West African Centre for Cell Biology of Infectious Pathogens (WACCBIP), University of Ghana, Legon-Accra 00233, Ghana.
Department of Biochemistry, Cell & Molecular Biology, University of Ghana, Legon-Accra 00233, Ghana.
Viruses. 2020 Jul 25;12(8):802. doi: 10.3390/v12080802.
Flaviviruses are constantly evolving diverse immune evasion strategies, and the exploitation of the functions of suppressors of cytokine signalling (SOCS) and protein inhibitors of activated STATs (PIAS) to favour virus replication has been described for Dengue and Japanese encephalitis viruses but not for yellow fever virus (YFV), which is still of global importance despite the existence of an effective vaccine. Some mechanisms that YFV employs to evade host immune defence has been reported, but the expression patterns of and in infected cells is yet to be determined. Here, we show that is down-regulated early in YFV-infected HeLa and HEK 293T cells, while and are not significantly altered, and mRNA expression appears to follow a rise-dip pattern akin to circadian-controlled genes. We also demonstrate that YFV evades interferon-β application to produce comparable viral titres. This report provides initial insight into the in vitro expression dynamics of and upon YFV infection and a basis for further investigation into expression and how these modulate the immune response in animal models.
黄病毒不断进化出多样化的免疫逃避策略,已描述登革热病毒和日本脑炎病毒利用细胞因子信号转导抑制因子(SOCS)和激活 STAT 蛋白抑制剂(PIAS)的功能来促进病毒复制,但黄热病病毒(YFV)除外,尽管存在有效的疫苗,但它仍然具有全球重要性。已经报道了 YFV 逃避宿主免疫防御的一些机制,但感染细胞中 和 的表达模式尚未确定。在这里,我们表明 YFV 感染的 HeLa 和 HEK 293T 细胞中早期下调 ,而 和 没有明显改变,并且 mRNA 表达似乎遵循类似昼夜节律控制基因的上升-下降模式。我们还证明 YFV 逃避干扰素-β的应用以产生可比的病毒滴度。本报告首次深入了解 YFV 感染后 和 在体外的表达动态,以及进一步研究 表达及其如何在动物模型中调节免疫反应的基础。