Search results for "reverse transcriptase"

showing 10 items of 715 documents

Real-Time RT-PCR assay to quantify the expression of fum1 and fum19 genes from the Fumonisin-producing Fusarium verticillioides

2007

Fumonisins are a group of mycotoxins produced by Fusarium species of the Gibberella fujikuroi species complex that contaminate food and feed products, and represent a risk for human and animal health. In this work, we have developed a specific real-time reverse transcription-PCR (RT-PCR) assay to quantify the level of expression of two genes of the fumonisin biosynthetic cluster in F. verticillioides: fum1 (that encodes a polyketide synthase enzyme) and the ABC transporter encoding gene fum19. The level of expression of both genes was compared with the amount of fumonisin B(1) (FB(1)), measured by HPLC, produced by several strains of F. verticillioides in liquid culture. The results indicat…

Microbiology (medical)FusariumbiologyReverse Transcriptase Polymerase Chain ReactionFungal geneticsfood and beveragesRNA Fungalbiology.organism_classificationFumonisinsMicrobiologyMicrobiologychemistry.chemical_compoundFusariumchemistryGene Expression Regulation FungalPolyketide synthaseGene expressionFumonisinbiology.proteinGibberella fujikuroiATP-Binding Cassette TransportersMycotoxinPolyketide SynthasesMolecular BiologyGeneJournal of Microbiological Methods
researchProduct

Detection of Norovirus Antigens from Recombinant Virus-Like Particles and Stool Samples by a Commercial Norovirus Enzyme-Linked Immunosorbent Assay K…

2006

ABSTRACT The commercial norovirus enzyme-linked immunosorbent assay kit was evaluated for its reactivity to recombinant virus-like particles and the detection of natural viruses from stool samples of Japanese infants and children with sporadic acute gastroenteritis compared to reverse transcription-PCR. The kit had a sensitivity of 76.3% and a specificity of 94.9%. Our results clearly indicated that the kit allows the detection of the most prevalent genotype, GII/4. In order to increase the sensitivity of the kit, the reactivity with norovirus of GII/3 and GII/6 genotypes needs to be improved.

Microbiology (medical)GenotypevirusesEnzyme-Linked Immunosorbent AssayBiologyRecombinant virusmedicine.disease_causeSensitivity and Specificitylaw.inventionFecesfluids and secretionsVirus-like particleAntigenlawVirologyGenotypemedicineHumansChildAntigens ViralFecesCaliciviridae Infectionschemistry.chemical_classificationReverse Transcriptase Polymerase Chain ReactionNorovirusvirus diseasesInfantVirologyGastroenteritisEnzymechemistryChild PreschoolRecombinant DNANorovirusReagent Kits Diagnostic
researchProduct

Real-time reverse transcription PCR analysis of expression of atrazine catabolism genes in two bacterial strains isolated from soil

2004

Abstract The level of expression of highly conserved, plasmid-borne, and widely dispersed atrazine catabolic genes ( atz ) was studied by RT-qPCR in two telluric atrazine-degrading microbes. RT-qPCR assays, based on the use of real-time PCR, were developed in order to quantify atzABCDEF mRNAs in Pseudomonas sp. ADP and atzABC mRNAs in Chelatobacter heintzii . atz gene expression was expressed as mRNA copy number per 10 6 16S rRNA. In Pseudomonas sp. ADP, atz genes were basally expressed. It confirmed atrazine-degrading kinetics indicating that catabolic activity starts immediately after adding the herbicide. atz gene expression increased transitorily in response to atrazine treatment. This …

Microbiology (medical)Microbiologychemistry.chemical_compoundPseudomonasRNA Ribosomal 16SProteobacteriaGene expressionSoil PollutantsRNA MessengerAtrazine[SDV.MP] Life Sciences [q-bio]/Microbiology and ParasitologyMolecular BiologyGeneSoil MicrobiologyMessenger RNAbiologyHerbicidesReverse Transcriptase Polymerase Chain ReactionCatabolismPseudomonasGene Expression Regulation Bacterialbiology.organism_classificationMolecular biologyReverse transcription polymerase chain reactionKinetics[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyBiodegradation EnvironmentalchemistryAtrazineBacteriaJournal of Microbiological Methods
researchProduct

Comparison of the BD Directigen Flu A+B Kit and the Abbott TestPack RSV with a multiplex RT-PCR ELISA for rapid detection of influenza viruses and re…

2005

ABSTRACTThe Directigen Flu A+B enzyme immunoassay and the Abbott TestPack RSV enzyme immunoassay were each compared with a multiplex RT-PCR ELISA by testing 635 nasopharyngeal aspirates collected from children aged < 16 years who had been hospitalised with acute respiratory tract infection during the epidemic season 2002–2003. In this study, the sensitivity of the Directigen Flu A+B assay was unacceptably low (29.3% and 10.0%, respectively) for the detection of influenza A and B viruses. The sensitivity of the Abbott TestPack RSV assay (77.4%) was acceptable and in agreement with the multiplex RT-PCR ELISA.

