Kuklin Nelly A, Pancari Gregory D, Tobery Timothy W, Cope Leslie, Jackson Jesse, Gill Charles, Overbye Karen, Francis Kevin P, Yu Jun, Montgomery Donna, Anderson Annaliesa S, McClements William, Jansen Kathrin U
Merck and Co, Inc, West Point, Pennsylvania 19486, USA.
Antimicrob Agents Chemother. 2003 Sep;47(9):2740-8. doi: 10.1128/AAC.47.9.2740-2748.2003.
Staphylococcal infections associated with catheter and prosthetic implants are difficult to eradicate and often lead to chronic infections. Development of novel antibacterial therapies requires simple, reliable, and relevant models for infection. Using bioluminescent Staphylococcus aureus, we have adapted the existing foreign-body and deep-wound mouse models of staphylococcal infection to allow real-time monitoring of the bacterial colonization of catheters or tissues. This approach also enables kinetic measurements of bacterial growth and clearance in each infected animal. Persistence of infection was observed throughout the course of the study until termination of the experiment at day 16 in a deep-wound model and day 21 in the foreign-body model, providing sufficient time to test the effects of antibacterial compounds. The usefulness of both animal models was assessed by using linezolid as a test compound and comparing bioluminescent measurements to bacterial counts. In the foreign-body model, a three-dose antibiotic regimen (2, 5, and 24 h after infection) resulted in a decrease in both luminescence and bacterial counts recovered from the implant compared to those of the mock-treated infected mice. In addition, linezolid treatment prevented the formation of subcutaneous abscesses, although it did not completely resolve the infection. In the thigh model, the same treatment regimen resulted in complete resolution of the luminescent signal, which correlated with clearance of the bacteria from the thighs.
与导管和人工植入物相关的葡萄球菌感染难以根除,且常常导致慢性感染。新型抗菌疗法的开发需要简单、可靠且相关的感染模型。利用生物发光金黄色葡萄球菌,我们对现有的葡萄球菌感染的异物和深部伤口小鼠模型进行了改进,以实现对导管或组织细菌定植的实时监测。这种方法还能够对每只感染动物体内细菌的生长和清除进行动力学测量。在整个研究过程中均观察到感染持续存在,直至在深部伤口模型中于第16天、在异物模型中于第21天实验终止,这为测试抗菌化合物的效果提供了足够的时间。通过使用利奈唑胺作为测试化合物,并将生物发光测量结果与细菌计数进行比较,对这两种动物模型的实用性进行了评估。在异物模型中,与未治疗的感染小鼠相比,三剂量抗生素方案(感染后2、5和24小时)导致从植入物中回收的发光和细菌计数均下降。此外,利奈唑胺治疗可预防皮下脓肿的形成,尽管它并未完全消除感染。在大腿模型中,相同的治疗方案导致发光信号完全消失,这与大腿中细菌的清除相关。