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dc.rights.licenseopenen_US
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorBELOTTI, P T
dc.contributor.authorTHABET, L
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorLAFARGUE, Aurelie
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorANDRE, C
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorCOULANGE-MAYONNOVE, L
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorARPIN, Corinne
IDREF: 093324626
dc.contributor.authorMESSADI, A
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorM’ZALI, Fatima
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorQUENTIN, C
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorDUBOIS, Veronique
dc.date.accessioned2023-12-01T10:09:01Z
dc.date.available2023-12-01T10:09:01Z
dc.date.issued2015-08-01
dc.identifier.issn1460-2091en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/186297
dc.description.abstractEnA burn unit of a hospital in Tunis underwent an endemic situation caused by imipenem-resistant Pseudomonas aeruginosa. For nine non-repetitive isolates of a clonal VIM-2-producing strain, the blaVIM-2 genetic background was characterized and the associated qnrVC1 gene molecularly analysed. The imipenem resistance mechanism was investigated by phenotypic and molecular tests, and resistance transfer was studied by conjugation and transformation experiments. The integron's structure was characterized by sequencing, and qnrVC1 expression was explored after cloning experiments. The nine VIM-2-producing strains were collected from eight patients and one environmental sample. All transfer assays failed, suggesting a chromosomal location of blaVIM-2. This latter was found to be part of a class 1 integron of ∼7500 bp, which also contains blaOXA-2, aadA1 and two copies of the aadB, arr-6 and qnrVC1 genes. qnrVC1 exhibited higher homology with the chromosomally encoded qnr genes of Vibrionaceae than with plasmid-mediated qnr genes of Enterobacteriaceae. The qnrVC1 gene cassette possesses a promoter allowing its expression, and it conferred decreased fluoroquinolone susceptibility to Escherichia coli. Additionally, on the same integron, genes encoding an uncommon group IIC-attC intron were detected. A VIM-2-producing P. aeruginosa outbreak led us to characterize an integron harbouring a qnrVC1 cassette and a new group IIC-attC intron. This is the first known description of a qnr determinant in a P. aeruginosa strain. Its presence conferred a low level of resistance to quinolones in E. coli, which might favour the emergence of highly resistant mutants.
dc.language.isoENen_US
dc.subject.enAnti-Bacterial Agents
dc.subject.enBurn Units
dc.subject.enBurns
dc.subject.enConjugation
dc.subject.enGenetic
dc.subject.enEndemic Diseases
dc.subject.enGene Expression Profiling
dc.subject.enGene Transfer
dc.subject.enHorizontal
dc.subject.enGenes
dc.subject.enBacterial
dc.subject.enHumans
dc.subject.enImipenem
dc.subject.enIntegrons
dc.subject.enIntrons
dc.subject.enMolecular Sequence Data
dc.subject.enPseudomonas Infections
dc.subject.enPseudomonas aeruginosa
dc.subject.enSequence Analysis
dc.subject.enDNA
dc.subject.enTransformation
dc.subject.enBacterial
dc.subject.enTunisia
dc.subject.enbeta-Lactam Resistance
dc.subject.enbeta-Lactamases
dc.title.enDescription of an original integron encompassing blaVIM-2, qnrVC1 and genes encoding bacterial group II intron proteins in Pseudomonas aeruginosa.
dc.title.alternativeJ Antimicrob Chemotheren_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1093/jac/dkv103en_US
dc.subject.halSciences du Vivant [q-bio]/Microbiologie et Parasitologieen_US
dc.identifier.pubmed25977399en_US
bordeaux.journalJournal of Antimicrobial Chemotherapyen_US
bordeaux.page2237-40en_US
bordeaux.volume70en_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.identifierhal-04317484
hal.version1
hal.date.transferred2023-12-01T10:09:03Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
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