Cellular protein profiles altered by PRRSV infection of porcine monocytes-derived dendritic cells

Yue Hu, Xiangju Wu, Wenhai Feng, Feng Li, Zhao Wang, Jing Qi, Yijun Du

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

Abstract

Dendritic cells (DCs) are potent antigen-presenting cells (APCs) that play an important role in inducing primary antigen-specific immune responses. Some viruses have evolved to specifically target DCs to circumvent the host immune responses for their persistence in the host. One example is porcine reproductive and respiratory syndrome virus (PRRSV) that causes a persistent infection in pigs through modulating DC-mediated antiviral response. To study the cellular protein responses in PRRSV-infected monocyte-derived dendritic cells (MoDCs), two-dimensional liquid chromatography-tandem mass spectrometry coupled with isobaric tags for relative and absolute quantification (iTRAQ) labeling was employed to quantitatively identify the differentially expressed proteins in PRRSV-infected MoDCs and the control cells. A total of 252 cellular proteins in MoDCs that were significantly altered at different time periods post-infection were identified. Differentially expressed proteins that are involved in the endocytosis pathway, actin cytoskeleton network, antigen processing and presentation, JAK-STAT signaling pathway and PRRSV receptors were identified and further analyzed. Among them, the expression changes of STAT1, Mx1, PICALM and SLA-DR were further verified by Western blotting. The protein profiles associated with PRRSV infection of MoDCs should offer novel insights to further investigation of PRRSV-mediated antiviral evasion mechanism and its pathobiology in swine.

Original languageEnglish
Pages (from-to)134-142
Number of pages9
JournalVeterinary Microbiology
Volume228
DOIs
StatePublished - Jan 2019

Bibliographical note

Publisher Copyright:
© 2018 Elsevier B.V.

Funding

We thank Dr. Ping Jiang, Nanjing Agricultural University, China, to provide the PRRSV SY0608 strain. This work was supported by The National Key Research and Development Program of China ( 2016YFD0501505 ), Young Taishan Scholars ( tsqn20161057 ), Agricultural Scientific and Technological Innovation Project of Shandong Academy of Agricultural Sciences ( CXGC2016C07 ), the National Natural Science Foundation of China ( 31672609 , 31702215 ).

FundersFunder number
major scientific and technological innovation project of Shandong Academy of Agricultural SciencesCXGC2016C07
Young Taishan Scholarstsqn20161057
National Natural Science Foundation of China (NSFC)31702215, 31672609
National Natural Science Foundation of China (NSFC)
National Basic Research Program of China (973 Program)2016YFD0501505
National Basic Research Program of China (973 Program)

    Keywords

    • Cellular network
    • MoDCs
    • PRRSV
    • iTRAQ

    ASJC Scopus subject areas

    • Microbiology
    • General Veterinary

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