Search results for "bacteria."

showing 10 items of 4757 documents

Electrophoretic analysis of heterogeneous lipopolysaccharides from various strains of Vibrio vulnificus biotypes 1 and 2 by silver staining and immun…

1992

Lipopolysaccharides (LPS) of 11 strains of Vibrio vulnificus biotypes 1 and 2, isolated from an eel farm, and of 10 reference strains, were examined by SDS-polyacrylamide gel electrophoresis coupled with silver staining and immunoblotting. LPS samples were obtained from whole-cell lysates, outer membrane fragments, and extracellular products. By silver staining, only a diffuse band of low-molecular weight could be visualized in all cases except for a biotype 1 strain isolated from water. However, immunoblotting with antisera obtained against strains of biotypes 1 and 2 from eels allowed visualization of multiple O-polysaccharide chains. All biotype 2 strains, independently of their origins,…

SerotypeLipopolysaccharidesSilver StainingBlotting WesternVibrio vulnificusApplied Microbiology and BiotechnologyMicrobiologyMicrobiologySilver stainSpecies SpecificityVibrionaceaeAgglutination TestsAnimalsVibrioGel electrophoresisAntiserumEelsbiologyPolysaccharides BacterialO AntigensGeneral Medicinebiology.organism_classificationMolecular biologyAntibodies BacterialElectrophoresis Polyacrylamide GelRabbitsBacterial outer membraneBacteriaCurrent microbiology
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Immunogenic antigens of the eel pathogen Vibrio vulnificus serovar E.

2003

Abstract The immunogenic antigens of Vibrio vulnificus serovar E were investigated in the eel. Fish were vaccinated by immersion with Vulnivaccine (V), revaccinated 2 years later by intraperitoneal injection (RV) and bath infected 15 days post-revaccination (RVI). The specific immune response in serum was followed in all groups, and selected sera were used for immunostaining of surface (SA) and extracellular antigens (ECA). Bacteria were grown in iron-rich (TSB and MSWYE) and iron-poor media (TSB and MSWYE plus human transferrin (TSB-T and MSWYE-T)) as well as eel serum (ES), and their SA and ECA were extracted and electrophoretically analysed. Cells grown in MSWYE-T and ES presented the sa…

SerotypeLipopolysaccharidesTime FactorsLipopolysaccharideIronImmunoblottingEnzyme-Linked Immunosorbent AssayVibrio vulnificusAquatic ScienceMicrobiologychemistry.chemical_compoundAntigenEnvironmental ChemistryAnimalsPathogenVibrio vulnificuschemistry.chemical_classificationAntigens BacterialbiologyImmune SeraGeneral Medicinebiology.organism_classificationAnguillachemistryTransferrinAntibody FormationBacterial VaccinesElectrophoresis Polyacrylamide GelBacterial outer membraneBacteriaBacterial Outer Membrane ProteinsFishshellfish immunology
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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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Plasmid-Mediated Resistance to Antimicrobial Agents among Listeriae

1998

The resistance to 14 antiseptic-disinfectant and dye compounds of 208 strains of Listeria (132 L. monocytogenes, 63 L. innocua, 8 L. seeligeri, 1 L. ivanovii, 1 L. welshimeri, and 3 Listeria spp.) was tested by the agar-dilution procedure. The Listeria strains were isolated from different varieties of foods, environments of cheese dairies, humans, and wild birds. A total of 14 (6.7%) Listeria strains (12 L. monocytogenes and 2 L. innocua) were resistant to benzalkonium chloride, hexamidine diisethionate, and ethidium bromide. This multiple resistance was observed more frequently from strains of Listeria spp. detected on carcasses of poultry (47%) than strains isolated from human listeriosis…

SerotypeListeriaMicrobial Sensitivity TestsDrug resistancemedicine.disease_causeMicrobiologyMicrobiologyBirdsmedicineAnimalsHumansFood microbiologyListeriosisSerotypingColoring AgentsBacteriophage TypingPhage typingbiologyDrug Resistance MicrobialPlasmid-mediated resistancebiology.organism_classificationDrug Resistance MultipleAnti-Bacterial AgentsStaphylococcus aureusConjugation GeneticFood MicrobiologyListeriaBacteriaCadmiumPlasmidsFood ScienceJournal of Food Protection
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Safety, tolerability, and immunologic noninferiority of a 13-valent pneumococcal conjugate vaccine compared to a 7-valent pneumococcal conjugate vacc…

2010

13-valent pneumococcal conjugate vaccine (PCV13) was compared to PCV7 in infants administered 4 doses. For the 7 common serotypes, PCV13- and PCV7-elicited responses showed comparable percent responders achieving 0.35mug/mL IgG threshold (exception 6B, 77.5% versus 87.1%, respectively) and OPA titers of 1:8; IgGs were lower than PCV7 but functional responses were generally comparable. For the 6 additional serotypes, PCV13-elicited IgG and functional OPA responses were notably greater than PCV7. The toddler dose boosted immune responses. Vaccines were comparable with regard to safety. PCV13 should be as effective as PCV7 in preventing pneumococcal disease caused by the common serotypes and m…

SerotypeMaleHeptavalent Pneumococcal Conjugate Vaccinemedicine.disease_causecomplex mixturesPneumococcal conjugate vaccinePneumococcal InfectionsPneumococcal Vaccinesstomatognathic systemDouble-Blind MethodGermanyStreptococcus pneumoniaemedicineHeptavalent Pneumococcal Conjugate VaccineHumansImmunization ScheduleVaccines ConjugateGeneral VeterinaryGeneral Immunology and Microbiologybusiness.industryImmunogenicityPublic Health Environmental and Occupational HealthInfantmedicine.diseaseAntibodies BacterialVaccinationPneumococcal infectionsInfectious DiseasesImmunizationImmunoglobulin GImmunologyMolecular MedicineFemalebusinessmedicine.drugVaccine
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Typhoid fever as a cause of opportunistic infection: case report.

