Yu Linyang, Dong Jianguo, Wang Yanwu, Zhang Pengfei, Liu Yanling, Zhang Leyi, Liang Pengshuai, Wang Lei, Song Changxu
Animal Science College/National Engineering Center for Swine Breeding Industry, South China Agriculture University, No. 483 Wushan Road, Tianhe District, Guangzhou, 510642, China.
School of Animal Husbandry and Medical Engineering, Xinyang Agriculture and Forestry University, No. 1 North Road, Pingqiao District, Xinyang, 464000, China.
Arch Virol. 2019 Apr;164(4):1147-1157. doi: 10.1007/s00705-019-04176-2. Epub 2019 Feb 24.
Porcine epidemic diarrhea virus (PEDV) causes severe economic loss in the pig industry each year. To better understand the relationship between cytokines and PEDV replication, in this study, pro-inflammatory cytokine and chemokine expression profiles in Vero cells infected with PEDV were analyzed. Real-time quantitative PCR assay indicated that IL-1α, IL-1β, TNF-α, CCL2, CCL5 and CXCL8 expression levels were significantly upregulated. Moreover, overexpression and siRNA silencing assays showed that overexpression of IL-1α, IL-1β, TNF-α, CCL2, CCL5 and CXCL8 could significantly inhibit PEDV replication, while silencing of IL-1α, IL-1β, TNF-α, CCL2, CCL5 and CXCL8 could significantly promote PEDV replication. Finally, a dual-luciferase reporter assay showed that nsp4 contributed to the expression of IL-1α, IL-1β, TNF-α, CCL2, CCL5 and CXCL8 via the NF-κB pathway. Together, these data determined that PEDV nsp4 could upregulate pro-inflammatory cytokine and chemokine expression, inhibiting viral replication in vitro. These results provided novel insights for understanding the roles of cytokines in PEDV replication.
猪流行性腹泻病毒(PEDV)每年给养猪业造成严重的经济损失。为了更好地理解细胞因子与PEDV复制之间的关系,在本研究中,分析了感染PEDV的Vero细胞中促炎细胞因子和趋化因子的表达谱。实时定量PCR分析表明,IL-1α、IL-1β、TNF-α、CCL2、CCL5和CXCL8的表达水平显著上调。此外,过表达和siRNA沉默试验表明,IL-1α、IL-1β、TNF-α、CCL2、CCL5和CXCL8的过表达可显著抑制PEDV复制,而IL-1α、IL-1β、TNF-α、CCL2、CCL5和CXCL8的沉默则可显著促进PEDV复制。最后,双荧光素酶报告基因试验表明,nsp4通过NF-κB途径促进IL-1α、IL-1β、TNF-α、CCL2、CCL5和CXCL8的表达。总之,这些数据表明PEDV nsp4可上调促炎细胞因子和趋化因子的表达,在体外抑制病毒复制。这些结果为理解细胞因子在PEDV复制中的作用提供了新的见解。