Search results for "Agglutination Tests"

showing 10 items of 20 documents

Circulating diphtheria antitoxin levels in children aged 11-14 years in relation to the vaccinal history.

1991

Diphtheria antitoxin level in serum samples obtained from 204 healthy children aged 11-14 years was determined by means of an indirect haemagglutination technique and related to the vaccinal history of the subjects. Irrespective of the time since the last toxoid inoculation, the mean antitoxin titre per ml of serum in the individuals who had received incomplete/irregular anti-diphtheria vaccination in childhood was significantly higher when the number of toxoid doses was higher (from two to more than four doses); the same was not observed for individuals given primary vaccination (three toxoid doses) according to the schedule for childhood vaccination in Italy (regular vaccinees) and one or…

HemagglutinationAdolescentDiphtheria ToxoidPhysiologycomplex mixturesSerologyMedicineHumansChildSicilyImmunization ScheduleGeneral VeterinaryGeneral Immunology and Microbiologybiologybusiness.industryDiphtheriaVaccinationPublic Health Environmental and Occupational HealthToxoidHemagglutination Testsmedicine.diseasebiology.organism_classificationDiphtheria AntitoxinVaccinationTiterInfectious DiseasesTasaImmunologyMolecular MedicineAntitoxinbusinessVaccine
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A novel galactose- and arabinose-specific lectin from the sponge Pellina semitubulosa: isolation, characterization and immunobiological properties.

1992

A new lectin from the sponge Pellina semitubulosa is derived which was extracted and purified to homogeneity. The purified lectin is probably a hexamer of polypeptide chains (each M(r) 34,000) which are covalently linked via disulfide linkages; the isoelectric point is 6.1. The lectin displays the following specificities: D-galactose (50% inhibition of hemagglutination at 0.2 mM) = L-arabinose (0.2 mM) greater than D-fucose (1.5 mM) greater than D-glucose (3.0 mM). It precipitates human erythrocytes (A1, A2, A1B, B, and O) with a titer between 2(8) and 2(11) and erythrocytes from sheep and rabbits with a titer between 2(5) and 2(10). The Pellina lectin displays a strong mitogenic effect on …

Interleukin 2HemagglutinationChemical PhenomenaLymphocyte ActivationBiochemistrySubstrate Specificitychemistry.chemical_compoundLectinsmedicineAnimalsLymphocytesAmino AcidsbiologyChemistry PhysicalMacrophagesInterleukinLectinGalactoseGeneral MedicineHemagglutination TestsMolecular biologyArabinosePoriferaTiterIsoelectric pointchemistryBiochemistryConcanavalin AGalactosebiology.proteinInterleukin-2medicine.drugInterleukin-1Biochimie
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Immune activation rapidly mirrored in a secondary sexual trait.

2003

A crucial assumption underlying most models of sexual selection is that sexual advertisements honestly reflect the phenotypic and/or genetic quality of their bearers ([1][1]). Here we show that experimental activation of the immune system is rapidly mirrored in the expression of a carotenoid-based

MaleBiologyXanthophyllsSongbirdsSexual Behavior AnimalImmune systemZeaxanthinsAnimalsCryptoxanthinsGeneticsMultidisciplinaryEcologyPigmentationLuteinBeakHemagglutination Testsbeta CarotenePhenotypeCarotenoidsMate choiceSexual selectionImmune SystemAntibody FormationTraitFemaleImmunizationImmune activationScience (New York, N.Y.)
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Arthus type inflammation with rat immunoglobulins.

1971

Etude comparative des proprietes biologiques des anticorps IgM, IgG1 et IgG2 du rat. Les resultats montrent que le pouvoir agglutinant et lytique des anticorps IgM est respectivement 37 et 100 fois superieur a celui des deux classes d'anticorps IgG. Par contre, en ce qui concerne le phenomene d'Arthus, les anticorps IgM sont moins actifs que les anticorps IgG, si les rapports sont exprimes en poids. Si l'on calcule les rapports par nombre de molecules, les anticorps IgM sont aussi, dans ce cas, plus actifs que les IgG.

