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Identification of an LGP2-associated MDA5 agonist in picornavirus-infected cells
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 enc...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3967861/ https://www.ncbi.nlm.nih.gov/pubmed/24550253 http://dx.doi.org/10.7554/eLife.01535 |
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author | 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 |
author_facet | 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 |
author_sort | Deddouche, Safia |
collection | PubMed |
description | 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 |
format | Online Article Text |
id | pubmed-3967861 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-39678612014-03-31 Identification of an LGP2-associated MDA5 agonist in picornavirus-infected cells 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 eLife Immunology 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 eLife Sciences Publications, Ltd 2014-02-18 /pmc/articles/PMC3967861/ /pubmed/24550253 http://dx.doi.org/10.7554/eLife.01535 Text en Copyright © 2014, Deddouche et al http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Immunology 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 Identification of an LGP2-associated MDA5 agonist in picornavirus-infected cells |
title | Identification of an LGP2-associated MDA5 agonist in picornavirus-infected cells |
title_full | Identification of an LGP2-associated MDA5 agonist in picornavirus-infected cells |
title_fullStr | Identification of an LGP2-associated MDA5 agonist in picornavirus-infected cells |
title_full_unstemmed | Identification of an LGP2-associated MDA5 agonist in picornavirus-infected cells |
title_short | Identification of an LGP2-associated MDA5 agonist in picornavirus-infected cells |
title_sort | identification of an lgp2-associated mda5 agonist in picornavirus-infected cells |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3967861/ https://www.ncbi.nlm.nih.gov/pubmed/24550253 http://dx.doi.org/10.7554/eLife.01535 |
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