Search results for "rase"

showing 10 items of 4343 documents

Fast and low-cost decentralized surveillance of transmission of tuberculosis based on strain-specific PCRs tailored from whole genome sequencing data…

2015

Molecular epidemiology has transformed our knowledge of how tuberculosis (TB) is transmitted. Whole genome sequencing (WGS) has reached unprecedented levels of accuracy. However, it has increased technical requirements and costs, and analysis of data delays results. Our objective was to find a way to reconcile speed and ease of implementation with the high resolution of WGS. The targeted regional allele-specific oligonucleotide PCR (TRAP) assay presented here is based on allele-specific PCR targeting strain-specific single nucleotide polymorphisms, identified from WGS, and makes it possible to track actively transmitted Mycobacterium tuberculosis strains. A TRAP assay was optimized to track…

DNA BacterialMicrobiology (medical)TuberculosisPopulationPilot ProjectsMinisatellite RepeatsComputational biologyBiologyPolymerase Chain ReactionPolymorphism Single NucleotideTRAPlaw.inventionMycobacterium tuberculosisTrap (computing)lawmedicineHumanseducationAllelesWhole genome sequencingMolecular Epidemiologywhole genome sequencingeducation.field_of_studyGeographyMolecular epidemiologytransmissionAllele-specific PCRMycobacterium tuberculosisSequence Analysis DNAGeneral Medicinemedicine.diseasebiology.organism_classificationVirologyInfectious DiseasesTransmission (mechanics)tuberculosisSpainPopulation SurveillanceVariants of PCRGenome Bacterial
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Distribution and diversity of type III secretion system-like genes in saprophytic and phytopathogenic fluorescent pseudomonads

2004

Type three secretion systems (TTSSs) are protein translocation mechanisms associated with bacterial pathogenicity in host plants, and hypersensitive reactions in non-host plants. Distribution and diversity of TTSS-like genes within a collection of saprophytic and phytopathogenic fluorescent pseudomonads were characterized. This collection included 16 strains belonging to 13 pathogenic species, and 87 strains belonging to five saprophytic species isolated from plant rhizosphere and soil. Presence of conserved hypersensitive reaction/pathogenicity (hrp) genes (hrc RST) was assessed both by PCR using primers designed to amplify the corresponding sequence and by dot-blot hybridization using a P…

DNA BacterialMolecular Sequence DataBiologyPlant RootsPolymerase Chain ReactionApplied Microbiology and BiotechnologyMicrobiologyFluorescenceMicrobiologyType three secretion systemlaw.inventionPSEUDOMOMAS FLUORESCENS03 medical and health sciencesBacterial ProteinslawPseudomonasRNA Ribosomal 16SGenotypeGene[SDV.MP] Life Sciences [q-bio]/Microbiology and ParasitologySoil MicrobiologyPolymerase chain reactionComputingMilieux_MISCELLANEOUSPlant Diseases030304 developmental biology2. Zero hungerGenetics0303 health sciencesEcology030306 microbiologyGenetic transferGenetic VariationSequence Analysis DNAPlants16S ribosomal RNAbiology.organism_classification[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyPOUVOIR PATHOGENERestriction fragment length polymorphismPolymorphism Restriction Fragment LengthBacteria
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Fast protocols for the 5S rDNA and ITS-2 based identification ofOenococcus oeni

2005

To identify specific marker sequences for the rapid identification of Oenococcus oeni, we sequenced the 23S-5S internal transcribed spacer (ITS-2) region and the 5S rDNA of five different O. oeni strains and three phylogenetically related lactic acid bacteria (LAB). Comparative analysis revealed 100% identity among the ITS-2 region of the O. oeni strains and remarkable differences in length and sequence compared to related LAB. These results enabled us to develop a primer set for a rapid PCR-identification of O. oeni within three hours. Moreover, the comparison of the 5S rDNA sequences and the highly conserved secondary structure provided the template for the design of three fluorescence-la…

DNA BacterialMolecular Sequence DataDNA RibosomalPolymerase Chain ReactionMicrobiologyRibosome5S ribosomal RNASequence Homology Nucleic AcidDNA Ribosomal SpacerGeneticsmedicineInternal transcribed spacerMolecular BiologyGeneIn Situ Hybridization FluorescenceOenococcus oeniGeneticsBase Sequencebiologymedicine.diagnostic_testOligonucleotideRNA Ribosomal 5Sbiology.organism_classificationGram-Positive CocciRNA BacterialGenes BacterialNucleic Acid ConformationPrimer (molecular biology)LeuconostocFluorescence in situ hybridizationFEMS Microbiology Letters
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Relative Abundances of Proteobacterial Membrane-Bound and Periplasmic Nitrate Reductases in Selected Environments

