Search results for "Bacteriological Techniques"

showing 10 items of 34 documents

Are pathogenic intestinal bacteria present in stool specimens from patients with chronic heart failure?

2018

It has been reported that patients with chronic heart failure exhibit an intestinal overgrowth of primary gut bacterial pathogens, such as Shigella spp., Salmonella spp., Campylobacter spp., and Yersinia enterocolitica. We failed to reproduce these findings in a cohort of 39 patients admitted to the hospital with decompensated heart failure by means of conventional stool bacterial cultures and a multiplexed polymerase chain reaction assay.

MaleMicrobiology (medical)SalmonellaMicrobiological culture030204 cardiovascular system & hematologymedicine.disease_causePolymerase Chain Reactionlaw.inventionMicrobiologyFeces03 medical and health sciences0302 clinical medicineEnterobacteriaceaelawmedicineHumansShigella030212 general & internal medicineYersinia enterocoliticaPolymerase chain reactionAgedAged 80 and overHeart FailureBacteriological Techniquesbiologybusiness.industryCampylobacterCampylobacterGeneral Medicinemedicine.diseasebiology.organism_classificationGastrointestinal MicrobiomeInfectious DiseasesHeart failureChronic DiseaseFemaleIntestinal bacteriabusinessDiagnostic Microbiology and Infectious Disease
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Biofilm development by potentially pathogenic non-pigmented rapidly growing mycobacteria

2008

Abstract Background A study to evaluate the biofilm-development ability in three different media (Middlebrook 7H9, sterile tap water and PBS-5% glucose) was performed with 19 collection strains from 15 different species on non-pigmented rapidly growing mycobacteria (NPRGM). A microtiter plate assay was developed to evaluate the percentage of covered surface of the microtiter plate wells in different days from day 1 to day 69. Results All strains were able to develop biofilm in all the tested media. Middlebrook 7H9 showed the fastest growth, followed by sterile tap water and PBS-5% glucose. A sigmoid growth curve was detected in all the strains both in Middlebrook 7H9 and in sterile tap wate…

Microbiology (medical)Bacteriological TechniquesMicroscopy ConfocalModels Statisticallcsh:QR1-502BiofilmBiologyMicrobiologyBacterial Adhesionlcsh:MicrobiologyCulture MediaMycobacteriumMicrobiologyMicrotiter plateTap waterBiofilmsResearch ArticleBMC Microbiology
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Development of a modified DNA extraction method for pulsed-field gel electrophoresis analysis of Staphylococcus aureus and enterococci without using …

2010

A modified pulsed-field gel electrophoresis (PFGE) protocol was developed and applied to clinical isolates of Staphylococcus aureus and enterococci to reduce the cost of using lysostaphin. This protocol reduces the expenses of PFGE typing of S. aureus and enterococci as it removes the use of lysostaphin during the spheroplast formation from these bacteria.

Microbiology (medical)DNA BacterialStaphylococcus aureusSettore MED/07 - Microbiologia E Microbiologia ClinicaMicrococcaceaemedicine.disease_causeMicrobiologyMicrobiologyPulsed-field gel electrophoresismedicineHumansMolecular BiologyGel electrophoresisBacteriological TechniquesbiologyLysostaphinbiochemical phenomena metabolism and nutritionSpheroplastStreptococcaceaebiology.organism_classificationBacterial Typing TechniquesElectrophoresis Gel Pulsed-FieldEnterococcusStaphylococcus aureusLysostaphinEnterococcusPulse-field gel electrophoresis(PFGE) MRSA VRE Nosocomial infections
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Nation-wide study of the occurrence of Listeria monocytogenes in French soils using culture-based and molecular detection methods

2013

Identifiant HAL : hal-01120618; International audience; Soil is a potential reservoir of human pathogens and a possible source of contamination of animals, crops and water. In order to study the distribution of Listeria monocytogenes in French soils, a real-time PCR TaqMan assay targeting the phosphoribosylpyrophosphate synthetase (prs) gene of L. monocytogenes was developed for the specific detection and quantification of this bacterium within a collection of 1315 soil DNAs originated from the French Soil Quality Monitoring Network. The prs real-time PCR TaqMan assay was specific for L. monocytogenes and could quantify accurately down to 104L. monocytogenes per gram of dry soil. Among the …

