The antibiotic resistome inEscherichia coliisolated from human, food, and animal sources

Author:

Rodrigues Isadora de Alcântara1,Ferrari Rafaela Gomes23,Panzenhagen Pedro2,Pereira dos Santos Anamaria Mota2,Rodrigues Grazielle Lima2,Junior Carlos Adam Conte124,Mano Sergio Borges1

Affiliation:

1. Molecular and Analytical Laboratory Center, Department of Food Technology, Faculty of Veterinary, Universidade Federal Fluminense , Rua Miguel de Frias 9, Niterói, RJ 24220-900 , Brazil

2. Chemistry Institute, Food Science Program, Universidade Federal do Rio de Janeiro , Av. Pasteur 250, Rio de Janeiro, RJ 21941-901 , Brazil

3. Laboratory for the Evaluation of Products of Animal Origin (LAPOA), Center for Agricultural Sciences, Department of Animal Science, Federal University of Paraíba , Cidade Universitária, João Pessoa, Areia, PB 58397-000 , Brazil

4. National Institute of Health Quality Control , Fundação Oswaldo Cruz, Rio de Janeiro, RJ 21040-900 , Brazil

Abstract

AbstractAimsThe aim of this study was to analyze and compare the prevalence and distribution of resistance genes in Escherichia coli genomes isolated from human clinical samples and animal-based foods worldwide.Methods and resultsWe download from NCBI Pathogen Detection Database the corresponding metadata of the 7,123 E. coli genome to access the information about the antimicrobial resistance gene content. The geographic location and the source of isolation were also obtained and compiled with the antimicrobial resistance gene for statistical analysis, results and discussion. Our criteria considered four groups for analyzing the antimicrobial resistance gene distribution. The first group of genomes from invasive clinical human (ICH) samples from countries with Human Development Index (HDI) ≥ 0.850; the second group of ICH from countries with an HDI ≤ 0.849; the third group of animal-based foods (ABF) from countries with HDI ≥ 0.850 and the fourth group of ABFs from countries with HDI ≤ 0.849. The most prevalent genes in the first group were blaCTX-M-134 (96.53%) and blaCTX-M-27 (86.35%). In the second group, ere(A) (95.96%), soxS (94.49%), qepA8 (90.81%), blaCTX-M-15 (85.66%), and fosA3 (80.88%). In the third group, the most frequently detected were aadA12 (98.5%), ant(3”) (89.92%), and blaCARB-2 (87.2%). In the fourth group, aadA12 and aac(3)-IV were identified in 100% of the analyzed genomes.ConclusionsIt was clear that the use of aminoglycosides in animal production is increasing the selective pressure on micro-organisms in both groups of countries since genes linked to aminoglycoside resistance are related to E. coli from ABF samples. The genomic profile of E. coli from HDI ≥ 0.850 countries indicates a selective pressure aimed at cephalosporins given the high prevalence in both sources.

Funder

Carlos Chagas Filho Foundation for Research Support in Rio de Janeiro

Publisher

Oxford University Press (OUP)

Subject

Applied Microbiology and Biotechnology,General Medicine,Biotechnology

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