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Duck Interleukin-22: Identification and Expression Analysis in Riemerella anatipestifer Infection

Riemerella anatipestifer is one of the most devastating pathogens affecting the global duck farms. Infection is involved in secretion of proinflammatory cytokines, including interleukin- (IL-) 17A. During the immune response to infection, IL-22 and IL-17A are often produced concurrently and at high...

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Autores principales: Flores, Rochelle A., Cammayo, Paula Leona T., Nguyen, Binh T., Fernandez-Colorado, Cherry P., Kim, Suk, Kim, Woo H., Min, Wongi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8601822/
https://www.ncbi.nlm.nih.gov/pubmed/34805416
http://dx.doi.org/10.1155/2021/3862492
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author Flores, Rochelle A.
Cammayo, Paula Leona T.
Nguyen, Binh T.
Fernandez-Colorado, Cherry P.
Kim, Suk
Kim, Woo H.
Min, Wongi
author_facet Flores, Rochelle A.
Cammayo, Paula Leona T.
Nguyen, Binh T.
Fernandez-Colorado, Cherry P.
Kim, Suk
Kim, Woo H.
Min, Wongi
author_sort Flores, Rochelle A.
collection PubMed
description Riemerella anatipestifer is one of the most devastating pathogens affecting the global duck farms. Infection is involved in secretion of proinflammatory cytokines, including interleukin- (IL-) 17A. During the immune response to infection, IL-22 and IL-17A are often produced concurrently and at high levels in inflamed tissues. Little is known about duck IL-22 (duIL-22) during R. anatipestifer infection. We describe the characterization of duIL-22 and its mRNA expression analysis in splenic lymphocytes and macrophages treated with heat-killed R. anatipestifer and in the spleens and livers of R. anatipestifer-infected ducks. Full-length cDNA of duIL-22 encoded 197 amino acids. The deduced amino acid sequence of duIL-22 shared a 30.4–40.5% similarity with piscine counterparts, 57.4–60.1% with mammalian homologs, and 93.4% similarity to the chicken. Duck IL-22 mRNA expression level was relatively high in the skin of normal ducks. It was increased in mitogen-stimulated splenic lymphocytes and in killed R. anatipestifer-activated splenic lymphocytes and macrophages. Compared with healthy ducks, IL-22 transcript expression was significantly upregulated in the livers and spleens on days 1 and 4 postinfection, but not on day 7. IL-17A was significantly increased in the spleens only on day 4 postinfection and in the livers at all time points. When splenic lymphocytes were stimulated with heat-killed R. anatipestifer, CD4(+) cells predominantly produced IL-22 while IL-17A was expressed both by CD4(+) and CD4(−) cells. These results suggested that IL-22 and IL-17A are likely expressed in different cell types during R. anatipestifer infection.
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spelling pubmed-86018222021-11-19 Duck Interleukin-22: Identification and Expression Analysis in Riemerella anatipestifer Infection Flores, Rochelle A. Cammayo, Paula Leona T. Nguyen, Binh T. Fernandez-Colorado, Cherry P. Kim, Suk Kim, Woo H. Min, Wongi J Immunol Res Research Article Riemerella anatipestifer is one of the most devastating pathogens affecting the global duck farms. Infection is involved in secretion of proinflammatory cytokines, including interleukin- (IL-) 17A. During the immune response to infection, IL-22 and IL-17A are often produced concurrently and at high levels in inflamed tissues. Little is known about duck IL-22 (duIL-22) during R. anatipestifer infection. We describe the characterization of duIL-22 and its mRNA expression analysis in splenic lymphocytes and macrophages treated with heat-killed R. anatipestifer and in the spleens and livers of R. anatipestifer-infected ducks. Full-length cDNA of duIL-22 encoded 197 amino acids. The deduced amino acid sequence of duIL-22 shared a 30.4–40.5% similarity with piscine counterparts, 57.4–60.1% with mammalian homologs, and 93.4% similarity to the chicken. Duck IL-22 mRNA expression level was relatively high in the skin of normal ducks. It was increased in mitogen-stimulated splenic lymphocytes and in killed R. anatipestifer-activated splenic lymphocytes and macrophages. Compared with healthy ducks, IL-22 transcript expression was significantly upregulated in the livers and spleens on days 1 and 4 postinfection, but not on day 7. IL-17A was significantly increased in the spleens only on day 4 postinfection and in the livers at all time points. When splenic lymphocytes were stimulated with heat-killed R. anatipestifer, CD4(+) cells predominantly produced IL-22 while IL-17A was expressed both by CD4(+) and CD4(−) cells. These results suggested that IL-22 and IL-17A are likely expressed in different cell types during R. anatipestifer infection. Hindawi 2021-11-11 /pmc/articles/PMC8601822/ /pubmed/34805416 http://dx.doi.org/10.1155/2021/3862492 Text en Copyright © 2021 Rochelle A. Flores et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Flores, Rochelle A.
Cammayo, Paula Leona T.
Nguyen, Binh T.
Fernandez-Colorado, Cherry P.
Kim, Suk
Kim, Woo H.
Min, Wongi
Duck Interleukin-22: Identification and Expression Analysis in Riemerella anatipestifer Infection
title Duck Interleukin-22: Identification and Expression Analysis in Riemerella anatipestifer Infection
title_full Duck Interleukin-22: Identification and Expression Analysis in Riemerella anatipestifer Infection
title_fullStr Duck Interleukin-22: Identification and Expression Analysis in Riemerella anatipestifer Infection
title_full_unstemmed Duck Interleukin-22: Identification and Expression Analysis in Riemerella anatipestifer Infection
title_short Duck Interleukin-22: Identification and Expression Analysis in Riemerella anatipestifer Infection
title_sort duck interleukin-22: identification and expression analysis in riemerella anatipestifer infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8601822/
https://www.ncbi.nlm.nih.gov/pubmed/34805416
http://dx.doi.org/10.1155/2021/3862492
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