A Mouse Model of Post-Arthroplasty Staphylococcus aureus Joint Infection to Evaluate In Vivo the Efficacy of Antimicrobial Implant Coatings

被引:168
作者
Bernthal, Nicholas M. [1 ]
Stavrakis, Alexandra I. [1 ]
Billi, Fabrizio [1 ]
Cho, John S. [2 ]
Kremen, Thomas J. [1 ]
Simon, Scott I. [3 ]
Cheung, Ambrose L. [4 ]
Finerman, Gerald A. [1 ]
Lieberman, Jay R. [5 ]
Adams, John S. [1 ]
Miller, Lloyd S. [1 ,2 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Orthopaed Surg, Orthopaed Hosp Res Ctr,Orthopaed Hosp, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Div Dermatol, Los Angeles, CA 90095 USA
[3] Univ Calif Davis, Dept Biomed Engn, Davis, CA 95616 USA
[4] Dartmouth Coll, Hitchcock Med Ctr, Dartmouth Med Sch, Dept Microbiol & Immunol, Hanover, NH 03756 USA
[5] Univ Connecticut, Ctr Hlth, Dept Orthopaed Surg, New England Musculoskeletal Inst, Farmington, CT USA
来源
PLOS ONE | 2010年 / 5卷 / 09期
基金
美国国家卫生研究院;
关键词
TOTAL HIP-ARTHROPLASTY; SURGICAL-SITE INFECTION; ANTIBIOTIC-IMPREGNATED CEMENT; TOTAL KNEE ARTHROPLASTY; REVISION TOTAL HIP; UNITED-STATES; NEUTROPHIL RECRUITMENT; TITANIUM IMPLANTS; CANINE MODEL; BIOFILMS;
D O I
10.1371/journal.pone.0012580
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: 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 5 x 10(3) and 5 x 10(4) CFUs developed increased bacterial counts with marked swelling of the affected leg, consistent with an acute joint infection. In contrast, mice inoculated with 5 x 10(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.
引用
收藏
页码:1 / 11
页数:11
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