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Duck MDA5 functions in innate immunity against H5N1 highly pathogenic avian influenza virus infections

Melanoma differentiation-associated gene 5 (MDA5) is an important intracellular receptor that recognizes long molecules of viral double-stranded RNA in innate immunity. To understand the mechanism of duck MDA5-mediated innate immunity, we cloned the MDA5 cDNA from the Muscovy duck (Cairina moschata)...

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Autores principales: Wei, Liangmeng, Cui, Jin, Song, Yafen, Zhang, Shuo, Han, Fei, Yuan, Runyu, Gong, Lang, Jiao, Peirong, Liao, Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4079828/
https://www.ncbi.nlm.nih.gov/pubmed/24939427
http://dx.doi.org/10.1186/1297-9716-45-66
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author Wei, Liangmeng
Cui, Jin
Song, Yafen
Zhang, Shuo
Han, Fei
Yuan, Runyu
Gong, Lang
Jiao, Peirong
Liao, Ming
author_facet Wei, Liangmeng
Cui, Jin
Song, Yafen
Zhang, Shuo
Han, Fei
Yuan, Runyu
Gong, Lang
Jiao, Peirong
Liao, Ming
author_sort Wei, Liangmeng
collection PubMed
description Melanoma differentiation-associated gene 5 (MDA5) is an important intracellular receptor that recognizes long molecules of viral double-stranded RNA in innate immunity. To understand the mechanism of duck MDA5-mediated innate immunity, we cloned the MDA5 cDNA from the Muscovy duck (Cairina moschata). Quantitative real-time PCR analysis indicates that duck MDA5 mRNA was constitutively expressed in all sampled tissues. A significant increase of MDA5 mRNA was detected in the brain, spleen and lungs of ducks after infection with an H5N1 highly pathogenic avian influenza virus (HPAIV). We investigated the role of the predicted functional domains of MDA5. The results indicate the caspase activation and recruitment domain (CARD) of duck MDA5 had a signal transmission function through IRF-7-dependent signaling pathway. Overexpression of the CARD strongly activated the chicken IFN-β promoter and upregulated the mRNA expression of antiviral molecules (such as OAS, PKR and Mx), proinflammatory cytokines (such as IL-2, IL-6, IFN-α and IFN-γ, but not IL-1β and IL-8) and retinoic acid-inducible gene I (RIG-I)-like receptors (RLR) (RIG-I and LGP2) without exogenous stimulation. We also demonstrate the NS1 of the H5N1 HPAIV inhibited the duck MDA5-mediated signaling pathway in vitro. These results suggest that duck MDA5 is an important receptor for inducing antiviral activity in the host immune response of ducks.
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spelling pubmed-40798282014-07-03 Duck MDA5 functions in innate immunity against H5N1 highly pathogenic avian influenza virus infections Wei, Liangmeng Cui, Jin Song, Yafen Zhang, Shuo Han, Fei Yuan, Runyu Gong, Lang Jiao, Peirong Liao, Ming Vet Res Research Melanoma differentiation-associated gene 5 (MDA5) is an important intracellular receptor that recognizes long molecules of viral double-stranded RNA in innate immunity. To understand the mechanism of duck MDA5-mediated innate immunity, we cloned the MDA5 cDNA from the Muscovy duck (Cairina moschata). Quantitative real-time PCR analysis indicates that duck MDA5 mRNA was constitutively expressed in all sampled tissues. A significant increase of MDA5 mRNA was detected in the brain, spleen and lungs of ducks after infection with an H5N1 highly pathogenic avian influenza virus (HPAIV). We investigated the role of the predicted functional domains of MDA5. The results indicate the caspase activation and recruitment domain (CARD) of duck MDA5 had a signal transmission function through IRF-7-dependent signaling pathway. Overexpression of the CARD strongly activated the chicken IFN-β promoter and upregulated the mRNA expression of antiviral molecules (such as OAS, PKR and Mx), proinflammatory cytokines (such as IL-2, IL-6, IFN-α and IFN-γ, but not IL-1β and IL-8) and retinoic acid-inducible gene I (RIG-I)-like receptors (RLR) (RIG-I and LGP2) without exogenous stimulation. We also demonstrate the NS1 of the H5N1 HPAIV inhibited the duck MDA5-mediated signaling pathway in vitro. These results suggest that duck MDA5 is an important receptor for inducing antiviral activity in the host immune response of ducks. BioMed Central 2014 2014-06-18 /pmc/articles/PMC4079828/ /pubmed/24939427 http://dx.doi.org/10.1186/1297-9716-45-66 Text en Copyright © 2014 Wei et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Wei, Liangmeng
Cui, Jin
Song, Yafen
Zhang, Shuo
Han, Fei
Yuan, Runyu
Gong, Lang
Jiao, Peirong
Liao, Ming
Duck MDA5 functions in innate immunity against H5N1 highly pathogenic avian influenza virus infections
title Duck MDA5 functions in innate immunity against H5N1 highly pathogenic avian influenza virus infections
title_full Duck MDA5 functions in innate immunity against H5N1 highly pathogenic avian influenza virus infections
title_fullStr Duck MDA5 functions in innate immunity against H5N1 highly pathogenic avian influenza virus infections
title_full_unstemmed Duck MDA5 functions in innate immunity against H5N1 highly pathogenic avian influenza virus infections
title_short Duck MDA5 functions in innate immunity against H5N1 highly pathogenic avian influenza virus infections
title_sort duck mda5 functions in innate immunity against h5n1 highly pathogenic avian influenza virus infections
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4079828/
https://www.ncbi.nlm.nih.gov/pubmed/24939427
http://dx.doi.org/10.1186/1297-9716-45-66
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