Microbiology (medical)DNA BacterialVeterinary medicineColony Count MicrobialFrench soil monitoring networkmedicine.disease_causeReal-Time Polymerase Chain ReactionMicrobiologyPasturecomplex mixturesTaqMan type probeMicrobiologyCulture-based detection03 medical and health sciencesListeria monocytogenesmedicineTaqMan[ SDU.ENVI ] Sciences of the Universe [physics]/Continental interfaces environmentRibose-Phosphate PyrophosphokinaseSerotyping[SDU.ENVI]Sciences of the Universe [physics]/Continental interfaces environmentMolecular BiologyMolecular detectionSoil Microbiology030304 developmental biologyGramDNA Primers2. Zero hunger0303 health sciencesgeography[ SDE.BE ] Environmental Sciences/Biodiversity and EcologyBacteriological Techniquesgeography.geographical_feature_categorybiology030306 microbiologyContaminationbiology.organism_classificationSoil qualityListeria monocytogenesBacterial Typing TechniquesSoil waterFrance[SDE.BE]Environmental Sciences/Biodiversity and EcologyBacteriaReal-time PCR
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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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Oligopeptide assimilation and transport by Oenococcus oeni

2008

International audience; Aims: Oenococcus oeni is a slow-growing wine bacterium with a low growth yield. It thrives better on complex nitrogen sources than on free amino-acid medium. We aimed to characterize the oligopeptide use of this micro-organism. Methods and Results: Several peptides of two to eight amino-acid residues were able to provide essential amino acids. The disappearance of various peptides from extracellular medium was assessed with whole cells. Initial rates of utilization varied with the peptide, and free amino acids were released into the medium. Conclusions: Oenococcus oeni was able to transport the oligopeptides with two to five amino-acid residues tested and to hydrolys…

NitrogenWinePeptideApplied Microbiology and Biotechnology[ CHIM ] Chemical SciencesIndustrial Microbiology03 medical and health sciencesHydrolysis[CHIM]Chemical Sciences030304 developmental biologyOenococcus oeniWinechemistry.chemical_classificationBacteriological Techniques0303 health sciencesOligopeptidebiology030306 microbiologyBiological TransportGeneral MedicineMetabolismbiology.organism_classificationCulture MediaAmino acidBiochemistrychemistryAmino Acids EssentialOligopeptidesLeuconostocBacteriaBiotechnology
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Rapid and specific detection of F17-related pilin and adhesin genes in diarrheic and septicemic Escherichia coli strains by multiplex PCR

1996

The F17-related adhesins are prevalent in Escherichia coli strains isolated from calves with diarrhea or septicemia and from lambs with nephropathy. The F17 family includes the F17a, F17b, F17c, and F111 fimbriae produced by bovine E. coli strains and the G agglutinin produced by human uropathogenic E. coli strains. An easy and inexpensive multiplex PCR method was developed to detect all the F17-related fimbriae and to identify four subtypes of structural subunit genes and two distinct subfamilies of adhesin genes by only two runs of amplification. A strict correlation was observed between the phenotypic assays and the multiplex PCR method when 166 pathogenic E. coli strains isolated from i…

OperonFimbriaBacteremiamedicine.disease_causePolymerase Chain ReactionPilusFimbriae ProteinsEscherichia coli InfectionsComputingMilieux_MISCELLANEOUS2. Zero hunger0303 health sciencesbiologyEnterobacteriaceae3. Good healthPhenotype[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyMultigene FamilyFimbriae ProteinsBacterial Outer Membrane ProteinsResearch ArticleDiarrheaMicrobiology (medical)Gene Transfer HorizontalCattle DiseasesSheep DiseasesMicrobiology03 medical and health sciencesSpecies SpecificityOperonEscherichia colimedicineAnimalsHumansAdhesins BacterialEscherichia coli[SDV.MP] Life Sciences [q-bio]/Microbiology and ParasitologyDNA Primers030304 developmental biologyBacteriological TechniquesSheepBase Sequence030306 microbiologyTOXINE CNF2biochemical phenomena metabolism and nutritionbiology.organism_classificationMolecular biologyFIMBRIAE F17Bacterial adhesinGenes BacterialPilinbiology.proteinbacteriaCattle
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Mutation of the oxaloacetate decarboxylase gene of Lactococcus lactis subsp. lactis impairs the growth during citrate metabolism

