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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.
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页码:5111 / 5119
页数:9
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