Nishizawa Mitsuhiro, Saleh Bahram, Marcucio Ralph, Morioka Kazuhito
Department of Orthopaedic Surgery, Orthopaedic Trauma Institute (OTI), University of California, San Francisco (UCSF).
Rosies Base, LLC.
J Vis Exp. 2025 Jun 6(220). doi: 10.3791/68067.
To develop a novel biomaterial with antibacterial properties for orthopedic surgical procedures, establishing an experimental animal model of implant-related infections that closely mimics the pathological state is crucial. Additionally, a quantitative comparison with control samples is required to assess biofilm formation on materials. However, current animal models, which involve implanting each individual with a single material, may yield inconsistent outcomes due to the heterogeneity of infection status among subjects. Furthermore, accurately quantifying biofilm formation on materials in vivo remains challenging, and the findings may lack reliability. To address these issues, this study demonstrated a unique mouse model of implant-related infection that enables the simultaneous incubation of two implants with bacteria in an enclosed environment within a single mouse, forming an encapsulated subcutaneous abscess. A mature air pouch was initially created beneath the skin of the back. Two stainless steel wires were connected and placed into the pouch, followed by the inoculation of Xen 36, a bioluminescent strain of Staphylococcus aureus. By 14 days after inoculation, a subcutaneous abscess had formed around the wires. The biofilm was completely removed from the surface of each wire, and the dissolved bacterial suspensions were accurately measured using optimized methods to assess biofilm formation on the implant, determine colony-forming units, and perform quantitative polymerase chain reaction analysis. By leveraging the lux operon of the bioluminescent bacteria, the relative expression levels of luxA and 16S rRNA were used to determine the bacterial load within the biofilm on each wire. This optimized comparative analytical approach enables precise assessments of biofilm formation on two wires under uniform infection conditions within a single mouse model and may facilitate the advancement of biomaterials with antibacterial properties.
为开发一种用于骨科手术的具有抗菌性能的新型生物材料,建立一个能紧密模拟病理状态的植入相关感染实验动物模型至关重要。此外,需要与对照样品进行定量比较,以评估材料上生物膜的形成情况。然而,目前的动物模型是给每只动物植入单一材料,由于个体间感染状态的异质性,可能会产生不一致的结果。此外,在体内准确量化材料上生物膜的形成仍然具有挑战性,其结果可能缺乏可靠性。为解决这些问题,本研究展示了一种独特的植入相关感染小鼠模型,该模型能在单只小鼠体内的封闭环境中同时将两个植入物与细菌一起孵育,形成一个被包裹的皮下脓肿。首先在背部皮肤下创建一个成熟的气袋。连接两根不锈钢丝并放入气袋中,随后接种金黄色葡萄球菌的生物发光菌株Xen 36。接种后14天,钢丝周围形成了皮下脓肿。将生物膜从每根钢丝表面完全去除,使用优化方法准确测量溶解的细菌悬液,以评估植入物上生物膜的形成、确定菌落形成单位并进行定量聚合酶链反应分析。通过利用生物发光细菌的lux操纵子,luxA和16S rRNA的相对表达水平被用于确定每根钢丝上生物膜内的细菌载量。这种优化的比较分析方法能够在单个小鼠模型的均匀感染条件下精确评估两根钢丝上生物膜的形成情况,并可能有助于推进具有抗菌性能的生物材料的发展。