Search results for "Protozoa"

showing 10 items of 222 documents

Inhibition of Eimeria tenella CDK-related kinase 2: From target identification to lead compounds.

2010

Apicomplexan parasites encompass several human- and animal-pathogenic protozoans such as Plasmodium falciparum, Toxoplasma gondii, and Eimeria tenella. E. tenella causes coccidiosis, a disease that afflicts chickens, leading to tremendous economic losses to the global poultry industry. The considerable increase in drug resistance makes it necessary to develop new therapeutic strategies against this parasite. Cyclin-dependent kinases (CDKs) are key molecules in cell-cycle regulation and are therefore prominent target proteins in parasitic diseases. Bioinformatics analysis revealed four potential CDK-like proteins, of which one—E. tenella CDK-related kinase 2 (EtCRK2)—has already been charact…

Molecular Sequence DataProtozoan ProteinsBiochemistryEimeriaArticleAdenosine TriphosphateCyclin-dependent kinaseDrug Discoveryparasitic diseasesAnimalsHumansComputer SimulationHomology modelingAmino Acid SequenceGeneral Pharmacology Toxicology and PharmaceuticsProtein Kinase InhibitorsPharmacologyVirtual screeningBinding SitesbiologyDrug discoveryKinaseCoccidiosisOrganic ChemistryCyclin-dependent kinase 2Cyclin-Dependent Kinase 2Plasmodium falciparumbiology.organism_classificationMolecular biologyBiochemistrybiology.proteinMolecular MedicineBenzimidazolesChickensSequence AlignmentEimeria tenellaChemMedChem
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Serological prevalence of toxoplasmosis in pregnant women in Luanda (Angola): Geospatial distribution and its association with socio-demographic and …

2020

We report a study on toxoplasmosis in pregnant women in Luanda, Angola, determining the seroprevalence, geospatial distribution and its association with socio-economic features, dietary habits and hygiene and health conditions. Anti-Toxoplasma gondii IgG and IgM were quantified in serum samples of women attended at the Lucrecia Paim Maternity Hospital between May 2016 and August 2017. The IgG avidity test and qPCR assay were used for dating the primary infection. Data were collected by questionnaire after written consent, and spatial distribution was assessed through a Kernel Density Function. The potential risk factors associated with Toxoplasma infection were evaluated using bivariate and…

Multivariate analysisEpidemiologyMaternal HealthAntibodies ProtozoanMiscarriageToxoplasma GondiiSerologyGeographical LocationsMedical ConditionsPregnancySeroepidemiologic StudiesPrevalenceMedicine and Health SciencesLongitudinal StudiesProtozoansMammalsMultidisciplinaryGeographybiologyCoinfectionObstetricsLiver DiseasesQRObstetrics and GynecologyEukaryotaMiddle AgedHepatitis BPopulation SurveillanceVertebratesMedicineFemaleToxoplasmaToxoplasmosisMaternal AgeResearch ArticleAdultmedicine.medical_specialtyAdolescentScienceGastroenterology and HepatologyLower riskYoung AdultParasitic DiseasesmedicineHumansAnimalsSeroprevalenceLiver Disease and PregnancyPregnancyProtozoan Infectionsbusiness.industryOrganismsBiology and Life SciencesToxoplasma gondiimedicine.diseasebiology.organism_classificationParasitic ProtozoansToxoplasmosisPregnancy ComplicationsCross-Sectional StudiesLogistic ModelsAngolaPregnancy Complications ParasiticMedical Risk FactorsPeople and PlacesAfricaAmniotesCatsWomen's HealthbusinessZoologyPLoS ONE
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What Could Be a Primary Cause of Multiple Sclerosis: Is It an Autoimmunity Triggered by Chronic Protozoan Infection?

2013

The generally accepted paradigm of multiple sclerosis is the autoimmune one; still, a body of evidence suggests that this disease may actually be triggered by an infectious factor. In this paper, it is hypothesized that multiple sclerosis may actually be a rare complication of a protozoan infection, which is usually asymptomatic but in some susceptible individuals is accompanied by autoimmune attack against the nervous tissue. If multiple sclerosis were actually caused by such an infection, then a microorganism responsible should exhibit several properties: it (i) is transmitted by an arthropod vector; (ii) is characterized by specific metabolism of the lipids; (iii) should be dependent on …

Nervous tissueMultiple sclerosisUsually asymptomaticDiseaseBiologymedicine.diseasemedicine.disease_causeAutoimmunitymedicine.anatomical_structureProtozoan infectionImmunologymedicineComplicationArthropod VectorJournal of Neuroparasitology
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Fasciola hepatica phenotypic characterization in Andean human endemic areas: Valley versus altiplanic patterns analysed in liver flukes from sheep fr…

