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Guanylate-binding protein 1 restricts avian coronavirus infectious bronchitis virus-infected HD11 cells

The Infectious Bronchitis Virus (IBV), a coronavirus, is a key avian pathogen that causes acute and highly infectious viral respiratory diseases. IBV is an enveloped, positive-sense RNA virus, and the host factors that restrict infection and replication of the virus remain poorly understood. Guanyla...

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Autores principales: Ma, Peng, Gu, Kui, Wen, Renqiao, Li, Chao, Zhou, Changyu, Zhao, Yu, Li, Hao, Lei, Changwei, Yang, Xin, Wang, Hongning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9731647/
https://www.ncbi.nlm.nih.gov/pubmed/36580763
http://dx.doi.org/10.1016/j.psj.2022.102398
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author Ma, Peng
Gu, Kui
Wen, Renqiao
Li, Chao
Zhou, Changyu
Zhao, Yu
Li, Hao
Lei, Changwei
Yang, Xin
Wang, Hongning
author_facet Ma, Peng
Gu, Kui
Wen, Renqiao
Li, Chao
Zhou, Changyu
Zhao, Yu
Li, Hao
Lei, Changwei
Yang, Xin
Wang, Hongning
author_sort Ma, Peng
collection PubMed
description The Infectious Bronchitis Virus (IBV), a coronavirus, is a key avian pathogen that causes acute and highly infectious viral respiratory diseases. IBV is an enveloped, positive-sense RNA virus, and the host factors that restrict infection and replication of the virus remain poorly understood. Guanylate-binding protein 1 (GBP1), an interferon-gamma (IFN-γ)-inducible guanosine triphosphatase (GTPase), is a major player in host immunity and provides defense against viral replication. However, the role of chicken GBP1 (chGBP1) in the IBV-life cycle is not well understood. Therefore, this study aimed to reveal the potential role of IFN-γ-induced chGBP1 in mediating host anti-IBV infection responses. We identified the host restriction factor, chGBP1, in IBV-infected chicken macrophages HD11 cell lines. We showed that chGBP1 was upregulated by treatment with both IFN-γ and IBV in HD11 cells. chGBP1 inhibited IBV replication in a dose-dependent manner and enhanced IFN-γ anti-IBV activity. Importantly, the GTPase domain of chGBP1 played a pivotal role in its anti-IBV activity. Furthermore, chGBP1 interacts with IBV Nucleocapsids protein to degrade IBV-N protein through the autophagy pathway. Taken together, our results demonstrate a critical role of chGBP1 in anti-IBV in macrophages HD11 cells.
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spelling pubmed-97316472022-12-09 Guanylate-binding protein 1 restricts avian coronavirus infectious bronchitis virus-infected HD11 cells Ma, Peng Gu, Kui Wen, Renqiao Li, Chao Zhou, Changyu Zhao, Yu Li, Hao Lei, Changwei Yang, Xin Wang, Hongning Poult Sci IMMUNOLOGY, HEALTH AND DISEASE The Infectious Bronchitis Virus (IBV), a coronavirus, is a key avian pathogen that causes acute and highly infectious viral respiratory diseases. IBV is an enveloped, positive-sense RNA virus, and the host factors that restrict infection and replication of the virus remain poorly understood. Guanylate-binding protein 1 (GBP1), an interferon-gamma (IFN-γ)-inducible guanosine triphosphatase (GTPase), is a major player in host immunity and provides defense against viral replication. However, the role of chicken GBP1 (chGBP1) in the IBV-life cycle is not well understood. Therefore, this study aimed to reveal the potential role of IFN-γ-induced chGBP1 in mediating host anti-IBV infection responses. We identified the host restriction factor, chGBP1, in IBV-infected chicken macrophages HD11 cell lines. We showed that chGBP1 was upregulated by treatment with both IFN-γ and IBV in HD11 cells. chGBP1 inhibited IBV replication in a dose-dependent manner and enhanced IFN-γ anti-IBV activity. Importantly, the GTPase domain of chGBP1 played a pivotal role in its anti-IBV activity. Furthermore, chGBP1 interacts with IBV Nucleocapsids protein to degrade IBV-N protein through the autophagy pathway. Taken together, our results demonstrate a critical role of chGBP1 in anti-IBV in macrophages HD11 cells. Elsevier 2022-12-09 /pmc/articles/PMC9731647/ /pubmed/36580763 http://dx.doi.org/10.1016/j.psj.2022.102398 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle IMMUNOLOGY, HEALTH AND DISEASE
Ma, Peng
Gu, Kui
Wen, Renqiao
Li, Chao
Zhou, Changyu
Zhao, Yu
Li, Hao
Lei, Changwei
Yang, Xin
Wang, Hongning
Guanylate-binding protein 1 restricts avian coronavirus infectious bronchitis virus-infected HD11 cells
title Guanylate-binding protein 1 restricts avian coronavirus infectious bronchitis virus-infected HD11 cells
title_full Guanylate-binding protein 1 restricts avian coronavirus infectious bronchitis virus-infected HD11 cells
title_fullStr Guanylate-binding protein 1 restricts avian coronavirus infectious bronchitis virus-infected HD11 cells
title_full_unstemmed Guanylate-binding protein 1 restricts avian coronavirus infectious bronchitis virus-infected HD11 cells
title_short Guanylate-binding protein 1 restricts avian coronavirus infectious bronchitis virus-infected HD11 cells
title_sort guanylate-binding protein 1 restricts avian coronavirus infectious bronchitis virus-infected hd11 cells
topic IMMUNOLOGY, HEALTH AND DISEASE
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9731647/
https://www.ncbi.nlm.nih.gov/pubmed/36580763
http://dx.doi.org/10.1016/j.psj.2022.102398
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