3.8 Article

Standardized quantification of biofilm in a novel rabbit model of periprosthetic joint infection

Journal

JOURNAL OF BONE AND JOINT INFECTION
Volume 7, Issue 2, Pages 91-99

Publisher

COPERNICUS GESELLSCHAFT MBH
DOI: 10.5194/jbji-7-91-2022

Keywords

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Funding

  1. Cleveland Clinic (SPARK)
  2. Cleveland Clinic (MSRC Pilot Project grant)
  3. Cleveland Clinic (Florida RPC grant)
  4. Case Western Reserve University (VPR Catalyst Award)
  5. National Science Foundation [DMR-1253358]

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This study developed a rabbit model of knee periprosthetic joint infection (PJI) that allows for reliable biofilm quantification and the study of PJI treatments. The model successfully produced quantifiable biofilm and showed that debridement, antibiotics, and implant retention (DAIR) treatment significantly reduced biofilm coverage. The model can be used to better understand the pathogenesis of PJI and evaluate treatment strategies.
Periprosthetic joint infection (PJI) is one of the most devastating complications of total joint arthroplasty. The underlying pathogenesis involves the formation of bacterial biofilm that protects the pathogen from the host immune response and antibiotics, making eradication difficult. The aim of this study was to develop a rabbit model of knee PJI that would allow reliable biofilm quantification and permit the study of treatments for PJI. In this work, New Zealand white rabbits (n = 19) underwent knee joint arthrotomy, titanium tibial implant insertion, and inoculation with Xen36 (bioluminescent Staphylococcus aureus) or a saline control after capsule closure. Biofilm was quantified via scanning electron microscopy (SEM) of the tibial explant 14 d after inoculation (n = 3 noninfected, n = 2 infected). Rabbits underwent debridement, antibiotics, and implant retention (DAIR) (n = 6) or sham surgery (n = 2 noninfected, n = 6 infected) 14 d after inoculation, and they were sacrificed 14 d post-treatment. Tibial explant and periprosthetic tissues were examined for infection. Laboratory assays supported bacterial infection in infected animals. No differences in weight or C-reactive protein (CRP) were detected after DAIR compared to sham treatment. Biofilm coverage was significantly decreased with DAIR treatment when compared with sham treatment (61.4% vs. 90.1 %, p < 0.0011) and was absent in noninfected control explants. In summary, we have developed an experimental rabbit hemiarthroplasty knee PJI model with bacterial infection that reliably produces quantifiable biofilm and provides an opportunity to introduce treatments at 14 d. This model may be used to better understand the pathogenesis of this condition and to measure treatment strategies for PJI.

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