2011

Fascioliasis is a zoonotic parasitic disease caused by Fasciola hepatica and Fasciola gigantica. Of both species, F. hepatica is the only one described in the Americas, mainly transmitted by lymnaeid snail vectors of the Galba/. Fossaria group. Human fascioliasis endemic areas are mainly located in high altitude areas of Andean countries. Given the necessity to characterize F. hepatica populations involved, the phenotypic features of fasciolid adults infecting sheep present in human fascioliasis endemic areas were analysed in the Cajamarca Valley and Mantaro Valley (valley transmission patterns) and the northern Bolivian Altiplano (altiplanic transmission pattern). A computer image analysis…

Ovis ariesorganisms by sizeRange (biology)GastropodaFasciola giganticageographic originFossariaLymnaeidaelaw.inventionlawPerucomparative studynon|phenotypeeducation.field_of_studybiologyEcologyparasite transmissionarticleLiver flukeEuropeFasciolidaemultivariate analysisPhenotypeInfectious DiseasesTransmission (mechanics)Parasitic diseasecomputer analysisaltitudeMicrobiology (medical)protozoal geneticsBoliviaFascioliasisFasciola giganticaPopulationPhenotypic characterizationSheep DiseasesZoology//purl.org/pe-repo/ocde/ford#3.03.08 [https]Microbiologyanimal tissueanimal parasitosisHuman endemic areasimage analysisHepaticaparasitic diseasesGeneticsmedicineAnimalsHumansFasciola hepaticacontrolled studyeducationMolecular Biologyendemic diseaseEcology Evolution Behavior and SystematicsSheeputerus|FascioliasisFasciola hepaticabiology.organism_classificationmedicine.diseasebreedingInfection, Genetics and Evolution
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Zschokkella hildae Auerbach, 1910: phylogenetic position, morphology, and location in cultured Atlantic cod.

2010

Abstract The myxozoan Zschokkella hildae Auerbach, 1910, was detected with a prevalence of 100% in cultured Atlantic cod, Gadus morhua L. aged 1+ from a culture facility on the west coast of Scotland. Sporogonic stages of Z. hildae, plasmodia producing 2–5 mature spores, were located predominantly in the collecting ducts and ureters of the kidney, and spores were present in the urine collected from the bladder. Less frequently, plasmodia were detected in the interstitial tissue of the kidney. The parasite prevalence in cultured fish was considerably higher than reported in wild fish but no obvious signs of pathology were detected. SSU rDNA sequencing and phylogenetic analysis showed that Z.…

Parasitic Diseases AnimalMolecular Sequence DataSpores ProtozoanUrinary BladderZoologyUrineDNA RibosomalHost-Parasite InteractionsFish DiseasesSpecies SpecificityPhylogeneticsparasitic diseasesParasite hostingGadusAnimalsMyxozoaRibosomal DNAPhylogenybiologyPhylogenetic treeBase SequenceEcologyfungiSequence Analysis DNADNA Protozoanbiology.organism_classificationTurbotInfectious DiseasesGadus morhuaRNA RibosomalMolecular phylogeneticsParasitologyUreterAtlantic codParasitology international
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Rapid quantitative method for measuring phagocytosis of Leishmania promastigotes using a double radiolabelling method.

1990

A double radiolabelling method is described for the measurement of phagocytosis of Leishmania major promastigotes in cultures of murine resident peritoneal macrophages. L. major promastigotes were radiolabelled during exponential growth in RPMI supplemented with [125I]5-iodo-2-deoxyuridine. They were used to infect sodium [51Cr]chromate-labelled macrophages. Phagocytosis was evaluated by measuring the radioactivity of the 125IUdR-labelled parasites detectable inside 51Cr-labelled macrophages by a Beckmann gamma 5500 counting system. This was able to count simultaneously, in two different windows the radioactivity of (a) the parasites and (b) the cells. The technique compares favorably with …

Pathologymedicine.medical_specialtyCell Membrane PermeabilityPhagocytosisImmunologyMice Inbred StrainsBiologyMicePhagocytosisIdoxuridinemedicineImmunology and AllergyMacrophageAnimalsLeishmania majorRadiometryLeishmaniasisPeritoneal CavityMicroscopyDouble labelingMacrophagesbiology.organism_classificationLeishmaniaMolecular biologyCell cultureLeishmania tropicaProtozoaJournal of immunological methods
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Visceral leishmaniasis in a patient with Down syndrome

2006

Pathologymedicine.medical_specialtyDown syndromeAntiprotozoal AgentsMEDLINEAntibodies ProtozoanAneuploidyAmphotericin BAnimalsHumansvisceral leishmaniasisMedicineProtozoal diseaseLeishmaniabusiness.industryInfantLeishmaniasismedicine.diseasePancytopeniaDermatologyVisceral leishmaniasisSplenomegalyPediatrics Perinatology and Child HealthLeishmaniasis VisceralDown SyndromebusinessTrisomyHepatomegalyEuropean Journal of Pediatrics
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Prediction of Aquatic Toxicity of Benzene Derivatives to Tetrahymena pyriformis According to OECD Principles

