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In vitro activity and rodent efficacy of clinafloxacin for bovine and swine respiratory disease
Clinafloxacin is a broad-spectrum fluoroquinolone that was originally developed and subsequently abandoned in the late 1990s as a human health antibiotic for respiratory diseases. The purpose of this study was to investigate the activity of clinafloxacin as a possible treatment for respiratory disea...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3682159/ https://www.ncbi.nlm.nih.gov/pubmed/23785362 http://dx.doi.org/10.3389/fmicb.2013.00154 |
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author | Sweeney, Michael T. Quesnell, Rebecca Tiwari, Raksha LeMay, Mary Watts, Jeffrey L. |
author_facet | Sweeney, Michael T. Quesnell, Rebecca Tiwari, Raksha LeMay, Mary Watts, Jeffrey L. |
author_sort | Sweeney, Michael T. |
collection | PubMed |
description | Clinafloxacin is a broad-spectrum fluoroquinolone that was originally developed and subsequently abandoned in the late 1990s as a human health antibiotic for respiratory diseases. The purpose of this study was to investigate the activity of clinafloxacin as a possible treatment for respiratory disease in cattle and pigs. Minimum inhibitory concentration (MIC) values were determined using Clinical and Laboratory Standards Institute recommended procedures with recent strains from the Zoetis culture collection. Rodent efficacy was determined in CD-1 mice infected systemically or intranasally with bovine Mannheimia haemolytica or Pasteurella multocida, or swine Actinobacillus pleuropneumoniae, and administered clinafloxacin for determination of ED(50) (efficacious dose-50%) values. The MIC(90) values for clinafloxacin against bovine P. multocida, M. haemolytica, Histophilus somni, and M. bovis were 0.125, 0.5, 0.125, and 1 μg/ml, respectively, and the MIC(90) values against swine P. multocida, A. pleuropneumoniae, S. suis, and M. hyopneumoniae were í0.03, í0.03, 0.125, and í0.008 μg/ml, respectively. Efficacy in mouse models showed average ED(50) values of 0.019 mg/kg/dose in the bovine M. haemolytica systemic infection model, 0.55 mg/kg in the bovine P. multocida intranasal lung challenge model, 0.08 mg/kg/dose in the bovine P. multocida systemic infection model, and 0.7 mg/kg/dose in the swine A. pleuropneumoniae systemic infection model. Clinafloxacin shows good in vitro activity and efficacy in mouse models and may be a novel treatment alternative for the treatment of respiratory disease in cattle and pigs. |
format | Online Article Text |
id | pubmed-3682159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-36821592013-06-19 In vitro activity and rodent efficacy of clinafloxacin for bovine and swine respiratory disease Sweeney, Michael T. Quesnell, Rebecca Tiwari, Raksha LeMay, Mary Watts, Jeffrey L. Front Microbiol Microbiology Clinafloxacin is a broad-spectrum fluoroquinolone that was originally developed and subsequently abandoned in the late 1990s as a human health antibiotic for respiratory diseases. The purpose of this study was to investigate the activity of clinafloxacin as a possible treatment for respiratory disease in cattle and pigs. Minimum inhibitory concentration (MIC) values were determined using Clinical and Laboratory Standards Institute recommended procedures with recent strains from the Zoetis culture collection. Rodent efficacy was determined in CD-1 mice infected systemically or intranasally with bovine Mannheimia haemolytica or Pasteurella multocida, or swine Actinobacillus pleuropneumoniae, and administered clinafloxacin for determination of ED(50) (efficacious dose-50%) values. The MIC(90) values for clinafloxacin against bovine P. multocida, M. haemolytica, Histophilus somni, and M. bovis were 0.125, 0.5, 0.125, and 1 μg/ml, respectively, and the MIC(90) values against swine P. multocida, A. pleuropneumoniae, S. suis, and M. hyopneumoniae were í0.03, í0.03, 0.125, and í0.008 μg/ml, respectively. Efficacy in mouse models showed average ED(50) values of 0.019 mg/kg/dose in the bovine M. haemolytica systemic infection model, 0.55 mg/kg in the bovine P. multocida intranasal lung challenge model, 0.08 mg/kg/dose in the bovine P. multocida systemic infection model, and 0.7 mg/kg/dose in the swine A. pleuropneumoniae systemic infection model. Clinafloxacin shows good in vitro activity and efficacy in mouse models and may be a novel treatment alternative for the treatment of respiratory disease in cattle and pigs. Frontiers Media S.A. 2013-06-14 /pmc/articles/PMC3682159/ /pubmed/23785362 http://dx.doi.org/10.3389/fmicb.2013.00154 Text en Copyright © Sweeney, Quesnell, Tiwari, LeMay and Watts. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc. |
spellingShingle | Microbiology Sweeney, Michael T. Quesnell, Rebecca Tiwari, Raksha LeMay, Mary Watts, Jeffrey L. In vitro activity and rodent efficacy of clinafloxacin for bovine and swine respiratory disease |
title | In vitro activity and rodent efficacy of clinafloxacin for bovine and swine respiratory disease |
title_full | In vitro activity and rodent efficacy of clinafloxacin for bovine and swine respiratory disease |
title_fullStr | In vitro activity and rodent efficacy of clinafloxacin for bovine and swine respiratory disease |
title_full_unstemmed | In vitro activity and rodent efficacy of clinafloxacin for bovine and swine respiratory disease |
title_short | In vitro activity and rodent efficacy of clinafloxacin for bovine and swine respiratory disease |
title_sort | in vitro activity and rodent efficacy of clinafloxacin for bovine and swine respiratory disease |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3682159/ https://www.ncbi.nlm.nih.gov/pubmed/23785362 http://dx.doi.org/10.3389/fmicb.2013.00154 |
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