Occurrence of plasmid-mediated quinolone resistance determinants among Escherichia coli strains isolated from animals in Tunisia: Specific pathovars acquired 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
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

50-55

Informations de copyright

Copyright © 2020 The Authors. Published by Elsevier Ltd.. All rights reserved.

Auteurs

Hajer Kilani (H)

Université de Tunis El Manar, Institut de la Recherché Vétérinaire de Tunisie, Tunis 1006, Tunisia; Université de Tunis El Manar, Faculté de Médecine de Tunis, LR99ES09 Laboratoire de Recherche 'Résistance aux Antimicrobiens', Tunis 1007, Tunisia.

Sana Ferjani (S)

Université de Tunis El Manar, Faculté de Médecine de Tunis, LR99ES09 Laboratoire de Recherche 'Résistance aux Antimicrobiens', Tunis 1007, Tunisia.

Riadh Mansouri (R)

Université de Tunis El Manar, Institut de la Recherché Vétérinaire de Tunisie, Tunis 1006, Tunisia.

Ilhem Boutiba-Benboubaker (I)

Université de Tunis El Manar, Faculté de Médecine de Tunis, LR99ES09 Laboratoire de Recherche 'Résistance aux Antimicrobiens', Tunis 1007, Tunisia; Hôpital Charles Nicolle, Service de Microbiologie, Tunis 1006, Tunisia.

Mohamed Salah Abbassi (MS)

Université de Tunis El Manar, Institut de la Recherché Vétérinaire de Tunisie, Tunis 1006, Tunisia; Université de Tunis El Manar, Faculté de Médecine de Tunis, LR99ES09 Laboratoire de Recherche 'Résistance aux Antimicrobiens', Tunis 1007, Tunisia. Electronic address: salahtoumi_mohamed@yahoo.com.

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Classifications MeSH