Transferable mechanisms of quinolone resistance are more frequent among enterotoxigenic Escherichia coli isolates displaying low-level quinolone resistance
- A. M. Medina,
- ,
- M. Riveros,
- T. J. Ochoa,
- ,
- J. Ruiz(corresponding author)
- Universidad Peruana Cayetano Heredia, Instituto de Medicina Tropical Alexander von Humboldt,
- ,
- Universidad Peruana Cayetano Heredia,
- Universidad Nacional Federico Villarreal,
- School of Public Health, University of Texas
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Publication Information
Output type
Original language
EnglishPages from-to (Number of pages)
Pages 183-187 (5 pages)Journal (Volume, Issue Number)
Tropical Biomedicine (Volume 40, Issue 2)Publication milestones
- Published - 06/2023
Publication status
ISSN
0127-5720Publication IDs
- Scopus: 85166512163
Abstract
This 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.
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