Susceptibility of canine and feline bacterial pathogens to pradofloxacin and comparison with other fluoroquinolones approved for companion animals

In this study, 908 bacterial pathogens from defined infections of dogs and cats were tested for their susceptibility to the novel fluoroquinolone pradofloxacin, which was approved in 2011 for use in cats and dogs. Most of the bacteria tested (Staphylococcus aureus, Staphylococcus pseudintermedius, E...

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Veröffentlicht in:Veterinary microbiology 2013-02, Vol.162 (1), p.119-126
Hauptverfasser: Schink, Anne-Kathrin, Kadlec, Kristina, Hauschild, Tomasz, Brenner Michael, Geovana, Dörner, Julia C., Ludwig, Carolin, Werckenthin, Christiane, Hehnen, Hans-Robert, Stephan, Bernd, Schwarz, Stefan
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container_end_page 126
container_issue 1
container_start_page 119
container_title Veterinary microbiology
container_volume 162
creator Schink, Anne-Kathrin
Kadlec, Kristina
Hauschild, Tomasz
Brenner Michael, Geovana
Dörner, Julia C.
Ludwig, Carolin
Werckenthin, Christiane
Hehnen, Hans-Robert
Stephan, Bernd
Schwarz, Stefan
description In this study, 908 bacterial pathogens from defined infections of dogs and cats were tested for their susceptibility to the novel fluoroquinolone pradofloxacin, which was approved in 2011 for use in cats and dogs. Most of the bacteria tested (Staphylococcus aureus, Staphylococcus pseudintermedius, Escherichia coli, β-haemolytic streptococci, Pasteurella multocida and Bordetella bronchiseptica) exhibited low pradofloxacin MIC90 values of ≤0.25μg/ml. Solely Proteus spp. and Pseudomonas aeruginosa had higher MIC90 values of ≥4μg/ml. Only six (3.4%) of 177 S. pseudintermedius and 12 (5.3%) of 227 E. coli isolates showed pradofloxacin MICs of ≥2μg/ml. Analysis of the quinolone resistance determining regions of the target genes identified double mutations in GyrA that resulted in amino acid exchanges S83L+D87N or S83L+D87Y and single or double mutations in ParC that resulted in amino acid exchanges S80I or S80I+E84G in all 12 E. coli isolates. The six S. pseudintermedius isolates exhibited amino acid exchanges S84L or E88K in GyrA and S80I in GrlA. Comparative analysis of the MICs of pradofloxacin and the MICs determined for enrofloxacin and its main metabolite ciprofloxacin, but also marbofloxacin, orbifloxacin, difloxacin and ibafloxacin was conducted for the target pathogens S. pseudintermedius, E. coli and P. multocida. This comparison confirmed that pradofloxacin MICs were significantly lower than those of the other tested fluoroquinolones.
doi_str_mv 10.1016/j.vetmic.2012.08.001
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Comparative analysis of the MICs of pradofloxacin and the MICs determined for enrofloxacin and its main metabolite ciprofloxacin, but also marbofloxacin, orbifloxacin, difloxacin and ibafloxacin was conducted for the target pathogens S. pseudintermedius, E. coli and P. multocida. 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Most of the bacteria tested (Staphylococcus aureus, Staphylococcus pseudintermedius, Escherichia coli, β-haemolytic streptococci, Pasteurella multocida and Bordetella bronchiseptica) exhibited low pradofloxacin MIC90 values of ≤0.25μg/ml. Solely Proteus spp. and Pseudomonas aeruginosa had higher MIC90 values of ≥4μg/ml. Only six (3.4%) of 177 S. pseudintermedius and 12 (5.3%) of 227 E. coli isolates showed pradofloxacin MICs of ≥2μg/ml. Analysis of the quinolone resistance determining regions of the target genes identified double mutations in GyrA that resulted in amino acid exchanges S83L+D87N or S83L+D87Y and single or double mutations in ParC that resulted in amino acid exchanges S80I or S80I+E84G in all 12 E. coli isolates. The six S. pseudintermedius isolates exhibited amino acid exchanges S84L or E88K in GyrA and S80I in GrlA. Comparative analysis of the MICs of pradofloxacin and the MICs determined for enrofloxacin and its main metabolite ciprofloxacin, but also marbofloxacin, orbifloxacin, difloxacin and ibafloxacin was conducted for the target pathogens S. pseudintermedius, E. coli and P. multocida. This comparison confirmed that pradofloxacin MICs were significantly lower than those of the other tested fluoroquinolones.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>22939523</pmid><doi>10.1016/j.vetmic.2012.08.001</doi><tpages>8</tpages></addata></record>
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subjects Animals
Anti-Bacterial Agents - pharmacology
Bordetella bronchiseptica
Cat Diseases - microbiology
Cats
Dog Diseases - microbiology
Dogs
Drug Resistance, Microbial
Escherichia coli
Fluoroquinolones - chemistry
Fluoroquinolones - pharmacology
Gram-Negative Bacteria - drug effects
Gram-Positive Bacteria - drug effects
Microbial Sensitivity Tests - veterinary
Minimum inhibitory concentration
Pasteurella multocida
Pets - microbiology
Proteus
Pseudomonas aeruginosa
Staphylococcus
Staphylococcus aureus
Target gene mutation
title Susceptibility of canine and feline bacterial pathogens to pradofloxacin and comparison with other fluoroquinolones approved for companion animals
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