Volume 27, Issue 10 pp. 1361-1365
Research Article
Free Access

Effects of vancomycin, daptomycin, fosfomycin, tigecycline, and ceftriaxone on Staphylococcus epidermidis biofilms

Stefan Hajdu

Stefan Hajdu

Department of Trauma Surgery, Medical University of Vienna, Vienna, Austria

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Andrea Lassnigg

Andrea Lassnigg

Department of Anaesthesia and General Intensive Care Medicine, Division of Cardiothoracic Anaesthesia, Medical University of Vienna, Vienna, Austria

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Wolfgang Graninger

Wolfgang Graninger

Department of Medicine I, Division of Infectious Diseases, Medical University of Vienna, Allgemeines Krankenhaus, Waehringer Guertel 18-20, 1090 Vienna, Austria

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Alexander M. Hirschl

Alexander M. Hirschl

Department of Medical Microbiology, Institute of Hygiene, Medical University of Vienna, Vienna, Austria

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Elisabeth Presterl

Corresponding Author

Elisabeth Presterl

Department of Medicine I, Division of Infectious Diseases, Medical University of Vienna, Allgemeines Krankenhaus, Waehringer Guertel 18-20, 1090 Vienna, Austria

Department of Medicine I, Division of Infectious Diseases, Medical University of Vienna, Allgemeines Krankenhaus, Waehringer Guertel 18-20, 1090 Vienna, Austria. T: +43 1 40400 4440; F: +43 1 40400 4418.Search for more papers by this author
First published: 24 April 2009
Citations: 37

Abstract

Infection of medical implanted material is associated with considerable morbidity and costs. In the following work, we investigated the effects of vancomycin, daptomycin, fosfomycin, tigecycline, and ceftriaxone on biofilms formed by Staphylococcus epidermidis isolates causative for implant infection and catheter-associated bacteremia. Biofilms were studied using the static microtiter plate model and incubated with the antibiotics increasing the concentration from 1× to 128× the minimal inhibitory concentration (MIC) of the respective isolate tested. To quantify the reduction of the biomass, the optical density ratio (ODr) of stained biofilms and the number of growing bacteria were determined. Incubation of the staphylococcal biofilms with the antibiotics decreased the biofilm ODr (at baseline = 1) for ceftriaxone (0.83 ± 0.48) but minimally only for fosfomycin (0.96 ± 0.64), daptomycin (1.05 ± 0.59), tigecycline (1.18 ± 0.66), and vancomycin (0.98 ± 0.44) at exceedingly high concentrations of 128 × MIC. The significant reduction of the bacterial growth was not achieved for all antibiotics, not even at the highest concentrations tested. Using higher doses of the antibiotics may be of some value in the treatment of biofilm-associated infections, although effects are seen only at clinically unachievable doses. However, to eradicate the staphylococcal biofilm, additional measures like debridement and/or removal of the implant are needed. © 2009 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 27:1361–1365, 2009

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