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蛋白质组学研究揭示真核翻译起始因子5A参与猪繁殖与呼吸综合征病毒感染

Proteomic Investigation Reveals Eukaryotic Translation Initiation Factor 5A Involvement in Porcine Reproductive and Respiratory Syndrome Virus Infection .

作者信息

Li Huawei, Wan Bo, Jiang Dawei, Ji Pengchao, Zhao Mengmeng, Li Xinfeng, Li Rui, Qiao Songlin

机构信息

Henan Key Laboratory of Innovation and Utilization of Unconventional Feed Resources, Henan University of Animal Husbandry and Economy, Zhengzhou, China.

College of Veterinary Medicine, Henan Agricultural University, Zhengzhou, China.

出版信息

Front Vet Sci. 2022 Apr 13;9:861137. doi: 10.3389/fvets.2022.861137. eCollection 2022.

DOI:10.3389/fvets.2022.861137
PMID:35498732
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9043857/
Abstract

Porcine reproductive and respiratory syndrome virus (PRRSV), one of the most serious animal pathogens in the world, has caused enormous global swine industry losses. An in-depth investigation of the PRRSV-host interaction would be beneficial for preventing and controlling PRRSV infections and transmission. In this study, we performed label-free quantitative proteomic assays to investigate proteome dynamics of porcine alveolar macrophages (PAMs) during infection with highly pathogenic PRRSV (HP-PRRSV) strain HN07-1. Analysis of the results led to identification of 269 significantly differentially expressed host cellular proteins, of which levels of proteins belonging to the eukaryotic translation initiation factor (eIF) family were found to be decreased in abundance in HP-PRRSV-infected PAMs. Furthermore, knockdown of eIF5A expression was demonstrated to markedly suppress HP-PRRSV propagation, as reflected by reduced progeny virus titers . These results highlight the importance of eIF5A in PRRSV infection, while also demonstrating that PAMs down-regulate eIF5A expression as a host cell antiviral strategy. Results of the current study deepen our understanding of PRRSV pathogenesis and provide novel insights to guide development of effective strategies to combat the virus.

摘要

猪繁殖与呼吸综合征病毒(PRRSV)是世界上最严重的动物病原体之一,已给全球养猪业造成巨大损失。深入研究PRRSV与宿主的相互作用将有助于预防和控制PRRSV的感染与传播。在本研究中,我们进行了无标记定量蛋白质组学分析,以研究高致病性PRRSV(HP-PRRSV)毒株HN07-1感染期间猪肺泡巨噬细胞(PAM)的蛋白质组动态变化。对结果的分析导致鉴定出269种显著差异表达的宿主细胞蛋白,其中发现属于真核翻译起始因子(eIF)家族的蛋白在HP-PRRSV感染的PAM中丰度降低。此外,eIF5A表达的敲低被证明能显著抑制HP-PRRSV的增殖,这通过子代病毒滴度降低得以体现。这些结果突出了eIF5A在PRRSV感染中的重要性,同时也表明PAM下调eIF5A表达作为一种宿主细胞抗病毒策略。本研究结果加深了我们对PRRSV发病机制的理解,并为指导开发对抗该病毒的有效策略提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cd4/9043857/5cedebf10d38/fvets-09-861137-g0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cd4/9043857/61d54b9ee2a8/fvets-09-861137-g0001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cd4/9043857/d6c405007840/fvets-09-861137-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cd4/9043857/b3ab5f9b789a/fvets-09-861137-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cd4/9043857/60c63615ee0c/fvets-09-861137-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cd4/9043857/5cedebf10d38/fvets-09-861137-g0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cd4/9043857/61d54b9ee2a8/fvets-09-861137-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cd4/9043857/c873ffcce5ee/fvets-09-861137-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cd4/9043857/361ace48910d/fvets-09-861137-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cd4/9043857/92acddea6ce4/fvets-09-861137-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cd4/9043857/d6c405007840/fvets-09-861137-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cd4/9043857/b3ab5f9b789a/fvets-09-861137-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cd4/9043857/60c63615ee0c/fvets-09-861137-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cd4/9043857/5cedebf10d38/fvets-09-861137-g0008.jpg

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