Antibiotics (Jan 2022)

Molecular and Genomic Insights of <i>mcr-1</i>-Producing <i>Escherichia coli</i> Isolates from Piglets

  • Jonathan Rodríguez-Santiago,
  • Nadia Rodríguez-Medina,
  • Elsa María Tamayo-Legorreta,
  • Jesús Silva-Sánchez,
  • Juan Téllez-Sosa,
  • Josefina Duran-Bedolla,
  • Alejandro Aguilar-Vera,
  • Alba Neri Lecona-Valera,
  • Ulises Garza-Ramos,
  • Celia Alpuche-Aranda

DOI
https://doi.org/10.3390/antibiotics11020157
Journal volume & issue
Vol. 11, no. 2
p. 157

Abstract

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The use of colistin in food-producing animals favors the emergence and spread of colistin-resistant strains. Here, we investigated the occurrence and molecular mechanisms of colistin resistance among E. coli isolates from a Mexican piglet farm. A collection of 175 cephalosporin-resistant colonies from swine fecal samples were recovered. The colistin resistance phenotype was identified by rapid polymyxin test and the mcr-type genes were screened by PCR. We assessed the colistin-resistant strains by antimicrobial susceptibility test, pulse-field gel electrophoresis, plasmid profile, and mating experiments. Whole-Genome Sequencing data was used to explore the resistome, virulome, and mobilome of colistin-resistant strains. A total of four colistin-resistant E. coli were identified from the cefotaxime-resistant colonies. All harbored the plasmid-borne mcr-1 gene, which was located on conjugative 170-kb IncHI-2 plasmid co-carrying ESBLs genes. Thus, high antimicrobial resistance rates were observed for several antibiotic families. In the RC2-007 strain, the mcr-1 gene was located as part of a prophage carried on non-conjugative 100-kb-plasmid, which upon being transformed into K. variicola strain increased the polymyxin resistance 2-fold. The genomic analysis showed a broad resistome and virulome. Our findings suggest that colistin resistance followed independent acquisition pathways as clonal and non-genetically related mcr-1-harboring strains were identified. These E. coli isolates represent a reservoir of antibiotic resistance and virulence genes in animals for human consumption which could be potentially propagated into other interfaces.

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