Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA; Institute for Immunology, University of Pennsylvania, Philadelphia, PA 19104, USA.
Department of Biochemistry and Biophysics, University of Pennsylvania, Philadelphia, PA 19104, USA.
Mol Cell. 2022 Oct 6;82(19):3729-3744.e10. doi: 10.1016/j.molcel.2022.08.030. Epub 2022 Sep 26.
Arthropod-borne viruses, including the alphavirus chikungunya virus (CHIKV), cause acute disease in millions of people and utilize potent mechanisms to antagonize and circumvent innate immune pathways including the type I interferon (IFN) pathway. In response, hosts have evolved antiviral counterdefense strategies that remain incompletely understood. Recent studies have found that long noncoding RNAs (lncRNAs) regulate classical innate immune pathways; how lncRNAs contribute to additional antiviral counterdefenses remains unclear. Using high-throughput genetic screening, we identified a cytoplasmic antiviral lncRNA that we named antiviral lncRNA prohibiting human alphaviruses (ALPHA), which is transcriptionally induced by alphaviruses and functions independently of IFN to inhibit the replication of CHIKV and its closest relative, O'nyong'nyong virus (ONNV), but not other viruses. Furthermore, we showed that ALPHA interacts with CHIKV genomic RNA and restrains viral RNA replication. Together, our findings reveal that ALPHA and potentially other lncRNAs can mediate non-canonical antiviral immune responses against specific viruses.
虫媒病毒,包括甲病毒中的基孔肯雅病毒(CHIKV),可导致数百万人罹患急性疾病,并利用强效机制拮抗和规避先天免疫途径,包括 I 型干扰素(IFN)途径。作为回应,宿主进化出了抗病毒的防御策略,但这些策略仍不完全清楚。最近的研究发现,长非编码 RNA(lncRNA)调控经典的先天免疫途径;lncRNA 如何有助于其他抗病毒防御尚不清楚。我们使用高通量遗传筛选,鉴定出一种细胞质抗病毒 lncRNA,我们将其命名为抗病毒 lncRNA 抑制人甲病毒(ALPHA),它可被甲病毒转录诱导,并独立于 IFN 发挥作用,抑制 CHIKV 及其最亲近的 O'nyong'nyong 病毒(ONNV)的复制,但不抑制其他病毒的复制。此外,我们还表明,ALPHA 与 CHIKV 基因组 RNA 相互作用并抑制病毒 RNA 复制。总之,我们的研究结果表明,ALPHA 和可能的其他 lncRNA 可以介导针对特定病毒的非典型抗病毒免疫反应。