Occurrence of plasmid-mediated quinolone resistance determinants among Escherichia coli strains isolated from animals in Tunisia: Specific pathovars acquired qnr genes.
Animals
Cattle
DNA Gyrase
/ genetics
DNA Topoisomerase IV
/ genetics
Drug Resistance, Multiple, Bacterial
Escherichia coli
/ classification
Escherichia coli Proteins
/ genetics
Feces
/ microbiology
Food Microbiology
Meat
/ microbiology
Microbial Sensitivity Tests
Mutation
Plasmids
/ genetics
Poultry
Quinolones
/ pharmacology
Tunisia
Virulence Factors
/ genetics
Animals
Escherichia coli
Integrons
qnr genes
Journal
Journal of global antimicrobial resistance
ISSN: 2213-7173
Titre abrégé: J Glob Antimicrob Resist
Pays: Netherlands
ID NLM: 101622459
Informations de publication
Date de publication:
03 2020
03 2020
Historique:
received:
07
01
2019
revised:
16
07
2019
accepted:
19
07
2019
pubmed:
1
8
2019
medline:
23
3
2021
entrez:
1
8
2019
Statut:
ppublish
Résumé
The aim of this study was to characterise Escherichia coli strains harbouring plasmid-mediated quinolone resistance (PMQR) genes recovered from various samples (n = 116) from healthy and diarrhoeic animals in Tunisia. All nalidixic acid-resistant E. coli isolates were screened for the presence of PMQR genes. Isolates positive for PMQR genes were investigated by PCR for chromosomal mutations in the quinolone resistance-determining regions (QRDRs) of GyrA and ParC, the presence of class 1 and class 2 integrons, genes encoding tetracycline and sulfonamide resistance, genes encoding virulence factors, and phylogenetic group. Genetic relationships was determined by pulsed-field gel electrophoresis (PFGE). Amongst 51 nalidixic acid-resistant isolates, 9 harboured PMQR genes (5 co-harbouredqnrS1 and qnrB1, 3 harboured qnrS1 and 1 harboured qnrB1). Two types of mutation in the QRDR of GyrA were observed: S83L and D87N (eight isolates) and S83L (one isolate). For the QRDR of ParC, the substitution S80I was observed in four isolates. A class 1 integron was found in six isolates. The tetA or tetB gene was observed in six isolates and both tetA and tetB were co-harboured by two isolates. The sul1, sul2 and sul3 genes were detected in six, four and one isolates, respectively. According to the presence of specific virulence genes, the nine strains were classified as UPEC (5), EAEC (3) and EPEC (1). Three isolates from turkey faeces were clonally related by PFGE. These findings highlight the plausible role of the avian industry as a reservoir of human pathogenic E. coli strains.
Identifiants
pubmed: 31365855
pii: S2213-7165(19)30189-4
doi: 10.1016/j.jgar.2019.07.023
pii:
doi:
Substances chimiques
Escherichia coli Proteins
0
Quinolones
0
Virulence Factors
0
DNA Topoisomerase IV
EC 5.99.1.-
DNA Gyrase
EC 5.99.1.3
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
50-55Informations de copyright
Copyright © 2020 The Authors. Published by Elsevier Ltd.. All rights reserved.