Search results for "LBIC"

showing 10 items of 361 documents

Different adhesins for type IV collagen on Candida albicans: identification of a lectin-like adhesin recognizing the 7S(IV) domain

2001

Adherence of the opportunistic pathogen Candida albicans to basement membrane (BM) proteins is considered a crucial step in the development of candidiasis. In this study the interactions of C. albicans yeast cells with the three main domains of type IV collagen, a major BM glycoprotein, were analysed. C. albicans adhered to the three immobilized domains by different mechanisms. Adhesion to the N-terminal cross-linking domain (7S) required the presence of divalent cations, whereas interaction with the central collagenous domain (CC) was cation-independent. Recognition of the C-terminal non-collagenous domain (NC1) was partially cation-dependent. Binding inhibition assays with the correspondi…

Collagen Type IVGlycosylationImmunoblottingOligosaccharidesBiologyMicrobiologyBasement MembraneType IV collagenOligosaccharide bindingCationsLectinsCandida albicansCell AdhesionAnimalsCandida albicanschemistry.chemical_classificationExtracellular Matrix ProteinsLectinOligosaccharidebiology.organism_classificationCorpus albicansBacterial adhesinchemistryBiochemistrybiology.proteinCattleGlycoproteinMicrobiology
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Complex Electromagnetic Fields Reduce Candida albicans Planktonic Growth and Its Adhesion to Titanium Surfaces

2021

This study evaluates the effects of different programs of complex electromagnetic fields (C.M.F.s) on Candida albicans, in planktonic and sessile phase and on human gingival fibroblasts (HGF cells). In vitro cultures of C. albicans ATCC 10231 and HGF cells were exposed to different cycles of C.M.F.s defined as: oxidative stress, oxidative stress/antibacterial, antibacterial, antibacterial/oxidative stress. Colony forming units (CFUs), metabolic activity, cells viability (live/dead), cell morphology, filamentation analysis, and cytotoxicity assay were performed. The broth cultures, exposed to the different C.M.F.s, were grown on titanium discs for 48 h. The quantity comparisons of adhered C.…

Colony-forming unitbiologyChemistryQH301-705.5BiofilmMedicine (miscellaneous)Germ tubecomplex electro-magnetic fields; <i>Candida albicans</i>; CFU; titanium; germ tube testmedicine.disease_causebiology.organism_classificationCell morphologyCFUGeneral Biochemistry Genetics and Molecular BiologyCorpus albicansMicrobiologycomplex electro-magnetic fields<i>Candida albicans</i>medicinetitaniumgerm tube testBiology (General)Candida albicansCytotoxicityOxidative stressBiomedicines
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High prevalence of oral potentially malignant disorders and risk factors in a semi-urban brazilian city: a population-based cross-sectional study

2021

Background Oral Potentially Malignant Disorders (OPMDs) are defined as lesions with a greater likelihood of progressing to cancer. Population-based studies that evaluate the prevalence of OPMDs are scarce in Brazil. The aim of the present study was to determine the prevalence of OPMDs and associated risk factors in a semi-urban Brazilian population. Material and Methods This is a cross-sectional study, whose universe included individuals aged 40 years or older residing in a medium-sized city of northeastern Brazil. Data collection was divided into two steps: interview and oral examination. The outcome variable was the presence of OPMDs. The predictor variables were sociodemographic characte…

Cross-sectional studyPopulationvirulence factorsc. albicansPopulation basedBivariate analysissymbols.namesakeRisk FactorsOral Cancer and Potentially malignant disordersPrevalenceMedicineHumansPoisson regressioneducationGeneral DentistryUNESCO:CIENCIAS MÉDICASeducation.field_of_studyHigh prevalenceSemi urbanbusiness.industryResearchConfidence intervalCross-Sectional StudiesgenotypingOtorhinolaryngologyleukoplakiasymbolsoral cavitySurgeryMouth NeoplasmsbusinessBrazilDemographyMedicina Oral, Patología Oral y Cirugía Bucal
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Molecular Identification of Yeasts Associated with Traditional Egyptian Dairy Products

