The therapeutic effect of tigecycline, unlike that of ceftazidime, is not influenced by whether the Klebsiella pneumoniae strain produces extended-spectrum β-lactamases in experimental pneumonia in rats

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Abstract

The efficacies of tigecycline and ceftazidime against fatal pneumonia in rats caused by an extended-spectrum β-lactamase (ESBL)-positive Klebsiella pneumoniae strain or its wild-type (WT) progenitor were compared. Ceftazidime at 12.5 or 50 mg/kg of body weight twice daily (b.i.d.) was effective (50% or 100% rat survival) in pneumonia caused by the WT isolate but unsuccessful (100% rat mortality) in pneumonia caused by the ESBL-positive variant. In contrast, tigecycline at 6.25, 12.5, or 25 mg/kg b.i.d. showed dosage-dependent efficacy up to 100% rat survival irrespective of the ESBL character of the infecting organism. Copyright © 2013, American Society for Microbiology. All Rights Reserved.

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Goessens, W. H. F., Mouton, J. W., Ten Kate, M. T., Sörgel, F., Kinzig, M., & Bakker-Woudenberg, I. A. J. M. (2013). The therapeutic effect of tigecycline, unlike that of ceftazidime, is not influenced by whether the Klebsiella pneumoniae strain produces extended-spectrum β-lactamases in experimental pneumonia in rats. Antimicrobial Agents and Chemotherapy, 57(1), 643–646. https://doi.org/10.1128/AAC.01154-12

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