Gil Laura H V G, Ansari Israrul H, Vassilev Ventzislav, Liang Delin, Lai Vicky C H, Zhong Weidong, Hong Zhi, Dubovi Edward J, Donis Ruben O
Department of Veterinary and Biomedical Sciences, University of Nebraska-Lincoln, 68583-0905, USA.
J Virol. 2006 Jan;80(2):900-11. doi: 10.1128/JVI.80.2.900-911.2006.
The alpha/beta interferon (IFN-alpha/beta) system is the first line of defense against viral infection and a critical link between the innate and adaptive immune responses. IFN-alpha/beta secretion is the hallmark of cellular responses to acute RNA virus infections. As part of their survival strategy, many viruses have evolved mechanisms to counteract the host IFN-alpha/beta response. Bovine viral diarrhea virus (BVDV) (genus Pestivirus) was reported to trigger interferon production in infected cultured cells under certain circumstances or to suppress it under others. Our studies with various cultured fibroblasts and epithelial bovine cells indicated that cytopathic (cp) BVDV induces IFN-alpha/beta very inefficiently. Using a set of engineered cp BVDVs expressing mutant Npro and appropriate controls, we found that the IFN-alpha/beta response to infection was dependent on Npro expression and independent of viral replication efficiency. In order to investigate whether the protease activity of Npro is required for IFN-alpha/beta antagonism, we engineered Npro mutants lacking protease activity by replacement of amino acid E22, H49, or C69. We found that E22 and H49 substitutions abolished the ability of Npro to suppress IFN, whereas C69 had no effect, suggesting that the structural integrity of the N terminus of Npro was more important than its catalytic activity for IFN-alpha/beta suppression. A catalytically active mutant with a change at a conserved Npro region near the N terminus (L8P) in both BVDV biotypes did not antagonize IFN-alpha/beta production, confirming its involvement in this process. Taken together, these results not only provide direct evidence for the role of Npro in blocking IFN-alpha/beta induction, but also implicate the amino-terminal domain of the protein in this function.
α/β干扰素(IFN-α/β)系统是抵御病毒感染的第一道防线,也是先天性免疫反应和适应性免疫反应之间的关键环节。IFN-α/β的分泌是细胞对急性RNA病毒感染作出反应的标志。作为其生存策略的一部分,许多病毒已经进化出对抗宿主IFN-α/β反应的机制。据报道,牛病毒性腹泻病毒(BVDV)(瘟病毒属)在某些情况下会在受感染的培养细胞中触发干扰素产生,而在其他情况下则会抑制它。我们对各种培养的成纤维细胞和牛上皮细胞的研究表明,致细胞病变(cp)的BVDV诱导IFN-α/β的效率非常低。使用一组表达突变Npro的工程化cp BVDV及其适当对照,我们发现对感染的IFN-α/β反应依赖于Npro表达,且与病毒复制效率无关。为了研究Npro的蛋白酶活性是否是IFN-α/β拮抗作用所必需的,我们通过替换氨基酸E22、H49或C69构建缺乏蛋白酶活性的Npro突变体。我们发现E22和H49的替换消除了Npro抑制IFN的能力,而C69的替换没有影响,这表明Npro N端的结构完整性对IFN-α/β抑制比其催化活性更重要。在两种BVDV生物型中,在靠近N端的保守Npro区域发生变化(L8P)的催化活性突变体并不拮抗IFN-α/β的产生,证实了其参与这一过程。综上所述,这些结果不仅为Npro在阻断IFN-α/β诱导中的作用提供了直接证据,也暗示了该蛋白的氨基末端结构域在这一功能中的作用。