Search results for " pulsed-field"

showing 10 items of 56 documents

Analysis of myxoma virus genome using pulsed-field gel electrophoresis

1996

A method is presented for the isolation of large quantities of myxoma virus DNA using pulsed-field gel electrophoresis (PFGE), and some preliminary applications of this technique.

Gel electrophoresisGeneral Veterinarybiology[SDV]Life Sciences [q-bio]Myxoma virusMyxoma virusGenome ViralPoxviridae InfectionsGeneral Medicinebiology.organism_classificationMicrobiologyGenomeDNA extractionVirologyMolecular biologyVirusElectrophoresis Gel Pulsed-Field[SDV] Life Sciences [q-bio]DNA Viralcardiovascular systemPulsed-field gel electrophoresisAnimalsPoxviridaeRabbitsLeporipoxvirus
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Identification of SCP2165, a new SCP2-derived plasmid of Streptomyces coelicolor A3(2).

2005

Aims:  Characterization of SCP2165, a plasmid identified in the Gram-positive bacterium Streptomyces coelicolor A3(2). Methods and Results:  Pulsed-field gel electrophoresis (PFGE) of mycelia of a S. coelicolor strain embedded in low melting agarose revealed the presence of a plasmid. Restriction enzyme mapping and sequence analysis of a 2·1 kb fragment revealed that this plasmid could be SCP2. SCP2 and its spontaneous derivative SCP2* are self-transmissible plasmids and have chromosome mobilizing ability (c.m.a.). SCP2* has a c. 1000-fold increased c.m.a. compared with SCP2. Interestingly the plasmid, named SCP2165, shows a c.m.a. from 5 × 10−2 to 1 × 10−1 which is 50–100-fold higher than …

Gel electrophoresisPlasmid preparationRecombination GeneticbiologyGene Transfer HorizontalSequence analysisStreptomycetaceaeStreptomyces coelicolorCloning vectorStreptomyces coelicolorbiology.organism_classificationApplied Microbiology and BiotechnologyStreptomycesMolecular biologyElectrophoresis Gel Pulsed-FieldPlasmidConjugative plasmids Pulsed-field gel electrophoresis SCP2 SCP2 derived plasmids Streptomyces coelicolorConjugation GeneticCrosses GeneticPlasmidsLetters in applied microbiology
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Karyotypic diversity among Blastocystis hominis isolates

1997

Fifteen Blastocystis hominis strains, 13 axenic and 2 monoxenic, have been included in the present study. The chromosomal pattern was analyzed by the contour-clamped homogeneous electric-field (CHEF) system. The number of chromosomes detected ranged between 9 and 13, with sizes from 2200 kbp to 260 kbp. Eleven karyotypic profiles, with a common pattern constituted by 8 chromosomes of 2200, 1280, 890, 840, 700, 650, 540 and 260 kbp, were observed. The Jaccard index demonstrated that the similarity between isolates ranged from 0.5714 to 1. The different isolates were clustered in 3 karyotypes (A: 8 isolates; B: 6 isolates and C: 1 isolate). All isolates grouped in karyotype A presented a char…

GeneticsBlastocystisbiologyGenetic VariationKaryotypeBlastocystis InfectionsDNA ProtozoanLoboseabiology.organism_classificationChromosomesElectrophoresis Gel Pulsed-FieldInfectious DiseasesHomogeneousKaryotypingBlastocystis InfectionsGenetic variationAnimalsCluster AnalysisHumansParasite hostingBlastocystis hominisParasitologyAxenicInternational Journal for Parasitology
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Pulsed field gel electrophoresis and genome size estimates

2015

Pulsed field gel electrophoresis (PFGE) is a quick and reliable procedure to resolve DNA molecules larger than 30 kb by applying an electric field that periodically changes direction. This technique can be used to estimate genome size of a microorganism, to reveal if a genome is circular or linear, to indicate the presence of megaplasmids, and to show if a strain contains only one or more chromosomes.

Genome sizeDNA BacterialMaterials scienceChromosomes ArchaealSettore BIO/19 - Microbiologia GeneraleGenomePlasmidchemistry.chemical_compoundPlasmidGeneticGenome ArchaealElectric fieldPulsed-field gel electrophoresisGenome sizeMolecular BiologyElectrophoresis Agar GelBase CompositionStrain (chemistry)BacteriaMulti-repliconMedicine (all)Physical Chromosome Mappingfood and beveragesChromosomes BacterialPhysical Chromosome MappingArchaeaElectrophoresis Gel Pulsed-FieldDNA ArchaealchemistryMegaplasmidBiological systemDNAGenome BacterialGenome topology
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High-resolution genotyping of Campylobacter strains isolated from poultry and humans with amplified fragment length polymorphism fingerprinting.

