Publicación:
Transferable mechanisms of quinolone resistance are more frequent among enterotoxigenic Escherichia coli isolates displaying low-level quinolone resistance

dc.contributor.authorMedina Prada, Anicia Magaly
dc.contributor.authorRivera Albinagorta, Fulton Paul
dc.contributor.authorRiveros Ramirez, Maribel Denise
dc.contributor.authorOchoa Woodell, Theresa Jean
dc.contributor.authorPons, M.J.
dc.contributor.authorRuiz, J.
dc.date.accessioned2023-10-09T17:09:20Z
dc.date.available2023-10-09T17:09:20Z
dc.date.issued2023
dc.description.abstractThis study analysed the mechanisms of quinolone resistance among enterotoxigenic Escherichia coli (ETEC) in a periurban area of Lima, Peru. The susceptibility to nalidixic acid and ciprofloxacin, the role of Phe-Arg-b-Naphtylamyde inhibitable-(PAbN) efflux pumps, the presence of mutations in gyrA and parC as well as the presence of aac(6’)Ib-cr, qepA, qnrA, qnrB, qnrC, qnrD, qnrVC and oqxAB were determined in 31 ETEC from previous case/control studies of children’s diarrhoea. Discordances between disk diffusion, with all isolates showing intermediate or fully resistance to nalidixic acid, and minimal inhibitory concentration (MIC), with 7 isolates being below considered resistance breakpoint, were observed. Twenty-one isolates possessed gyrA mutations (19 S83L, 2 S83A). AAC(6’) Ib-cr, QnrS, QnrB and QepA were found in 7, 6, 2 and 1 isolates respectively, with 3 isolates presenting 2 transferable mechanisms of quinolone resistance (TMQR) concomitantly. TMQR were more frequent among isolates with MIC to nalidixic acid ranging from 2 to 16 mg/L (p=0.03), while gyrA mutations were more frequent among isolates with nalidixic acid MIC > 128 mg/L (p=0.0002). In summary, the mechanisms of quinolone resistance present in ETEC isolates in Peru have been described. Differences in the prevalence of underlying mechanisms associated with final MIC levels were observed. The results suggest two different evolutive strategies to survive in the presence of quinolones related to specific bacterial genetic background.en_US
dc.description.sponsorshipEste trabajo fue financiado por FONDECYT [número de contrato 08-2019].es_PE
dc.identifier.doihttps://doi.org/10.47665/tb.40.2.009
dc.identifier.urihttps://hdl.handle.net/20.500.12866/14246
dc.language.isoeng
dc.publisherThe Malaysian Society of Parasitology and Tropical Medicine
dc.relation.ispartofurn:issn:2521-9855
dc.relation.ispartofseriesTropical Biomedicine
dc.relation.issn2521-9855
dc.rightshttps://purl.org/coar/access_right/c_16ec
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/deed.es
dc.subjectEpidemiologyen_US
dc.subjectPublic healthen_US
dc.subjectGyrAen_US
dc.subjectQnren_US
dc.subjectDiarrheogenic Escherichia colien_US
dc.subject.ocdehttps://purl.org/pe-repo/ocde/ford#3.03.06
dc.titleTransferable mechanisms of quinolone resistance are more frequent among enterotoxigenic Escherichia coli isolates displaying low-level quinolone resistanceen_US
dc.typehttp://purl.org/coar/resource_type/c_6501
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dspace.entity.typePublication

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