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A Novel Inhibitor of the NF-κB Signaling Pathway Encoded by the Parapoxvirus Orf Virus

机译:副痘病毒Orf病毒编码的新型NF-κB信号通路抑制剂。

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摘要

The parapoxvirus orf virus (ORFV) is a pathogen of sheep and goats that has been used as a preventive and therapeutic immunomodulatory agent in several animal species. However, the functions (genes, proteins, and mechanisms of action) evolved by ORFV to modulate and manipulate immune responses are poorly understood. Here, the novel ORFV protein ORFV024 was shown to inhibit activation of the NF-κB signaling pathway, an important modulator of early immune responses against viral infections. Infection of primary ovine cells with an ORFV024 deletion mutant virus resulted in a marked increase in expression of NF-κB-regulated chemokines and other proinflammatory host genes. Expression of ORFV024 in cell cultures significantly decreased lipopolysaccharide (LPS)- and tumor necrosis factor alpha (TNF-α)-induced NF-κB-responsive reporter gene expression. Further, ORFV024 expression decreased TNF-α-induced phosphorylation and nuclear translocation of NF-κB-p65, phosphorylation, and degradation of IκBα, and phosphorylation of IκB kinase (IKK) subunits IKKα and IKKβ, indicating that ORFV024 functions by inhibiting activation of IKKs, the bottleneck for most NF-κB activating stimuli. Although ORFV024 interferes with activation of the NF-κB signaling pathway, its deletion from the OV-IA82 genome had no significant effect on disease severity, progression, and time to resolution in sheep, indicating that ORFV024 is not essential for virus virulence in the natural host. This represents the first description of a NF-κB inhibitor encoded by a parapoxvirus.
机译:副痘病毒orf病毒(ORFV)是绵羊和山羊的病原体,已在几种动物物种中用作预防和治疗性免疫调节剂。但是,人们对ORFV进化出的调节和操纵免疫应答的功能(基因,蛋白质和作用机制)了解甚少。在这里,新的ORFV蛋白ORFV024被证明可以抑制NF-κB信号通路的激活,NF-κB信号通路是针对病毒感染的早期免疫反应的重要调节剂。用ORFV024缺失突变病毒感染原代绵羊细胞会导致NF-κB调节的趋化因子和其他促炎宿主基因的表达显着增加。细胞培养物中ORFV024的表达显着降低了脂多糖(LPS)和肿瘤坏死因子α(TNF-α)诱导的NF-κB反应性报告基因的表达。此外,ORFV024的表达降低了TNF-α诱导的NF-κB-p65的磷酸化和核易位,IκBα的磷酸化和降解以及IκB激酶(IKK)亚基IKKα和IKKβ的磷酸化,表明ORFV024通过抑制IKK的激活而发挥作用。 ,这是大多数NF-κB激活刺激的瓶颈。尽管ORFV024干扰NF-κB信号通路的激活,但从OV-IA82基因组中删除对绵羊的疾病严重性,进展和消退时间没有明显影响,这表明ORFV024对于天然的病毒毒力不是必需的主办。这是对副痘病毒编码的NF-κB抑制剂的首次描述。

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