2005

Abstract Background Typhoid fever is a systemic infection caused by the bacterium Salmonella enterica subspecies enterica serotype typhi, which is acquired by ingestion of contaminated food and water. Each year the disease affects at least 16 million persons world-wide, most of whom reside in the developing countries of Southeast Asia and Africa. In Italy the disease is uncommon with a greater number of cases in Southern regions than in Northern ones. Case presentation We report on a 57-year-old Sri-Lankan male affected by typhoid fever, the onset of which was accompanied by oropharyngeal candidiasis. This clinical sign was due to a transient cell-mediated immunity depression (CD4+ cell cou…

SerotypeMalemedicine.medical_specialtyOpportunistic infectionCase ReportDiseaseOpportunistic InfectionsTyphoid feverlcsh:Infectious and parasitic diseasesMicrobiologythiphoidMedical microbiologyAnti-Infective AgentsCandidiasis OralmedicineHumanslcsh:RC109-216Typhoid FeverSri Lankabiologybusiness.industryMiddle Agedbiology.organism_classificationmedicine.diseasebacterial infections and mycosesVirologyInfectious DiseasesParasitologySalmonella entericaTropical medicinebusinessBMC infectious 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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Salmonella serovars identified at the centre for enterobacteriaceae of palermo over the 5-year period 1983-87

1990

Salmonellosis is become an increasing public health problem in many countries. Serotyping and assessment of antibiotic resistance are useful tools, which assist in understanding the epidemiology of Salmonella infections. In this respect, the Centre of Enterobacteriaceae of Southern Italy provides helpful information on the changing pattern of Salmonella serovars in this geographic area. This paper reports the distribution of serovars and their antibiotic susceptibility in the years 1983-1987. In particular, because of their peculiar trends during this 5-year period, epidemiological features of Mbandaka, Corvallis, Dublin, Infantis and Wien serovars are described.

SerotypeSalmonella Infections Animalmedicine.medical_specialtySalmonellaAntiinfective agentbiologyEpidemiologybusiness.industryPublic healthMicrobial Sensitivity TestsDrug resistancebiology.organism_classificationmedicine.disease_causeEnterobacteriaceaeMicrobiologyAntibiotic resistanceItalySalmonellaEnvironmental healthSalmonella InfectionsEpidemiologymedicineAnimalsHumansbusinessEuropean Journal of Epidemiology
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Pheno-genotyping of Salmonella enterica serotype Enteritidis isolates identified in Sicily during a reemergence period.

2005

After an upward trend paralleling that occurring in most European countries, including Italy, since October 2002 Salmonella enterica serotype Enteritidis (S. Enteritidis) has again gained the first position among outbreak and sporadic human isolates of Salmonella in Sicily. Because phage typing of S. Enteritidis has many technical and epidemiological limitations and molecular methods have proved to be poorly discriminative for this organism, multiple typing, using phage typing together with pulsed field gel electrophoresis (PFGE) and plasmid profiling on a sample of fifty human and poultry isolates identified during the period October 2002 to May 2003 in Sicily, was chosen as the most valua…

SerotypeSalmonellaGenotypeSalmonella enteritidisEggsBiologymedicine.disease_causeApplied Microbiology and BiotechnologyMicrobiologyMicrobiologyDisease OutbreaksmedicinePulsed-field gel electrophoresisAnimalsHumansTypingSicilyPhylogenyPhage typingBacterial Typing Techniques Eggs microbiology Plasmids genetics Salmonella Food oisoning epidemiology Salmonella enteritidis isolation & purificationMolecular EpidemiologyMolecular epidemiologybiology.organism_classificationVirologyBacterial Typing TechniquesElectrophoresis Gel Pulsed-FieldPhenotypeSalmonella enteritidisSalmonella entericaFood MicrobiologyAnimal Science and ZoologySalmonella Food PoisoningChickensFood SciencePlasmidsFoodborne pathogens and disease
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Use of TaqMan® real-time PCR for rapid detection of Salmonella enterica serovar Typhi

2014

We evaluated the performances of a newly designed real-time polymerase chain reaction (PCR) assay using TaqMan® probes to detectSalmonellaTyphi. TaqMan® real-time PCR assays were performed by designed primers and probe based on thestaGgene for detectingS.Typhi. The specificity of the assay was evaluated on 15Salmonellaserovars. The analytical specificity was evaluated on 20 non-Salmonellamicroorganisms. The analytical sensitivity was assessed using decreasing DNA quantities ofS.Typhi ATCC 19430. Finally the detection capability of the TaqMan® real-time PCR assay on isolates recovered from patients withSalmonellainfections was compared to the conventional PCR assay. OnlyS.Typhi strain had po…

SerotypeSalmonellaSettore MED/07 - Microbiologia E Microbiologia ClinicaBiologySalmonella typhimedicine.disease_causeReal-Time Polymerase Chain ReactionSettore MED/42 - Igiene Generale E ApplicataRapid detectionSensitivity and Specificitylaw.inventionlawTaqManmedicineHumansTyphoid FeverPolymerase chain reactionreal time typhoid fever diagnosisDNA PrimersGeneral Immunology and MicrobiologyGeneral MedicineSalmonella typhiVirologyMolecular biologyBacterial Typing TechniquesReal-time polymerase chain reactionSalmonella enterica serovar TyphiGenes Bacterial
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