Search results for "techniques"

showing 10 items of 4426 documents

Freezing and storage at -20 °C provides adequate preservation of Toxoplasma gondii DNA for retrospective molecular analysis.

2014

Equipe EA MERS; International audience; Nucleic acid-based testing has become crucial for toxoplasmosis diagnosis. For retrospective (forensic or scientific) studies, optimal methods must be employed for DNA long-term storage. We compared Toxoplasma gondii detection before and after DNA storage using real-time PCR. No significant differences were found depending on duration or storage conditions at -20 °C or -80 °C.

Microbiology (medical)Time Factors[SDV]Life Sciences [q-bio]educationBiologyReal-Time Polymerase Chain ReactionSpecimen HandlingToxoplasma gondii DNAchemistry.chemical_compoundparasitic diseasesFreezingmedicineRetrospective Studiestoxoplasma gondiiDNA storageToxoplasma gondiiamniotic fluidGeneral MedicineDNA Protozoanmedicine.diseasebiology.organism_classificationVirologyToxoplasmosisDna storageMolecular analysisInfectious DiseasesReal-time polymerase chain reaction[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologychemistryMolecular Diagnostic Techniquescongenital toxoplasmosisNucleic acidMESH: DNA Protozoan/isolation&purification; Freezing; Molecular Diagnostic Technics/methods; Specimen Handling/methods; Toxoplasmosis/diagnosisreal-Time PCRToxoplasmaDNAToxoplasmosisDiagnostic microbiology and infectious disease
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Class 1 integrons in environmental and clinical isolates of Pseudomonas aeruginosa.

2011

The aims of this study were to ascertain the presence and spread of class 1 integrons amongst environmental and clinical isolates of Pseudomonas aeruginosa and to characterise their variable regions. A total of 76 isolates (56 clinical and 20 environmental) were studied. The presence of plasmids was explored, and polymerase chain reaction (PCR) was used for integron detection. All amplicons were sequenced. PCR detected class 1 integrons in 26 of the 56 clinical isolates; environmental isolates were integron-free. No plasmids were found, thus all the integrons found are possibly on the chromosome. Most isolates presented one amplicon, except PA110514 and PA116136, which showed two PCR produc…

Microbiology (medical)Transposable elementDNA BacterialMicrobial Sensitivity TestsBiologymedicine.disease_causeIntegronPolymerase Chain Reactionlaw.inventionMicrobiologyIntegronsPlasmidAntibiotic resistancelawDrug Resistance Multiple BacterialmedicineHumansPharmacology (medical)Pseudomonas InfectionsPolymerase chain reactionGeneticsPseudomonas aeruginosaGeneral Medicinebiochemical phenomena metabolism and nutritionAmpliconAnti-Bacterial AgentsBacterial Typing TechniquesInfectious DiseasesFomitesHorizontal gene transferPseudomonas aeruginosabiology.proteinbacteriaWater MicrobiologyPlasmidsInternational journal of antimicrobial agents
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Evaluation of the Amplex eazyplex Loop-Mediated Isothermal Amplification Assay for Rapid Diagnosis of Pneumocystis jirovecii Pneumonia

2020

ABSTRACT Quantitative PCR (qPCR) assays are the gold standard for diagnosis of Pneumocystis jirovecii pneumonia (PCP). However, they are laborious and require skilled personnel. Therefore, execution outside regular working hours of the molecular biology laboratory is limited. The eazyplex P. jirovecii assay (PJA) uses loop-mediated isothermal amplification for detection of P. jirovecii. It is performed directly with respiratory specimens, without the need for special skills, and delivers a result within 3 to 25 min. The goal of our study was to compare the performance of the eazyplex PJA with that of established P. jirovecii qPCR assays. All archived bronchoalveolar lavage fluid (BALF) samp…

Microbiology (medical)Working hoursmedicine.diagnostic_testbusiness.industryPneumonia PneumocystisPneumocystis jirovecii PneumoniaLoop-mediated isothermal amplificationTime to resultMycologyGold standard (test)Pneumocystis cariniiSensitivity and SpecificityMicrobiologyReal-time polymerase chain reactionBronchoalveolar lavageMolecular Diagnostic TechniquesPneumocystis cariniiparasitic diseasesHumansMedicineProspective StudiesbusinessBronchoalveolar Lavage FluidNucleic Acid Amplification TechniquesRetrospective StudiesJournal of Clinical Microbiology
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Application of fnbA gene as new target for the species-specific and quantitative detection of Staphylococcus aureus directly from lower respiratory t…

