Role of topoisomerase mutations, plasmid mediated resistance (qnr) and acrAB efflux pump in fluoroquinolone resistant clinical isolates of avian Escherichia coli
- Autores: Yaqoob M.1, Wang L.P.1, Memon J.1, Kashif J.1, Umar S.1, Naseer Z.1, Iqbal M.F.1, Fiaz M.1, Lu C.P.1
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Afiliações:
- Department of Veterinary Medicine
- Edição: Volume 32, Nº 1 (2017)
- Páginas: 49-54
- Seção: Experimental Works
- URL: https://journals.rcsi.science/0891-4168/article/view/178174
- DOI: https://doi.org/10.3103/S0891416817010116
- ID: 178174
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Resumo
We investigated the role of topoisomerase mutations, increased level of the multidrug efflux pump AcrAB, and the plasmid-borne genes (qnr) in the fluoroquinolone (FQ) resistant avian Escherichia coli simultaneously.
Here, we used four FQs (ciprofloxacin, enrofloxacin, ofloxacin and pefloxacin) and eight clinical isolates of E. coli containing six fluoroquinolone-resistant and two fluoroquinolone- susceptible. PCR and direct sequencing methods were used to detect the role of regulator/ repressor gene (acrR).
The objective of this study was to determine the relationship of these resistance mechanisms for fluoroquinolone resistance.
The results showed that (i) all four fluoroquinolone- resistant isolates have topoisomerase mutation and plasmid borne genes qnrS and aac(6')-Ib; (ii) three FQ (enrofloxacin, ofloxacin and pefloxacin) resistant isolates harboring qnrS genes; (iii) two FQ (ciprofloxacin and pefloxacin) resistant isolates had topoisomerase mutation and plasmid borne gene qnrS; (iv) all fluoroquinolone susceptible were not harboring qnrS gene and topoisomerase mutation (v) All isolates were negative for qnrA and qnrB.
We found that FQs resistance combination was correlated with synergistically contribution of these resistance mechanisms. Plasmid mediated resistance by qnrS was correlated to pefloxacin resistance but did not correlate to ofloxacin, enrofloxacin and ciprofloxacin. This mechanism might be account for the pefloxacin resistance in avian E. coli.
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Sobre autores
M. Yaqoob
Department of Veterinary Medicine
Email: lucp@njau.edu.cn
Paquistão, Rawalpindi
L. Wang
Department of Veterinary Medicine
Email: lucp@njau.edu.cn
República Popular da China, Nanjing
J. Memon
Department of Veterinary Medicine
Email: lucp@njau.edu.cn
Paquistão, Rawalpindi
J. Kashif
Department of Veterinary Medicine
Email: lucp@njau.edu.cn
Paquistão, Rawalpindi
S. Umar
Department of Veterinary Medicine
Email: lucp@njau.edu.cn
Paquistão, Rawalpindi
Z. Naseer
Department of Veterinary Medicine
Email: lucp@njau.edu.cn
Paquistão, Rawalpindi
M. Iqbal
Department of Veterinary Medicine
Email: lucp@njau.edu.cn
Paquistão, Rawalpindi
M. Fiaz
Department of Veterinary Medicine
Email: lucp@njau.edu.cn
Paquistão, Rawalpindi
C. Lu
Department of Veterinary Medicine
Autor responsável pela correspondência
Email: lucp@njau.edu.cn
República Popular da China, Nanjing
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