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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2014
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
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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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