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Quantitative Proteomic Analysis of BHK-21 Cells Infected with Foot-and-Mouth Disease Virus Serotype Asia 1

机译:感染口蹄疫病毒亚洲血清型1的BHK-21细胞的定量蛋白质组学分析

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摘要

Stable isotope labeling with amino acids in cell culture (SILAC) was used to quantitatively study the host cell gene expression profile, in order to achieve an unbiased overview of the protein expression changes in BHK-21 cells infected with FMDV serotype Asia 1. The SILAC-based approach identified overall 2,141 proteins, 153 of which showed significant alteration in the expression level 6 h post FMDV infection (57 up-regulated and 96 down-regulated). Among these proteins, six cellular proteins, including three down-regulated (VPS28, PKR, EVI5) and three up-regulated (LYPLA1, SEC62 and DARs), were selected according to the significance of the changes and/or the relationship with PKR. The expression level and pattern of the selected proteins were validated by immunoblotting and confocal microscopy. Furthermore, the functions of these cellular proteins were assessed by small interfering RNA-mediated depletion, and their functional importance in the replication of FMDV was demonstrated by western blot, reverse transcript PCR (RT-PCR) and 50% Tissue Culture Infective Dose (TCID50). The results suggest that FMDV infection may have effects on the expression of specific cellular proteins to create more favorable conditions for FMDV infection. This study provides novel data that can be utilized to understand the interactions between FMDV and the host cell.
机译:为了稳定地概述感染了FMDV亚洲型1型血清型的BHK-21细胞的蛋白表达变化,使用了细胞培养物中氨基酸的稳定同位素标记(SILAC)来定量研究宿主细胞的基因表达谱。基于方法的方法共鉴定了2,141种蛋白质,其中153种在FMDV感染后6小时显示出表达水平的显着改变(上调了57种,下调了96种)。在这些蛋白质中,根据变化的重要性和/或与PKR的关系,选择了六种细胞蛋白质,包括三种下调的蛋白质(VPS28,PKR,EVI5)和三种上调的蛋白质(LYPLA1,SEC62和DARs)。通过免疫印迹和共聚焦显微镜验证所选蛋白的表达水平和模式。此外,这些细胞蛋白的功能通过小干扰RNA介导的耗竭来评估,其蛋白在FMDV复制中的功能重要性已通过蛋白质印迹,逆转录PCR(RT-PCR)和50%组织培养物感染剂量(TCID50)证明)。结果表明,FMDV感染可能会影响特定细胞蛋白的表达,从而为FMDV感染创造更有利的条件。这项研究提供了新颖的数据,可用于了解FMDV与宿主细胞之间的相互作用。

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