Key Laboratory of Animal Diseases Diagnostic and Immunology, Ministry of Agriculture, College of Veterinary Medicine, Nanjing Agricultural University, Nanjing 210095, China.
Key Laboratory of Animal Diseases Diagnostic and Immunology, Ministry of Agriculture, College of Veterinary Medicine, Nanjing Agricultural University, Nanjing 210095, China.
Virus Res. 2014 Aug 30;189:235-42. doi: 10.1016/j.virusres.2014.05.024. Epub 2014 Jun 4.
Porcine circovirus type 2 (PCV2) has been identified as the etiologic agent which causing postweaning multisystemic wasting syndrome in swine farms in the world. Some quantitative proteomic studies showed that many proteins significantly changed in PCV2-infected cells. To explore the role of cellular chaperones during PCV2 infection, cytoprotective chaperone Hsp27 was analyzed in PCV2-infected PK-15 cells in this study. The results showed that Hsp27 could up-regulate and accumulate in phosphorylated forms in the nuclear zone during PCV2 replication. Suppression of Hsp27 phosphorylation with specific chemical inhibitors or downregulation of all forms of Hsp27 via RNA interference significantly reduced the virus replication. Meanwhile, over-expression of Hsp27 enhanced PCV2 genome replication and virion production. It indicated that Hsp27 was required for PCV2 production in PK-15 cells culture. It should be helpful for understanding the mechanism of replication and pathogenesis of PCV2 and development of novel antiviral therapies in the future.
猪圆环病毒 2 型(PCV2)已被确定为引起世界范围内猪养殖场断奶后多系统消耗综合征的病原体。一些定量蛋白质组学研究表明,PCV2 感染细胞中许多蛋白质发生了显著变化。为了探讨细胞伴侣在 PCV2 感染过程中的作用,本研究分析了 PCV2 感染 PK-15 细胞中的细胞保护性伴侣热休克蛋白 27(Hsp27)。结果表明,Hsp27 在 PCV2 复制过程中可以在核区上调并以磷酸化形式积累。用特异性化学抑制剂抑制 Hsp27 磷酸化或通过 RNA 干扰下调所有形式的 Hsp27,均可显著降低病毒复制。同时,Hsp27 的过表达增强了 PCV2 基因组复制和病毒粒子的产生。这表明 Hsp27 是 PCV2 在 PK-15 细胞培养中产生所必需的。这将有助于理解 PCV2 的复制机制和发病机制,并为未来开发新型抗病毒疗法提供帮助。