Microbiology (medical)Paramyxoviridaerespiratory syncytial virusrespiratory tract infectionEnzyme-Linked Immunosorbent AssayPolymerase Chain ReactionSensitivity and Specificityinfluenza virusVirusAssaysMicrobiologyPneumovirinaeNasopharynxMultiplex polymerase chain reactionmedicineMultiplexProspective StudiesMononegaviralesbiologymedicine.diagnostic_testReverse Transcriptase Polymerase Chain Reactionvirus diseasesGeneral Medicinebiology.organism_classificationenzyme immunoassayVirologyInfluenza B virusInfectious Diseasesmultiplex RT-PCRInfluenza A virusRespiratory Syncytial Virus HumanImmunoassayReagent Kits DiagnosticViral diseaseClinical Microbiology and Infection
researchProduct

Performance of the COBAS AMPLICOR HCV MONITOR Test, Version 2.0, an Automated Reverse Transcription-PCR Quantitative System for Hepatitis C Virus Loa…

2000

ABSTRACT A clinical evaluation of an automated quantitative PCR assay, the COBAS AMPLICOR HCV MONITOR test, version 2.0 (v2.0), was carried out to assess the performance of this test in comparison with that of the previous, manual version, the AMPLICOR HCV MONITOR test, and with that of nested PCR. Serial dilutions of serum samples infected with genotype 1b, 2a, or 3, as well as synthetic RNA transcripts and serum samples derived from 87 patients with chronic hepatitis C and infected with genotype 1a, 1b, 2a, 2b, 3a, 3b, 4, or 5, were analyzed to determine the ability of the system to efficiently quantify various hepatitis C virus (HCV) genotypes. These experiments showed that the COBAS AMP…

Microbiology (medical)Serial dilutionHepacivirusHepatitis C virusViremiaHepacivirusmedicine.disease_causePolymerase Chain ReactionFlaviviridaeVirologymedicineHumansbiologyReverse Transcriptase Polymerase Chain Reactionvirus diseasesReproducibility of ResultsHepatitis CHepatitis C ChronicViral Loadbiology.organism_classificationmedicine.diseaseVirologyImmunologyRNA ViralReagent Kits DiagnosticNested polymerase chain reactionViral loadJournal of Clinical Microbiology
researchProduct

Rapid Selective Detection of Potentially Infectious Porcine Epidemic Diarrhea Coronavirus Exposed to Heat Treatments Using Viability RT-qPCR

2020

Coronaviruses (CoVs) cause severe respiratory, enteric, and systemic infections in a wide range of hosts, including humans and animals. Porcine epidemic diarrhea virus (PEDV), a member of the Coronaviridae family, is the etiological agent of porcine epidemic diarrhea (PED), a highly contagious intestinal disease affecting pigs of all ages. In this study, we optimized a viability real-time reverse transcriptase polymerase chain reaction (RT-qPCR) for the selective detection of infectious and heat-inactivated PEDV. PEMAX™, EMA™, and PMAxx™ photoactivable dyes along with PtCl4 and CDDP platinum compounds were screened as viability markers using two RT-qPCR assays: firstly, on PEDV purified RNA…

Microbiology (medical)lcsh:QR1-502Microbiologiamedicine.disease_causeMicrobiologylcsh:MicrobiologyViruslaw.inventionThermal inactivation03 medical and health scienceslawmedicineCoronaviridaePolymerase chain reactionOriginal Research030304 developmental biologyCoronavirusInfectivity0303 health sciencesViability RT-qPCRbiology030306 microbiologyPorcine epidemic diarrhea virusOutbreakbiology.organism_classificationVirologyReverse transcriptaseCoronavirusInfectivityPorcine epidemic diarrhea virusFrontiers in Microbiology
researchProduct

Molecular Epidemiology of Caliciviruses Causing Outbreaks and Sporadic Cases of Acute Gastroenteritis in Spain

2002

ABSTRACT The molecular epidemiology of human caliciviruses (HuCVs) causing sporadic cases and outbreaks of acute gastroenteritis around eastern Spain (Catalonia and the Valencian Community) was studied by reverse transcription-PCR (RT-PCR) and by sequencing part of the RNA polymerase gene in open reading frame 1. HuCVs were detected in 44 of 310 stool specimens (14.19%) negative for other enteric pathogens obtained from children with acute gastroenteritis. Norwalk-like viruses (NLVs) were the most common cause of the gastroenteritis outbreaks investigated here. They were detected in 14 out of 25 (56%) outbreaks with an identified pathogen. Genotypes producing both sporadic cases and outbrea…

Microbiology (medical)virusesMolecular Sequence DataBiologySapovirusVirusDisease Outbreakslaw.inventionlawVirologyGenotypeHumansPathogenGenePhylogenyPolymerase chain reactionFecesCaliciviridae InfectionsMolecular EpidemiologyMolecular epidemiologyReverse Transcriptase Polymerase Chain ReactionNorovirusOutbreakDNA-Directed RNA PolymerasesSequence Analysis DNAVirologyGastroenteritisSpainChild PreschoolAcute DiseaseCaliciviridaeJournal of Clinical Microbiology
researchProduct

Mitochondrial interference by anti-HIV drugs: mechanisms beyond Pol-γ inhibition.

