Quantitative Proteomic Analysis of BHK-21 Cells Infected with Foot-and-Mouth Disease Virus Serotype Asia 1

PLoS One. 2015 Jul 10;10(7):e0132384. doi: 10.1371/journal.pone.0132384. eCollection 2015.

Abstract

Stable isotope labeling with amino acids in cell culture (SILAC) was used to quantitatively study the host cell gene expression profile, in order to achieve an unbiased overview of the protein expression changes in BHK-21 cells infected with FMDV serotype Asia 1. The SILAC-based approach identified overall 2,141 proteins, 153 of which showed significant alteration in the expression level 6 h post FMDV infection (57 up-regulated and 96 down-regulated). Among these proteins, six cellular proteins, including three down-regulated (VPS28, PKR, EVI5) and three up-regulated (LYPLA1, SEC62 and DARs), were selected according to the significance of the changes and/or the relationship with PKR. The expression level and pattern of the selected proteins were validated by immunoblotting and confocal microscopy. Furthermore, the functions of these cellular proteins were assessed by small interfering RNA-mediated depletion, and their functional importance in the replication of FMDV was demonstrated by western blot, reverse transcript PCR (RT-PCR) and 50% Tissue Culture Infective Dose (TCID50). The results suggest that FMDV infection may have effects on the expression of specific cellular proteins to create more favorable conditions for FMDV infection. This study provides novel data that can be utilized to understand the interactions between FMDV and the host cell.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Cell Line
  • Chromatography, Liquid
  • Computational Biology
  • Down-Regulation
  • Foot-and-Mouth Disease / virology*
  • Foot-and-Mouth Disease Virus / genetics
  • Foot-and-Mouth Disease Virus / physiology*
  • Gene Knockdown Techniques
  • Genes, Viral
  • Immunoblotting
  • Isotope Labeling
  • Mass Spectrometry
  • Metabolic Networks and Pathways
  • Proteome / metabolism
  • Proteomics / methods*
  • RNA Interference
  • RNA, Small Interfering / metabolism
  • Reproducibility of Results
  • Subcellular Fractions / metabolism
  • Time Factors
  • Transfection
  • Up-Regulation
  • Viral Proteins / metabolism

Substances

  • Proteome
  • RNA, Small Interfering
  • Viral Proteins

Grants and funding

This research was supported by grants from the National Science and Technology Support Program (2013BAD12B00), International Science &Technology Cooperation Program of China (2014DFA31890), the Fundamental Research Funds for the Chinese Academy of Agricultural Sciences (2015ZL062), and the "Twelfth Five-Year" National Science and technology program in rural areas (2011AA10A211). Guangzhou Fitgene biotechnology Co. Ltd. provided support in the form of salaries for author [XJL], but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific roles of this author are articulated in the ‘author contributions’ section.