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

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...

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Main Authors: Guo, Hui-Chen, Jin, Ye, Han, Shi-Chong, Sun, Shi-Qi, Wei, Yan-Quan, Liu, Xian-Ji, Feng, Xia, Liu, Ding Xiang, Liu, Xiang-Tao
Other Authors: Jin, Dong-Yan
Format: Article
Language:English
Published: 2015
Online Access:https://hdl.handle.net/10356/103360
http://hdl.handle.net/10220/38736
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1033602023-02-28T16:56:28Z Quantitative Proteomic Analysis of BHK-21 Cells Infected with Foot-and-Mouth Disease Virus Serotype Asia 1 Guo, Hui-Chen Jin, Ye Han, Shi-Chong Sun, Shi-Qi Wei, Yan-Quan Liu, Xian-Ji Feng, Xia Liu, Ding Xiang Liu, Xiang-Tao Jin, Dong-Yan School of Biological Sciences 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. Published version 2015-09-23T04:11:48Z 2019-12-06T21:10:52Z 2015-09-23T04:11:48Z 2019-12-06T21:10:52Z 2015 2015 Journal Article Guo, H.-C., Jin, Y., Han, S.-C., Sun, S.-Q., Wei, Y.-Q., Liu, X.-J., et al. (2015). Quantitative Proteomic Analysis of BHK-21 Cells Infected with Foot-and-Mouth Disease Virus Serotype Asia 1. PLOS ONE, 10(7), e0132384-. 1932-6203 https://hdl.handle.net/10356/103360 http://hdl.handle.net/10220/38736 10.1371/journal.pone.0132384 26161868 en PLOS ONE © 2015 Guo et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
description 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.
author2 Jin, Dong-Yan
author_facet Jin, Dong-Yan
Guo, Hui-Chen
Jin, Ye
Han, Shi-Chong
Sun, Shi-Qi
Wei, Yan-Quan
Liu, Xian-Ji
Feng, Xia
Liu, Ding Xiang
Liu, Xiang-Tao
format Article
author Guo, Hui-Chen
Jin, Ye
Han, Shi-Chong
Sun, Shi-Qi
Wei, Yan-Quan
Liu, Xian-Ji
Feng, Xia
Liu, Ding Xiang
Liu, Xiang-Tao
spellingShingle Guo, Hui-Chen
Jin, Ye
Han, Shi-Chong
Sun, Shi-Qi
Wei, Yan-Quan
Liu, Xian-Ji
Feng, Xia
Liu, Ding Xiang
Liu, Xiang-Tao
Quantitative Proteomic Analysis of BHK-21 Cells Infected with Foot-and-Mouth Disease Virus Serotype Asia 1
author_sort Guo, Hui-Chen
title Quantitative Proteomic Analysis of BHK-21 Cells Infected with Foot-and-Mouth Disease Virus Serotype Asia 1
title_short Quantitative Proteomic Analysis of BHK-21 Cells Infected with Foot-and-Mouth Disease Virus Serotype Asia 1
title_full Quantitative Proteomic Analysis of BHK-21 Cells Infected with Foot-and-Mouth Disease Virus Serotype Asia 1
title_fullStr Quantitative Proteomic Analysis of BHK-21 Cells Infected with Foot-and-Mouth Disease Virus Serotype Asia 1
title_full_unstemmed Quantitative Proteomic Analysis of BHK-21 Cells Infected with Foot-and-Mouth Disease Virus Serotype Asia 1
title_sort quantitative proteomic analysis of bhk-21 cells infected with foot-and-mouth disease virus serotype asia 1
publishDate 2015
url https://hdl.handle.net/10356/103360
http://hdl.handle.net/10220/38736
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