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定量蛋白质组学研究宿主对毒力和减毒伪狂犬病病毒感染小鼠大脑的反应。

Quantitative proteomics study of host response to virulent and attenuated pseudorabies virus infection in mouse brain.

机构信息

Department of Laboratory Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

State Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan, China.

出版信息

Biochim Biophys Acta Proteins Proteom. 2018 Feb;1866(2):307-315. doi: 10.1016/j.bbapap.2017.11.010. Epub 2017 Nov 23.

DOI:10.1016/j.bbapap.2017.11.010
PMID:29174846
Abstract

Bartha, the pseudorabies virus (PRV) vaccine strain, is widely used in studies of neuronal circuit-tracing, due to its attenuated virulence and retrograde spreading. However, we know little regarding the molecular mechanisms of PRV infection and spreading between structurally connected neurons. In this study, we systematically analyzed the host brain proteomes after acute infection with PRV, attempting to identified the proteins involved in the processes. Mice were injected with PRV-Bartha and PRV-Becker (PRV-Bartha's wild-type parent strain) in the olfactory system, the proteomes of the brain and synaptosome were analyzed and compared at various infection intervals using mass spectrometry-based proteomics techniques. In all, we identified >100 PRV-infection regulated proteins at the whole-tissue level and the synaptosome level. While at whole-tissue level, bioinformatics analyses mapped most of the regulations to the inflammation pathways, at the synaptosome level, most of those to synaptic transmission, cargo transport and cytoskeleton organization. We established regulated protein networks demonstrating distinct cellular regulation pattern between the global and the synaptosome levels. Moreover, we identified a series of potentially PRV-strain-specific regulated proteins with diverse biological functions. This study may provide new clues for molecular mechanisms for PRV infection and spread.

摘要

巴氏伪狂犬病病毒(PRV)疫苗株由于其毒力减弱和逆行传播,被广泛应用于神经元回路示踪研究。然而,我们对 PRV 感染和在结构连接的神经元之间传播的分子机制知之甚少。在本研究中,我们系统地分析了 PRV 急性感染后宿主大脑的蛋白质组,试图鉴定参与该过程的蛋白质。我们将 PRV-Bartha 和 PRV-Becker(PRV-Bartha 的野生型亲本株)注射到小鼠的嗅觉系统中,然后使用基于质谱的蛋白质组学技术,在不同的感染时间点分析和比较大脑和突触体的蛋白质组。总的来说,我们在全组织水平和突触体水平上鉴定了>100 种 PRV 感染调控蛋白。虽然在全组织水平上,生物信息学分析将大多数调控映射到炎症途径,但在突触体水平上,大多数调控涉及突触传递、货物运输和细胞骨架组织。我们建立了调控蛋白网络,展示了全局和突触体水平之间不同的细胞调控模式。此外,我们还鉴定了一系列具有不同生物学功能的潜在 PRV 株特异性调控蛋白。这项研究可能为 PRV 感染和传播的分子机制提供新的线索。

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