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激光捕获显微切割评估感染神经毒力猴免疫缺陷病毒的猕猴中枢神经系统中的病毒区室化。

Laser capture microdissection assessment of virus compartmentalization in the central nervous systems of macaques infected with neurovirulent simian immunodeficiency virus.

机构信息

Laboratory of Molecular Microbiology, NIAID, NIH, Bethesda, Maryland, USA.

出版信息

J Virol. 2013 Aug;87(16):8896-908. doi: 10.1128/JVI.00874-13. Epub 2013 May 29.

Abstract

Nonhuman primate-simian immunodeficiency virus (SIV) models are powerful tools for studying the pathogenesis of human immunodeficiency virus type 1 (HIV-1) in the brain. Our laboratory recently isolated a neuropathogenic viral swarm, SIVsmH804E, a derivative of SIVsmE543-3, which was the result of sequential intravenous passages of viruses isolated from the brains of rhesus macaques with SIV encephalitis. Animals infected with SIVsmH804E or its precursor (SIVsmH783Br) developed SIV meningitis and/or encephalitis at high frequencies. Since we observed macaques with a combination of meningitis and encephalitis, as well as animals in which meningitis or encephalitis was the dominant component, we hypothesized that distinct mechanisms could be driving the two pathological states. Therefore, we assessed viral populations in the meninges and the brain parenchyma by laser capture microdissection. Viral RNAs were isolated from representative areas of the meninges, brain parenchyma, terminal plasma, and cerebrospinal fluid (CSF) and from the inoculum, and the SIV envelope fragment was amplified by PCR. Phylogenetic analysis of envelope sequences from the conventional progressors revealed compartmentalization of viral populations between the meninges and the parenchyma. In one of these animals, viral populations in meninges were closely related to those from CSF and shared signature truncations in the cytoplasmic domain of gp41, consistent with a common origin. Apart from magnetic resonance imaging (MRI) and positron-emission tomography (PET) imaging, CSF is the most accessible assess to the central nervous system for HIV-1-infected patients. However, our results suggest that the virus in the CSF may not always be representative of viral populations in the brain and that caution should be applied in extrapolating between the properties of viruses in these two compartments.

摘要

非人类灵长类动物-猴免疫缺陷病毒(SIV)模型是研究人类免疫缺陷病毒 1(HIV-1)在大脑中发病机制的有力工具。我们实验室最近分离出一种神经致病性病毒群,SIVsmH804E,是 SIVsmE543-3 的衍生物,它是从患有 SIV 脑炎的恒河猴大脑中分离出的病毒连续静脉传代的结果。感染 SIVsmH804E 或其前体(SIVsmH783Br)的动物以高频率发生 SIV 脑膜炎和/或脑炎。由于我们观察到同时患有脑膜炎和脑炎的猕猴,以及以脑膜炎或脑炎为主的动物,我们假设不同的机制可能会导致这两种病理状态。因此,我们通过激光捕获显微切割评估脑膜和脑实质中的病毒群体。从代表性的脑膜、脑实质、终末血浆和脑脊液(CSF)区域以及接种物中分离病毒 RNA,并通过 PCR 扩增 SIV 包膜片段。对常规进展者包膜序列的系统发育分析表明,病毒群体在脑膜和实质之间存在区室化。在其中一只动物中,脑膜中的病毒群体与 CSF 中的病毒群体密切相关,并且在 gp41 的细胞质结构域中共享特征性截断,这与共同起源一致。除了磁共振成像(MRI)和正电子发射断层扫描(PET)成像外,CSF 是 HIV-1 感染患者最容易进入中枢神经系统的方法。然而,我们的结果表明,CSF 中的病毒并不总是代表大脑中的病毒群体,在推断这两个隔室中病毒的特性时应谨慎。

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