1999

ABSTRACT For epidemiological studies of Campylobacter infections, molecular typing methods that can differentiate campylobacters at the strain level are needed. In this study we used a recently developed genotyping method, amplified fragment length polymorphism (AFLP), which is based on selective amplification of restriction fragments of chromosomal DNA, for genetic typing of Campylobacter jejuni and Campylobacter coli strains derived from humans and poultry. We developed an automated AFLP fingerprinting method in which restriction endonucleases Hin dIII and Hha I were used in combination with one set of selective PCR primers. This method resulted in evenly distributed band patterns for amp…

GenotypeGenetics and Molecular BiologyCampylobacter coliDeoxyribonuclease HindIIImedicine.disease_causeApplied Microbiology and BiotechnologyCampylobacter jejuniPolymerase Chain ReactionPoultryMicrobiologyRestriction fragmentCampylobacter jejuniGenotypeCampylobacter InfectionsmedicineAnimalsDeoxyribonucleases Type II Site-SpecificGenotypingDNA PrimersGeneticsEcologybiologyCampylobacterfood and beveragesReproducibility of ResultsCampylobacterbiology.organism_classificationDNA FingerprintingBacterial Typing TechniquesElectrophoresis Gel Pulsed-FieldDNA profilingCampylobacter colibiology.proteinAmplified fragment length polymorphismFood ScienceBiotechnologyApplied and environmental microbiology
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No association between Helicobacter pylori genotypes and antibiotic resistance phenotypes within families.

2002

Background. Triple therapy combining a proton pump inhibitor with two antibiotics, e.g. clarythromycin (CLR), metronidazole (MTZ) or amoxicillin (AMX), represents the standard in Helicobacter pylori eradication regimens. Resistance to antimicrobial agents, particularly MTZ (up to 56% in Western countries) and CLR (up to 15% in southern Europe), is frequently observed and may be associated with treatment failure [1]. Recently, several studies indicated that individual H. pylori colonies from a single anatomic site may not always yield identical genotypes, or the identical patterns of susceptibility to antibiotics [2–5]. Representative for every single patient we analyzed 27 H. pylori antrum …

Genotypemedicine.drug_classAntibioticsDrug resistanceMicrobial Sensitivity TestsPolymerase Chain ReactionMicrobiologyHelicobacter InfectionsAntibiotic resistanceDrug Resistance BacterialmedicineHelicobacterbiologyHelicobacter pyloriGastroenterologyGeneral MedicineAmoxicillinHelicobacter pyloribiology.organism_classificationAntimicrobialAnti-Bacterial AgentsElectrophoresis Gel Pulsed-FieldMetronidazoleInfectious DiseasesPhenotypePolymorphism Restriction Fragment Lengthmedicine.drugHelicobacter
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Induction of apoptosis in the blue mussel Mytilus galloprovincialis by tri-n-butyltin chloride

2001

Induction of apoptosis by tri-n-butyltin (TBT) in gill tissue of the mussel Mytilus galloprovincialis was investigated. The terminal dUTP nick-end labeling technique (TUNEL) was used to detect cells displaying DNA fragmentation within gill structures. Genomic DNA fragmentation was detected as characteristically ladder-like pattern of DNA fragments induced by single injection of different doses of TBT (1-5 microg/g) below the mantle, directly into the pallial fluid, after 24 h of incubation. DNA degradation of higher order DNA structure, as well as reduced G(0)/G(1) cell cycle region (the sub-G(1) region) was detectable after 1.5 h of TBT incubation. Presence of apoptotic cells in mussels' g…

GillsGillanimal structuresDNA damageHealth Toxicology and MutagenesisApoptosisDNA FragmentationAquatic ScienceBiologychemistry.chemical_compoundIn Situ Nick-End LabelingAnimalsTUNEL assayCell CyclefungiMusselAnatomyFlow Cytometrybiology.organism_classificationImmunohistochemistryMolecular biologyMytilusBivalviaElectrophoresis Gel Pulsed-FieldchemistryTributyltinDNA damage; apoptosis; tributyltin; musselDNA fragmentationTrialkyltin CompoundsWater Pollutants ChemicalBlue musselAquatic Toxicology
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Outbreak of IMI-1 Carbapenemase-producing colistin-resistant Enterobacter cloacae on the French island of Mayotte (Indian Ocean)

2018

International audience; The spread of carbapenemase-producing Enterobacteriaceae in the Southwest Indian Ocean islands is poorly known. Here we describe an outbreak of colistin-resistant Enterobacter cloacae harbouring blaIMI-1 in the French overseas department of Mayotte. Between October 2015 and January 2017, all isolates of imipenem-non-susceptible E. cloacae at Mayotte Medical Center and University Hospital of Reunion Island were screened for carbapenemase production. Positive isolates were typed by pulsed-field gel electrophoresis and whole-genome sequencing (WGS)-based multilocus sequence typing (MLST), and all β-lactamase genes were identified by PCR and sequencing. Resistance profil…

