8 + or - 1 nm long and correspond to single Caf1 proteins. Short polymers often form circles, presumably by DSE. We also provide the first images of proteins bound to alhydrogel adjuvant. Caf1, hemocyanin and anthrax PA are all resolved clearly and Caf1 exhibits adjuvant bound stretches with long intervening loops draped from the edges.

Models MolecularProtein FoldingPolymersVirulence FactorsYersinia pestismedicine.medical_treatmentVirulence factorMicrobiologychemistry.chemical_compoundProtein structureAdjuvants ImmunologicBacterial ProteinsMicroscopy Electron TransmissionmedicineProtein Structure QuaternaryBacterial Capsuleschemistry.chemical_classificationAntigens BacterialPlaguePlague VaccineGeneral VeterinaryGeneral Immunology and MicrobiologybiologyPublic Health Environmental and Occupational HealthHemocyaninPolymerbiology.organism_classificationInfectious DiseasesMonomerYersinia pestischemistryBiophysicsMolecular MedicinePlague vaccineProtein foldingVaccine
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Tools for Pathogen Proteomics: Fishing with Biomimetic Nanosponges

2017

The identification of the major virulence factors that drive pathogenicity is critical for gaining insight into the underlying molecular mechanisms of diseases. Although genetic approaches combined with functional analyses have markedly increased the rate of virulence factor discovery, the divergence between genome and proteome can impair the identification of important markers, in particular, of those that act in concert or depend on specific environmental factors. Recently, membrane-coated nanomaterials mimicking source cells of interest have emerged as powerful tools that can be used for improved tumor targeting and as "nanotraps" to capture chemokines and bacterial toxins. In this issue…

Proteomics0301 basic medicineProteomeVirulence FactorsBacterial ToxinsQuantitative proteomicsGeneral EngineeringGeneral Physics and AstronomyVirulenceComputational biologyBiologyProteomicsBioinformaticsGenomeVirulence factor03 medical and health sciences030104 developmental biologyBiomimeticsProteomeGeneral Materials ScienceIdentification (biology)PathogenACS Nano
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N-acyl-homoserine-lactone quorum sensing in tomato phytopathogenic Pseudomonas spp. is involved in the regulation of lipodepsipeptide production

2012

Pseudomonas corrugata and Pseudomonas mediterranea are two closely related phytopathogenic bacteria both causal agents of tomato pith necrosis. P. corrugata produces phytotoxic and antimicrobial cationic lipodepsipeptides (LDPs) which are thought to act as major virulence factors. Previous studies have demonstrated that P. corrugata CFBP 5454 has an N-acyl homoserine lactone (AHL) quorum sensing (QS) system PcoI/PcoR and that LDP production occurs at high population densities. No molecular studies on virulence have thus far been reported for P. mediterranea. In this study, we show that P. mediterranea also produces LDPs as well as possessing an AHL-dependent QS system, designated PmeI/PmeR,…

Pseudomonas mediterraneaVirulence FactorsLipoproteinsPlant DiseaseHomoserineVirulenceBioengineeringBiologyAcyl-ButyrolactonesPseudomonaAcyl-ButyrolactoneApplied Microbiology and BiotechnologyTomatoMicrobiologychemistry.chemical_compoundSolanum lycopersicumVirulence FactorDepsipeptidesPseudomonasLycopersicon esculentumLipoproteinPromoter Regions GeneticDepsipeptidePlant DiseasesAntimicrobial Cationic PeptideVirulencePseudomonasGeneral MedicineLipodepsipeptidesbiology.organism_classificationPseudomonas corrugataQuorum sensingPseudomonas corrugataQuorum sensingN-Acyl homoserine lactonePhenotypechemistryPseudomonas mediterranea; Pseudomonas corrugata; Quorum sensing; Lipodepsipeptides; Virulence; TomatoMutationLipodepsipeptidePseudomonas mediterraneaBacteriaBiotechnologyAntimicrobial Cationic PeptidesJournal of Biotechnology
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Salmonella bongori Provides Insights into the Evolution of the Salmonellae

2011

The genus Salmonella contains two species, S. bongori and S. enterica. Compared to the well-studied S. enterica there is a marked lack of information regarding the genetic makeup and diversity of S. bongori. S. bongori has been found predominantly associated with cold-blooded animals, but it can infect humans. To define the phylogeny of this species, and compare it to S. enterica, we have sequenced 28 isolates representing most of the known diversity of S. bongori. This cross-species analysis allowed us to confidently differentiate ancestral functions from those acquired following speciation, which include both metabolic and virulence-associated capacities. We show that, although S. bongori…

Salmonellamedicine.disease_causeSettore MED/42 - Igiene Generale E ApplicataTranslocation GeneticEnteropathogenic Escherichia coli1108 Medical MicrobiologySalmonellaCOMPLETE GENOME SEQUENCEIII SECRETION SYSTEMBiology (General)PATHOGENICITY ISLAND 2PhylogenyGenetics0303 health sciencesbiologyVirulenceEffectorPARASITOLOGYENTERICA SEROVAR TYPHIMURIUMSalmonella entericaGenomicsSalmonella bongori evolutionary genomicsBiological EvolutionUREIDOGLYCOLLATE LYASEInfectious DiseasesSalmonella enterica1107 ImmunologyQR180MedicineKLEBSIELLA-PNEUMONIAELife Sciences & BiomedicineResearch Article0605 MicrobiologySalmonella bongoriMICROBIOLOGYESCHERICHIA-COLI K-12Genomic IslandsQH301-705.5Sequence analysisVirulence FactorsImmunologyVirulenceVIROLOGYENCODED EFFECTORsalmonella; salmonella bongori; evoluzione geneticaMicrobiologyQH30103 medical and health sciencesVirologyGeneticsmedicineMICROARRAY ANALYSISAnimalsHumansEnteropathogenic Escherichia coliBiologyMolecular BiologyGene030304 developmental biologyEvolutionary BiologyScience & Technology030306 microbiologyANTIBIOTIC-RESISTANCESequence Analysis DNARC581-607biology.organism_classificationGenes BacterialImmunologic diseases. Allergy
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