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dc.rights.licenseopenen_US
hal.structure.identifierBoRdeaux Institute in onCology [Inserm U1312 - BRIC]
dc.contributor.authorFABRE, Adrien
hal.structure.identifierInfection à helicobacter, inflammation et cancer
dc.contributor.authorOLEASTRO, Monica
dc.contributor.authorNUNES, Alexandra
dc.contributor.authorSANTOS, Andrea
hal.structure.identifierInfection à helicobacter, inflammation et cancer
hal.structure.identifierUniversité de Bordeaux [UB]
hal.structure.identifierBoRdeaux Institute in onCology [Inserm U1312 - BRIC]
dc.contributor.authorSIFRE, Elodie
hal.structure.identifierBoRdeaux Institute in onCology [Inserm U1312 - BRIC]
dc.contributor.authorBENEJAT, Lucie
hal.structure.identifierUniversité de Bordeaux [UB]
hal.structure.identifierBoRdeaux Institute in onCology [Inserm U1312 - BRIC]
dc.contributor.authorBUISSONNIÈRE, Alice
hal.structure.identifierBoRdeaux Institute in onCology [Inserm U1312 - BRIC]
dc.contributor.authorFLOCH, Pauline
hal.structure.identifierBoRdeaux Institute in onCology [Inserm U1312 - BRIC]
dc.contributor.authorMÉGRAUD, Francis
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorDUBOIS, Veronique
hal.structure.identifierBoRdeaux Institute in onCology [Inserm U1312 - BRIC]
dc.contributor.authorLEHOURS, Philippe
dc.date.accessioned2023-11-21T14:43:43Z
dc.date.available2023-11-21T14:43:43Z
dc.date.issued2018-09-01
dc.identifier.issn1098-660Xen_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/186019
dc.description.abstractEnA whole-genome sequencing (WGS) approach was conducted in order to identify the molecular determinants associated with antimicrobial resistance in 12 multidrug-resistant and isolates, with a focus on aminoglycoside resistance determinants. Two variants of a new aminoglycoside phosphotransferase gene [(″)- and (″)- ] putatively associated with gentamicin resistance were found. In addition, the following new genes were identified for the first time in : a lincosamide nucleotidyltransferase gene [(G)], likely associated with lincomycin resistance, and two resistance enzyme genes ( and ) similar to those found in , which may confer spectinomycin and gentamicin resistance, respectively. A C1192T mutation of the 16S rRNA gene that may be involved in spectinomycin resistance was also found in a isolate. Genes identified in the present study were located either on the bacterial chromosome or on plasmids that could be transferred naturally. Their role in aminoglycoside resistance remains to be supported by genetic studies. Regarding the other antimicrobial agents studied, i.e., ampicillin, ciprofloxacin, erythromycin, and tetracycline, a perfect correlation between antimicrobial phenotypes and genotypes was found. Overall, our data suggest that WGS analysis is a powerful tool for identifying resistance determinants in and can disclose the full genetic elements associated with resistance, including antimicrobial compounds not tested routinely in antimicrobial susceptibility testing.
dc.language.isoENen_US
dc.subject.enAminoglycosides
dc.subject.enAnimals
dc.subject.enAnti-Bacterial Agents
dc.subject.enBacterial Proteins
dc.subject.enCampylobacter
dc.subject.enCampylobacter Infections
dc.subject.enCampylobacter coli
dc.subject.enCampylobacter jejuni
dc.subject.enDNA
dc.subject.enBacterial
dc.subject.enDrug Resistance
dc.subject.enMultiple
dc.subject.enBacterial
dc.subject.enGenome
dc.subject.enBacterial
dc.subject.enHumans
dc.subject.enMutation
dc.subject.enPhylogeny
dc.subject.enPlasmids
dc.subject.enRNA
dc.subject.enRibosomal
dc.subject.en16S
dc.subject.enRed Meat
dc.subject.enSequence Analysis
dc.subject.enDNA
dc.title.enWhole-Genome Sequence Analysis of Multidrug-Resistant Campylobacter Isolates: a Focus on Aminoglycoside Resistance Determinants.
dc.title.alternativeJ Clin Microbiolen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1128/JCM.00390-18en_US
dc.subject.halSciences du Vivant [q-bio]/Microbiologie et Parasitologieen_US
dc.identifier.pubmed29976591en_US
bordeaux.journalJournal of Clinical Microbiologyen_US
bordeaux.volume56en_US
bordeaux.hal.laboratoriesMFP (Laboratoire Microbiologie Fondamentale et Pathogénicité) - UMR 5234en_US
bordeaux.issue9en_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04298096
hal.version1
hal.date.transferred2023-11-21T14:43:46Z
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%20Clinical%20Microbiology&rft.date=2018-09-01&rft.volume=56&rft.issue=9&rft.eissn=1098-660X&rft.issn=1098-660X&rft.au=FABRE,%20Adrien&OLEASTRO,%20Monica&NUNES,%20Alexandra&SANTOS,%20Andrea&SIFRE,%20Elodie&rft.genre=article


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