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羔羊严重腹泻和脑膜脑炎大肠杆菌致血脑屏障破坏的机制。

Mechanism of blood-brain barrier disruption by an Escherichia coli from lambs with severe diarrhea and meningoencephalitis.

机构信息

College of Veterinary Medicine, Jilin University, Changchun, Jilin, China.

College of Veterinary Medicine, Jilin University, Changchun, Jilin, China; Key Laboratory for Zoonosis, Ministry of Education, Changchun, Jilin, China.

出版信息

Microb Pathog. 2020 Oct;147:104288. doi: 10.1016/j.micpath.2020.104288. Epub 2020 Jun 1.

Abstract

Escherichia coli (E. coli) is a common conditional pathogen that is associated with a variety of infections in humans and animals. Although there are increasing reports regarding the infection of E. coli to domestic animals and poultry, the infection of E. coli in lambs is relatively less reported, especially on meningoencephalitis. Here, we reported the isolation of an E. coli strain designated as NMGCF-19 from lambs characterized with severe diarrhea and neurological disorder, and demonstrated that NMGCF-19 as the causative agent has the ability to disrupt the blood-brain barrier (BBB) to cause the meningoencephalitis using a mouse model. Investigation on the mechanism regarding the NMGCF-19-related meningoencephalitis revealed a significant decreased expression of ZO-1 and occludin in mouse brain tissue in comparison with the control mice. Moreover, infection of NMGCF-19 increased the expression of proinflammatory cytokines TNF-α, IL-6, IL-1β and IL-18, up-regulated HMGB1 level, and activated TLR2/TLR4/MyD88 and NLRP3 inflammasome pathways. These findings indicated that NMGCF-19 likely invades the brain tissue by disrupting the tight junction (TJ) architecture and causes the meningoencephalitis via increasing inflammatory response and activating TLR2/TLR4/MyD88 and NLRP3 inflammasome pathways.

摘要

大肠杆菌(E. coli)是一种常见的条件性病原体,与人类和动物的多种感染有关。尽管越来越多的报道涉及大肠杆菌感染家畜和家禽,但羔羊感染大肠杆菌的报道相对较少,尤其是在脑膜炎方面。在这里,我们从患有严重腹泻和神经紊乱的羔羊中分离出一株大肠杆菌菌株,命名为 NMGCF-19,并证明 NMGCF-19 作为病原体具有破坏血脑屏障(BBB)导致脑膜炎的能力,使用小鼠模型进行了验证。对 NMGCF-19 相关脑膜炎的机制进行调查发现,与对照小鼠相比,小鼠脑组织中 ZO-1 和闭合蛋白的表达显著降低。此外,NMGCF-19 的感染增加了促炎细胞因子 TNF-α、IL-6、IL-1β 和 IL-18 的表达,上调了 HMGB1 水平,并激活了 TLR2/TLR4/MyD88 和 NLRP3 炎症小体途径。这些发现表明,NMGCF-19 可能通过破坏紧密连接(TJ)结构侵犯脑组织,并通过增加炎症反应和激活 TLR2/TLR4/MyD88 和 NLRP3 炎症小体途径导致脑膜炎。

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