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Updated: Apr 20, 2026

In Vivo Mouse Model of Spinal Implant Infection
Published on: June 23, 2020
Daptomycin plus fosfomycin, a synergistic combination in experimental implant-associated osteomyelitis due to
Tilman Lingscheid1, Wolfgang Poeppl1, Dominik Bernitzky1
1Department of Internal Medicine I, Division of Infectious Diseases and Tropical Medicine, Medical University of Vienna, Vienna, Austria.
Abstract:
The aim of this study was to evaluate the combination of daptomycin and fosfomycin in experimental chronic implant-associated osteomyelitis due to methicillin-resistant Staphylococcus aureus (MRSA). Infection was induced in the tibiae of rats by the insertion of a bacterial inoculum (1 to 5×10(8) CFU/ml) of a clinical MRSA isolate and a titanium wire. Four weeks after infection, each animal was assigned to a treatment group: daptomycin monotherapy at 60 mg/kg of body weight once daily (n=10), fosfomycin monotherapy at 40 mg/kg once daily (n=10), or daptomycin and fosfomycin combined at 60 mg/kg and 40 mg/kg, respectively, once daily (n=9). Ten animals were left untreated. After a 3-week treatment period, the animals were euthanized, and the infected tibiae and implants were processed for quantitative bacterial cultures. The bacterial cultures from bones were positive for MRSA in all animals in the untreated group, the daptomycin group, and the fosfomycin group, with median bacterial counts of 2.34×10(6) CFU/g bone, 1.57×10(6) CFU/g bone, and 3.48×10(2) CFU/g bone, respectively. In the daptomycin-fosfomycin group, 6 out of 9 animals were positive for MRSA, with a median count of 7.92 CFU/g bone. Bacterial cultures derived from the titanium wires were negative in the fosfomycin- and daptomycin-fosfomycin-treated groups. Based on bacterial counts in bones, treatment with daptomycin-fosfomycin was statistically significantly superior to all that of the other groups (P≤0.003). Fosfomycin was superior to daptomycin and no treatment (P<0.0001). No development of resistance was observed in any treatment arm. The combination of daptomycin and fosfomycin demonstrated synergism against MRSA in experimental implant-associated osteomyelitis.
Insights
The combination of daptomycin and fosfomycin effectively treats experimental implant-associated osteomyelitis caused by methicillin-resistant Staphylococcus aureus (MRSA). This antibiotic combination demonstrated synergistic effects, significantly reducing bacterial burden in bone and on implants.
Area of Science:
- Infectious Diseases
- Pharmacology
- Orthopedic Surgery
Background:
- Implant-associated osteomyelitis is a challenging infection often caused by multidrug-resistant bacteria like methicillin-resistant Staphylococcus aureus (MRSA).
- Current treatment options for chronic implant-associated osteomyelitis are limited, necessitating the exploration of novel therapeutic strategies.
Purpose of the Study:
- To evaluate the efficacy of combining daptomycin and fosfomycin against experimental chronic implant-associated osteomyelitis caused by MRSA.
- To assess the synergistic potential of daptomycin and fosfomycin in this infection model.
Main Methods:
- An experimental model of chronic implant-associated osteomyelitis was established in rats using MRSA and titanium implants.
- Animals were treated with daptomycin monotherapy, fosfomycin monotherapy, or a combination of both antibiotics.
- Quantitative bacterial cultures of bone and implants were performed post-treatment to assess bacterial burden.
Main Results:
- The combination of daptomycin and fosfomycin was statistically superior in reducing bacterial counts in bone compared to monotherapy or no treatment (P≤0.003).
- Bacterial cultures from implants were negative in the daptomycin-fosfomycin and fosfomycin monotherapy groups.
- No development of antibiotic resistance was observed during the study.
Conclusions:
- Daptomycin and fosfomycin combination therapy demonstrates significant efficacy and potential synergism against MRSA in experimental implant-associated osteomyelitis.
- This combination therapy offers a promising therapeutic option for challenging bone infections involving MRSA and implants.
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