2009

This study aimed to examine the diversity and ecology of yeasts associated with traditional Egyptian dairy products employing molecular techniques in yeast identification. A total of 120 samples of fresh and stored Domiati cheese, kariesh cheese, and "Matared" cream were collected from local markets and examined. Forty yeast isolates were cultured from these samples and identified using the restriction-fragment length polymorphism (RFLPs) of 5.8S-ITS rDNA region and sequencing of the domains D1 and D2 of the 26S rRNA gene. Yeasts were identified as Issatchenkia orientalis (13 isolates), Candida albicans (4 isolates), Clavispora lusitaniae (Candida lusitaniae) (9 isolates), Kodamaea ohmeri (…

Cultured Milk ProductsFood HandlingColony Count MicrobialDNA RibosomalPolymerase Chain ReactionMicrobiologyFoodborne DiseasesKluyveromyces marxianusCheeseYeastsAnimalsFood microbiologyFood scienceSodium Chloride DietaryMycological Typing TechniquesCandida albicansPhylogenybiologyCandida lusitaniaeWaterHydrogen-Ion ConcentrationRibosomal RNAbiology.organism_classificationCorpus albicansYeastKodamaea ohmeriRNA RibosomalFood MicrobiologyEgyptPolymorphism Restriction Fragment LengthFood ScienceJournal of Food Science
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Quantitative analysis of opsonophagocytosis and of killing of Candida albicans by human peripheral blood leukocytes by using flow cytometry

1991

We describe a simple, rapid, automated procedure for measuring opsonophagocytosis and killing of Candida albicans by human peripheral blood leukocytes. Yeast cells are labelled by allowing uptake and cleavage of membrane-permeable bis-carboxyethyl-carboxyfluorescein pentaacetoxymethylester to its membrane-impermeable fluorescent derivative bis-carboxyethyl-carboxyfluorescein. The yeast cells are added to cell-rich plasma obtained after dextran sedimentation of erythrocytes. Opsonophagocytosis and killing are quantified by using automated fluorescent cell analysis, and the following parameters can be obtained: (i) relative percentage of phagocytes that participate in opsonophagocytosis, (ii)…

Cytotoxicity ImmunologicMicrobiology (medical)Phagocytemedicine.drug_classPhagocytosisIn Vitro TechniquesMonoclonal antibodyMicrobiologyFlow cytometryPhagocytosisCandida albicansLeukocytesmedicineHumansCandida albicansPhagocytesbiologymedicine.diagnostic_testOpsonin ProteinsFlow Cytometrybiology.organism_classificationMolecular biologyYeastCorpus albicansAntibody opsonizationmedicine.anatomical_structureEvaluation Studies as TopicResearch ArticleJournal of Clinical Microbiology
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Oligonucleotide-capped mesoporous silica nanoparticles as DNA-responsive dye delivery systems for genomic DNA detection

2015

[EN] New hybrid oligonucleotide-capped mesoporous silica nanoparticles able to detect genomic DNA were designed.

DNA BacterialINGENIERIA DE LA CONSTRUCCIONDesignControlled-releaseSupportsOligonucleotidesNanoparticleNanotechnologyCatalysisLegionella pneumophilachemistry.chemical_compoundQUIMICA ORGANICAhemic and lymphatic diseasesCandida albicansBIOQUIMICA Y BIOLOGIA MOLECULARMaterials ChemistryMycoplasma fermentansColoring AgentsStimuliRhodaminesOligonucleotideChemistryQUIMICA INORGANICAMetals and AlloysGenomicsGeneral ChemistryMesoporous silicaSilicon DioxideControlled releaseDrug-deliverySurfaces Coatings and FilmsElectronic Optical and Magnetic Materialsgenomic DNADrug deliveryCeramics and CompositesNanoparticlesDNAChemical Communications
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Cloning of a cDNA fragment encoding part of the protein moiety of the 58-kDa fibrinogen-binding mannoprotein of Candida albicans

2006

Immunoscreening of a Candida albicans expression library with antibodies against the 58 kDa fibrinogen-binding mannoprotein (mp58) of the fungus resulted in the isolation of clones encoding the protein moiety of this molecule. Sequence of the 0.9 kb cDNA of one of the clones selected for further analysis, revealed an open reading frame coding for 292 amino acids, which displays sequence similarity to proteins belonging to a family of immunodominant antigens of Aspergillus spp. The gene corresponding to this cDNA was named FBP1 (fibrinogen-binding protein). These results represent the first report on the identification of C. albicans genes encoding surface receptors for host proteins.

