Identification of an LGP2-associated MDA5 agonist in picornavirus-infected cells

被引:97
作者
Deddouche, Safia [1 ]
Goubau, Delphine [1 ]
Rehwinkel, Jan [1 ]
Chakravarty, Probir [2 ]
Begum, Sharmin [3 ]
Maillard, Pierre V. [1 ]
Borg, Annabel [4 ]
Matthews, Nik [3 ]
Feng, Qian [5 ]
van Kuppeveld, Frank J. M. [5 ]
Reis e Sousa, Caetano [1 ]
机构
[1] London Res Inst, Canc Res UK, Immunobiol Lab, London, England
[2] London Res Inst, Canc Res UK, Bioinformat Lab, London, England
[3] London Res Inst, Canc Res UK, Clonal Sequencing Lab, London, England
[4] London Res Inst, Canc Res UK, Prot Purificat Lab, London, England
[5] Univ Utrecht, Dept Infect Dis & Immunol, Virol Div, Utrecht, Netherlands
基金
欧洲研究理事会; 英国医学研究理事会;
关键词
DOUBLE-STRANDED-RNA; INTERFERON REGULATORY FACTOR-3; RIG-I; ANTIVIRAL RESPONSES; LEADER PROTEIN; 5'-TRIPHOSPHATE RNA; STIMULATED GENES; DENDRITIC CELLS; VIRAL-INFECTION; MESSENGER-RNA;
D O I
10.7554/eLife.01535
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
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页数:20
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