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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]
hal.structure.identifierUniversité de Bordeaux [UB]
dc.contributor.authorCOUZIGOU, Celia
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorFITTON-OUHABI, Valerie
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorBITEAU, Nicolas
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorNOEL, Thierry
dc.date.accessioned2023-11-21T14:07:41Z
dc.date.available2023-11-21T14:07:41Z
dc.date.issued2019-03-01
dc.identifier.issn1460-2091en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/186017
dc.description.abstractEnA strain of the opportunistic pathogenic yeast Candida lusitaniae was genetically engineered for full-length replacement of the FKS1 gene encoding the target of echinocandin antifungals in order to assess the impact of FKS mutations on echinocandin resistance and reduced echinocandin susceptibility (RES). FKS1 allelic exchange was achieved by transforming C. lusitaniae with two DNA fragments covering the entire FKS1 ORF. Both fragments overlap a 40 bp region where SNPs or small indels of interest were inserted. To target integration at the FKS1 locus, each DNA fragment was fused with split auxotrophic markers of which complementary truncated parts were previously inserted into the chromosomal regions flanking FKS1, allowing selection on minimal medium. Three SNPs described in the FKS1 hotspot (HS) regions HS1 or HS2 of clinical isolates of Candida albicans were expressed at an equivalent position in C. lusitaniae and were confirmed to confer either reduced susceptibility (F641V) or full resistance (S645P and R1361G) to caspofungin. The F659 deletion reported in an FKS2 allele of Candida glabrata and the naturally occurring P660A substitution in FKS1 of Candida parapsilosis were shown to confer a 256-fold and 6-fold increase in caspofungin MIC, respectively, when introduced into an FKS1 allele of C. lusitaniae. We have successfully developed a C. lusitaniae strain for the expression of full-length FKS1 alleles harbouring known mutations contributing to reduced susceptibility or resistance to caspofungin, thus opening the way for the screening of other FKS1/FKS2 mutations potentially involved in RES.
dc.language.isoENen_US
dc.subject.enAlleles
dc.subject.enAntifungal Agents
dc.subject.enCandida
dc.subject.enCaspofungin
dc.subject.enDrug Resistance
dc.subject.enFungal
dc.subject.enGlucosyltransferases
dc.subject.enMicrobial Sensitivity Tests
dc.subject.enPolymorphism
dc.subject.enSingle Nucleotide
dc.subject.enRecombination
dc.subject.enGenetic
dc.title.enChallenging SNP impact on caspofungin resistance by full-length FKS1 allele replacement in Candida lusitaniae.
dc.title.alternativeJ Antimicrob Chemotheren_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1093/jac/dky475en_US
dc.subject.halSciences du Vivant [q-bio]/Microbiologie et Parasitologieen_US
dc.identifier.pubmed30517635en_US
bordeaux.journalJournal of Antimicrobial Chemotherapyen_US
bordeaux.page618-624en_US
bordeaux.volume74en_US
bordeaux.hal.laboratoriesMFP (Laboratoire Microbiologie Fondamentale et Pathogénicité) - UMR 5234en_US
bordeaux.issue3en_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04297934
hal.version1
hal.date.transferred2023-11-21T14:07:44Z
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=Journal%20of%20Antimicrobial%20Chemotherapy&rft.date=2019-03-01&rft.volume=74&rft.issue=3&rft.spage=618-624&rft.epage=618-624&rft.eissn=1460-2091&rft.issn=1460-2091&rft.au=ACCOCEBERRY,%20Isabelle&COUZIGOU,%20Celia&FITTON-OUHABI,%20Valerie&BITEAU,%20Nicolas&NOEL,%20Thierry&rft.genre=article


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