0000000000002701

AUTHOR

O. Vagner

showing 6 related works from this author

Optimization of the preanalytical steps of matrix-assisted laser desorption ionization-time of flight mass spectrometry identification provides a fle…

2012

ABSTRACT We report here that modifications of the preanalytical steps of matrix-assisted laser desorption ionization–time of flight mass spectrometry (MALDI-TOF MS) identification of yeasts, with regard to the original protocol provided by the manufacturers, appear to be efficient for the reliable routine identification of clinical yeast isolates in medical laboratories. Indeed, when one colony was sampled instead of five and the protein extraction protocol was modified, the performance of MALDI-TOF MS was superior to that of the API ID 32C method (discrepancies were confirmed by using molecular identification), allowing the correct identification of 94% of the 335 clinical isolates prospec…

Microbiology (medical)Microbiological TechniquesTime Factorsmedical laboratories[SDV]Life Sciences [q-bio]clinical yeast isolatesMatrix assisted laser desorption ionization time of flightMycologyMass spectrometrySpecimen Handlingflight mass spectrometry03 medical and health sciencesYeastsHumansionization-time030304 developmental biologyMolecular identification0303 health sciencesChromatography030306 microbiologyChemistryYeastCulture MediaIdentification (information)Mycosesmatrix-assisted laserSpectrometry Mass Matrix-Assisted Laser Desorption-Ionization[SDE]Environmental SciencesidentificationJournal of clinical microbiology
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Détection et identification de Fusarium spp. dans le réseau hydrique d’un centre hospitalier universitaire

2012

Infectious Diseasesbusiness.industryMedicinebusinessJournal de Mycologie Médicale
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Profiles and seasonal distribution of airborne fungi in indoor and outdoor environments at a French hospital

2009

International audience; A one-year prospective survey of fungal air contamination was conducted in outdoor air and inside two haematological units of a French hospital. Air was sampled with a portable Air System Impactor. During this period of survey, the mean viable fungal load was 122.1 cfu/m(3) in outdoor air samples, and 4.1 and 3.9 cfu/m(3) in samples from adult and pediatric haematology units, respectively. In outdoor samples, Cladosporium was the dominant genus (55%) while in the clinical units, Penicillium sp. (23 to 25%), Aspergillus sp. (15 to 23%) and Bjerkandera adusta (11 to 13%) were the most frequently recovered airborne fungi. The outdoor fungal load was far higher in autumn…

Veterinary medicineEnvironmental EngineeringSeasonal distributionAir Microbiology010501 environmental sciences01 natural sciences03 medical and health sciencesBjerkandera adusta[ SDV.MP ] Life Sciences [q-bio]/Microbiology and ParasitologymedicineEnvironmental ChemistryHospital Design and ConstructionWaste Management and DisposalAir quality indexAirborne fungi Outdoor and indoor air Hospital Haematology units Seasonal variations Aspergillus0105 earth and related environmental sciences0303 health sciencesAspergillusbiology030306 microbiologyEcologyFungiFungi imperfectiSeasonalitybiology.organism_classificationmedicine.diseasePollution[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyAir Pollution IndoorPenicilliumParticulate MatterFranceSeasonsEnvironmental MonitoringCladosporium
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Dynamics of fungal colonization in a new medical mycology laboratory

2012

International audience; Objective of the study. - Study of the spatio-temporal fungal colonization in a new medical mycology laboratory. Methods. - A 17-month survey of airborne fungal contamination was conducted in a new medical mycology laboratory at a tertiary care university hospital. This survey was implemented at three different periods: before the new premises were occupied (period A), during the move into the new laboratory (period B) and after resumption of the mycological activities in these new premises (period C). Results. - During period A, the airborne fungal load ranged from 2.3 to 6 cfu/m(3). The most frequently recovered airborne fungi were Penicillium spp. (75 to 100%). Du…

Fungal contaminationFilamentous fungiMedical mycology[SDV]Life Sciences [q-bio]Fungal contaminationAir MicrobiologyColony Count MicrobialMycologyAspergillus fumigatusConidiumMicrobiology03 medical and health sciences0302 clinical medicineFungal colonization[SDV.BV]Life Sciences [q-bio]/Vegetal BiologyHumansMedical mycology laboratory030212 general & internal medicine0303 health sciencesAspergillusbiology030306 microbiologyAspergillus fumigatusFungiPenicilliumLaboratories Hospitalbiology.organism_classificationPenicillium chrysogenumAspergillusInfectious DiseasesPenicillium spp.[SDE]Environmental SciencesPenicilliumHospital UnitsEnvironmental MonitoringJournal de Mycologie Médicale
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Failure to differentiate Cryptosporidium parvum from C. meleagridis based on PCR amplification of eight DNA sequences.

1998

ABSTRACT In order to determine the specificities of PCR-based assays used for detecting Cryptosporidium parvum DNA, eight pairs of previously described PCR primers targeting six distinct regions of the Cryptosporidium genome were evaluated for the detection of C. parvum , the agent of human cryptosporidiosis, and C. muris , C. baileyi , and C. meleagridis , three Cryptosporidium species that infect birds or mammals but are not considered to be human pathogens. The four Cryptosporidium species were divided into two groups: C. parvum and C. meleagridis , which gave the same-sized fragments with all the reactions, and C. muris and C. baileyi , which gave positive results with primer pairs targ…

animal diseases030231 tropical medicineGenes ProtozoanCryptosporidiumApplied Microbiology and BiotechnologyGenomePolymerase Chain ReactionSensitivity and SpecificityDNA sequencing18S ribosomal RNAMicrobiologylaw.invention03 medical and health sciences0302 clinical medicineSpecies Specificitylawparasitic diseasesTECHNIQUE PCRAnimalsHumansGenePolymerase chain reactionComputingMilieux_MISCELLANEOUSDNA Primers[SDV.EE]Life Sciences [q-bio]/Ecology environmentCryptosporidium parvum0303 health sciencesEcologybiologyBase Sequence030306 microbiologyCryptosporidiumDNA Protozoanbiology.organism_classificationVirologyBacterial Typing Techniques[SDV.EE] Life Sciences [q-bio]/Ecology environmentCryptosporidium parvumEnvironmental and Public Health MicrobiologyPrimer (molecular biology)Water MicrobiologyFood ScienceBiotechnologyApplied and environmental microbiology
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Evaluation of CandiSelect4, a new chromogenic medium for isolation and presumptive identification of Candida species from clinical specimens

2008

Abstract In clinical laboratories, isolation of Candida species is generally based on the culture of specimens on Sabouraud dextrose agar. This strategy does not allow species identification on primary culture and makes it difficult to detect mixed cultures. Chromogenic media contain substrates that react specifically with different Candida species, and partly overcome these difficulties. Objectives The aim of this study was to compare two chromogenic media: (i) CandiSelect4 (C4), a new medium developed for direct identification of C. albicans and presumptive identification of C. krusei , C. tropicalis and C. glabrata (ii) CHROMagar Candida (CH), a medium licensed for direct identification …

food.ingredientChromogenicFungi imperfectiBiologyIsolation (microbiology)biology.organism_classificationCorpus albicansMicrobiologyInfectious DiseasesfoodAgarSpecies identificationChromagar candidaIdentification (biology)Journal de Mycologie Médicale
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