2013

Staphylococcus aureus is a significant cause of hospital-acquired pneumonia (HAP), particularly in mechanically ventilated patients. We used the fibronectin-binding protein A gene (fnbA) for the species-specific and quantitative detection of S. aureus directly from lower respiratory tract (LRT) specimens by a Taq Man real time PCR. For this reason, a total of 269 lower respiratory tract (LRT) specimens collected from patients with hospital-acquired pneumonia were assayed. Amplification of fnbA in serial dilutions ranged from 10(9) CFU/ ml to 10(2) CFU/ml. Standard curve of triplicate every dilution had slope 3.34±0.1 and R2>0.99 with SD 0.1. Based on these data, the sensitivity and specif…

Microbiology (medical)fnbA Gene real time PCR respiratory infection Staphylococcus aureusSettore MED/07 - Microbiologia E Microbiologia ClinicaStaphylococcus aureusSerial dilutionRespiratory Systemlcsh:QR1-502medicine.disease_causeReal-Time Polymerase Chain ReactionSensitivity and SpecificityfnbA Genelcsh:MicrobiologyPathology and Forensic MedicineMicrobiologyrespiratory infectionPneumonia StaphylococcalmedicineTaqManlcsh:PathologyHumansAdhesins BacterialCross InfectionbiologyStaphylococcus. aureusRespiratory infectionGeneral Medicinemedicine.diseasePneumoniareal time PCRmedicine.anatomical_structureReal-time polymerase chain reactionMolecular Diagnostic TechniquesStaphylococcus aureusbiology.proteinProtein ARespiratory tractlcsh:RB1-214Indian journal of pathologymicrobiology
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In vitro activity of LY333328, a new glycopeptide, against extracellular and intracellular vancomycin-resistant enterococci.

2000

The objectives of the study were to observe the activity of LY333328, a new semisynthetic glycopeptide, compared to that of vancomycin against six strains of Enterococcus faecium and Enterococcus faecalis, including four vancomycin-resistant strains. Bacteria ingested by polymorphonuclear leukocytes (PMN) as well as extracellular bacteria were studied using a colony count method. The activity against intracellular bacteria was tested with the drugs present in the extracellular medium, as well as after preincubating the PMN and removal of the drugs. LY333328 is active against the tested enterococci, regardless of their susceptibility to vancomycin, with MICs of 1-2 mg/l. It is bacteriostatic…

Microbiology (medical)medicine.drug_classAntibioticsEnterococcus faeciumCell Culture TechniquesMicrobial Sensitivity TestsEnterococcus faecalisMicrobiologymedicineExtracellularEnterococcus faecalisHumansGram-Positive Bacterial InfectionsAntibacterial agentbiologyDose-Response Relationship DrugGlycopeptidesLipoglycopeptidesVancomycin ResistanceGeneral Medicinebiochemical phenomena metabolism and nutritionbiology.organism_classificationStreptococcaceaeGlycopeptideAnti-Bacterial AgentsInfectious DiseasesVancomycinmedicine.drugEnterococcus faeciumInfection
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Foci of degeneration produced by measles virus in cell cultures with antibody-free liquid medium

1974

Measles virus produces discrete foci of degeneration in monkey kidney cell and HeLa cell cultures with antibody-free liquid medium. The number of sharply defined “foci” is directly proportional to the relative virus dilution. The technique for enumeration of infective units of measles virus by “foci” count is described. The self-limiting spread of measles virusin vitro and some possible advantages over the standard plaque method are discussed.

Microbiology (medical)medicine.medical_specialtyImmunologyKidneyMeaslesAntibodiesVirusMeasles virusHeLaMedical microbiologymedicineAnimalsHumansImmunology and AllergyCells CulturedBacteriological TechniquesbiologyImmune SeraHaplorhiniGeneral Medicinemedicine.diseasebiology.organism_classificationVirologyIn vitroCulture MediaMeasles virusCell culturebiology.proteinFemaleAntibodyHeLa CellsMedical Microbiology and Immunology
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PCR ITS-RFLP: A useful method for identifying filamentous fungi isolates on grapes.

