The Heilongjiang Key Laboratory of Immunity and Infection, Heilongjiang, China.
Biochem Biophys Res Commun. 2013 Sep 6;438(4):619-23. doi: 10.1016/j.bbrc.2013.08.006. Epub 2013 Aug 11.
The expression of type I interferon (IFN) is one of the most potent innate defences against viral infection in higher vertebrates. Borna disease virus (BDV) establishes persistent, noncytolytic infections in animals and in cultured cells. Early studies have shown that the BDV phosphoprotein can inhibit the activation of type I IFN through the TBK1-IRF3 pathway. The function of the BDV nucleoprotein in the inhibition of IFN activity is not yet clear. In this study, we demonstrated IRF7 activation and increased IFN-α/β expression in a BDV-persistently infected human oligodendroglia cell line following RNA interference-mediated BDV nucleoprotein silencing. Furthermore, we showed that BDV nucleoprotein prevented the nuclear localisation of IRF7 and inhibited endogenous IFN induction by poly(I:C), coxsackie virus B3 and IFN-β. Our findings provide evidence for a previously undescribed mechanism by which the BDV nucleoprotein inhibits type I IFN expression by interfering with the IRF7 pathway.
I 型干扰素(IFN)的表达是高等脊椎动物对抗病毒感染的最有效先天防御机制之一。博尔纳病病毒(BDV)在动物和培养细胞中建立持续的非细胞溶解感染。早期研究表明,BDV 磷蛋白可通过 TBK1-IRF3 途径抑制 I 型 IFN 的激活。BDV 核蛋白在抑制 IFN 活性中的功能尚不清楚。在这项研究中,我们证明了在 BDV 持续感染的人少突胶质细胞系中,通过 RNA 干扰介导的 BDV 核蛋白沉默后,IRF7 的激活和 IFN-α/β 的表达增加。此外,我们还表明,BDV 核蛋白阻止了 IRF7 的核定位,并抑制了 poly(I:C)、柯萨奇病毒 B3 和 IFN-β 诱导的内源性 IFN。我们的发现为 BDV 核蛋白通过干扰 IRF7 途径抑制 I 型 IFN 表达提供了以前未描述的机制的证据。