In vivo Mouse Model of Spinal Implant Infection

体内 植入 生物发光成像 离体 生物发光 病理 医学 临床前影像学 生物医学工程 金黄色葡萄球菌 生物 细菌 外科 荧光素酶 细胞培养 生态学 遗传学 生物技术 转染
作者
Benjamin V. Kelley,Stephen D. Zoller,Danielle Greig,Kellyn R. Hori,Nicolas Cevallos,Chad R. Ishmael,Peter P. Hsiue,Rishi Trikha,Troy Sekimura,Thomas E. Olson,Ameen Chaudry,Michael M Le,Anthony A. Scaduto,Kevin P. Francis,Nicholas M. Bernthal
出处
期刊:Journal of Visualized Experiments [MyJoVE Corporation]
卷期号: (160) 被引量:5
标识
DOI:10.3791/60560
摘要

Spine implant infections portend poor outcomes as diagnosis is challenging and surgical eradication is at odds with mechanical spinal stability. The purpose of this method is to describe a novel mouse model of spinal implant infection (SII) that was created to provide an inexpensive, rapid, and accurate in vivo tool to test potential therapeutics and treatment strategies for spinal implant infections. In this method, we present a model of posterior-approach spinal surgery in which a stainless-steel k-wire is transfixed into the L4 spinous process of 12-week old C57BL/6J wild-type mice and inoculated with 1 x 103 CFU of a bioluminescent strain of Staphylococcus aureus Xen36 bacteria. Mice are then longitudinally imaged for bioluminescence in vivo on post-operative days 0, 1, 3, 5, 7, 10, 14, 18, 21, 25, 28, and 35. Bioluminescence imaging (BLI) signals from a standardized field of view are quantified to measure in vivo bacterial burden. To quantify bacteria adhering to implants and peri-implant tissue, mice are euthanized and the implant and surrounding soft tissue are harvested. Bacteria are detached from the implant by sonication, cultured overnight and then colony forming units (CFUs) are counted. The results acquired from this method include longitudinal bacterial counts as measured by in vivo S. aureus bioluminescence (mean maximum flux) and CFU counts following euthanasia. While prior animal models of instrumented spine infection have involved invasive, ex vivo tissue analysis, the mouse model of SII presented in this paper leverages noninvasive, real time in vivo optical imaging of bioluminescent bacteria to replace static tissue study. Applications of the model are broad and may include utilizing alternative bioluminescent bacterial strains, incorporating other types of genetically engineered mice to contemporaneously study host immune response, and evaluating current or investigating new diagnostic and therapeutic modalities such as antibiotics or implant coatings.
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