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dc.rights.licenseopenen_US
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorPEREYRE, Sabine
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorHÉNIN, Nadège
dc.contributor.authorDOLZY, Amandine
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorGUIRAUD, Jennifer
dc.contributor.authorLAURIER-NADALIÉ, Cécile
dc.contributor.authorGARDETTE, Marie
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorBÉBÉAR, Cécile
dc.date.accessioned2024-10-31T09:00:51Z
dc.date.available2024-10-31T09:00:51Z
dc.date.issued2024-07-16
dc.identifier.issn1098-660Xen_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/203073
dc.description.abstractEnAntimicrobial susceptibility testing (AST) of human mycoplasmas using microdilution is time-consuming. In this study, we compared the performance of MICRONAUT-S plates (Biocentric-Bruker) designed for AST of , , and with the results using the Clinical & Laboratory Standards Institute (CLSI) reference method. Then, we investigated the prevalence and mechanisms of resistance to tetracyclines, fluoroquinolones, and macrolides in France in 2020 and 2021. The two methods were compared using 60 strains. For the resistance prevalence study, -, -, and -positive clinical specimens were collected for 1 month each year in 22 French diagnostic laboratories. MICs were determined using the MICRONAUT-S plates. The (M) gene was screened using PCR, and fluoroquinolone resistance-associated mutations were screened using PCR and Sanger sequencing. Comparing the methods, 99.5% (679/680) MICs obtained using the MICRONAUT-S plates concurred with those obtained using the CLSI reference method. For 90 . isolates, the tetracycline, levofloxacin, and moxifloxacin resistance rates were 11.1%, 2.2%, and 2.2%, respectively, with no clindamycin resistance. For 248 . isolates, the levofloxacin and moxifloxacin resistance rates were 5.2% and 0.8%, respectively; they were 2.9% and 1.5% in 68 . isolates. Tetracycline resistance in (11.8%) was significantly ( < 0.001) higher than in (1.2%). No macrolide resistance was observed. Overall, the customized MICRONAUT-S plates are a reliable, convenient tool for AST of human mycoplasmas. Tetracycline and fluoroquinolone resistance remain limited in France. However, the prevalence of levofloxacin and moxifloxacin resistance has increased significantly in spp. from 2010 to 2015 and requires monitoring. Antimicrobial susceptibility testing of human urogenital mycoplasmas using the CLSI reference broth microdilution method is time-consuming and requires the laborious preparation of antimicrobial stock solutions. Here, we validated the use of reliable, convenient plates designed for antimicrobial susceptibility testing that allows the simultaneous determination of the MICs of eight antibiotics of interest. We then investigated the prevalence and mechanisms of resistance of each of these bacteria to tetracyclines, fluoroquinolones, and macrolides in France in 2020 and 2021. We showed that the prevalence of levofloxacin and moxifloxacin resistance has increased significantly in spp. from 2010 to 2015 and requires ongoing monitoring.
dc.language.isoENen_US
dc.subject.enHumans
dc.subject.enMycoplasma hominis
dc.subject.enMicrobial Sensitivity Tests
dc.subject.enFrance
dc.subject.enUreaplasma
dc.subject.enAnti-Bacterial Agents
dc.subject.enUreaplasma Infections
dc.subject.enMycoplasma Infections
dc.subject.enUreaplasma urealyticum
dc.subject.enDrug Resistance
dc.subject.enBacterial
dc.subject.enPrevalence
dc.subject.enFluoroquinolones
dc.subject.enMacrolides
dc.title.enEvaluation of commercial, customized microdilution plates for Ureaplasma parvum, Ureaplasma urealyticum, and Mycoplasma hominis antimicrobial susceptibility testing and determination of antimicrobial resistance prevalence in France
dc.title.alternativeJ Clin Microbiolen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1128/jcm.00226-24en_US
dc.subject.halSciences du Vivant [q-bio]/Médecine humaine et pathologieen_US
dc.identifier.pubmed38832769en_US
bordeaux.journalJournal of Clinical Microbiologyen_US
bordeaux.pagee0022624en_US
bordeaux.volume62en_US
bordeaux.hal.laboratoriesMFP (Laboratoire Microbiologie Fondamentale et Pathogénicité) - UMR 5234en_US
bordeaux.issue7en_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04761432
hal.version1
hal.date.transferred2024-10-31T09:00:53Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&amp;rft_val_fmt=info:ofi/fmt:kev:mtx:journal&amp;rft.jtitle=Journal%20of%20Clinical%20Microbiology&amp;rft.date=2024-07-16&amp;rft.volume=62&amp;rft.issue=7&amp;rft.spage=e0022624&amp;rft.epage=e0022624&amp;rft.eissn=1098-660X&amp;rft.issn=1098-660X&amp;rft.au=PEREYRE,%20Sabine&amp;H%C3%89NIN,%20Nad%C3%A8ge&amp;DOLZY,%20Amandine&amp;GUIRAUD,%20Jennifer&amp;LAURIER-NADALI%C3%89,%20C%C3%A9cile&amp;rft.genre=article


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