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Autores principales: Hu, Yang, Wang, Huan, Wang, Zixuan, Zhang, Xu, Liu, Lei, Chen, Jiong
Formato: Artículo científico
Lenguaje:en
Publicado: Fish & shellfish immunology 2025
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Acceso en línea:https://pubmed.ncbi.nlm.nih.gov/40089086/
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author Hu, Yang
Wang, Huan
Wang, Zixuan
Zhang, Xu
Liu, Lei
Chen, Jiong
author_facet Hu, Yang
Wang, Huan
Wang, Zixuan
Zhang, Xu
Liu, Lei
Chen, Jiong
Hu, Yang
Wang, Huan
Wang, Zixuan
Zhang, Xu
Liu, Lei
Chen, Jiong
collection PubMed - marine biology
contents Antiviral potential of the arctigenin derivative COA in reducing viral adhesion to the epithelial cell surface against IHNV infection. Hu, Yang Wang, Huan Wang, Zixuan Zhang, Xu Liu, Lei Chen, Jiong Animals Antiviral Agents Lignans Fish Diseases Furans Infectious hematopoietic necrosis virus Rhabdoviridae Infections Oncorhynchus mykiss Virus Attachment Epithelial Cells Cell Line Infectious hematopoietic necrosis virus (IHNV) is a major aquaculture threat, highlighting the need for effective antiviral agents. This study evaluates the arctigenin derivative COA for its antiviral potential against IHNV. COA demonstrated no cytotoxicity to EPC cells at concentrations up to 10 μM and inhibited over 90 % of IHNV gene expression in vitro. It preserved normal nuclear morphology in infected cells, reduced viral titers, and completely blocked IHNV infection at 10 μM. Time-gradient assays identified COA's antiviral action during early infection, specifically inhibiting viral adsorption (82 %) and internalization (92 %). Using DiO-labeled IHNV particles, we visualized COA preventing viral entry into EPC cells, marking a novel finding for arctigenin derivatives. COA remained stable in water for over four days, enhancing its suitability for aquaculture applications. In vivo, COA improved survival rates of IHNV-infected rainbow trout by 46 % (injection) and 22 % (immersion) while significantly reducing IHNV gene expression and viral titers in spleen and kidney. It also upregulated interferon genes, activating antiviral responses and effectively reducing horizontal transmission of IHNV. These results highlight COA's potential as an antiviral agent, providing insights for developing targeted therapies against rhabdoviruses in aquaculture.
format Artículo científico
id pubmed_40089086
institution PubMed
language en
publishDate 2025
publisher Fish & shellfish immunology
record_format pubmed
spellingShingle Antiviral potential of the arctigenin derivative COA in reducing viral adhesion to the epithelial cell surface against IHNV infection.
Hu, Yang
Wang, Huan
Wang, Zixuan
Zhang, Xu
Liu, Lei
Chen, Jiong
Animals
Antiviral Agents
Lignans
Fish Diseases
Furans
Infectious hematopoietic necrosis virus
Rhabdoviridae Infections
Oncorhynchus mykiss
Virus Attachment
Epithelial Cells
Cell Line
Antiviral potential of the arctigenin derivative COA in reducing viral adhesion to the epithelial cell surface against IHNV infection. Hu, Yang Wang, Huan Wang, Zixuan Zhang, Xu Liu, Lei Chen, Jiong Animals Antiviral Agents Lignans Fish Diseases Furans Infectious hematopoietic necrosis virus Rhabdoviridae Infections Oncorhynchus mykiss Virus Attachment Epithelial Cells Cell Line Infectious hematopoietic necrosis virus (IHNV) is a major aquaculture threat, highlighting the need for effective antiviral agents. This study evaluates the arctigenin derivative COA for its antiviral potential against IHNV. COA demonstrated no cytotoxicity to EPC cells at concentrations up to 10 μM and inhibited over 90 % of IHNV gene expression in vitro. It preserved normal nuclear morphology in infected cells, reduced viral titers, and completely blocked IHNV infection at 10 μM. Time-gradient assays identified COA's antiviral action during early infection, specifically inhibiting viral adsorption (82 %) and internalization (92 %). Using DiO-labeled IHNV particles, we visualized COA preventing viral entry into EPC cells, marking a novel finding for arctigenin derivatives. COA remained stable in water for over four days, enhancing its suitability for aquaculture applications. In vivo, COA improved survival rates of IHNV-infected rainbow trout by 46 % (injection) and 22 % (immersion) while significantly reducing IHNV gene expression and viral titers in spleen and kidney. It also upregulated interferon genes, activating antiviral responses and effectively reducing horizontal transmission of IHNV. These results highlight COA's potential as an antiviral agent, providing insights for developing targeted therapies against rhabdoviruses in aquaculture.
title Antiviral potential of the arctigenin derivative COA in reducing viral adhesion to the epithelial cell surface against IHNV infection.
topic Animals
Antiviral Agents
Lignans
Fish Diseases
Furans
Infectious hematopoietic necrosis virus
Rhabdoviridae Infections
Oncorhynchus mykiss
Virus Attachment
Epithelial Cells
Cell Line
url https://pubmed.ncbi.nlm.nih.gov/40089086/