Department of Molecular Genetics & Microbiology, Duke University Medical Center, Durham, North Carolina, USA.
W. Harry Feinstone Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
J Virol. 2014 Jul;88(14):8065-76. doi: 10.1128/JVI.00985-14. Epub 2014 May 7.
The issue of whether viruses are subject to restriction by endogenous microRNAs (miRNAs) and/or by virus-induced small interfering RNAs (siRNAs) in infected human somatic cells has been controversial. Here, we address this question in two ways. First, using deep sequencing, we demonstrate that infection of human cells by the RNA virus dengue virus (DENV) or West Nile virus (WNV) does not result in the production of any virus-derived siRNAs or viral miRNAs. Second, to more globally assess the potential of small regulatory RNAs to inhibit virus replication, we used gene editing to derive human cell lines that lack a functional Dicer enzyme and that therefore are unable to produce miRNAs or siRNAs. Infection of these cells with a wide range of viruses, including DENV, WNV, yellow fever virus, Sindbis virus, Venezuelan equine encephalitis virus, measles virus, influenza A virus, reovirus, vesicular stomatitis virus, human immunodeficiency virus type 1, or herpes simplex virus 1 (HSV-1), failed to reveal any enhancement in the replication of any of these viruses, although HSV-1, which encodes at least eight Dicer-dependent viral miRNAs, did replicate somewhat more slowly in the absence of Dicer. We conclude that most, and perhaps all, human viruses have evolved to be resistant to inhibition by endogenous human miRNAs during productive replication and that dependence on a cellular miRNA, as seen with hepatitis C virus, is rare. How viruses have evolved to avoid inhibition by endogenous cellular miRNAs, which are generally highly conserved during metazoan evolution, remains to be determined. Importance: Eukaryotic cells express a wide range of small regulatory RNAs, including miRNAs, that have the potential to inhibit the expression of mRNAs that show sequence complementarity. Indeed, previous work has suggested that endogenous miRNAs have the potential to inhibit viral gene expression and replication. Here, we demonstrate that the replication of a wide range of pathogenic viruses is not enhanced in human cells engineered to be unable to produce miRNAs, indicating that viruses have evolved to be resistant to inhibition by miRNAs. This result is important, as it implies that manipulation of miRNA levels is not likely to prove useful in inhibiting virus replication. It also focuses attention on the question of how viruses have evolved to resist inhibition by miRNAs and whether virus mutants that have lost this resistance might prove useful, for example, in the development of attenuated virus vaccines.
病毒是否会受到内源性 microRNAs(miRNAs)和/或感染人体体细胞中的病毒诱导的小干扰 RNA(siRNA)的限制,这一问题一直存在争议。在这里,我们通过两种方法来解决这个问题。首先,我们通过深度测序证明,RNA 病毒登革热病毒(DENV)或西尼罗河病毒(WNV)感染人类细胞不会产生任何病毒衍生的 siRNA 或病毒 miRNA。其次,为了更全面地评估小调控 RNA 抑制病毒复制的潜力,我们使用基因编辑技术衍生出缺乏功能性 Dicer 酶的人类细胞系,从而无法产生 miRNA 或 siRNA。将这些细胞感染广泛的病毒,包括 DENV、WNV、黄热病病毒、辛德毕斯病毒、委内瑞拉马脑炎病毒、麻疹病毒、甲型流感病毒、呼肠孤病毒、水疱性口炎病毒、人类免疫缺陷病毒 1 或单纯疱疹病毒 1(HSV-1),并未发现这些病毒中的任何一种复制能力增强,尽管 HSV-1 至少编码 8 种依赖 Dicer 的病毒 miRNA,但在缺乏 Dicer 的情况下,它的复制速度略有减慢。我们得出结论,大多数(如果不是全部的话)人类病毒在有效复制过程中已经进化到对内源性人类 miRNA 的抑制具有抗性,而像丙型肝炎病毒那样依赖细胞 miRNA 的情况则很少见。病毒如何进化以避免被真核生物进化过程中普遍高度保守的内源性细胞 miRNA 抑制,仍有待确定。重要性:真核细胞表达广泛的小调控 RNA,包括 miRNA,这些 RNA 具有抑制与序列互补的 mRNA 表达的潜力。事实上,先前的研究表明,内源性 miRNA 具有抑制病毒基因表达和复制的潜力。在这里,我们证明,在经过基因工程改造而无法产生 miRNA 的人类细胞中,广泛的致病性病毒的复制并没有增强,这表明病毒已经进化到对 miRNA 的抑制具有抗性。这一结果很重要,因为这意味着操纵 miRNA 水平不太可能对抑制病毒复制有用。它还将注意力集中在病毒如何进化以抵抗 miRNA 的抑制以及失去这种抗性的病毒突变体是否可能有用的问题上,例如在开发减毒病毒疫苗方面。