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Yellow Fever Virus Down-Regulates mRNA Expression of SOCS1 in the Initial Phase of Infection in Human Cell Lines

机译:黄热病病毒下调SOCS1的mRNA表达在人体细胞系中感染的初始阶段

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摘要

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 SOCS and PIAS in infected cells is yet to be determined. Here, we show that SOCS1 is down-regulated early in YFV-infected HeLa and HEK 293T cells, while SOCS3 and SOCS5 are not significantly altered, and PIAS 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 SOCS and PIAS upon YFV infection and a basis for further investigation into SOCS/PIAS expression and how these modulate the immune response in animal models.
机译:黄病毒不断发展不同的免疫逃避策略,并针对登革热和日本脑炎病毒描述了抑制细胞因子信号传导(SOC)和激活统计数据(PIAS)的蛋白质抑制剂的抑制剂的功能,以便是黄热病的尽管存在有效疫苗,但病毒(YFV)仍然是全球重要性。据报道,某些机制用于逃避宿主免疫防御,但尚未确定感染细胞中的SOC和胶合的表达模式。在这里,我们表明SOCS1在YFV感染的HELA和HEK 293T细胞中较早调节,而SOCS3和SOCS5没有显着改变,并且胶结mRNA表达似乎遵循类似于昼夜循环控制基因的升高模式。我们还证明YFV逃避干扰素-β应用以产生可比较的病毒滴度。本报告提供了对SOCS和PIAS对YFV感染的体外表达动态的初步见解,以及进一步调查SOCS / PIAS表达以及这些调节动物模型中的免疫应答的基础。

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