一种监测细菌感染和中性粒细胞活性的新动物模型

Q4 Engineering
N. Zulaziz, N. Himeno, H. Miyazaki, D. Saitoh, A. Azhim, Y. Morimoto
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引用次数: 0

摘要

为了同时监测炎症过程中中性粒细胞在体内的迁移,我们利用携带荧光阳性中性粒细胞和生物发光耐甲氧西林金黄色葡萄球菌(MRSA)的转基因小鼠建立了一种新的皮下软组织感染动物模型。方法:8 ~ 9周龄雄性lys-EGFP C57BL/6麻醉(50 mg/kg戊巴比比钠,ip),皮下注射1.0 ×107 CFU生物发光MRSA (Xen31, PerkinElmer)。对照组注射PBS,治疗组经尾静脉滴注阿贝卡星(25 mg/kg)。为了评估MRSA活性和中性粒细胞积累,使用了一种体内成像系统(as -4000, GE)。结果:两组表现相似,MRSA生物荧光明显下降,中性粒细胞荧光在第1天达到峰值。治疗组细菌感染在第6天完全消失,中性粒细胞荧光逐渐下降。结论:该动物模型可作为评估皮下软组织感染的有效方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Novel Animal Model for Monitoring Bacterial Infection and Neutrophil Activity
In order to simultaneously monitor neutrophil migration in vivo during inflammation, we developed a novel animal model for subcutaneous soft tissue infection using transgenic mouse bearing fluorescence-positive neutrophils and bioluminescent methicillin-resistant Staphylococcus aureus (MRSA). Methods: Eight to nine-week-old male lys-EGFP C57BL/6 were anesthetized (50 mg/kg pentobarbital sodium, ip) and 1.0 ×107 CFU of bioluminescent MRSA (Xen31, PerkinElmer) were subcutaneously injected. Control group was injected with PBS while the treatment group was given Arbekacin (25 mg/kg) intravenously via tail vein. For the evaluation of MRSA activity and neutrophil accumulation, an in vivo imaging system (LAS-4000, GE) was performed. Results: Both groups displayed similar pattern with significant drop in MRSA bioluminescence and neutrophil fluorescence peaked on day 1. However, bacterial infection completely resolved in treatment group by day 6 with gradual decline in neutrophil fluorescence. Conclusions: This animal model could be a competent method for assessment of subcutaneous soft tissue infections.
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