2010

Restriction digestion analysis of the ITS products was tested as an easy method to identify isolates of filamentous fungi on grapes. Endonucleases SduI, HinfI, MseI, HaeIII were used. Endonucleases BfmI, Cfr9I, Hpy188I, MaeII or PspGI were used as necessary to complete discrimination. The 43 species studied generated 42 different composite profiles. Only the species P. thomii and P. glabrum gave the same composite profile. 96.3% strains tested could be differentiated to the species level with only four enzymes. Hundred ninety nine strains of filamentous fungi were isolated from various vineyards in Burgundy and identified by this method. Penicillium (58.5%) was the genus the most frequently…

MicrobiologyVineyardPolymerase Chain ReactionMicrobiologylaw.inventionHaeIIIFungal ProteinsGenuslawBotanymedicineVitisAmplified Fragment Length Polymorphism AnalysisMycological Typing TechniquesPolymerase chain reactionAspergillusbiologyFungibiology.organism_classificationPenicilliumRestriction digestDNA IntergenicRestriction fragment length polymorphismPolymorphism Restriction Fragment LengthFood Sciencemedicine.drugFood microbiology
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Biosensing of microcystins in water samples; recent advances

2020

Safety and quality of water are significant matters for agriculture, animals and human health. Microcystins, as secondary metabolite of cyanobacteria (blue-green algae) and cyclic heptapeptide cyanotoxin, are one of the main marine toxins in continental aquatic ecosystems. More than 100 microcystins have been identified, of which MC-LR is the most important type due to its high toxicity and common detection in the environment. Climate change is an impressive factor with effects on cyanobacterial blooms as source of microcystins. The presence of this cyanotoxin in freshwater, drinking water, water reservoir supplies and food (vegetable, fish and shellfish) has created a common phenomenon in …

MicrocystinsBiomedical EngineeringBiophysicsBiosensing Techniques02 engineering and technologyMicrocystin01 natural sciencesFreshwater ecosystemHuman healthWater reservoirpolycyclic compoundsElectrochemistryAnimalsHumansEcosystemchemistry.chemical_classificationAquatic ecosystem010401 analytical chemistryReproducibility of ResultsWaterGeneral MedicineCyanotoxin021001 nanoscience & nanotechnology0104 chemical scienceschemistryEnvironmental chemistryEnvironmental science0210 nano-technologyEutrophicationMarine toxinBiotechnologyBiosensors and Bioelectronics
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Access to Phylogeny from Voltammetric Fingerprints of Seeds: the Apsparagus Case

2016

A methodology for characterizing vegetal taxonomic groups from the voltammetric fingerprints of polyphenolic components of seeds is described. It is based on recording the voltammetric response of microparticulate films deposited on glassy carbon electrodes from seed extracts using different organic solvents. The obtained responses in contact with aqueous electrolytes provided characteristic voltammetric profiles at the level of genera/subgenera and/or families using bivariant and multivariant chemometric methods. The voltammograms of 14 species from 5 different families provided family-characteristic patterns. Analysis of voltammetric responses for a set of 20 species of the Asparagus genu…

MicroextractionChromatographybiologyChemistryAsparagusVoltammetry of microparticles010401 analytical chemistryfood and beverages02 engineering and technologyAqueous electrolyteGlassy carbon021001 nanoscience & nanotechnologybiology.organism_classification01 natural sciences0104 chemical sciencesAnalytical ChemistryChemotaxonomyChemometric techniquesChemotaxonomyPhylogeneticsElectrochemistryMyrsiphyllumAsparagusSubgenus0210 nano-technology
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Green Analytical Chemistry Past, Present and Perspectives

2019

The book explains the principles and fundamentals of Green Analytical Chemistry (GAC) and highlights the current developments and future potential of the analytical green chemistry-oriented applications of various solutions. The book consists of sixteen chapters, including the history and milestones of GAC; issues related to teaching of green analytical chemistry and greening the university laboratories; evaluation of impact of analytical activities on the environmental and human health, direct techniques of detection, identification and determination of trace constituents; new achievements in the field of extraction of trace analytes from samples characterized by complex composition of the…

MicroextractionPassive techniquesPollution remote monitoringGreen chromatographyDerivatization processGreen solventsGreen analytical techniquesGreen sorption materialsGreen Analytical ChemistryDirect techniques
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