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Label‐Free Quantitative Proteomic Analysis of Differentially Expressed Membrane Proteins of Pulmonary Alveolar Macrophages Infected with Highly Pathogenic Porcine Reproductive and Respiratory Syndrome Virus and Its Attenuated Strain

机译:高致病性猪繁殖与呼吸综合征病毒及其减毒株感染的肺泡巨噬细胞差异表达膜蛋白的无标签定量蛋白质组分析

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摘要

Significant differences exist between the highly pathogenic (HP) porcine reproductive and respiratory syndrome virus (PRRSV) and its attenuated pathogenic (AP) strain in the ability to infect host cells. The mechanisms by which different virulent strains invade host cells remain relatively unknown. In this study, pulmonary alveolar macrophages (PAMs) are infected with HP‐PRRSV (HuN4) and AP‐PRRSV (HuN4‐F112) for 24 h, then harvested and subjected to label‐free quantitative MS. A total of 2849 proteins are identified, including 95 that are differentially expressed. Among them, 26 proteins are located on the membrane. The most differentially expressed proteins are involved in response to stimulus, metabolic process, and immune system process, which mainly have the function of binding and catalytic activity. Cluster of differentiation CD163, vimentin (VIM), and nmII as well as detected proteins are assessed together by string analysis, which elucidated a potentially different infection mechanism. According to the function annotations, PRRSV with different virulence may mainly differ in immunology, inflammation, immune evasion as well as cell apoptosis. This is the first attempt to explore the differential characteristics between HP‐PRRSV and its attenuated PRRSV infected PAMs focusing on membrane proteins which will be of great help to further understand the different infective mechanisms of HP‐PRRSV and AP‐PRRSV.
机译:高致病性(HP)猪繁殖与呼吸综合征病毒(PRRSV)与减毒的致病性(AP)株之间感染宿主细胞的能力存在显着差异。尚不清楚不同毒株侵袭宿主细胞的机制。在这项研究中,肺泡巨噬细胞(PAM)被HP-PRRSV(HuN4)和AP-PRRSV(HuN4-F112)感染了24小时,然后收获并进行了无标记定量MS。总共鉴定出2849种蛋白质,其中95种差异表达。其中,有26种蛋白质位于膜上。表达最差异的蛋白质参与对刺激,代谢过程和免疫系统过程的响应,其主要具有结合和催化活性的功能。通过字符串分析一起评估分化CD163,波形蛋白(VIM)和nmII以及检测到的蛋白质的簇,这阐明了潜在的不同感染机制。根据功能注释,具有不同毒力的PRRSV在免疫学,炎症,免疫逃逸以及细胞凋亡方面可能主要不同。这是探索HP‐PRRSV及其减毒的PRRSV感染的PAM(以膜蛋白为中心)之间差异特征的首次尝试,这将有助于进一步了解HP‐PRRSV和AP‐PRRSV的不同感染机制。

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