Deddouche Safia, Goubau Delphine, Rehwinkel Jan, Chakravarty Probir, Begum Sharmin, Maillard Pierre V, Borg Annabel, Matthews Nik, Feng Qian, van Kuppeveld Frank J M, Reis e Sousa Caetano
Immunobiology Laboratory, Cancer Research UK, London Research Institute, London, United Kingdom.
Elife. 2014 Feb 18;3:e01535. doi: 10.7554/eLife.01535.
The RIG-I-like receptors RIG-I, LGP2, and MDA5 initiate an antiviral response that includes production of type I interferons (IFNs). The nature of the RNAs that trigger MDA5 activation in infected cells remains unclear. Here, we purify and characterise LGP2/RNA complexes from cells infected with encephalomyocarditis virus (EMCV), a picornavirus detected by MDA5 and LGP2 but not RIG-I. We show that those complexes contain RNA that is highly enriched for MDA5-stimulatory activity and for a specific sequence corresponding to the L region of the EMCV antisense RNA. Synthesis of this sequence by in vitro transcription is sufficient to generate an MDA5 stimulatory RNA. Conversely, genomic deletion of the L region in EMCV generates viruses that are less potent at stimulating MDA5-dependent IFN production. Thus, the L region antisense RNA of EMCV is a key determinant of innate immunity to the virus and represents an RNA that activates MDA5 in virally-infected cells. DOI: http://dx.doi.org/10.7554/eLife.01535.001.
视黄酸诱导基因I样受体RIG-I、LGP2和MDA5启动抗病毒反应,其中包括I型干扰素(IFN)的产生。在受感染细胞中触发MDA5激活的RNA的性质仍不清楚。在这里,我们从感染脑心肌炎病毒(EMCV)的细胞中纯化并鉴定LGP2/RNA复合物,EMCV是一种小核糖核酸病毒,可被MDA5和LGP2检测到,但不能被RIG-I检测到。我们发现这些复合物含有高度富集MDA5刺激活性以及与EMCV反义RNA的L区域相对应的特定序列的RNA。通过体外转录合成该序列足以产生一种MDA5刺激RNA。相反,EMCV中L区域的基因组缺失产生的病毒在刺激依赖MDA5的IFN产生方面效力较低。因此,EMCV的L区域反义RNA是对该病毒先天免疫的关键决定因素,并且代表一种在病毒感染细胞中激活MDA5的RNA。DOI: http://dx.doi.org/10.7554/eLife.01535.001。