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Determination of the Mutant Selection Window and Evaluation of the Killing of Mycoplasma gallisepticum by Danofloxacin, Doxycycline, Tilmicosin, Tylvalosin and Valnemulin

Mycoplasma gallisepticum is a common etiological cause of a chronic respiratory disease in chickens; its increasing antimicrobial resistance compromises the use of tetracyclines, macrolides and quinolones in the farm environment. Mutant selection window (MSW) determination was used to investigate th...

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Autores principales: Zhang, Nan, Ye, Xiaomei, Wu, Yuzhi, Huang, Zilong, Gu, Xiaoyan, Cai, Qinren, Shen, Xiangguang, Jiang, Hongxia, Ding, Huanzhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5215565/
https://www.ncbi.nlm.nih.gov/pubmed/28052123
http://dx.doi.org/10.1371/journal.pone.0169134
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author Zhang, Nan
Ye, Xiaomei
Wu, Yuzhi
Huang, Zilong
Gu, Xiaoyan
Cai, Qinren
Shen, Xiangguang
Jiang, Hongxia
Ding, Huanzhong
author_facet Zhang, Nan
Ye, Xiaomei
Wu, Yuzhi
Huang, Zilong
Gu, Xiaoyan
Cai, Qinren
Shen, Xiangguang
Jiang, Hongxia
Ding, Huanzhong
author_sort Zhang, Nan
collection PubMed
description Mycoplasma gallisepticum is a common etiological cause of a chronic respiratory disease in chickens; its increasing antimicrobial resistance compromises the use of tetracyclines, macrolides and quinolones in the farm environment. Mutant selection window (MSW) determination was used to investigate the propensity for future resistance induction by danofloxacin, doxycycline, tilmicosin, tylvalosin and valnemulin. Killing of M. gallisepticum strain S6 by these antimicrobials was also studied by incubating M. gallisepticum into medium containing the compounds at the minimal concentration that inhibits colony formation by 99% (MIC(99)) and the mutant prevention concentration (MPC). Based on the morphology and colony numbers of M. gallisepticum on agar plates, the four kinds of sera in the order of the applicability for culturing M. gallisepticum were swine serum > horse serum > bovine serum > mixed serum. The MPC/MIC(99) values for each agent were as follows: danofloxacin > tilmicosin > tylvalosin > doxycycline > valnemulin. MPC generated more rapid and greater magnitude killing than MIC(99) against M. gallisepticum. Under exposure of 10(5)–10(9) CFU/mL at MPC drug levels, valnemulin had the slowest rate of reduction in viable organisms and danofloxacin had the highest rate of reduction.
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spelling pubmed-52155652017-01-19 Determination of the Mutant Selection Window and Evaluation of the Killing of Mycoplasma gallisepticum by Danofloxacin, Doxycycline, Tilmicosin, Tylvalosin and Valnemulin Zhang, Nan Ye, Xiaomei Wu, Yuzhi Huang, Zilong Gu, Xiaoyan Cai, Qinren Shen, Xiangguang Jiang, Hongxia Ding, Huanzhong PLoS One Research Article Mycoplasma gallisepticum is a common etiological cause of a chronic respiratory disease in chickens; its increasing antimicrobial resistance compromises the use of tetracyclines, macrolides and quinolones in the farm environment. Mutant selection window (MSW) determination was used to investigate the propensity for future resistance induction by danofloxacin, doxycycline, tilmicosin, tylvalosin and valnemulin. Killing of M. gallisepticum strain S6 by these antimicrobials was also studied by incubating M. gallisepticum into medium containing the compounds at the minimal concentration that inhibits colony formation by 99% (MIC(99)) and the mutant prevention concentration (MPC). Based on the morphology and colony numbers of M. gallisepticum on agar plates, the four kinds of sera in the order of the applicability for culturing M. gallisepticum were swine serum > horse serum > bovine serum > mixed serum. The MPC/MIC(99) values for each agent were as follows: danofloxacin > tilmicosin > tylvalosin > doxycycline > valnemulin. MPC generated more rapid and greater magnitude killing than MIC(99) against M. gallisepticum. Under exposure of 10(5)–10(9) CFU/mL at MPC drug levels, valnemulin had the slowest rate of reduction in viable organisms and danofloxacin had the highest rate of reduction. Public Library of Science 2017-01-04 /pmc/articles/PMC5215565/ /pubmed/28052123 http://dx.doi.org/10.1371/journal.pone.0169134 Text en © 2017 Zhang et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Zhang, Nan
Ye, Xiaomei
Wu, Yuzhi
Huang, Zilong
Gu, Xiaoyan
Cai, Qinren
Shen, Xiangguang
Jiang, Hongxia
Ding, Huanzhong
Determination of the Mutant Selection Window and Evaluation of the Killing of Mycoplasma gallisepticum by Danofloxacin, Doxycycline, Tilmicosin, Tylvalosin and Valnemulin
title Determination of the Mutant Selection Window and Evaluation of the Killing of Mycoplasma gallisepticum by Danofloxacin, Doxycycline, Tilmicosin, Tylvalosin and Valnemulin
title_full Determination of the Mutant Selection Window and Evaluation of the Killing of Mycoplasma gallisepticum by Danofloxacin, Doxycycline, Tilmicosin, Tylvalosin and Valnemulin
title_fullStr Determination of the Mutant Selection Window and Evaluation of the Killing of Mycoplasma gallisepticum by Danofloxacin, Doxycycline, Tilmicosin, Tylvalosin and Valnemulin
title_full_unstemmed Determination of the Mutant Selection Window and Evaluation of the Killing of Mycoplasma gallisepticum by Danofloxacin, Doxycycline, Tilmicosin, Tylvalosin and Valnemulin
title_short Determination of the Mutant Selection Window and Evaluation of the Killing of Mycoplasma gallisepticum by Danofloxacin, Doxycycline, Tilmicosin, Tylvalosin and Valnemulin
title_sort determination of the mutant selection window and evaluation of the killing of mycoplasma gallisepticum by danofloxacin, doxycycline, tilmicosin, tylvalosin and valnemulin
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5215565/
https://www.ncbi.nlm.nih.gov/pubmed/28052123
http://dx.doi.org/10.1371/journal.pone.0169134
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