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dc.rights.licenseopenen_US
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorACCOCEBERRY, Isabelle
IDREF: 075520818
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorROUGERON, Amandine
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorBITEAU, Nicolas
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorCHEVREL, Pauline
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorFITTON-OUHABI, Valerie
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorNOËL, Thierry
dc.date.accessioned2023-11-17T15:53:46Z
dc.date.available2023-11-17T15:53:46Z
dc.date.issued2018-01-01
dc.identifier.issn1098-6596en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/184829
dc.description.abstractEnA strain of the opportunistic pathogenic yeast was genetically modified for use as a cellular model for assessing by allele replacement the impact of lanosterol C14α-demethylase mutations on azole resistance. was chosen because it is susceptible to azole antifungals, it belongs to the CTG clade of yeast, which includes most of the species pathogenic for humans, and it is haploid and easily amenable to genetic transformation and molecular modeling. In this work, allelic replacement is targeted at the locus by the reconstitution of a functional auxotrophic marker in the 3' intergenic region of Homologous and heterologous alleles are expressed from the resident promoter of , allowing accurate comparison of the phenotypic change in azole susceptibility. As a proof of concept, we successfully expressed in different alleles, either bearing or not bearing mutations retrieved from a clinical context, from two phylogenetically distant yeasts, and constitutes a high-fidelity expression system, giving specific Erg11p-dependent fluconazole MICs very close to those observed with the donor strain. This work led us to characterize the phenotypic effect of two kinds of mutation: mutation conferring decreased fluconazole susceptibility in a species-specific manner and mutation conferring fluconazole resistance in several yeast species. In particular, a missense mutation affecting amino acid K143 of Erg11p in species, and the equivalent position K151 in , plays a critical role in fluconazole resistance.
dc.language.isoENen_US
dc.subject.enAntifungal Agents
dc.subject.enCandida
dc.subject.enDrug Resistance
dc.subject.enFungal
dc.subject.enFluconazole
dc.subject.enHumans
dc.subject.enMicrobial Sensitivity Tests
dc.subject.enMutation
dc.subject.enPhylogeny
dc.subject.enSterol 14-Demethylase
dc.title.enA CTG Clade Candida Yeast Genetically Engineered for the Genotype-Phenotype Characterization of Azole Antifungal Resistance in Human-Pathogenic Yeasts.
dc.title.alternativeAntimicrob Agents Chemotheren_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1128/AAC.01483-17en_US
dc.subject.halSciences du Vivant [q-bio]/Microbiologie et Parasitologieen_US
dc.identifier.pubmed29038279en_US
bordeaux.journalAntimicrobial Agents and Chemotherapyen_US
bordeaux.volume62en_US
bordeaux.hal.laboratoriesMFP (Laboratoire Microbiologie Fondamentale et Pathogénicité) - UMR 5234en_US
bordeaux.issue1en_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04292501
hal.version1
hal.date.transferred2023-11-17T15:53:49Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Antimicrobial%20Agents%20and%20Chemotherapy&rft.date=2018-01-01&rft.volume=62&rft.issue=1&rft.eissn=1098-6596&rft.issn=1098-6596&rft.au=ACCOCEBERRY,%20Isabelle&ROUGERON,%20Amandine&BITEAU,%20Nicolas&CHEVREL,%20Pauline&FITTON-OUHABI,%20Valerie&rft.genre=article


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