2007

ABSTRACT Dissimilatory nitrate reduction is catalyzed by a membrane-bound and a periplasmic nitrate reductase. We set up a real-time PCR assay to quantify these two enzymes, using the narG and napA genes, encoding the catalytic subunits of the two types of nitrate reductases, as molecular markers. The narG and napA gene copy numbers in DNA extracted from 18 different environments showed high variations, with most numbers ranging from 2 × 10 2 to 6.8 × 10 4 copies per ng of DNA. This study provides evidence that, in soil samples, the number of proteobacteria carrying the napA gene is often as high as that of proteobacteria carrying the narG gene. The high correlation observed between narG an…

DNA BacterialMolecular Sequence DataEnvironmentNitrate reductaseNitrate ReductasePlant RootsPolymerase Chain ReactionApplied Microbiology and BiotechnologyMicrobial Ecologychemistry.chemical_compoundBacterial ProteinsNitrateProteobacteriaGeneSoil Microbiology[SDV.EE]Life Sciences [q-bio]/Ecology environmentNAPAEcologybiologyMembrane ProteinsPeriplasmic spacebiology.organism_classificationBiochemistrychemistryPeriplasmic ProteinsProteobacteriaBacteriaDNAFood ScienceBiotechnologyApplied and Environmental Microbiology
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Nested PCR method for rapid and sensitive detection of Vibrio vulnificus in fish, sediments, and water

1995

A nested PCR for the detection of Vibrio vulnificus in fish farms was developed as an alternative to cultural methods by using universal primers flanking the V. vulnificus-specific sequences directed against 23S rRNA genes. This specific assay detected 10 fg of DNA or 12 to 120 cells in artificially inoculated samples without enrichment and within 24 h.

DNA BacterialMolecular Sequence DataVibrio vulnificusPolymerase Chain ReactionSensitivity and SpecificityApplied Microbiology and Biotechnologylaw.inventionMicrobiologylawVibrionaceae23S ribosomal RNAAnimalsRibosomal DNAPolymerase chain reactionDNA PrimersVibrioBase SequenceEcologybiologyFishesRibosomal RNAbiology.organism_classificationMolecular biologyVibrioRNA Ribosomal 23SEvaluation Studies as TopicGenes BacterialWater MicrobiologyNested polymerase chain reactionResearch ArticleFood ScienceBiotechnology
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Description of Enterovibrio nigricans sp. nov., reclassification of Vibrio calviensis as Enterovibrio calviensis comb. nov. and emended description o…

2009

Eleven strains of halophilic, facultative anaerobes isolated from healthy and diseased Dentex dentex and Sparus aurata (bony fishes) cultured in Spanish Mediterranean fisheries have been studied by a polyphasic approach that included a wide phenotypic characterization, DNA-DNA hybridization and phylogenetic analysis using 16S rRNA, recA and rpoD gene sequences. All strains were phylogenetically related to Enterovibrio species and Vibrio calviensis. On the basis of sequence analysis and DNA-DNA hybridization data, eight of the strains were identified as Enterovibrio coralii. The remaining three strains formed a tight, independent clade in all sequence analyses and showed less than 70 % DNA-D…

DNA BacterialMolecular Sequence DataVibrionaceaeSigma FactorDNA RibosomalMicrobiologyMicrobiologyVibrionaceaePhylogeneticsRNA Ribosomal 16SSequence Homology Nucleic AcidAnimalsCluster AnalysisPhylogenyEcology Evolution Behavior and SystematicsGeneticsbiologyPhylogenetic treeNucleic Acid HybridizationDentex dentexDNA-Directed RNA PolymerasesSequence Analysis DNAGeneral MedicineRibosomal RNAbiology.organism_classification16S ribosomal RNAVibrioBacterial Typing TechniquesPerciformesRec A RecombinasesSpainTaxonomy (biology)International Journal of Systematic and Evolutionary Microbiology
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Rapid differentiation and in situ detection of 16 sourdough lactobacillus species by multiplex PCR.

