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Johannes Maximilian Wagner, Hannah Zöllner, Christoph Wallner, Britta Ismer, Jessica Schira, Stephanie Abraham, Kamran Harati, Marcus Lehnhardt, Björn Behr

• \(\bf{Introduction}\) Bone infections after trauma, \(\textit{i.e.}\) posttraumatic osteomyelitis, pose one of the biggest problems of orthopedic surgery. Even after sufficient clinical therapy including vast debridement of infected bone and antibiotic treatment, regeneration of postinfectious bone seems to be restricted. One explanation includes the large sized defects resulting from sufficient debridement. Furthermore, it remains unclear if inflammatory processes after bone infection do affect bone regeneration. For continuing studies in this field, an animal model is needed where bone regeneration after sufficient treatment can be studied in detail. \(\bf{Methods}\) For this purpose we created a stable infection in murine tibiae by \(\textit{Staphylococcus aureus}\) inoculation. Thereafter, osteomyelitic bones were debrided thoroughly and animals were subsequently treated with antibiotics. Controls included debrided, non-infected, as well as infected animals exclusively treated with antibiotics. To verify sufficient treatment of infected bone, different assessments detecting \(\textit{S. aureus}\) were utilized: agar plates, histology and RT-qPCR. \(\bf{Results}\) All three detection methods revealed massive reduction or eradication of \(\textit{S.aureus}\) within debrided bones 1 and 2 weeks postoperatively, whereas sole antibiotic therapy could not provide sufficient treatment of osteomyelitic bones. Debrided, previously infected bones showed significantly decreased bone formation, compared to debrided, non-infected controls. \(\bf{Discussion}\) Thus, the animal model presented herein provides a reliable and fascinating tool to study posttraumatic osteomyelitis for clinical therapies.