Comparison of in vitro activities of plazomicin and other aminoglycosides against clinical isolates of Klebsiella pneumoniae and Escherichia coli

dc.contributor.authorInce, Gizem
dc.contributor.authorMirza, Hasan Cenk
dc.contributor.authorGuclu, Aylin Uskudar
dc.contributor.authorGumus, Hale
dc.contributor.authorErol, Cigdem
dc.contributor.authorBasustaoglu, Ahmet
dc.contributor.orcID0000-0001-9071-9606en_US
dc.contributor.orcID0000-0002-1872-028Xen_US
dc.contributor.orcID0000-0002-2535-2534en_US
dc.contributor.orcID0000-0002-8853-3893en_US
dc.contributor.pubmedID34499728en_US
dc.contributor.researcherIDAAJ-2108-2021en_US
dc.contributor.researcherIDAAU-6196-2020en_US
dc.contributor.researcherIDAAJ-1219-2021en_US
dc.contributor.researcherIDF-1232-2015en_US
dc.date.accessioned2022-06-23T12:03:54Z
dc.date.available2022-06-23T12:03:54Z
dc.date.issued2021
dc.description.abstractObjectives: To compare the in vitro activity of plazomicin and two older aminoglycosides (gentamicin and amikacin) against 180 isolates of Escherichia coli and Klebsiella pneumoniae, including subsets of 60 non-ESBL-producing, 60 ESBL-producing and 60 carbapenem-resistant (46 carrying bla(OXA-48), 11 carrying bla(NDM) and 3 carrying bla(OXA-48) and bla(NDM)) strains. Methods: MICs of plazomicin, gentamicin and amikacin were determined by a gradient diffusion method. Gentamicin and amikacin MICs were interpreted according to CLSI criteria and EUCAST breakpoint tables. Plazomicin MICs were interpreted using FDA-defined breakpoints. Results: All non-ESBL-producing and ESBL-producing isolates were susceptible to plazomicin. The plazomicin susceptibility rate (71.7%) in carbapenem-resistant isolates was significantly higher than those observed for gentamicin (45%) and amikacin (56.7% and 51.7% according to CLSI and EUCAST breakpoints, respectively). Gentamicin, amikacin and plazomicin susceptibility rates (35.6% for gentamicin; 44.4% and 37.8% for amikacin according to CLSI and EUCAST breakpoints, respectively; 64.4% for plazomicin) in carbapenem-resistant K. pneumoniae were significantly lower than those observed for carbapenem-resistant E. coli isolates (73.3% for gentamicin; 93.3% for amikacin and plazomicin). Gentamicin, amikacin and plazomicin susceptibility rates for bla(NDM)-positive isolates were lower than those observed for bla(OXA-48)-positive isolates, but differences were not statistically significant. Among the isolates that were non-susceptible to both gentamicin and amikacin, the plazomicin susceptibility rate was less than 30%. Conclusions: Although plazomicin showed excellent in vitro activity against carbapenem-susceptible isolates, the plazomicin resistance rate increased to 35.6% among carbapenem-resistant K. pneumoniae and further increased to 45.5% among bla(NDM)-positive isolates.en_US
dc.identifier.endpage3196en_US
dc.identifier.issn0305-7453en_US
dc.identifier.issue12en_US
dc.identifier.scopus2-s2.0-85121056577en_US
dc.identifier.startpage3192en_US
dc.identifier.urihttp://hdl.handle.net/11727/7137
dc.identifier.volume76en_US
dc.identifier.wos000728183500015en_US
dc.language.isoengen_US
dc.relation.isversionof10.1093/jac/dkab331en_US
dc.relation.journalJOURNAL OF ANTIMICROBIAL CHEMOTHERAPYen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergien_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCARBAPENEMASEen_US
dc.titleComparison of in vitro activities of plazomicin and other aminoglycosides against clinical isolates of Klebsiella pneumoniae and Escherichia colien_US
dc.typeArticleen_US

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