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Differential innate immune responses induced by classical and variant infectious bronchitis viruses in specific pathogen free chicks

Avian infectious bronchitis virus (IBV) continues to cause serious economic losses in global chicken production. Concurrent circulation of both classic and variant IBVs have been identified in most parts of the world, raising major challenges to global prevention and control efforts. Therefore, immu...

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Autores principales: Chhabra, Rajesh, Ball, Christopher, Chantrey, Julian, Ganapathy, Kannan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7173069/
https://www.ncbi.nlm.nih.gov/pubmed/29751011
http://dx.doi.org/10.1016/j.dci.2018.04.026
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author Chhabra, Rajesh
Ball, Christopher
Chantrey, Julian
Ganapathy, Kannan
author_facet Chhabra, Rajesh
Ball, Christopher
Chantrey, Julian
Ganapathy, Kannan
author_sort Chhabra, Rajesh
collection PubMed
description Avian infectious bronchitis virus (IBV) continues to cause serious economic losses in global chicken production. Concurrent circulation of both classic and variant IBVs have been identified in most parts of the world, raising major challenges to global prevention and control efforts. Therefore, immunopathogenesis, particularly early host responses, needs to be better understood for effective control of diseases caused by different strains of IBVs. We investigated differing immunopathogenesis in chickens following infection with IS/885/00-like (885), QX-like (QX) and M41 IBV strains. We confirmed that the histopathological changes, proinflammatory and innate immune gene responses were induced to different magnitudes, depending on the IBV strain. Results indicated that upregulation of proinflammatory cytokines (such as IL-6 and IL-1β) and lipopolysaccharide-induced tumor necrosis factor-alpha factor (LITAF) expression is induced by IBV M41 in the trachea and by IBV 885 and QX in the kidney, which mainly coincides with tracheal and renal histopathological lesions respectively caused by these strains. In addition, elevated levels of TLR3, MDA5 and IFN-β expression occurred concurrently with greater lesion severity in IBV infected trachea and kidney tissues. Overall, this study reports marked differences in the activation of early host responses by pathogenic IBV strains.
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spelling pubmed-71730692020-04-22 Differential innate immune responses induced by classical and variant infectious bronchitis viruses in specific pathogen free chicks Chhabra, Rajesh Ball, Christopher Chantrey, Julian Ganapathy, Kannan Dev Comp Immunol Article Avian infectious bronchitis virus (IBV) continues to cause serious economic losses in global chicken production. Concurrent circulation of both classic and variant IBVs have been identified in most parts of the world, raising major challenges to global prevention and control efforts. Therefore, immunopathogenesis, particularly early host responses, needs to be better understood for effective control of diseases caused by different strains of IBVs. We investigated differing immunopathogenesis in chickens following infection with IS/885/00-like (885), QX-like (QX) and M41 IBV strains. We confirmed that the histopathological changes, proinflammatory and innate immune gene responses were induced to different magnitudes, depending on the IBV strain. Results indicated that upregulation of proinflammatory cytokines (such as IL-6 and IL-1β) and lipopolysaccharide-induced tumor necrosis factor-alpha factor (LITAF) expression is induced by IBV M41 in the trachea and by IBV 885 and QX in the kidney, which mainly coincides with tracheal and renal histopathological lesions respectively caused by these strains. In addition, elevated levels of TLR3, MDA5 and IFN-β expression occurred concurrently with greater lesion severity in IBV infected trachea and kidney tissues. Overall, this study reports marked differences in the activation of early host responses by pathogenic IBV strains. Elsevier Ltd. 2018-10 2018-05-08 /pmc/articles/PMC7173069/ /pubmed/29751011 http://dx.doi.org/10.1016/j.dci.2018.04.026 Text en © 2018 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Chhabra, Rajesh
Ball, Christopher
Chantrey, Julian
Ganapathy, Kannan
Differential innate immune responses induced by classical and variant infectious bronchitis viruses in specific pathogen free chicks
title Differential innate immune responses induced by classical and variant infectious bronchitis viruses in specific pathogen free chicks
title_full Differential innate immune responses induced by classical and variant infectious bronchitis viruses in specific pathogen free chicks
title_fullStr Differential innate immune responses induced by classical and variant infectious bronchitis viruses in specific pathogen free chicks
title_full_unstemmed Differential innate immune responses induced by classical and variant infectious bronchitis viruses in specific pathogen free chicks
title_short Differential innate immune responses induced by classical and variant infectious bronchitis viruses in specific pathogen free chicks
title_sort differential innate immune responses induced by classical and variant infectious bronchitis viruses in specific pathogen free chicks
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7173069/
https://www.ncbi.nlm.nih.gov/pubmed/29751011
http://dx.doi.org/10.1016/j.dci.2018.04.026
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