2005

ABSTRACT A two-step multiplex PCR-based method was designed for the rapid detection of 16 species of lactobacilli known to be commonly present in sourdough. The first step of multiplex PCR was developed with a mixture of group-specific primers, while the second step included three multiplex PCR assays with a mixture of species-specific primers. Primers were derived from sequences that specify the 16S rRNA, the 16S-23S rRNA intergenic spacer region, and part of the 23S rRNA gene. The primer pairs designed were shown to exclusively amplify the targeted rrn operon fragment of the corresponding species. Due to the reliability of simultaneously identifying Lactobacillus plantarum , Lactobacillus…

DNA BacterialPCR multiplex batteri lattici impasti acidiTime FactorsMolecular Sequence DataLactobacillus pentosusLactobacillus paraplantarumApplied Microbiology and BiotechnologyPolymerase Chain Reactionlaw.inventionSpecies Specificity23S ribosomal RNAlawLactobacillusRNA Ribosomal 16SMultiplex polymerase chain reactionDNA Ribosomal SpacerPolymerase chain reactionPhylogenyDNA PrimersEcologybiologyBase Sequencefood and beveragesBreadSequence Analysis DNAbiology.organism_classificationMolecular biologyBacterial Typing TechniquesLactobacillusRNA Ribosomal 23SFood MicrobiologySequence AlignmentLactobacillus plantarumFood ScienceBiotechnologyIn silico PCRSettore AGR/16 - Microbiologia AgrariaApplied and environmental microbiology
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Microbial diversity in a thermophilic aerobic biofilm process: analysis by length heterogeneity PCR (LH-PCR).

2003

A two-stage pilot-scale thermophilic aerobic suspended carrier biofilm process (SCBP) was set up for the on-site treatment of pulp and paper mill whitewater lining. The microbial diversity in this process was analyzed by length heterogeneity analysis of PCR-amplified 16S ribosomal DNA. The primer pair selected for PCR amplification was first evaluated by a computational analysis of fragment lengths in ten main phylogenetical eubacterial groups. The fragment contained the first third of the 16S rRNA gene, which was shown to vary naturally between 465 and 563 bp in length. The length heterogeneity analysis of polymerase chain reaction (LH-PCR) profile of the biomass attached to carrier elemen…

DNA BacterialPaperEnvironmental EngineeringFlexibacterMicroorganismPopulationPopulation DynamicsIndustrial WastePolymerase Chain ReactionWaste Disposal FluidMicrobiologyRNA Ribosomal 16SBiomasseducationWaste Management and DisposalRibosomal DNAWater Science and TechnologyCivil and Structural Engineeringeducation.field_of_studybiologyBacteriaEcological ModelingThermophileBiofilmTemperature16S ribosomal RNAbiology.organism_classificationPollutionCytophagaBiofilmsWater research
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Multiple Site-Specific Binding of Fis Protein to Escherichia coli nuoA-N Promoter DNA and its Impact on DNA Topology Visualised by Means of Scanning …

2004

DNA BacterialPlasma protein bindingMicroscopy Atomic Forcemedicine.disease_causeBiochemistryBacterial geneticsMitochondrial Proteinschemistry.chemical_compoundScanning probe microscopyMicroscopyEscherichia coliImage Processing Computer-AssistedmedicinePromoter Regions GeneticMolecular BiologyEscherichia coliDNA PrimersReverse Transcriptase Polymerase Chain ReactionOrganic ChemistryMembrane ProteinsPromoterMolecular biologyMembrane proteinchemistryMolecular MedicineDNAProtein BindingChemBioChem
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Phylogenetic analysis of the genera Proteus, Morganella and Providencia by comparison of rpoB sequences of type and clinical strains suggests the cla…

2010

Phylogenetic analysis of partial rpoB gene sequences of type and clinical strains belonging to different 16S rRNA gene-fingerprinting ribogroups within 11 species of enterobacteria of the genera Proteus, Morganella and Providencia was performed and allowed the definition of rpoB clades, supported by high bootstrap values and confirmed by ≥2.5 % nucleotide divergence. None of the resulting clades included strains belonging to different species and the majority of the species were confirmed as discrete and homogeneous. However, more than one distinct rpoB clade could be defined among strains belonging to the species Proteus vulgaris (two clades), Providencia alcalifaciens (two clades) and Pro…

DNA BacterialProteus myxofacienSettore MED/07 - Microbiologia E Microbiologia ClinicaMolecular Sequence DataProteus vulgarisZoologyProvidenciaBiologyProvidenciaMicrobiologyMorganellaGenusCosenzaea myxofaciensRNA Ribosomal 16SProteuProteus myxofaciensPhylogenyEcology Evolution Behavior and SystematicsGeneticsMorganellaCosenzaeaProvidencia rettgeriDNA-Directed RNA PolymerasesSequence Analysis DNAGeneral MedicineProteusbiology.organism_classificationrpoBBacterial Typing TechniquesProteusclassificationGenes BacterialbacteriarpoB
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