Christopher S. Bond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA.
Department of Molecular Microbiology and Immunology, School of Medicine, University of Missouri, Columbia, MO 65212, USA.
Viruses. 2019 Jul 17;11(7):651. doi: 10.3390/v11070651.
Moloney leukemia virus 10 (MOV10) is an RNA helicase that has been shown to affect the replication of several viruses. The effect of MOV10 on Hepatitis B virus (HBV) infection is not known and its role on the replication of this virus is poorly understood. We investigated the effect of MOV10 down-regulation and MOV10 over-expression on HBV in a variety of cell lines, as well as in an infection system using a replication competent virus. We report that MOV10 down-regulation, using siRNA, shRNA, and CRISPR/Cas9 gene editing technology, resulted in increased levels of HBV DNA, HBV pre-genomic RNA, and HBV core protein. In contrast, MOV10 over-expression reduced HBV DNA, HBV pre-genomic RNA, and HBV core protein. These effects were consistent in all tested cell lines, providing strong evidence for the involvement of MOV10 in the HBV life cycle. We demonstrated that MOV10 does not interact with HBV-core. However, MOV10 binds HBV pgRNA and this interaction does not affect HBV pgRNA decay rate. We conclude that the restriction of HBV by MOV10 is mediated through effects at the level of viral RNA.
莫洛尼鼠白血病病毒 10(MOV10)是一种 RNA 解旋酶,已被证明会影响几种病毒的复制。MOV10 对乙型肝炎病毒(HBV)感染的影响尚不清楚,其对该病毒复制的作用也知之甚少。我们研究了 MOV10 下调和 MOV10 过表达对多种细胞系以及使用复制型病毒的感染系统中 HBV 的影响。我们报告说,使用 siRNA、shRNA 和 CRISPR/Cas9 基因编辑技术下调 MOV10 会导致 HBV DNA、HBV 前基因组 RNA 和 HBV 核心蛋白水平升高。相比之下,MOV10 的过表达会降低 HBV DNA、HBV 前基因组 RNA 和 HBV 核心蛋白。这些影响在所有测试的细胞系中都是一致的,为 MOV10 参与 HBV 生命周期提供了强有力的证据。我们证明 MOV10 不与 HBV 核心相互作用。然而,MOV10 结合 HBV pgRNA,并且这种相互作用不会影响 HBV pgRNA 降解率。我们的结论是,MOV10 通过对病毒 RNA 水平的影响来限制 HBV。