Laboratory of Experimental Virology, Department of Medical Microbiology, University of Amsterdam, Amsterdam, The Netherlands.
Curr Opin Virol. 2018 Oct;32:9-14. doi: 10.1016/j.coviro.2018.07.008. Epub 2018 Jul 14.
RNA interference (RNAi) was discovered in plants where it functions as the main antiviral pathway and this antiviral role was subsequently extended to invertebrates. But it remained hotly debated whether RNAi fulfils a similar role in mammals that already have a potent innate immune system based on interferon and an elaborate adaptive immune system. On the one hand, mammalian cells do encode most of the RNAi machinery, but this could be used exclusively to control cellular gene expression via micro RNAs (miRNAs). But on the other hand, virus-derived small interfering RNAs, the hallmark of RNAi involvement, could not be readily detected upon virus infection of mammalian cells. However, recent studies have indicated that these signature molecules are generated in virus-infected embryonic cell types of mammals and that viruses actively suppress such responses by means of potent RNAi suppressor proteins. Thus, the tide seems to be changing in favor of RNAi as accessory antiviral defense mechanism in humans. Intriguingly, recent studies indicate that insects have also developed an additional innate immune system that collaborates with the RNAi response in the fight against invading viral pathogens. Thus, the presence of multiple antiviral response mechanisms seems standard outside the plant world and we will specifically discuss the interactions between these antiviral programs.
RNA 干扰 (RNAi) 最初在植物中被发现,它是植物体内主要的抗病毒途径,随后这一抗病毒作用被扩展到无脊椎动物中。但是,关于 RNAi 是否在已经具有基于干扰素的强大先天免疫系统和精细的适应性免疫系统的哺乳动物中发挥类似作用,仍存在激烈的争论。一方面,哺乳动物细胞确实编码了 RNAi 机制的大部分,但这可能仅用于通过 microRNAs (miRNAs) 来控制细胞基因表达。另一方面,病毒衍生的小干扰 RNA 是 RNAi 参与的标志,在哺乳动物细胞被病毒感染时,无法轻易检测到这些小干扰 RNA。然而,最近的研究表明,在哺乳动物胚胎细胞类型中,这些特征分子是在病毒感染时产生的,并且病毒通过有效的 RNAi 抑制蛋白积极抑制这种反应。因此,RNAi 似乎正在成为人类辅助抗病毒防御机制的潮流。有趣的是,最近的研究表明,昆虫也已经开发出一种额外的先天免疫系统,与 RNAi 反应协同作用,抵御入侵的病毒病原体。因此,在植物界之外,存在多种抗病毒反应机制似乎是标准的,我们将专门讨论这些抗病毒程序之间的相互作用。