Bostian Phillip A, Karnes Jonathan M, Cui Shari, Robinson Lisa J, Daffner Scott D, Witt Michelle R, Emery Sanford E
Department of Orthopaedics, West Virginia University, P.O. Box 9196, Morgantown, West Virginia 26506-9196.
Department of Pathology, West Virginia University, Lab Room 2156, HSC North, Morgantown, West Virginia 26506.
J Orthop Res. 2017 Sep;35(9):2075-2081. doi: 10.1002/jor.23497. Epub 2017 Mar 15.
Management of spondylodiscitis is a challenging clinical problem requiring medical and surgical treatment strategies. The purpose of this study was to establish a rat model of spondylodiscitis that utilizes bioluminescent Staphylococcus aureus (S. aureus), thus permitting in vivo surveillance of infection intensity. Inocula of the bioluminescent S. aureus strain XEN36 were created in concentrations of 10 CFU/0.1 ml, 10 CFU/0.1 ml, and 10 CFU/0.1 ml. Three groups of rats were injected with the bacteria in the most proximal intervertebral tail segment. The third most proximal tail segment was injected with saline as a control. Bioluminescence was measured at baseline, 3 days, and weekly for a total of 6 weeks. Detected bioluminescence for each group peaked at day 3 and returned to baseline in 21 days. The average intensity was highest for the experimental group injected with the most concentrated bacterial solution (10 CFU/0.1 ml). Radiographic analysis revealed loss of intervertebral disc space and evidence of osseous bridging. Saline-injected spaces exhibited no decrease in intervertebral spacing as compared to distal sites. Histologic analysis revealed neutrophilic infiltrates, destruction of the annulus fibrosus and nucleus pulposus, destruction of vertebral endplates, and osseous bridging. Saline-injected discs exhibited preserved annulus fibrosus and nucleus pulposus on histology. This study demonstrates that injection of bioluminescent S. aureus into the intervertebral disc of a rat tail is a viable animal model for spondylodiscitis research. This model allows for real-time, in vivo quantification of infection intensity, which may decrease the number of animals required for infection studies of the intervertebral disc. © 2017 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 35:2075-2081, 2017.
脊柱椎间盘炎的治疗是一个具有挑战性的临床问题,需要医学和外科治疗策略。本研究的目的是建立一种利用生物发光金黄色葡萄球菌(金葡菌)的脊柱椎间盘炎大鼠模型,从而能够在体内监测感染强度。制备了浓度为10⁵CFU/0.1 ml、10⁶CFU/0.1 ml和10⁷CFU/0.1 ml的生物发光金葡菌菌株XEN36接种物。三组大鼠在最靠近尾端的椎间节段注射细菌。将第三靠近尾端的节段注射生理盐水作为对照。在基线、第3天以及总共6周的时间内每周测量生物发光。每组检测到的生物发光在第3天达到峰值,并在21天内恢复到基线水平。注射最浓缩菌液(10⁷CFU/0.1 ml)的实验组平均强度最高。影像学分析显示椎间盘间隙变窄和骨桥形成的证据。与远端部位相比,注射生理盐水的间隙椎间盘间隙没有减小。组织学分析显示有中性粒细胞浸润、纤维环和髓核破坏、椎体终板破坏以及骨桥形成。组织学上,注射生理盐水的椎间盘纤维环和髓核保存完好。本研究表明,将生物发光金葡菌注射到大鼠尾巴的椎间盘中是一种可行的脊柱椎间盘炎研究动物模型。该模型允许对感染强度进行实时、体内定量,这可能会减少椎间盘感染研究所需的动物数量。© 2017年骨科研究协会。由威利期刊公司出版。《矫形外科研究杂志》2017年第35卷:2075 - 2081页 。