4.5 Article

ITRAQ-based quantitative proteomics reveals the proteome profiles of MDBK cells infected with bovine viral diarrhea virus

期刊

VIROLOGY JOURNAL
卷 18, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12985-021-01592-2

关键词

BVDV; Virus infection; Proteomics; iTRAQ; MDBK cells

类别

资金

  1. National Natural Science Foundation of China (NSFC) [31660718, U1803111]
  2. Bingtuan Science and Technology Project [2018BC011, 2019AB034]
  3. Young innovative talents [2017CB003, CXRC201603, CXRC201806]
  4. foundation of state key laboratory for sheep genetic improvement and healthy production [MYSKLKF201901]

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The study analyzed the pathogenic mechanisms of Bovine viral diarrhea virus (BVDV) by comparing protein expression levels in infected host cells. Different proteins were found to be differentially expressed at different time points post-infection, mainly involved in metabolic processes, biological regulation, and localization. Various signaling pathways related to BVDV infection and host resistance were enriched at different stages of infection.
BackgroundBovine viral diarrhea (BVD) which is caused by Bovine viral diarrhea virus (BVDV), is an acute, contagious disease. In spite of the use of vaccines and elimination projects, BVDV still causes severe economic losses to the cattle industry for the past few years. The current study presents a preliminary analysis of the pathogenic mechanisms from the perspective of protein expression levels in infected host cells at different points in time to elucidate the infection process associated with BVDV.MethodsWe used the isobaric tags for relative and absolute quantitation (iTRAQ) technology coupled with liquid chromatography-tandem mass spectrometric (LC-MS/MS) approach for a quantitative proteomics comparison of BVDV NADL-infected MDBK cells and non-infected cells. The functions of the proteins were deduced by functional annotation and their involvement in metabolic processes explored by KEGG pathway analysis to identify their interactions.ResultsThere were 357 (47.6% downregulated, 52.4% upregulated infected vs. control), 101 (52.5% downregulated, 47.5% upregulated infected vs. control), and 66 (21.2% downregulated, 78.8% upregulated infected vs. control) proteins were differentially expressed (fold change>1.5 or<0.67) in the BVDV NADL-infected MDBK cells at 12, 24, and 48 h after infection. GO analysis showed that the differentially expressed proteins (DEPs) are mainly involved in metabolic processes, biological regulation and localization. KEGG enrichment analysis showed that some signaling pathways that involved in the regulation of BVDV NADL-infection and host resistance are significantly (P<0.05) enriched at different stages of the BVDV NADL-infection, such as Endocytosis signaling pathway, FoxO signaling pathway, Homologous recombination signaling pathway and Lysosome pathway.ConclusionsThese results revealed that the DEPs in BVDV NADL-infected MDBK cells have a wide range of regulatory effects; in addition, they provide a lot of resources for the study of host cell proteomics after BVDV infection.

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