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Plasmidic resistance to colistin mediated by mcr-1 gene in Escherichia coli clinical isolates in Argentina

A retrospective study, 2012–2018

Bibliographic Data

ID14965743
AuthorsDiego Faccone (0009-0000-2688-8229, Buenos Aires), Melina Rapoport (0000-0001-6961-640X, Buenos Aires), Ezequiel Albornoz (Buenos Aires), Federico Celaya (Buenos Aires), Juan De Mendieta (Buenos Aires), Denise De Belder (0000-0002-5568-4804, National Council on Scientific and Technical Research (CONICET), Buenos Aires, Argentina.), Celeste Lucero (0000-0003-3890-8930, Buenos Aires), Sonia Gómez (0000-0001-9106-1762, National Council on Scientific and Technical Research (CONICET), Buenos Aires, Argentina.), Diego Danze (Buenos Aires), Fernando Pasteran (0000-0001-5840-5869, Buenos Aires), Alejandra Corso (0000-0003-1183-6746, [email protected], corresponding author)
Year2020
Volume44
Pages1
Publication date2020-09-23
Open AccessYes
TypeARTICLE
VenueRevista Panamericana de Salud Pública (JOURNAL)
Journal identifiersISSN: 1020-4989 • E-ISSN: 1680-5348
PublisherPan American Health Organization (PUBLISHER • US)
DOI10.26633/rpsp.2020.55
PMID32973904
OpenAlexW3088203841
LanguageEN
Citations received1
References cited28

Objective. To describe the resistance profile and the genetic characteristics of Escherichia coli isolates that harbor the mobilizable colistin resistance gene mcr-1 in Argentina. Methods. This was a retrospective study of 192 E. coli isolates positive for mcr-1 obtained from 69 hospitals of Buenos Aires City and 14 Argentinean provinces in 2012 – 2018. The antimicrobial susceptibility was performed by agar diffusion, broth macrodilution, and/or agar dilution. Standard polymerase chain reaction (PCR) was performed to detect resistance genes and incompatibility groups; specific PCR was applied to discriminate between blaCTX-M allelic groups and mcr-1.5 variant. The genetic relatedness among isolates was evaluated by XbaI-pulsed field gel electrophoresis and multilocus sequence typing in a subset of isolates. Results. All E. coli isolates showed minimal inhibitory concentrations to colistin = 4μg/mL; nearly 50% were resistant to third-generation cephalosporins, with CTX-M-2 being the main extended-spectrum β-lactamase detected. Five E. coli were carbapenemase-producers (3 NDM, 2 KPC). The mcr-1.5 variant was detected in 13.5% of the isolates. No genetic relationship was observed among the mcr-1-positive E. coli clinical isolates, but a high proportion (164/192; 85.4%) of IncI2 plasmids was detected. Conclusions. The presence of IncI2 plasmids among highly diverse E. coli clones suggests that the mcr-1 gene’s wide distribution in Argentina may be driven by the horizontal transmission of IncI2 plasmids

Agar · Agar dilution · Antimicrobial · Bacteria · Biology · Colistin · Enterobacteriaceae · Escherichia coli · Gene · Genotype · MCR-1 · Minimum inhibitory concentration · Multilocus sequence typing · Plasmid · Polymerase chain reaction · Pulsed-field gel electrophoresis · Typing · Antibiotic Resistance in Bacteria · Antibiotics Pharmacokinetics and Efficacy · Pharmaceutical and Antibiotic Environmental Impacts · Genetics · Microbiology

  • Mcr-1 Gene in Latin America

    Open Access•Silvia Adriana Mayer Lentz, Tanise Vendruscolo Dalmolin et al.•Frontiers in Public Health•2021

Citations per year0.2
Citation span2021 - 2021 (1)
Highly citedNo

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