2007

 ; Aims: Citrate metabolism generates metabolic energy through the generation of a membrane potential and a pH gradient. The purpose of this work was to study the influence of oxaloacetate decarboxylase in citrate metabolism and intracellular pH maintenance in relation to acidic conditions. Methods and Results: A Lactococcus lactis oxaloacetate decarboxylase mutant [ILCitM (pFL3)] was constructed by double homologous recombination. During culture with citrate, and whatever the initial pH, the growth rate of the mutant was lower. In addition, the production of diacetyl and acetoin was altered in the mutant strain. However, our results indicated no relationship with a change in the maintenanc…

Oxaloacetic AcidATP citrate lyaseCarboxy-LyasesCITRATE METABOLISMIntracellular pHMolecular Sequence DataDiacetylACIDE LACTIQUEApplied Microbiology and BiotechnologyCitric Acidchemistry.chemical_compoundLACTIC ACID BACTERIAOxaloacetic acidCitrate synthaseBacteriological TechniquesBase SequencebiologyOXALOACETATE DECARBOXYLASEAcetoinLactococcus lactisGeneral MedicineHydrogen-Ion Concentrationbiology.organism_classificationLactococcus lactis[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyOxaloacetate decarboxylaseBiochemistrychemistryGenes BacterialFermentationMutationINTRACELLULAR PHFood Microbiologybiology.proteinGenetic EngineeringCitric acidPhosphoenolpyruvate carboxykinaseBiotechnologyJournal of Applied Microbiology
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Protocol for Specific Isolation of Virulent Strains of Vibrio vulnificus Serovar E (Biotype 2) from Environmental Samples

2004

ABSTRACT The eel pathogen Vibrio vulnificus biotype 2 comprises at least three serovars, with serovar E being the only one involved in both epizootics of eel vibriosis and sporadic cases of human infections. The virulent strains of this serovar (VSE) have only been recovered from clinical (mainly eel tissue) sources. The main objective of this work was to design and validate a new protocol for VSE-specific isolation from environmental samples. The key element of the new protocol is the broth used for the first step (saline eel serum broth [SEB]), which contains eel serum as a nutritive and selective component. This approach takes advantage of the ability of VSE cells to grow in eel serum an…

Serotypeanimal structuresPlating efficiencyfood.ingredientVirulenceFresh WaterPublic Health MicrobiologyVibrio vulnificusApplied Microbiology and BiotechnologyMicrobiologyFish DiseasesMicefoodVibrionaceaeAnimalsHumansAgarSeawaterSerotypingVibrio vulnificusPathogenBacteriological TechniquesMice Inbred BALB CEelsVirulenceEcologybiologybiology.organism_classificationCulture MediaVibrio InfectionsWater MicrobiologyBacteriaFood ScienceBiotechnologyApplied and Environmental Microbiology
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Recommended minimal standards for describing new taxa of the family Halomonadaceae

2007

Following Recommendation 30b of the Bacteriological Code (1990 Revision), a proposal of minimal standards for describing new taxa within the family Halomonadaceae is presented. An effort has been made to evaluate as many different approaches as possible, not only the most conventional ones, to ensure that a rich polyphasic characterization is given. Comments are given on the advantages of each particular technique. The minimal standards are considered as guidelines for authors to prepare descriptions of novel taxa. The proposals presented here have been endorsed by the International Committee on Systematics of Prokaryotes Subcommittee on the Taxonomy of Halomonadaceae.

SystematicsBacteriological TechniquesbiologyManagement scienceEcologyGeneral MedicineClassificationbiology.organism_classificationMicrobiologyFamily HalomonadaceaeHalomonadaceaeHalomonadaceaeTaxonMolecular BiologyEcology Evolution Behavior and SystematicsInternational Journal of Systematic and Evolutionary Microbiology
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