2011

The combined pharmacological approach to the treatment of HIV infection, known as highly active antiretroviral therapy (HAART), has dramatically reduced AIDS-related morbidity and mortality. However, its use has been associated with serious adverse reactions, of which those resulting from mitochondrial dysfunction are particularly widespread. Nucleos(t)ide-reverse transcriptase inhibitors (NRTIs) have long been considered the main source of HAART-related mitochondrial toxicity due to their ability to inhibit Pol-γ, the DNA polymerase responsible for the synthesis of mitochondrial DNA. Nevertheless, accumulating evidence points to a more complex relationship between these organelles and NRTI…

Mitochondrial DNAMitochondrial DiseasesNucleic Acid Synthesis InhibitorDNA polymeraseAnti-HIV Agentsmedicine.medical_treatmentDNA-Directed DNA PolymeraseMitochondrionPharmacologyToxicologyAntiretroviral Therapy Highly ActivemedicineAnimalsHumansNucleic Acid Synthesis InhibitorsPharmacologyProteasebiologyvirus diseasesmedicine.diseaseReverse transcriptaseDNA Polymerase gammaMitochondriaMitochondrial toxicityToxicitybiology.proteinReverse Transcriptase InhibitorsTrends in pharmacological sciences
researchProduct

Digitalis purpurea P5 beta R2, encoding steroid 5 beta-reductase, is a novel defense-related gene involved in cardenolide biosynthesis.

2009

The stereospecific 5 beta-reduction of progesterone is a required step for cardiac glycoside biosynthesis in foxglove plants. Recently, we have isolated the gene P5 beta R, and here we investigate the function and regulation of P5 beta R2, a new progesterone 5 beta-reductase gene from Digitalis purpurea. P5 beta R2 cDNA was isolated from a D. purpurea cDNA library and further characterized at the biochemical, structural and physiological levels. Like P5 beta R, P5 beta R2 catalyzes the 5 beta-reduction of the Delta(4) double bond of several steroids and is present in all plant organs. Under stress conditions or on treatment with chemical elicitors, P5 beta R expression does not vary, wherea…

Models MolecularDNA ComplementaryPhysiologyMolecular Sequence DataPlant ScienceBiologyGenes Plantchemistry.chemical_compoundBiosynthesisGene Expression Regulation PlantComplementary DNACardenolidemedicineAmino Acid SequenceRNA MessengerCloning MolecularBeta (finance)Cardiac glycosideRegulation of gene expressionDigitaliscDNA libraryReverse Transcriptase Polymerase Chain ReactionGene Expression ProfilingDigitalis purpureaSequence Analysis DNAbiology.organism_classificationCardenolidesKineticschemistryBiochemistryOxidoreductasesMetabolic Networks and Pathwaysmedicine.drugThe New phytologist
researchProduct

Docking and multivariate methods to explore HIV-1 drug-resistance: a comparative analysis

2007

In this paper we describe a comparative analysis between multivariate and docking methods in the study of the drug resistance to the reverse transcriptase and the protease inhibitors. In our early papers we developed a simple but efficient method to evaluate the features of compounds that are less likely to trigger resistance or are effective against mutant HIV strains, using the multivariate statistical procedures PCA and DA. In the attempt to create a more solid background for the prediction of susceptibility or resistance, we carried out a comparative analysis between our previous multivariate approach and molecular docking study. The intent of this paper is not only to find further supp…

Models MolecularMultivariate statisticsMultivariate analysisAnti-HIV AgentsCombined useHuman immunodeficiency virus (HIV)Computational biologyDrug resistanceBiologyLigandsBioinformaticsmedicine.disease_causeHIV ProteaseMolecular descriptorDrug Resistance ViralDrug DiscoverymedicineHumansDOCKINGPhysical and Theoretical ChemistryBinding SitesHIV Protease InhibitorsSettore CHIM/08 - Chimica FarmaceuticaHIV Reverse TranscriptaseComputer Science ApplicationsDRUG RESISTANCEDocking (molecular)Drug DesignMultivariate AnalysisMutationHIV-1Computer-Aided DesignReverse Transcriptase InhibitorsMultivariate statisticalJournal of Computer-Aided Molecular Design
researchProduct