Search results for "Real-Time"

showing 10 items of 881 documents

SCAR-based real time PCR to identify a biocontrol strain (T1) of Trichoderma atroviride and study its population dynamics in soils.

2006

Strains of Trichoderma spp. are known for their antagonistic properties against plant pathogens, some are already on the market, others are under development. In order to launch a strain on the market its perfect identification at the species and strain levels is needed. The aim of this study is to (i) design a SCAR marker for specific identification of strain T1 of Trichoderma atroviride and (ii) monitor population dynamics of this strain in soil by real time PCR. A primer pair targeting a 141-bp fragment enabled specific detection of this strain without cross detection of autochthonous populations of Trichoderma in several field soils. In two soils, population dynamics assessed by real ti…

Microbiology (medical)PopulationBiologycomplex mixturesMicrobiologyPolymerase Chain Reactionlaw.inventionlawREAL-TIME PCReducationDNA FungalMolecular BiologyPolymerase chain reactionSoil MicrobiologyTrichodermaeducation.field_of_studyStrain (chemistry)business.industryFungal geneticsfood and beveragesFungi imperfectiSequence Analysis DNAbiology.organism_classificationDNA FingerprintingSOILSBiotechnologyRandom Amplified Polymorphic DNA TechniquePOPULATION DYNAMICSSCAR[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyTrichodermabusinessSoil microbiologySpecific identificationJournal of microbiological methods
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Clinical significance of Pneumocystis jirovecii DNA detection by real-time PCR in hematological patient respiratory specimens

2020

Microbiology (medical)Simplexvirusfood.ingredientbusiness.industryPneumonia PneumocystisDNAPneumocystis cariniiReal-Time Polymerase Chain Reactionmedicine.diseaseVirologyImmunocompromised Hostchemistry.chemical_compoundPneumoniaInfectious DiseasesfoodReal-time polymerase chain reactionchemistryPneumocystis jirovecii DNAHumansSimplexvirusMedicineClinical significanceRespiratory systembusinessDNAJournal of Infection
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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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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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Comparison of the new Abbott Real Time CMV assay and the Abbott CMV PCR Kit for the quantitation of plasma cytomegalovirus DNAemia

2012

CMV DNA loads measured by the new Abbott RealTime CMV PCR were significantly higher than those quantitated by the Abbott CMV PCR kit (approximately 1 log(10)), and provided a better estimate of the actual CMV load present in plasma specimens as inferred by the use of the WHO standard.

Microbiology (medical)business.industryCongenital cytomegalovirus infectionCytomegalovirusvirus diseasesGeneral Medicinemedicine.diseasePolymerase Chain ReactionVirologylaw.inventionInfectious DiseasesReal-time polymerase chain reactionlawCytomegalovirus InfectionsDNA ViralLinear ModelsmedicineHumansCytomegalovirus infectionsDna viralbusinessPolymerase chain reactionDiagnostic Microbiology and Infectious Disease
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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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Local response of bacterial densities and enzyme activities to elevated atmospheric CO2 and different N supply in the rhizosphere of Phaseolus vulgar…

2008

Publication Inra prise en compte dans l'analyse bibliométrique des publications scientifiques mondiales sur les Fruits, les Légumes et la Pomme de terre. Période 2000-2012. http://prodinra.inra.fr/record/256699; Altered flux of labile C from plant roots into soil is thought to influence growth and maintenance of microbial communities under elevated atmospheric CO2 concentrations. We studied the abundance and function of the soil microbial community at two levels of spatial resolution to assess the response of microorganisms in the rhizosphere of the whole root system and of apical root zones of Phaseolus vulgaris L. to elevated CO2 and high or low N supply. At the coarser resolution, microb…

MicroorganismSoil biologySoil ScienceRoot systemPHASEOLUS VULGARIS L.[SDV.SA.SDS]Life Sciences [q-bio]/Agricultural sciences/Soil studyMicrobiologySOIL ENZYMESDenitrifying bacteriaBotanyREAL-TIME PCRRELATION PLANTE-MICROORGANISMERhizospherebiologyfood and beveragesRHIZOSPHEREDENITRIFICATIONPLFASHARICOTbiology.organism_classificationRELATION SOL-PLANTE-ATMOSPHEREMicrobial population biologySoil waterSIRPhaseolusELEVATED CO2Soil Biology and Biochemistry
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Single-tube nested quantitative PCR: a rational and sensitive technique for detection of retroviral DNA. Application to RERV-H/HRV-5 and confirmation…

2003

It was reported earlier that a few patients suffering from non-Hodgkin's lymphoma had low amounts of DNA from the so-called fifth human exogenous retrovirus, HRV-5. A sensitive and rational method for large-scale screening for HRV-5 DNA was therefore developed. It is a single-tube nested quantitative PCR (stnQPCR), which uses two functionally isolated primer pairs and one probe target distinct from related endogenous retroviral sequences, yet encompassing known HRV-5 variation, allowing optimal use of sequence conservation. DNA from lymphoma, myeloma, and follicular dendritic cell lines was tested for HRV-5 positivity, as was DNA from whole blood of blood donors, non-Hodgkin's lymphoma and …

Mitochondrial DNAMolecular Sequence DataAntibodies ViralDNA MitochondrialPolymerase Chain ReactionCell LineArthritis RheumatoidRetrovirusProvirusesVirologymedicineAnimalsHumansLupus Erythematosus SystemicbiologyBase SequenceLymphoma Non-HodgkinEndogenous Retrovirusesmedicine.diseasebiology.organism_classificationVirologyLymphomaReal-time polymerase chain reactionRetroviridaeDNA ContaminationEvaluation Studies as TopicDNA Viralbiology.proteinLeukocytes MononuclearRabbitsAntibodyPrimer (molecular biology)Nested polymerase chain reactionJournal of virological methods
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Radio network aspects

2006

Publisher Summary This chapter reviews the mobile radio access network reference scenarios (MORANS)—used to study the performance of the radio cellular networks related to UMTS and the methodologies for the radio network performance evaluation, including the theoretical connectivity models,. It discusses the techniques for radio network optimization such as the packet scheduling for cellular systems or system capacity maximization through the use of multiple antennas. . In order to perform system simulations, reference values for the main parameters characterizing a WCDMA network, are required. MORANS is used for the identification of such parameters. The parameters are classified in two gr…

Mobile radioAccess networkComputer sciencebusiness.industryCall Admission ControlComputerSystemsOrganization_COMPUTER-COMMUNICATIONNETWORKSReal-time computingNetwork congestionUMTS Terrestrial Radio Access NetworkCellular networkRadio resource managementbusinessUMTS frequency bandsComputer network
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Correlation-Based Cell Degradation Detection for Operational Fault Detection in Cellular Wireless Base-Stations

2013

The management and troubleshooting of faults in mobile radio networks are challenging as the complexity of radio networks is increasing. A proactive approach to system failures is needed to reduce the number of outages and to reduce the duration of outages in the operational network in order to meet operator’s requirements on network availability, robustness, coverage, capacity and service quality. Automation is needed to protect the operational expenses of t he network. Through a good performance of the network element and a low failure probability the network can operate more efficiently reducing the necessity for equipment investments. We present a new method that utilizes the correlatio…

Mobile radioBase stationNetwork elementbusiness.industryRobustness (computer science)Computer scienceReal-time computingWirelessTroubleshootingbusinessFault detection and isolationFault management
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