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新生大鼠神经致病性大肠杆菌感染的非侵入性模型

Non-invasive model of neuropathogenic Escherichia coli infection in the neonatal rat.

作者信息

Dalgakiran Fatma, Witcomb Luci A, McCarthy Alex J, Birchenough George M H, Taylor Peter W

机构信息

School of Pharmacy, University College London.

Mucin Biology Group, University of Gothenburg.

出版信息

J Vis Exp. 2014 Oct 29(92):e52018. doi: 10.3791/52018.

Abstract

Investigation of the interactions between animal host and bacterial pathogen is only meaningful if the infection model employed replicates the principal features of the natural infection. This protocol describes procedures for the establishment and evaluation of systemic infection due to neuropathogenic Escherichia coli K1 in the neonatal rat. Colonization of the gastrointestinal tract leads to dissemination of the pathogen along the gut-lymph-blood-brain course of infection and the model displays strong age dependency. A strain of E. coli O18:K1 with enhanced virulence for the neonatal rat produces exceptionally high rates of colonization, translocation to the blood compartment and invasion of the meninges following transit through the choroid plexus. As in the human host, penetration of the central nervous system is accompanied by local inflammation and an invariably lethal outcome. The model is of proven utility for studies of the mechanism of pathogenesis, for evaluation of therapeutic interventions and for assessment of bacterial virulence.

摘要

只有当所采用的感染模型能够复制自然感染的主要特征时,对动物宿主与细菌病原体之间相互作用的研究才有意义。本方案描述了新生大鼠因神经致病性大肠杆菌K1导致的全身感染的建立和评估程序。胃肠道的定植会导致病原体沿着肠道-淋巴-血液-脑感染途径传播,并且该模型显示出很强的年龄依赖性。一株对新生大鼠具有增强毒力的大肠杆菌O18:K1在穿过脉络丛后,会产生极高的定植率、向血液腔室的转移率和脑膜侵袭率。与人类宿主一样,中枢神经系统的穿透伴随着局部炎症和必然致命的结果。该模型在发病机制研究、治疗干预评估和细菌毒力评估方面已被证明具有实用性。

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