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对伯氏疏螺旋体进行改造以过量产生外膜蛋白A(OspA)或可变主要表面蛋白E(VlsE)会改变其感染行为。

Modification of Borrelia burgdorferi to overproduce OspA or VlsE alters its infectious behaviour.

作者信息

Xu Qilong, McShan Kristy, Liang Fang Ting

机构信息

Department of Pathobiological Sciences, Louisiana State University, Baton Rouge, LA 70803, USA.

出版信息

Microbiology (Reading). 2008 Nov;154(Pt 11):3420-3429. doi: 10.1099/mic.0.2008/019737-0.

Abstract

The surface lipoproteins of the Lyme disease spirochaete Borrelia burgdorferi directly interact with tissue microenvironments during mammalian infection, and thus potentially affect various aspects of infection. To investigate the influence of surface antigen synthesis on infectious behaviour, B. burgdorferi was modified to constitutively produce the well-characterized surface lipoproteins OspA and invariant VlsE. Although increasing OspA or VlsE production did not significantly affect synthesis of other surface lipoproteins or spirochaetal growth in vitro, overexpressing vlsE resulted in increased ospA but decreased ospC expression, and overexpressing ospA led to decreased ospC and vlsE expression in severe combined immunodeficient (SCID) mice. Increasing the expression of either ospA or vlsE did not alter the ID(50), but affected spirochaetal dissemination and significantly reduced tissue spirochaete loads in SCID mice. In immunocompetent mice, increased vlsE expression resulted in quick clearance of infection, while constitutive ospA expression led to a substantial ID(50) increase and severely impaired dissemination. Furthermore, B. burgdorferi with constitutive ospA expression persisted in the skin tissue but was cleared from both heart and joints of chronically infected immunocompetent mice. Taken together, the study indicates that increasing production of OspA or invariant VlsE influences lipoprotein gene expression in the murine host and alters the infectious behaviour of B. burgdorferi.

摘要

莱姆病螺旋体伯氏疏螺旋体的表面脂蛋白在哺乳动物感染期间直接与组织微环境相互作用,因此可能影响感染的各个方面。为了研究表面抗原合成对感染行为的影响,对伯氏疏螺旋体进行了改造,使其组成性产生特征明确的表面脂蛋白OspA和恒定的VlsE。虽然增加OspA或VlsE的产量对其他表面脂蛋白的合成或体外螺旋体生长没有显著影响,但在严重联合免疫缺陷(SCID)小鼠中,过表达vlsE导致ospA增加但ospC表达降低,而过表达ospA导致ospC和vlsE表达降低。增加ospA或vlsE的表达均未改变半数感染剂量(ID50),但影响螺旋体的播散,并显著降低SCID小鼠组织中的螺旋体载量。在免疫健全的小鼠中,增加vlsE表达导致感染迅速清除,而组成性表达ospA导致ID50大幅增加并严重损害播散。此外,组成性表达ospA的伯氏疏螺旋体在皮肤组织中持续存在,但在慢性感染的免疫健全小鼠的心脏和关节中均被清除。综上所述,该研究表明增加OspA或恒定VlsE的产量会影响小鼠宿主中的脂蛋白基因表达,并改变伯氏疏螺旋体 的感染行为。

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