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HPAI-resistant Ri chickens exhibit elevated antiviral immune-related gene expression

BACKGROUND: Highly pathogenic avian influenza viruses (HPAIVs) is an extremely contagious and high mortality rates in chickens resulting in substantial economic impact on the poultry sector. Therefore, it is necessary to elucidate the pathogenic mechanism of HPAIV for infection control. OBJECTIVE: G...

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Autores principales: Vu, Thi Hao, Heo, Jubi, Hong, Yeojin, Kang, Suyeon, Tran, Ha Thi Thanh, Dang, Hoang Vu, Truong, Anh Duc, Hong, Yeong Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Veterinary Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9899939/
https://www.ncbi.nlm.nih.gov/pubmed/36726278
http://dx.doi.org/10.4142/jvs.22229
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author Vu, Thi Hao
Heo, Jubi
Hong, Yeojin
Kang, Suyeon
Tran, Ha Thi Thanh
Dang, Hoang Vu
Truong, Anh Duc
Hong, Yeong Ho
author_facet Vu, Thi Hao
Heo, Jubi
Hong, Yeojin
Kang, Suyeon
Tran, Ha Thi Thanh
Dang, Hoang Vu
Truong, Anh Duc
Hong, Yeong Ho
author_sort Vu, Thi Hao
collection PubMed
description BACKGROUND: Highly pathogenic avian influenza viruses (HPAIVs) is an extremely contagious and high mortality rates in chickens resulting in substantial economic impact on the poultry sector. Therefore, it is necessary to elucidate the pathogenic mechanism of HPAIV for infection control. OBJECTIVE: Gene set enrichment analysis (GSEA) can effectively avoid the limitations of subjective screening for differential gene expression. Therefore, we performed GSEA to compare HPAI-infected resistant and susceptible Ri chicken lines. METHODS: The Ri chickens Mx(A)/BF2(B21) were chosen as resistant, and the chickens Mx(G)/BF2(B13) were selected as susceptible by genotyping the Mx and BF2 genes. The tracheal tissues of HPAIV H5N1 infected chickens were collected for RNA sequencing followed by GSEA analysis to define gene subsets to elucidate the sequencing results. RESULTS: We identified four differentially expressed pathways, which were immune-related pathways with a total of 78 genes. The expression levels of cytokines (IL-1β, IL-6, IL-12), chemokines (CCL4 and CCL5), type interferons and their receptors (IFN-β, IFNAR1, IFNAR2, and IFNGR1), Jak-STAT signaling pathway genes (STAT1, STAT2, and JAK1), MHC class I and II and their co-stimulatory molecules (CD80, CD86, CD40, DMB2, BLB2, and B2M), and interferon stimulated genes (EIF2AK2 and EIF2AK1) in resistant chickens were higher than those in susceptible chickens. CONCLUSIONS: Resistant Ri chickens exhibit a stronger antiviral response to HPAIV H5N1 compared with susceptible chickens. Our findings provide insights into the immune responses of genetically disparate chickens against HPAIV.
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spelling pubmed-98999392023-02-14 HPAI-resistant Ri chickens exhibit elevated antiviral immune-related gene expression Vu, Thi Hao Heo, Jubi Hong, Yeojin Kang, Suyeon Tran, Ha Thi Thanh Dang, Hoang Vu Truong, Anh Duc Hong, Yeong Ho J Vet Sci Original Article BACKGROUND: Highly pathogenic avian influenza viruses (HPAIVs) is an extremely contagious and high mortality rates in chickens resulting in substantial economic impact on the poultry sector. Therefore, it is necessary to elucidate the pathogenic mechanism of HPAIV for infection control. OBJECTIVE: Gene set enrichment analysis (GSEA) can effectively avoid the limitations of subjective screening for differential gene expression. Therefore, we performed GSEA to compare HPAI-infected resistant and susceptible Ri chicken lines. METHODS: The Ri chickens Mx(A)/BF2(B21) were chosen as resistant, and the chickens Mx(G)/BF2(B13) were selected as susceptible by genotyping the Mx and BF2 genes. The tracheal tissues of HPAIV H5N1 infected chickens were collected for RNA sequencing followed by GSEA analysis to define gene subsets to elucidate the sequencing results. RESULTS: We identified four differentially expressed pathways, which were immune-related pathways with a total of 78 genes. The expression levels of cytokines (IL-1β, IL-6, IL-12), chemokines (CCL4 and CCL5), type interferons and their receptors (IFN-β, IFNAR1, IFNAR2, and IFNGR1), Jak-STAT signaling pathway genes (STAT1, STAT2, and JAK1), MHC class I and II and their co-stimulatory molecules (CD80, CD86, CD40, DMB2, BLB2, and B2M), and interferon stimulated genes (EIF2AK2 and EIF2AK1) in resistant chickens were higher than those in susceptible chickens. CONCLUSIONS: Resistant Ri chickens exhibit a stronger antiviral response to HPAIV H5N1 compared with susceptible chickens. Our findings provide insights into the immune responses of genetically disparate chickens against HPAIV. The Korean Society of Veterinary Science 2023-01-11 /pmc/articles/PMC9899939/ /pubmed/36726278 http://dx.doi.org/10.4142/jvs.22229 Text en © 2023 The Korean Society of Veterinary Science 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 (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
Vu, Thi Hao
Heo, Jubi
Hong, Yeojin
Kang, Suyeon
Tran, Ha Thi Thanh
Dang, Hoang Vu
Truong, Anh Duc
Hong, Yeong Ho
HPAI-resistant Ri chickens exhibit elevated antiviral immune-related gene expression
title HPAI-resistant Ri chickens exhibit elevated antiviral immune-related gene expression
title_full HPAI-resistant Ri chickens exhibit elevated antiviral immune-related gene expression
title_fullStr HPAI-resistant Ri chickens exhibit elevated antiviral immune-related gene expression
title_full_unstemmed HPAI-resistant Ri chickens exhibit elevated antiviral immune-related gene expression
title_short HPAI-resistant Ri chickens exhibit elevated antiviral immune-related gene expression
title_sort hpai-resistant ri chickens exhibit elevated antiviral immune-related gene expression
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9899939/
https://www.ncbi.nlm.nih.gov/pubmed/36726278
http://dx.doi.org/10.4142/jvs.22229
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