In vitro activity and rodent efficacy of clinafloxacin for bovine and swine respiratory disease

被引:7
作者
Sweeney, Michael T. [1 ]
Quesnell, Rebecca [1 ]
Tiwari, Raksha [1 ]
LeMay, Mary [1 ]
Watts, Jeffrey L. [1 ]
机构
[1] Zoetis, Global Therapeut Res, Kalamazoo, MI 49007 USA
关键词
clinafloxacin; respiratory diseases; minimum inhibitory concentration; efficacy; mouse models; veterinary medicine; FLUOROQUINOLONES; SUSCEPTIBILITY; RESISTANCE; PATHOGENS;
D O I
10.3389/fmicb.2013.00154
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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 ED50 (efficacious dose-50%) values. The MIC90 values for clinafloxacin against bovine P. multocida, M. haemolytica, Histophilus somni, and M. bovis were 0.125, 0.5, 0.125, and 1 mu g/ml, respectively, and the MIC90 values against swine P. multocida, A. pleuropneumoniae, S. suis, and M. hyopneumoniae were <= 0.03, <= 0.03, 0.125, and <= 0.008 mu g/ml, respectively. Efficacy in mouse models showed average ED50 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.
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页数:6
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