{"title":"伪狂犬病毒感染PK-15细胞的蛋白质组学分析","authors":"Shuaiwei Wang, Xiaoyong Chen, Houqiang Luo, Meng Wang, Junyu Liu, Qingsong Han","doi":"10.30466/vrf.2024.2026963.4239","DOIUrl":null,"url":null,"abstract":"<p><p>Pseudorabies virus (PRV) heavily depends on host machinery to support its life cycle. Investigating the interaction between PRV and host could aid in the understandings of viral pathogenesis. In this study, we performed a 4D label free proteomic method to examine the differentially expressed proteins in porcine kidney PK-15 cells with PRV infection. The results showed that the levels of 661 proteins were significantly elevated and 693 proteins were markedly reduced. Furthermore, these altered proteins were primarily enriched in spliceosome, protein processing in endoplasmic reticulum (ER), RNA transport, and protein export. To ensure the reliability of the proteomic results, the protein levels of formin binding protein 11 and wolfram syndrome 1as components of spliceosome and ER were verified via western blotting and the results were consistent. Together, our data shed light on a new protein profiling induced by PRV infection and highlighted the importance of spliceosome and ER in PRV replication which could promote understandings of host-PRV interplay.</p>","PeriodicalId":23989,"journal":{"name":"Veterinary Research Forum","volume":"16 3","pages":"141-147"},"PeriodicalIF":0.8000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12085936/pdf/","citationCount":"0","resultStr":"{\"title\":\"Proteomic profiling of pseudorabies virus-infected PK-15 cells based on 4D label free analysis.\",\"authors\":\"Shuaiwei Wang, Xiaoyong Chen, Houqiang Luo, Meng Wang, Junyu Liu, Qingsong Han\",\"doi\":\"10.30466/vrf.2024.2026963.4239\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Pseudorabies virus (PRV) heavily depends on host machinery to support its life cycle. Investigating the interaction between PRV and host could aid in the understandings of viral pathogenesis. In this study, we performed a 4D label free proteomic method to examine the differentially expressed proteins in porcine kidney PK-15 cells with PRV infection. The results showed that the levels of 661 proteins were significantly elevated and 693 proteins were markedly reduced. Furthermore, these altered proteins were primarily enriched in spliceosome, protein processing in endoplasmic reticulum (ER), RNA transport, and protein export. To ensure the reliability of the proteomic results, the protein levels of formin binding protein 11 and wolfram syndrome 1as components of spliceosome and ER were verified via western blotting and the results were consistent. Together, our data shed light on a new protein profiling induced by PRV infection and highlighted the importance of spliceosome and ER in PRV replication which could promote understandings of host-PRV interplay.</p>\",\"PeriodicalId\":23989,\"journal\":{\"name\":\"Veterinary Research Forum\",\"volume\":\"16 3\",\"pages\":\"141-147\"},\"PeriodicalIF\":0.8000,\"publicationDate\":\"2025-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12085936/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Veterinary Research Forum\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://doi.org/10.30466/vrf.2024.2026963.4239\",\"RegionNum\":4,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/3/15 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"ZOOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Veterinary Research Forum","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.30466/vrf.2024.2026963.4239","RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/15 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"ZOOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
伪狂犬病毒(PRV)严重依赖宿主机制来支持其生命周期。研究PRV与宿主的相互作用有助于了解病毒的发病机制。在本研究中,我们采用4D无标记蛋白质组学方法检测猪肾PK-15细胞中PRV感染的差异表达蛋白。结果表明,661蛋白水平显著升高,693蛋白水平显著降低。此外,这些改变的蛋白质主要富集在剪接体、内质网(ER)的蛋白质加工、RNA转运和蛋白质输出中。为了保证蛋白质组学结果的可靠性,通过western blotting对剪接体和内质网组成部分formin binding protein 11和wolfram syndrome 1的蛋白水平进行了验证,结果一致。总之,我们的数据揭示了由PRV感染诱导的一种新的蛋白质谱,并强调了剪接体和ER在PRV复制中的重要性,这可以促进对宿主-PRV相互作用的理解。
Proteomic profiling of pseudorabies virus-infected PK-15 cells based on 4D label free analysis.
Pseudorabies virus (PRV) heavily depends on host machinery to support its life cycle. Investigating the interaction between PRV and host could aid in the understandings of viral pathogenesis. In this study, we performed a 4D label free proteomic method to examine the differentially expressed proteins in porcine kidney PK-15 cells with PRV infection. The results showed that the levels of 661 proteins were significantly elevated and 693 proteins were markedly reduced. Furthermore, these altered proteins were primarily enriched in spliceosome, protein processing in endoplasmic reticulum (ER), RNA transport, and protein export. To ensure the reliability of the proteomic results, the protein levels of formin binding protein 11 and wolfram syndrome 1as components of spliceosome and ER were verified via western blotting and the results were consistent. Together, our data shed light on a new protein profiling induced by PRV infection and highlighted the importance of spliceosome and ER in PRV replication which could promote understandings of host-PRV interplay.
期刊介绍:
Veterinary Research Forum (VRF) is a quarterly international journal committed to publish worldwide contributions on all aspects of veterinary science and medicine, including anatomy and histology, physiology and pharmacology, anatomic and clinical pathology, parasitology, microbiology, immunology and epidemiology, food hygiene, poultry science, fish and aquaculture, anesthesia and surgery, large and small animal internal medicine, large and small animal reproduction, biotechnology and diagnostic imaging of domestic, companion and farm animals.