Identification of mcr-1 Genes and Characterization of Resistance Mechanisms to Colistin in Escherichia coli Isolates from Colombian Hospitals

Author:

De La Cadena Elsa1ORCID,Mahecha Mateo2,Velandia Ana María2,García-Betancur Juan Carlos1ORCID,Rojas Laura J.34,Porras Jessica1ORCID,Pallares Christian15,Villegas María Virginia15ORCID

Affiliation:

1. Grupo de Investigación en Resistencia Antimicrobiana y Epidemiologia Hospitalaria, Universidad El Bosque, Bogotá 110121, Colombia

2. Grupo de Investigación REMA, Facultad de Ciencias de la Salud, Programa de Bacteriología y Laboratorio Clínico, Universidad Colegio Mayor de Cundinamarca, Bogotá 110311, Colombia

3. Department of Microbiology and Molecular Biology, Case Western Reserve University, Cleveland, OH 44106-7164, USA

4. Research Service, Louis Stokes Veterans Affairs Medical Center, Cleveland, OH 44106-7164, USA

5. Comité de Infecciones y Vigilancia Epidemiológica, Clínica Imbanaco, Cali 760031, Colombia

Abstract

We report the presence of the mcr-1 gene among 880 Escherichia coli clinical isolates collected in 13 hospitals from 12 Colombian cities between 2016 and 2019. Seven (0.8%) isolates were colistin resistant (MIC ≥ 4 µg/mL). These colistin-resistant isolates were screened for the presence of the mcr-1 gene; five carried the gene. These five isolates were subjected to whole genome sequencing (WGS) to identify additional resistomes and their ST. In addition, antimicrobial susceptibility testing revealed that all E. coli isolates carrying mcr-1 were susceptible to third generation-cephalosporin and carbapenems, except one, which carried an extended-spectrum β-lactamase (CTX-M-55), along with the fosfomycin resistance encoding gene, fosA. WGS indicated that these isolates belonged to four distinct sequence types (ST58, ST46, ST393, and a newly described ST14315) and to phylogroups B1, A, and D. In this geographic region, the spread of mcr-1 in E. coli is low and has not been inserted into high-risk clones such as ST131, which has been present in the country longer.

Funder

Pfizer Co.

Publisher

MDPI AG

Subject

Pharmacology (medical),Infectious Diseases,Microbiology (medical),General Pharmacology, Toxicology and Pharmaceutics,Biochemistry,Microbiology

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