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Daptomycin as adjunctive treatment for experimental infection by Acinetobacter baumannii with resistance to colistin
Authors:Garyfallia Poulakou  Georgios Renieris  Labros Sabrakos  Olympia Zarkotou  Katherine Themeli-Digalaki  Efstathia Perivolioti  Eleni Kraniotaki  Evangelos J. Giamarellos-Bourboulis  Nikolaos Zavras
Affiliation:1. 3rd Department of Internal Medicine, National and Kapodistrian University of Athens, Medical School, Athens 115 27, Greece;2. 4th Department of Internal Medicine, National and Kapodistrian University of Athens, Medical School, Athens 12462, Greece;3. Department of Microbiology, Tzaneio Hospital, Piraeus 185 36, Greece;4. Department of Microbiology, Evangelismos Athens General Hospital, Athens, Greece;5. Department of Children''s Surgery, National and Kapodistrian University of Athens, Medical School, Athens 124 62, Greece
Abstract:The emergence of Acinetobacter baumannii with resistance to colistin (ABRC) led to the investigation of daptomycin as an adjunctive to colistin for these isolates. In this study, one ABRC carbapenemase-producing bloodstream isolate was examined. Minimum inhibitory concentrations (MICs) were >512, >512 and 8 µg/mL for imipenem, daptomycin and colistin, respectively. First, a ‘humanised’ model of the pharmacokinetics of daptomycin and colistin was developed in 18 male C57BL/6 mice. Then, 112 mice were infected by intraperitoneal injection of the ABRC isolate and were randomly assigned into four groups of once-daily treatment for 7 days: group A, controls treated with saline; group B, treated with 20 mg/kg colistin; group C, treated with 50 mg/kg daptomycin; and group D, treated with both agents. Survival was recorded for 7 days in ten mice per group. The remaining mice were sacrificed at regular time intervals following bacterial challenge and the bacterial outgrowth in the liver, lung and right kidney was determined. Mean serum concentrations of daptomycin at 15, 30 and 60 min post-dose were 121.8, 110.3 and 100.4 µg/mL, respectively. The respective concentrations of colistin were 13.9, 9.1 and 7.5 µg/mL. The 7-day mortality in groups A, B, C and D was 100%, 50%, 100% and 0%, respectively. Tissue outgrowth of the right kidney was significantly decreased in group D compared with group B after 72 h. Daptomycin used in combination with colistin leads to prolonged survival in an experimental infection by ABRC. Failure of colistin alone is probably related to rebound of tissue outgrowth.
Keywords:Colistin  Daptomycin  Resistance
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