MaleImmunodiffusioneducationFreund's AdjuvantImmunoglobulinsInflammationHemolysisChromatography DEAE-CelluloseAntigen-Antibody ReactionsCellular and Molecular NeurosciencemedicineArthus ReactionAnimalsMolecular BiologyPharmacologybiologyChemistryImmune SeraSerum Albumin BovineCell BiologyHemagglutination TestsMolecular biologyRatsMolecular WeightImmunoglobulin Gbiology.proteinMolecular MedicineImmunizationmedicine.symptomAntibodyExperientia
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Occurrence of Edwardsiella tarda in wild European eels Anguilla anguilla from Mediterranean Spain

2007

Pure cultures of Edwarsiella tarda were isolated from body ulcers and internal organs of wild European eels caught in a Mediterranean freshwater coastal lagoon (Albufera Lake, Valencia, Spain) over a 1 yr period. Overall, the E. tarda isolation rate from wild eels was 9%, but this increased to 22.8% in diseased individuals. All 22 E. tarda isolates belonged to the 'wild-type' biogroup of the species and were virulent for eels (lethal dose that kills 50% of exposed individuals [LD50 dose]: 10(4.85) to 10(6.83) CFU ind.(-1)), and therefore represented the aetiological agent of the haemorrhagic disease observed in wild European eels. The E. tarda isolates and E. tarda CECT 894T type strain wer…

Mediterranean climatecongenital hereditary and neonatal diseases and abnormalitiesendocrine systemanimal structuresPopulationZoologyVirulenceMicrobial Sensitivity TestsAquatic ScienceIsolation rateFish DiseasesMediterranean seaAnti-Infective AgentsAnguillidaeAgglutination TestsMediterranean SeaPrevalenceAnimalsskin and connective tissue diseaseseducationEdwardsiella tardaEcology Evolution Behavior and SystematicsAntigens Bacterialeducation.field_of_studyVirulencebiologyEcologyEdwardsiella tardaLethal doseEnterobacteriaceae InfectionsAnguillabiology.organism_classificationPhenotypeSpainDiseases of Aquatic Organisms
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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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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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A serum fucolectin isolated and characterized from sea bass Dicentrarchus labrax

2001

A lectin specific for fucose and galactose was isolated by affinity chromatography on Sepharose CL-6B from the serum of Dicentrarchus labrax. The hemagglutinating activity against rabbit erythrocytes was calcium-independent, and reached its maximum at 37 degrees C. Two protein components were found in the hemagglutinating fractions eluted from the Sepharose column. Only the 34 kDa component (DLL2) eluted from the polyacrylamide gels (SDS-PAGE) showed agglutinating activity against rabbit erythrocytes. SDS-PAGE, in non-reducing conditions, revealed a single 66 kDa protein that reacted with antibodies to the 34 kDa component. Therefore, a dimeric structure stabilized by disulfide bonds can be…

SerumImmunoblottingCarbohydratesSettore BIO/05 - ZoologiaBiophysicsHemagglutinin (influenza)CentrifugationBiochemistryFucoseSepharosechemistry.chemical_compoundAffinity chromatographyLectinsAnimalsDicentrarchus labraxHemagglutininSea bassMolecular BiologybiologyLectinHemagglutination Testsbiology.organism_classificationFishchemistryBiochemistryGalactosebiology.proteinBassElectrophoresis Polyacrylamide GelDicentrarchusFucolectinBiochimica et Biophysica Acta (BBA) - General Subjects
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Serological and molecular characteristics of Vibrio vulnificus biotype 3: evidence for high clonality.

2007

Vibrio vulnificus biotype 3 has been implicated as the causative pathogen of an ongoing disease outbreak that erupted in Israel in 1996. Recent work based on multi-locus sequence typing (MLST) showed that V. vulnificus biotype 3 is genetically homogeneous. The aim of this study was to investigate the existence of subpopulations within this homogeneous biotype by characterizing the surface antigens and analysing the sequence diversity of selected outer-membrane protein (OMP)-encoding genes. Rabbit antisera were prepared against biotype 1, 2 and 3 strains. The results of the slide-agglutination test, dot-blot assay (using fresh and boiled cells), and immunoblotting of lipopolysaccharides (LPS…

clone (Java method)DNA BacterialLipopolysaccharidesPopulationImmunoblottingMolecular Sequence DataSequence HomologyBiologyMicrobiologyDNA sequencingMicrobiologyEvolution MolecularAgglutination TestsCluster AnalysisHumansTypingIsraeleducationGenePathogenVibrio vulnificuseducation.field_of_studyAntigens BacterialMolecular EpidemiologyBase SequenceStrain (biology)Genetic Variationbacterial infections and mycosesVibrio InfectionsbacteriaMultilocus sequence typingBacterial Outer Membrane ProteinsMicrobiology (Reading, England)
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Amebiasis autóctona española. ¿Enfermedad emergente o endémica?

2004

medicine.medical_specialtybusiness.industryInternal medicineTreatment outcomemedicineMEDLINEGeneral MedicineEndemic diseasesbusinessmedicine.diseaseGastroenterologyHemagglutination testsLiver abscessMedicina Clínica
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