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Study of in vivo catheter biofilm infections using pediatric central venous catheter implanted in rat

机译:用小儿中心静脉导管植入大鼠体内导管生物膜感染的研究

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Venous access catheters used in clinics are prone to biofilm contamination, contributing to chronic and nosocomial infections. Although several animal models for studying device-associated biofilms were previously described, only a few detailed protocols are currently available. Here we provide a protocol using totally implantable venous access ports (TIVAPAPs) implanted in rats. This model recapitulates all phenomena observed in the clinic, and it allows bacterial biofilm development and physiology to be studied. After TIVAPAP implantation and inoculation with luminescent pathogens, in vivo biofilm formation can be monitored in situ, and biofilm biomass can be recovered from contaminated TIVAPAP and organs. We used this protocol to study host responses to biofilm infection, to evaluate preventive and curative antibiofilm strategies and to study fundamental biofilm properties. For this procedure, one should expect similar to 3 h of hands-on time, including the implantation in one rat followed by in situ luminescence monitoring and bacterial load estimation.
机译:临床中使用的静脉通路导管容易受到生物膜的污染,从而导致慢性和医院感染。尽管先前已经描述了用于研究与设备相关的生物膜的几种动物模型,但是目前只有一些详细的协议可用。在这里,我们提供了一种使用植入大鼠的完全可植入静脉通路(TIVAPAP)的协议。该模型概括了在临床中观察到的所有现象,并且可以研究细菌生物膜的发育和生理学。植入TIVAPAP并接种发光病原体后,可以原位监测体内生物膜的形成,并可以从受污染的TIVAPAP和器官中回收生物膜的生物量。我们使用此协议来研究宿主对生物膜感染的反应,评估预防性和治疗性抗生物膜策略以及研究基本生物膜特性。对于此程序,应该期望接近3小时的动手时间,包括将其植入一只大鼠中,然后进行原位发光监测和细菌负荷估算。

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