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Ascending unobstructed urinary tract infection in mice caused by pyelonephritogenic Escherichia coli of human origin.

机译:人源性发源性幽门螺杆菌引起的小鼠上行畅通性尿路感染。

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摘要

A model for ascending unobstructed urinary tract infection was developed in mice to study the pathogenesis of urinary tract infection induced by Escherichia coli associated with urinary tract infection in humans. Specifically, the model was designed to monitor the initial stages of the infectious process, e.g., bacterial adhesion. Mice were selected since the specificity and intensity of bacterial attachment of pyelonephritogenic E. coli strains to human and mouse uroepithelial cells were similar. Female mice were infected by urethral catheterization and installation of bacteria in the urinary bladder. To maximize clearance of unattached bacteria, no obstructive manipulations were performed. After sacrifice, the persistence of bacteria in kidneys and bladder was determined by viable counts on homogenized tissues. The experimental infection was standardized by using one pyelonephritis (HU734) and one normal fecal (414) E. coli isolate. With both strains all of the bladders became infected, but E. coli 414 was eliminated more rapidly than HU734. The percentage of positive kidney cultures increased with the bacterial inoculum concentration and volume. An inoculum of 0.05 ml containing 10(10) bacteria per ml was selected, giving the highest percentage of positive kidney cultures without detectable bacterial spread to the blood stream. The variation in the percentage of positive kidney cultures possibly depended on the degree of vesicoureteric reflux in the individual animals. Both in the kidneys and in the urinary bladders, strain HU734 yielded higher numbers of bacteria at 24 h and persisted longer than did strain 414. Several E. coli pyelonephritis isolates with properties associated with virulence in the human urinary tract consistently were recovered from mouse kidneys and bladders in higher numbers than E. coli strains of human fecal origin lacking those properties. The role of bacterial adhesion per se is the topic of the accompanying paper.
机译:在小鼠中建立了用于提升无障碍性尿路感染的模型,以研究由大肠杆菌诱导的与人的尿路感染有关的尿路感染的发病机理。具体而言,该模型被设计为监测感染过程的初始阶段,例如细菌粘附。之所以选择小鼠,是因为pyelonephritogenic大肠杆菌菌株与人和小鼠尿道上皮细胞的细菌附着的特异性和强度相似。雌性小鼠通过尿道导管插入术和在膀胱中安装细菌感染。为了最大程度地清除未附着细菌,没有进行任何阻塞性操作。处死后,通过均质化组织上的活菌计数确定细菌在肾脏和膀胱中的持久性。通过使用一种肾盂肾炎(HU734)和一种正常粪便(414)大肠杆菌分离株对实验性感染进行标准化。两种菌株都感染了所有膀胱,但是大肠杆菌414的清除速度比HU734更快。肾培养阳性率随细菌接种物浓度和体积的增加而增加。选择每毫升含10(10)个细菌的0.05毫升接种物,可得到最高百分比的阳性肾脏培养物,而没有可检测到的细菌扩散到血流中。阳性肾脏培养物百分比的变化可能取决于各个动物中膀胱输尿管返流的程度。在肾脏和膀胱中,HU734菌株在24 h产生的细菌数量更多,并且比414菌株持续更长的时间。从小鼠肾脏中一直回收到数种与人尿道中毒力有关的大肠杆菌肾盂肾炎分离株。和膀胱的数量要比缺乏这些特性的人类粪便来源的大肠杆菌菌株高。细菌粘附本身的作用是随附论文的主题。

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