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Species Specific Antiviral Activity of Porcine Interferon-α8 (IFNα8)

Interferons (IFNs) have been known as antiviral genes and they are classified by type 1, type 2, and type 3 IFN. The type 1 IFN consists of IFNα, IFNβ, IFNτ, and IFNω whereas the type 2 IFN consists of only IFNγ, which is a key cytokine driving T helper cell type 1 immunity. IFNλ belongs to the type...

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Autores principales: Kim, Eunhye, Jhun, Hyunjhung, Kim, Joohee, Park, Unjoo, Jo, Seunghyun, Kwak, Areum, Kim, Sinae, Nguyen, Tam T., Kang, Yongsun, Choi, Insoo, Lee, Joongbok, Kim, Heijun, Kim, Younghyun, Lee, Siyoung, Kim, Soohyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Association of Immunologists 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5746612/
https://www.ncbi.nlm.nih.gov/pubmed/29302255
http://dx.doi.org/10.4110/in.2017.17.6.424
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author Kim, Eunhye
Jhun, Hyunjhung
Kim, Joohee
Park, Unjoo
Jo, Seunghyun
Kwak, Areum
Kim, Sinae
Nguyen, Tam T.
Kang, Yongsun
Choi, Insoo
Lee, Joongbok
Kim, Heijun
Kim, Younghyun
Lee, Siyoung
Kim, Soohyun
author_facet Kim, Eunhye
Jhun, Hyunjhung
Kim, Joohee
Park, Unjoo
Jo, Seunghyun
Kwak, Areum
Kim, Sinae
Nguyen, Tam T.
Kang, Yongsun
Choi, Insoo
Lee, Joongbok
Kim, Heijun
Kim, Younghyun
Lee, Siyoung
Kim, Soohyun
author_sort Kim, Eunhye
collection PubMed
description Interferons (IFNs) have been known as antiviral genes and they are classified by type 1, type 2, and type 3 IFN. The type 1 IFN consists of IFNα, IFNβ, IFNτ, and IFNω whereas the type 2 IFN consists of only IFNγ, which is a key cytokine driving T helper cell type 1 immunity. IFNλ belongs to the type 3 IFN, which is also known as IL-28 and IL-29 possessing antiviral activities. Type 1 IFN is produced by viral infection whereas type 2 IFN is induced by mitogenic or antigenic T-cell stimuli. The IFNτ of bovine was first discovered in an ungulate ruminant recognition hormone. IFNτ belongs to the type 1 IFN with the common feature of type 1 IFN such as antiviral activity. IFNs have been mostly studied for basic research and clinical usages therefore there was no effort to investigate IFNs in industrial animals. Here we cloned porcine IFNα8 from peripheral blood mononuclear cells of Korean domestic pig (Sus scrofa domestica). The newly cloned IFNα8 amino acid sequence from Korean domestic pig shares 98.4% identity with the known porcine IFNα8 in databank. The recombinant porcine IFNα8 showed potent antiviral activity and protected bovine Madin-Darby bovine kidney epithelial (MDBK) cells from the cytopathic effect of vesicular stomatitis virus, but it failed to protect human Wistar Institute Susan Hayflick (WISH) cells and canine Madin-Darby canine kidney epithelial-like (MDCK) cells. The present study demonstrates species specific antiviral activity of porcine IFNα8.
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spelling pubmed-57466122018-01-04 Species Specific Antiviral Activity of Porcine Interferon-α8 (IFNα8) Kim, Eunhye Jhun, Hyunjhung Kim, Joohee Park, Unjoo Jo, Seunghyun Kwak, Areum Kim, Sinae Nguyen, Tam T. Kang, Yongsun Choi, Insoo Lee, Joongbok Kim, Heijun Kim, Younghyun Lee, Siyoung Kim, Soohyun Immune Netw Original Article Interferons (IFNs) have been known as antiviral genes and they are classified by type 1, type 2, and type 3 IFN. The type 1 IFN consists of IFNα, IFNβ, IFNτ, and IFNω whereas the type 2 IFN consists of only IFNγ, which is a key cytokine driving T helper cell type 1 immunity. IFNλ belongs to the type 3 IFN, which is also known as IL-28 and IL-29 possessing antiviral activities. Type 1 IFN is produced by viral infection whereas type 2 IFN is induced by mitogenic or antigenic T-cell stimuli. The IFNτ of bovine was first discovered in an ungulate ruminant recognition hormone. IFNτ belongs to the type 1 IFN with the common feature of type 1 IFN such as antiviral activity. IFNs have been mostly studied for basic research and clinical usages therefore there was no effort to investigate IFNs in industrial animals. Here we cloned porcine IFNα8 from peripheral blood mononuclear cells of Korean domestic pig (Sus scrofa domestica). The newly cloned IFNα8 amino acid sequence from Korean domestic pig shares 98.4% identity with the known porcine IFNα8 in databank. The recombinant porcine IFNα8 showed potent antiviral activity and protected bovine Madin-Darby bovine kidney epithelial (MDBK) cells from the cytopathic effect of vesicular stomatitis virus, but it failed to protect human Wistar Institute Susan Hayflick (WISH) cells and canine Madin-Darby canine kidney epithelial-like (MDCK) cells. The present study demonstrates species specific antiviral activity of porcine IFNα8. The Korean Association of Immunologists 2017-12 2017-12-19 /pmc/articles/PMC5746612/ /pubmed/29302255 http://dx.doi.org/10.4110/in.2017.17.6.424 Text en Copyright © 2017. The Korean Association of Immunologists https://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kim, Eunhye
Jhun, Hyunjhung
Kim, Joohee
Park, Unjoo
Jo, Seunghyun
Kwak, Areum
Kim, Sinae
Nguyen, Tam T.
Kang, Yongsun
Choi, Insoo
Lee, Joongbok
Kim, Heijun
Kim, Younghyun
Lee, Siyoung
Kim, Soohyun
Species Specific Antiviral Activity of Porcine Interferon-α8 (IFNα8)
title Species Specific Antiviral Activity of Porcine Interferon-α8 (IFNα8)
title_full Species Specific Antiviral Activity of Porcine Interferon-α8 (IFNα8)
title_fullStr Species Specific Antiviral Activity of Porcine Interferon-α8 (IFNα8)
title_full_unstemmed Species Specific Antiviral Activity of Porcine Interferon-α8 (IFNα8)
title_short Species Specific Antiviral Activity of Porcine Interferon-α8 (IFNα8)
title_sort species specific antiviral activity of porcine interferon-α8 (ifnα8)
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5746612/
https://www.ncbi.nlm.nih.gov/pubmed/29302255
http://dx.doi.org/10.4110/in.2017.17.6.424
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