A Mouse Model of Multi-Drug Resistant Staphylococcus aureus-induced Ocular Disease

N. Broekema, I. Larsen, E. S. Naruzawa, M. Filutowicz, A. Kolb, L. Teixeira, C. Brandt
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引用次数: 2

Abstract

Staphylococcus aureus infection of the cornea is a significant threat to vision. The percentage of bacterial isolates resistant to antibiotics is increasing as is the percentage of infections caused by methicillin resistant isolates. There is a critical need for additional therapeutic approaches and their development will require the use of animal models to test efficacy. Two mouse models of S. aureus keratitis have been described but only quantified stromal keratitis (corneal clouding and perforation). We have extended these models using the methicillin resistant S. aureus USA300 LAC strain and show that eyelid inflammation and swelling (blepharitis) and corneal neovascularization can be quantified. This expanded model should prove useful in assessing additional effects of antibacterial therapies and additional pathological mechanisms involved in bacterial ocular infection.
多重耐药金黄色葡萄球菌所致眼部疾病小鼠模型
金黄色葡萄球菌感染角膜是对视力的重大威胁。对抗生素耐药的细菌分离株的百分比正在增加,由耐甲氧西林分离株引起的感染百分比也在增加。迫切需要更多的治疗方法,它们的发展将需要使用动物模型来测试疗效。已经描述了两种金黄色葡萄球菌角膜炎的小鼠模型,但仅量化了间质角膜炎(角膜混浊和穿孔)。我们使用耐甲氧西林金黄色葡萄球菌USA300 LAC菌株扩展了这些模型,并表明眼睑炎症和肿胀(眼炎)和角膜新生血管可以量化。这个扩展的模型在评估抗菌治疗的其他效果和与细菌性眼部感染有关的其他病理机制方面应该证明是有用的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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