Differential Proteome Analysis of Host Cells Infected with Porcine Circovirus Type 2

被引:55
|
作者
Zhang, Xin [1 ]
Zhou, Jiyong [1 ,2 ]
Wu, Yongping [1 ,2 ]
Zheng, Xiaojuan [1 ,2 ]
Ma, Guangpeng [3 ]
Wang, Zhongtian [4 ]
Jin, Yulan [1 ,2 ]
He, Jialing [1 ,2 ]
Yan, Yan [1 ]
机构
[1] Zhejiang Univ, Minist Agr, Key Lab Anim Epidem Etiol & Immunol Prevent, Hangzhou 310029, Zhejiang, Peoples R China
[2] Zhejiang Univ, Affiliated Hosp 1, State Key Lab Diag & Treatment Infect Dis, Hangzhou 310003, Zhejiang, Peoples R China
[3] China Rural Technol Dev Ctr, Beijing 100045, Peoples R China
[4] Chinese Inst Vet Drug Control, Beijing 100081, Peoples R China
基金
中国国家自然科学基金;
关键词
porcine circovirus type 2; proteome analysis; two-dimensional gel electrophoresis; MALDI-TOF/TOF; PK-15; cell; BURSAL DISEASE VIRUS; SWINE-FEVER VIRUS; MASS-SPECTROMETRY; CAPSID PROTEIN; CELLULAR-RESPONSES; ESCHERICHIA-COLI; VIRAL PROTEOMICS; BIOPSY SPECIMENS; TRANSFER-RNA; IDENTIFICATION;
D O I
10.1021/pr900488q
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Porcine circovirus type 2 (PCV2) is the primary causative agent of postweaning multisystemic wasting syndrome, which is an emerging swine immunosuppressive disease. To uncover cellular protein responses in PCV2-infected PK-15 cells, the comprehensive proteome profiles were analyzed utilizing two-dimensional gel electrophoresis (2-DE) coupled with MALDI-TOF/TOF identification. Multiple comparisons of 2-DE revealed that the majority of changes in protein expression occurred at 48-96 h after PCV2 infection A total of 34 host-encoded proteins, including 15 up-regulated and 19 down-regulated proteins, were identified by MALDI-TOF/TOF analysis According to cellular function, the differential expression proteins could be sorted into several groups cytoskeleton proteins, stress response, macromolecular biosynthesis, energy metabolism, ubiquitin-proteasome pathway, signal transduction, gene regulation. Western blot analysis demonstrated the changes of a tubulin, beta actin, and cytokeratin 8 during infection. Colocalization and coimmunoprecipitation analyses confirmed that the cellular alpha tubulin Interacts with the Cap protein of PCV2 in the infected PK-15 cells. These identified cellular constituents have important implications for understanding the host interactions with PCV2 and brings us a step closer to defining the cellular requirements for the underlying mechanism of PCV2 replication and pathogenesis.
引用
收藏
页码:5111 / 5119
页数:9
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