Institute of Medical Virology, University of Zurich, Winterthurerstrasse 190, 8057, Zürich, Switzerland.
Life Science Zurich Graduate School, Winterthurerstrasse 190, 8057, Zürich, Switzerland.
Nat Commun. 2018 May 17;9(1):1980. doi: 10.1038/s41467-018-04379-2.
The type I interferon (IFN) system plays an important role in controlling herpesvirus infections, but it is unclear which IFN-mediated effectors interfere with herpesvirus replication. Here we report that human myxovirus resistance protein B (MxB, also designated Mx2) is a potent human herpesvirus restriction factor in the context of IFN. We demonstrate that ectopic MxB expression restricts a range of herpesviruses from the Alphaherpesvirinae and Gammaherpesvirinae, including herpes simplex virus 1 and 2 (HSV-1 and HSV-2), and Kaposi's sarcoma-associated herpesvirus (KSHV). MxB restriction of HSV-1 and HSV-2 requires GTPase function, in contrast to restriction of lentiviruses. MxB inhibits the delivery of incoming HSV-1 DNA to the nucleus and the appearance of empty capsids, but not the capsid delivery to the cytoplasm or tegument dissociation from the capsid. Our study identifies MxB as a potent pan-herpesvirus restriction factor which blocks the uncoating of viral DNA from the incoming viral capsid.
I 型干扰素(IFN)系统在控制疱疹病毒感染方面发挥着重要作用,但尚不清楚哪种 IFN 介导的效应物会干扰疱疹病毒的复制。在这里,我们报告人源弹状病毒抗性蛋白 B(MxB,也称为 Mx2)是 IFN 背景下的一种有效的人类疱疹病毒限制因子。我们证明,异位表达 MxB 可限制来自 Alphaherpesvirinae 和 Gammaherpesvirinae 的多种疱疹病毒,包括单纯疱疹病毒 1 型和 2 型(HSV-1 和 HSV-2)和卡波西肉瘤相关疱疹病毒(KSHV)。MxB 对 HSV-1 和 HSV-2 的限制需要 GTPase 功能,这与对慢病毒的限制不同。MxB 抑制了进入的 HSV-1 DNA 向核内的传递和空衣壳的出现,但不影响衣壳向细胞质的传递或衣壳与囊膜的分离。我们的研究确定 MxB 是一种有效的泛疱疹病毒限制因子,可阻止从进入的病毒衣壳中释放病毒 DNA。