Male0301 basic medicineImipenembla(IMI-1)Carbapenem-resistant enterobacteriaceaeComorosDisease Outbreaks[ SDV.MP ] Life Sciences [q-bio]/Microbiology and ParasitologyPharmacology (medical)Enterobacteriaceae InfectionsGeneral MedicineMiddle AgedFrench overseas islandAnti-Bacterial AgentsElectrophoresis Gel Pulsed-Field3. Good healthInfectious Diseases[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyFemalemedicine.drugAdultErtapenemMicrobiology (medical)Adolescent030106 microbiologyMayotteMicrobial Sensitivity TestsBiologybeta-LactamasesMicrobiologyCarbapenemaseYoung Adult03 medical and health sciencesBacterial Proteins[ SDV.MHEP ] Life Sciences [q-bio]/Human health and pathologyEnterobacter cloacaePulsed-field gel electrophoresismedicineHumansEtestColistinOutbreakOutbreakbiology.organism_classificationCephalosporinsImipenemCarbapenem-Resistant EnterobacteriaceaeCarbapenemsColistinMultilocus sequence typingEnterobacter cloacaeGenome BacterialMultilocus Sequence Typing
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Cluster of cases of Salmonella enterica serotype Rissen infection in a general hospital, Italy, 2007.

2009

In 2007, three strains of Salmonella enterica serotype Rissen (S. Rissen) were isolated in the laboratory of diagnostic microbiology of the General Hospital of Prato, Tuscany, Italy, over a 1 month and half interval of time. The first isolate was recovered on January 26 from an outpatient with enteritis. Then, two strains were isolated on February 16 and March 11 respectively, from central venous catheters of patients who were being hospitalized in two departments of the Hospital. An epidemiologically linked cluster of cases of salmonellosis was suspected. The three strains were submitted to single enzyme-amplified fragment length polymorphism (SE-AFLP) and XbaI macrorestriction and pulsed-…

MaleCross InfectionMolecular EpidemiologySalmonella RissenInfantSalmonella entericaMiddle AgedSettore MED/42 - Igiene Generale E ApplicataHospitals GeneralBacterial Typing TechniquesElectrophoresis Gel Pulsed-Fieldmolecular subtypingFecesItalyOutpatientsSalmonella Infectionscase clusterAnimalsCluster AnalysisHumansepidemiologyFemaleAmplified Fragment Length Polymorphism AnalysisAgedZoonoses and public health
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CTX-M β-Lactamase-Producing Escherichia coli in French Hospitals: Prevalence, Molecular Epidemiology, and Risk Factors▿

2007

ABSTRACT In 2004, 65 CTX-M-producing Escherichia coli isolates were collected from infected patients in four French hospitals. The bla CTX-M-15 genes were predominant. Pulsed-field gel electrophoresis highlighted a clonal propagation of CTX-M-15-producing strains belonging to phylogenetic group B2, notably in the community. The main risk factors for acquiring these isolates were urinary tract infections or the presence of a urinary catheter in diabetic or renal failure patients.

MaleMESH : Escherichia coliMESH : PrevalenceEpidemiologyMESH : AgedMESH: beta-LactamasesMESH: Urinary Tract Infectionsmedicine.disease_causeMESH: Risk Factors[SDV.MHEP.MI]Life Sciences [q-bio]/Human health and pathology/Infectious diseasesRisk FactorsGenotypePrevalenceMESH : Urinary Tract InfectionsMESH : FemaleMESH: PhylogenyEscherichia coli InfectionsPhylogenyGel electrophoresisMESH: Aged0303 health sciencesMolecular EpidemiologybiologyMESH: Escherichia coliMESH : beta-LactamasesMESH: HospitalsEnterobacteriaceaeMESH : Risk FactorsHospitals3. Good healthElectrophoresis Gel Pulsed-FieldMESH : Hospitals[ SDV.MHEP.MI ] Life Sciences [q-bio]/Human health and pathology/Infectious diseasesMESH: Electrophoresis Gel Pulsed-FieldMESH : Escherichia coli InfectionsUrinary Tract Infections[SDV.MHEP.MI] Life Sciences [q-bio]/Human health and pathology/Infectious diseasesFemaleFranceMicrobiology (medical)Urinary systemMESH : Malebeta-LactamasesMicrobiologyMESH : Epidemiology Molecular03 medical and health sciencesMESH: Epidemiology MolecularmedicineEscherichia coliHumansRisk factorMESH : FranceEscherichia coliMESH: Prevalence030304 developmental biologyMESH : Electrophoresis Gel Pulsed-FieldMESH: Escherichia coli InfectionsAgedMESH: HumansMolecular epidemiology030306 microbiologyMESH : HumansMESH : Phylogenybiology.organism_classificationMESH: MaleMESH: FranceMESH: FemaleBacteria
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