2016

Background: Many QSAR studies have been developed to predict acute toxicity over several biomarkers like Pimephales promelas, Daphnia magna and Tetrahymena pyriformis. Regardless of the progress made in this field there are still some gaps to be resolved such as the prediction of aquatic toxicity over the protozoan T. pyriformis still lack a QSAR study focused in accomplish the OECD principles. Methods: Atom-based quadratic indices are used to obtain quantitative structure-activity relationship (QSAR) models for the prediction of aquatic toxicity. Our models agree with the principles required by the OECD for QSAR models to regulatory purposes. The database employed consists of 392 substitut…

PharmacologyQuantitative structure–activity relationshipTetrahymena pyriformisAntiprotozoal AgentsQuantitative Structure-Activity Relationship010501 environmental sciencesBiology01 natural sciencesAcute toxicity0104 chemical sciencesAquatic toxicologyToxicology010404 medicinal & biomolecular chemistryParasitic Sensitivity TestsTest setDrug DiscoveryBenzene derivativesLinear regressionTetrahymena pyriformisBenzene DerivativesBiological systemMonte Carlo MethodAlgorithmsBootstrapping (statistics)0105 earth and related environmental sciencesCurrent Pharmaceutical Design
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TLR4 abrogates the Th1 immune response through IRF1 and IFN-β to prevent immunopathology during L. infantum infection

2020

A striking feature of human visceral leishmaniasis (VL) is chronic inflammation in the spleen and liver, and VL patients present increased production levels of multiple inflammatory mediators, which contribute to tissue damage and disease severity. Here, we combined an experimental model with the transcriptional profile of human VL to demonstrate that the TLR4-IFN-β pathway regulates the chronic inflammatory process and is associated with the asymptomatic form of the disease. Tlr4-deficient mice harbored fewer parasites in their spleen and liver than wild-type mice. TLR4 deficiency enhanced the Th1 immune response against the parasite, which was correlated with an increased activation of de…

PhysiologyGene ExpressionWhite Blood CellsMiceCell SignalingAnimal CellsImmune PhysiologyZoonosesImmunopathologyMedicine and Health SciencesMembrane Receptor SignalingBiology (General)Immune ResponseLeishmaniasisProtozoansLeishmaniaMice Knockout0303 health sciencesbiologyT Cells030302 biochemistry & molecular biologyEukaryotaImmune Receptor SignalingInfectious Diseasesmedicine.anatomical_structureLeishmaniasis VisceralCellular Typesmedicine.symptomLeishmania infantumResearch ArticleSignal TransductionNeglected Tropical DiseasesQH301-705.5Leishmania InfantumImmune CellsImmunologySpleenInflammationLEISHMANIOSE VISCERALMicrobiology03 medical and health sciencesImmune systemVirologyParasitic DiseasesGeneticsmedicineAnimalsMolecular Biology030304 developmental biologyInflammationProtozoan InfectionsBlood CellsOrganismsBiology and Life SciencesCell BiologyInterferon-betaTh1 CellsRC581-607Tropical Diseasesmedicine.diseasebiology.organism_classificationParasitic ProtozoansToll-Like Receptor 4IRF1Visceral leishmaniasisImmunologyTLR4ParasitologyImmunologic diseases. AllergySpleenInterferon Regulatory Factor-1
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Paratransgenic manipulation of a tsetse microRNA alters the physiological homeostasis of the fly’s midgut environment

2021

Tsetse flies are vectors of parasitic African trypanosomes, the etiological agents of human and animal African trypanosomoses. Current disease control methods include fly-repelling pesticides, fly trapping, and chemotherapeutic treatment of infected people and animals. Inhibiting tsetse’s ability to transmit trypanosomes by strengthening the fly’s natural barriers can serve as an alternative approach to reduce disease. The peritrophic matrix (PM) is a chitinous and proteinaceous barrier that lines the insect midgut and serves as a protective barrier that inhibits infection with pathogens. African trypanosomes must cross tsetse’s PM in order to establish an infection in the fly, and PM struc…

PhysiologyGenes InsectBiochemistryAnimals Genetically ModifiedMedical ConditionsGene expressionMedicine and Health SciencesHomeostasisPeritrophic matrixBiology (General)Protozoans0303 health sciencesbiologyGene OntologiesSodalis glossinidiusEukaryotaCardiaGenomicsBody FluidsCell biologyIntestinesNucleic acidsBloodDigestionAnatomyResearch ArticleSymbiotic bacteriaTrypanosomaTsetse FliesQH301-705.5ImmunologyParatransgenesisMicrobiology03 medical and health sciencesVirologyParasitic DiseasesGeneticsAnimalsNon-coding RNAMolecular Biology030304 developmental biologyNatural antisense transcripts030306 microbiologyfungiOrganismsBiology and Life SciencesComputational BiologyTsetse flyMidgutRC581-607Genome Analysisbiology.organism_classificationParasitic ProtozoansGastrointestinal MicrobiomeInsect VectorsGene regulationGastrointestinal TractMicroRNAsTrypanosomiasis AfricanTrypanosomaRNAParasitologyGene expressionImmunologic diseases. AllergyPhysiological ProcessesDigestive SystemPLOS Pathogens
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