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The impact of inoculation parameters on the pathogenesis of contact lens-related infectious keratitis.

机译:接种参数对隐形眼镜相关感染性角膜炎发病机制的影响。

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PURPOSE: Contact lens wear predisposes to Pseudomonas aeruginosa keratitis, but the mechanisms involved remain unclear. An in vivo model was used to study lens inoculation conditions enabling disease. METHODS: Custom-made hydrogel contact lenses were fitted to rats after incubation in P. aeruginosa approximately 10(11) cfu/mL (3 hours) or approximately 10(3) cfu/mL (24 hours). Another group was inadvertently inoculated with a suction pen previously used with high inocula, but rinsed in ethanol and stored dry (6 months). Some corneas were tissue paper-blotted to cause fluorescein staining before lens fitting. Contralateral eyes were untreated. Twenty-four hours after disease detection, lenses were transferred to naive rats or examined by confocal microscopy before homogenization to quantify viable bacteria. After lens removal, corneas were washed to collect nonadherent bacteria and were analyzed by immunohistochemistry. RESULTS: All eyes challenged with unworn contaminated lenses developed keratitis after approximately 7 to 10 days. Disease delay and severity were unaffected by inoculum parameters or tissue blotting but occurred sooner with lenses transferred from infected eyes ( approximately 2 days). Worn lenses and corneal washes contained infecting bacteria. Posterior, not anterior, lens surfaces harbored P. aeruginosa biofilms that penetrated the lens matrix. Diseased corneas showed an infiltration of phagocytes and T-lymphocytes. CONCLUSIONS: P. aeruginosa induces keratitis in this lens-wearing model after a single inoculation. Delayed disease onset was interesting considering the greater keratitis risk during extended wear. Infection did not require the disruption of corneal barrier function before lens wear and occurred without exposure to lens care solutions. The data suggest that keratitis involves biofilm formation or other bacterial adaptations in vivo.
机译:目的:隐形眼镜磨损易于伪装铜绿假单胞菌角膜炎,但涉及的机制仍然不清楚。在体内模型中用于研究患有疾病的镜片接种条件。方法:在铜绿假单胞菌孵育大约10(11)CFU / mL(3小时)或约10(3)CFU / mL(24小时)后,定制的水凝胶隐形眼镜在大鼠孵育后安装到大鼠。用先前与高海地使用的吸入笔无意中接种另一组,但在乙醇中冲洗并储存干燥(6个月)。一些玉米饼是组织纸 - 涂上镜片配件前的荧光素染色。对侧眼没有治疗。疾病检测后二十四小时,将晶状体转移到幼稚大鼠或通过共聚焦显微镜检查均质化以量化活细菌。去除晶状体后,洗涤玉米羚以收集非闭合细菌,并通过免疫组化分析。结果:所有眼睛遇到未磨损的污染镜片在大约7到10天后开发出角膜炎。疾病延迟和严重程度不受接种参数或组织印迹的影响,而是发生从感染眼睛(约2天)转移的镜片较早发生。磨损的镜片和角膜洗涤含有感染细菌。后部,而不是前部,透镜表面覆盖P. eruginosa生物膜穿透透镜矩阵。患病的玉米羚表现出吞噬吞噬细胞和T淋巴细胞。结论:P. Aeruginosa在单一接种后诱导该镜片磨损模型的角膜炎。考虑到延长磨损期间的角膜炎风险,延迟疾病发病是有趣的。感染在镜片磨损前并未发生在镜片磨损前的角膜屏障功能的破坏,而不会暴露于镜片护理解决方案。数据表明角膜炎涉及生物膜形成或体内的其他细菌适应。

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