Institute for Molecular Virology and McArdle Laboratory for Cancer Research, University of Wisconsin-Madison, Madison, WI 53706, USA.
Sci Adv. 2015 Nov 27;1(10):e1501164. doi: 10.1126/sciadv.1501164. eCollection 2015 Nov.
Intrinsic immune defenses mediated by restriction factors inhibit productive viral infections. Select viruses rapidly establish latent infections and, with gene expression profiles that imply cell-autonomous intrinsic defenses, may be the most effective immune control measure against latent reservoirs. We illustrate that lysine-specific demethylases (KDMs) are restriction factors that prevent human cytomegalovirus from establishing latency by removing repressive epigenetic modifications from histones associated with the viral major immediate early promoter (MIEP), stimulating the expression of a viral lytic phase target of cell-mediated adaptive immunity. The viral UL138 protein negates this defense by preventing KDM association with the MIEP. The presence of an intrinsic defense against latency and the emergence of a cognate neutralizing viral factor indicate that "arms races" between hosts and viruses over lifelong colonization exist at the cellular level.
先天免疫防御机制通过限制因子来抑制病毒的有效感染。部分病毒会迅速建立潜伏感染,这些病毒的基因表达谱暗示了细胞自主的先天防御机制,它们可能是对抗潜伏库最有效的免疫控制措施。我们的研究表明,赖氨酸特异性去甲基酶(KDMs)是一种限制因子,通过去除与病毒主要早期即刻启动子(MIEP)相关的组蛋白上的抑制性表观遗传修饰,来阻止人类巨细胞病毒建立潜伏,从而刺激细胞介导的适应性免疫的病毒裂解期靶标表达。病毒 UL138 蛋白通过阻止 KDM 与 MIEP 的结合来否定这种防御。针对潜伏的内在防御机制的存在和与之对应的中和病毒因子的出现表明,在细胞水平上,宿主和病毒之间存在着针对终身定植的“军备竞赛”。