Orthopaedic Hospital Research Center, Orthopaedic Hospital Department of Orthopaedic Surgery, David Geffen School of Medicine at University of California Los Angeles, Los Angeles, California, USA.
PLoS One. 2010 Sep 7;5(9):e12580. doi: 10.1371/journal.pone.0012580.
Post-arthroplasty infections represent a devastating complication of total joint replacement surgery, resulting in multiple reoperations, prolonged antibiotic use, extended disability and worse clinical outcomes. As the number of arthroplasties in the U.S. will exceed 3.8 million surgeries per year by 2030, the number of post-arthroplasty infections is projected to increase to over 266,000 infections annually. The treatment of these infections will exhaust healthcare resources and dramatically increase medical costs.
METHODOLOGY/PRINCIPAL FINDINGS: To evaluate novel preventative therapeutic strategies against post-arthroplasty infections, a mouse model was developed in which a bioluminescent Staphylococcus aureus strain was inoculated into a knee joint containing an orthopaedic implant and advanced in vivo imaging was used to measure the bacterial burden in real-time. Mice inoculated with 5x10(3) and 5x10(4) CFUs developed increased bacterial counts with marked swelling of the affected leg, consistent with an acute joint infection. In contrast, mice inoculated with 5x10(2) CFUs developed a low-grade infection, resembling a more chronic infection. Ex vivo bacterial counts highly correlated with in vivo bioluminescence signals and EGFP-neutrophil fluorescence of LysEGFP mice was used to measure the infection-induced inflammation. Furthermore, biofilm formation on the implants was visualized at 7 and 14 postoperative days by variable-pressure scanning electron microscopy (VP-SEM). Using this model, a minocycline/rifampin-impregnated bioresorbable polymer implant coating was effective in reducing the infection, decreasing inflammation and preventing biofilm formation.
CONCLUSIONS/SIGNIFICANCE: Taken together, this mouse model may represent an alternative pre-clinical screening tool to evaluate novel in vivo therapeutic strategies before studies in larger animals and in human subjects. Furthermore, the antibiotic-polymer implant coating evaluated in this study was clinically effective, suggesting the potential for this strategy as a therapeutic intervention to combat post-arthroplasty infections.
关节置换术后感染是全关节置换手术的一种毁灭性并发症,导致多次再手术、延长抗生素使用、延长残疾时间和更差的临床结果。随着美国每年接受关节置换手术的人数将超过 380 万,预计每年关节置换术后感染人数将增加到 26.6 万以上。这些感染的治疗将耗尽医疗资源,并大幅增加医疗费用。
方法/主要发现:为了评估针对关节置换术后感染的新型预防治疗策略,我们开发了一种小鼠模型,在该模型中,将发光的金黄色葡萄球菌菌株接种到含有骨科植入物的膝关节中,并使用先进的体内成像技术实时测量细菌负荷。接种 5x10(3)和 5x10(4)CFUs 的小鼠的细菌计数增加,受影响的腿部明显肿胀,与急性关节感染一致。相比之下,接种 5x10(2)CFUs 的小鼠发展为低度感染,类似于更慢性感染。体外细菌计数与体内生物发光信号高度相关,并用 LysEGFP 小鼠的 EGFP-中性粒细胞荧光来测量感染引起的炎症。此外,还通过可变压力扫描电子显微镜(VP-SEM)在术后 7 天和 14 天观察到植入物上的生物膜形成。使用该模型,载有米诺环素/利福平的可生物降解聚合物植入物涂层在减少感染、减轻炎症和防止生物膜形成方面非常有效。
结论/意义:综上所述,这种小鼠模型可能代表一种替代的临床前筛选工具,可在更大动物和人体研究之前评估新的体内治疗策略。此外,本研究中评估的抗生素-聚合物植入物涂层在临床上是有效的,表明这种策略有作为治疗干预措施来对抗关节置换术后感染的潜力。