DNA ComplementaryGenes FungalMolecular Sequence DataSequence alignmentMicrobiologyFungal ProteinsCell WallComplementary DNAImmunoscreeningCandida albicansCell AdhesionGeneticsAmino Acid SequenceCloning MolecularCandida albicansMolecular BiologyPeptide sequenceBase SequenceSequence Homology Amino AcidbiologyFibrinogenFibrinogen bindingbiology.organism_classificationMolecular biologyCorpus albicansMolecular WeightBlotting SouthernOpen reading frameCell Adhesion MoleculesSequence AlignmentFEMS Microbiology Letters
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Molecular cloning and characterization of aCandida albicansgene (EFB1) coding for the elongation factor EF-1β

1996

A Candida albicans gene homologous to Saccharomyces cerevisiae elongation factor 1 beta was isolated by screening a genomic DNA library using a C. albicans cDNA as a probe. This cDNA was previously obtained by immunoscreening of an expression library with polyclonal antibodies raised against candidal cell wall components. Sequence analysis of the cDNA and the whole C. albicans gene (EMBL accession number X96517) revealed an intron-interrupted open reading frame of 639 base pairs that encodes a 213 amino acid protein. Exon sequences are highly homologous (74%) to S. cerevisiae EFB1, whereas intron sequence is less conserved (34% identity), and the predicted amino acid sequence shares about 7…

DNA ComplementarySequence analysisGenes FungalMolecular Sequence DataSaccharomyces cerevisiaeMolecular cloningMicrobiologyFungal ProteinsPeptide Elongation Factor 1ImmunoscreeningComplementary DNACandida albicansGeneticsAnimalsCloning MolecularCandida albicansMolecular BiologyPeptide sequenceGeneGeneticsGenomeBase SequenceSequence Homology Amino AcidbiologySequence Analysis DNABlotting NorthernPeptide Elongation Factorsbiology.organism_classificationMolecular biologyElongation factorBlotting SouthernRabbitsFEMS Microbiology Letters
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A new ecdysteroid and other constituents from two Dioscorea species

2008

Phytochemical investigation of the rhizome of Dioscorea dumetorum has led to the isolation by several chromatographic steps on normal and reversed phase silica gel of a new ecdysteroid, (20R)-5β,11α,20-trihydroxyecdysone (1), and two known ecdysteroids, ajugasterone C (2) and herkesterone (3). Their structures were determined by spectroscopic methods including 1D- and 2D-NMR (COSY, TOCSY, HSQC and HMBC). This is the first report on the occurrence of phytoecdysteroids in the Dioscoreaceae family. These compounds were devoid of antifungal activity against three Candida species (Candida albicans, Candida glabrata and Candida tropicalis, MIC > 200 μg/ml).

Dioscoreaceae01 natural sciencesBiochemistryCandida tropicalischemistry.chemical_compoundDioscoreaceaeCandida albicansDioscorea schimperianaDioscorea dumetorumEcology Evolution Behavior and SystematicsEcdysteroidChromatographybiologyCandida glabrata010405 organic chemistryEcdysteroidsbiology.organism_classification0104 chemical sciences3. Good healthRhizome010404 medicinal & biomolecular chemistrychemistryPhytochemicalBiochemistry[SDV.SP.PHARMA]Life Sciences [q-bio]/Pharmaceutical sciences/PharmacologyDioscorea2D-NMR
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Viability of microorganisms in novel antineoplastic and antiviral drug solutions

1998

Introduction. In determining the expiration-dates of ready-to-use antineoplastic and antiviral drug solu tions, microbiological aspects must be considered. This is especially true because many antineoplastic drugs introduced into the market are already known to lack antimicrobial activity. The purpose of this study is to evaluate the growth of four different microorganisms in ready-to-use solutions of 14 differ ent novel antineoplastic and antiviral drugs. Methods. The lowest concentrations of 14 dif ferent antineoplastic and antiviral drugs prescribed in our hospital were prepared in polyvinyl chloride bags or a polyethylene container (paclitaxel) containing 0.9% sodium chloride or 5% dex…

Drugmedicine.drug_classPseudomonas aeruginosamedia_common.quotation_subjectSodiumchemistry.chemical_elementBiologyPharmacologyAntimicrobialbiology.organism_classificationmedicine.disease_causeMicrobiology03 medical and health sciences0302 clinical medicineOncologychemistryStaphylococcus aureus030220 oncology & carcinogenesismedicinePharmacology (medical)Antiviral drugCandida albicansBacteria030215 immunologymedia_commonJournal of Oncology Pharmacy Practice
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