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dc.rights.licenseopenen_US
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorGABRIEL, Frédéric
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorSABRA, Ayman
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorEL-KIRAT-CHATEL, Sofiane
dc.contributor.authorPUJOL, Sophie
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorFITTON-OUHABI, Valérie
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorBRÈTHES, Daniel
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorDEMENTHON, Karine
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorACCOCEBERRY, Isabelle
IDREF: 075520818
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorNOËL, Thierry
dc.date.accessioned2024-09-30T10:58:56Z
dc.date.available2024-09-30T10:58:56Z
dc.date.issued2014-08-01
dc.identifier.issn1098-6596en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/202035
dc.description.abstractEnWe characterized two additional membrane transporters (Fur4p and Dal4p) of the nucleobase cation symporter 1 (NCS1) family involved in the uptake transport of pyrimidines and related molecules in the opportunistic pathogenic yeast Candida lusitaniae. Simple and multiple null mutants were constructed by gene deletion and genetic crosses. The function of each transporter was characterized by supplementation experiments, and the kinetic parameters of the uptake transport of uracil were measured using radiolabeled substrate. Fur4p specifically transports uracil and 5-fluorouracil. Dal4p is very close to Fur4p and transports allantoin (glyoxyldiureide). Deletion of the FUR4 gene confers resistance to 5-fluorouracil as well as cross-resistance to triazoles and imidazole antifungals when they are used simultaneously with 5-fluorouracil. However, the nucleobase transporters are not involved in azole uptake. Only fluorinated pyrimidines, not pyrimidines themselves, are able to promote cross-resistance to azoles by both the salvage and the de novo pathway of pyrimidine synthesis. A reinterpretation of the data previously obtained led us to show that subinhibitory doses of 5-fluorocytosine, 5-fluorouracil, and 5-fluorouridine also were able to trigger resistance to fluconazole in susceptible wild-type strains of C. lusitaniae and of different Candida species. Our results suggest that intracellular fluorinated nucleotides play a key role in azole resistance, either by preventing azoles from targeting the lanosterol 14-alpha-demethylase or its catalytic site or by acting as a molecular switch for the triggering of efflux transport.
dc.language.isoENen_US
dc.subject.enAntifungal Agents
dc.subject.enAzoles
dc.subject.enBiological Transport
dc.subject.enCandida
dc.subject.enCrosses
dc.subject.enGenetic
dc.subject.enDrug Antagonism
dc.subject.enDrug Resistance
dc.subject.enFungal
dc.subject.enFlucytosine
dc.subject.enFluorouracil
dc.subject.enFungal Proteins
dc.subject.enGene Deletion
dc.subject.enGene Expression Regulation
dc.subject.enFungal
dc.subject.enMicrobial Sensitivity Tests
dc.subject.enNucleobase Transport Proteins
dc.subject.enNucleotide Transport Proteins
dc.subject.enSterol 14-Demethylase
dc.subject.enUracil
dc.subject.enUridine
dc.title.enDeletion of the uracil permease gene confers cross-resistance to 5-fluorouracil and azoles in Candida lusitaniae and highlights antagonistic interaction between fluorinated nucleotides and fluconazole.
dc.title.alternativeAntimicrob Agents Chemotheren_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1128/aac.00009-14en_US
dc.subject.halSciences du Vivant [q-bio]/Microbiologie et Parasitologieen_US
dc.identifier.pubmed24867971en_US
bordeaux.journalAntimicrobial Agents and Chemotherapyen_US
bordeaux.page4476-85en_US
bordeaux.volume58en_US
bordeaux.hal.laboratoriesMFP (Laboratoire Microbiologie Fondamentale et Pathogénicité) - UMR 5234en_US
bordeaux.issue8en_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exportfalse
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=2014-08-01&rft.volume=58&rft.issue=8&rft.spage=4476-85&rft.epage=4476-85&rft.eissn=1098-6596&rft.issn=1098-6596&rft.au=GABRIEL,%20Fr%C3%A9d%C3%A9ric&SABRA,%20Ayman&EL-KIRAT-CHATEL,%20Sofiane&PUJOL,%20Sophie&FITTON-OUHABI,%20Val%C3%A9rie&rft.genre=article


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