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Dynamics of Quinolone Resistance in Fecal Escherichia coli of Finishing Pigs after Ciprofloxacin Administration
Escherichia coli resistance to quinolones has now become a serious issue in large-scale pig farms of China. It is necessary to study the dynamics of quinolone resistance in fecal Escherichia coli of pigs after antimicrobial administration. Here, we present the hypothesis that the emergence of resist...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society of Veterinary Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4197147/ https://www.ncbi.nlm.nih.gov/pubmed/24919413 http://dx.doi.org/10.1292/jvms.14-0025 |
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author | HUANG, Kang XU, Chang-Wen ZENG, Bo XIA, Qing-Qing ZHANG, An-Yun LEI, Chang-Wei GUAN, Zhong-Bin CHENG, Han WANG, Hong-Ning |
author_facet | HUANG, Kang XU, Chang-Wen ZENG, Bo XIA, Qing-Qing ZHANG, An-Yun LEI, Chang-Wei GUAN, Zhong-Bin CHENG, Han WANG, Hong-Ning |
author_sort | HUANG, Kang |
collection | PubMed |
description | Escherichia coli resistance to quinolones has now become a serious issue in large-scale pig farms of China. It is necessary to study the dynamics of quinolone resistance in fecal Escherichia coli of pigs after antimicrobial administration. Here, we present the hypothesis that the emergence of resistance in pigs requires drug accumulation for 7 days or more. To test this hypothesis, 26 pigs (90 days old, about 30 kg) not fed any antimicrobial after weaning were selected and divided into 2 equal groups: the experimental (EP) group and control (CP) group. Pigs in the EP group were orally treated daily with 5 mg ciprofloxacin/kg of body weight for 30 days, and pigs in the CP group were fed a normal diet. Fresh feces were collected at 16 time points from day 0 to day 61. At each time point, ten E. coli clones were tested for susceptibility to quinolones and mutations of gyrA and parC. The results showed that the minimal inhibitory concentration (MIC) for ciprofloxacin increased 16-fold compared with the initial MIC (0.5 µg/ml) after ciprofloxacin administration for 3 days and decreased 256-fold compared with the initial MIC (0.5 µg/ml) after ciprofloxacin withdrawal for 26 days. GyrA (S83L, D87N/ D87Y) and parC (S80I) substitutions were observed in all quinolone-resistant E. coli (QREC) clones with an MIC ≥8 µg/ml. This study provides scientific theoretical guidance for the rational use of antimicrobials and the control of bacterial resistance. |
format | Online Article Text |
id | pubmed-4197147 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The Japanese Society of Veterinary Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41971472014-10-17 Dynamics of Quinolone Resistance in Fecal Escherichia coli of Finishing Pigs after Ciprofloxacin Administration HUANG, Kang XU, Chang-Wen ZENG, Bo XIA, Qing-Qing ZHANG, An-Yun LEI, Chang-Wei GUAN, Zhong-Bin CHENG, Han WANG, Hong-Ning J Vet Med Sci Bacteriology Escherichia coli resistance to quinolones has now become a serious issue in large-scale pig farms of China. It is necessary to study the dynamics of quinolone resistance in fecal Escherichia coli of pigs after antimicrobial administration. Here, we present the hypothesis that the emergence of resistance in pigs requires drug accumulation for 7 days or more. To test this hypothesis, 26 pigs (90 days old, about 30 kg) not fed any antimicrobial after weaning were selected and divided into 2 equal groups: the experimental (EP) group and control (CP) group. Pigs in the EP group were orally treated daily with 5 mg ciprofloxacin/kg of body weight for 30 days, and pigs in the CP group were fed a normal diet. Fresh feces were collected at 16 time points from day 0 to day 61. At each time point, ten E. coli clones were tested for susceptibility to quinolones and mutations of gyrA and parC. The results showed that the minimal inhibitory concentration (MIC) for ciprofloxacin increased 16-fold compared with the initial MIC (0.5 µg/ml) after ciprofloxacin administration for 3 days and decreased 256-fold compared with the initial MIC (0.5 µg/ml) after ciprofloxacin withdrawal for 26 days. GyrA (S83L, D87N/ D87Y) and parC (S80I) substitutions were observed in all quinolone-resistant E. coli (QREC) clones with an MIC ≥8 µg/ml. This study provides scientific theoretical guidance for the rational use of antimicrobials and the control of bacterial resistance. The Japanese Society of Veterinary Science 2014-06-12 2014-09 /pmc/articles/PMC4197147/ /pubmed/24919413 http://dx.doi.org/10.1292/jvms.14-0025 Text en ©2014 The Japanese Society of Veterinary Science http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. |
spellingShingle | Bacteriology HUANG, Kang XU, Chang-Wen ZENG, Bo XIA, Qing-Qing ZHANG, An-Yun LEI, Chang-Wei GUAN, Zhong-Bin CHENG, Han WANG, Hong-Ning Dynamics of Quinolone Resistance in Fecal Escherichia coli of Finishing Pigs after Ciprofloxacin Administration |
title | Dynamics of Quinolone Resistance in Fecal Escherichia coli
of Finishing Pigs after Ciprofloxacin Administration |
title_full | Dynamics of Quinolone Resistance in Fecal Escherichia coli
of Finishing Pigs after Ciprofloxacin Administration |
title_fullStr | Dynamics of Quinolone Resistance in Fecal Escherichia coli
of Finishing Pigs after Ciprofloxacin Administration |
title_full_unstemmed | Dynamics of Quinolone Resistance in Fecal Escherichia coli
of Finishing Pigs after Ciprofloxacin Administration |
title_short | Dynamics of Quinolone Resistance in Fecal Escherichia coli
of Finishing Pigs after Ciprofloxacin Administration |
title_sort | dynamics of quinolone resistance in fecal escherichia coli
of finishing pigs after ciprofloxacin administration |
topic | Bacteriology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4197147/ https://www.ncbi.nlm.nih.gov/pubmed/24919413 http://dx.doi.org/10.1292/jvms.14-0025 |
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