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Ethanol extract from Artemisia argyi leaves inhibits HSV-1 infection by destroying the viral envelope
Herpes simplex virus type 1 (HSV-1) is a widely disseminated virus that establishes latency in the brain and causes occasional but fatal herpes simplex encephalitis. Currently, acyclovir (ACV) is the main clinical drug used in the treatment of HSV-1 infection, and the failure of therapy in immunocom...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9841929/ https://www.ncbi.nlm.nih.gov/pubmed/36647143 http://dx.doi.org/10.1186/s12985-023-01969-5 |
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author | Liu, Ping Zhong, Lishan Xiao, Ji Hu, Yuze Liu, Tao Ren, Zhe Wang, Yifei Zheng, Kai |
author_facet | Liu, Ping Zhong, Lishan Xiao, Ji Hu, Yuze Liu, Tao Ren, Zhe Wang, Yifei Zheng, Kai |
author_sort | Liu, Ping |
collection | PubMed |
description | Herpes simplex virus type 1 (HSV-1) is a widely disseminated virus that establishes latency in the brain and causes occasional but fatal herpes simplex encephalitis. Currently, acyclovir (ACV) is the main clinical drug used in the treatment of HSV-1 infection, and the failure of therapy in immunocompromised patients caused by ACV-resistant HSV-1 strains necessitates the requirement to develop novel anti-HSV-1 drugs. Artemisia argyi, a Traditional Chinese Medicine, has been historically used to treat inflammation, bacterial infection, and cancer. In this study, we demonstrated the antiviral effect and mechanism of ethanol extract of A. argyi leaves (hereafter referred to as ‘AEE’). We showed that AEE at 10 μg/ml exhibits potent antiviral effects on both normal and ACV-resistant HSV-1 strains. AEE also inhibited the infection of HSV-2, rotavirus, and influenza virus. Transmission electron microscopy revealed that AEE destroys the membrane integrity of HSV-1 viral particles, resulting in impaired viral attachment and penetration. Furthermore, mass spectrometry assay identified 12 major components of AEE, among which two new flavones, deoxysappanone B 7,3ʹ-dimethyl ether, and 3,7-dihydroxy-3′,4ʹ-dimethoxyflavone, exhibited the highest binding affinity to HSV-1 glycoprotein gB at the surface site critical for gB–gH–gL interaction and gB-mediated membrane fusion, suggesting their involvement in inactivating virions. Therefore, A. argyi is an important source of antiviral drugs, and the AEE may be a potential novel antiviral agent against HSV-1 infection. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12985-023-01969-5. |
format | Online Article Text |
id | pubmed-9841929 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-98419292023-01-17 Ethanol extract from Artemisia argyi leaves inhibits HSV-1 infection by destroying the viral envelope Liu, Ping Zhong, Lishan Xiao, Ji Hu, Yuze Liu, Tao Ren, Zhe Wang, Yifei Zheng, Kai Virol J Research Herpes simplex virus type 1 (HSV-1) is a widely disseminated virus that establishes latency in the brain and causes occasional but fatal herpes simplex encephalitis. Currently, acyclovir (ACV) is the main clinical drug used in the treatment of HSV-1 infection, and the failure of therapy in immunocompromised patients caused by ACV-resistant HSV-1 strains necessitates the requirement to develop novel anti-HSV-1 drugs. Artemisia argyi, a Traditional Chinese Medicine, has been historically used to treat inflammation, bacterial infection, and cancer. In this study, we demonstrated the antiviral effect and mechanism of ethanol extract of A. argyi leaves (hereafter referred to as ‘AEE’). We showed that AEE at 10 μg/ml exhibits potent antiviral effects on both normal and ACV-resistant HSV-1 strains. AEE also inhibited the infection of HSV-2, rotavirus, and influenza virus. Transmission electron microscopy revealed that AEE destroys the membrane integrity of HSV-1 viral particles, resulting in impaired viral attachment and penetration. Furthermore, mass spectrometry assay identified 12 major components of AEE, among which two new flavones, deoxysappanone B 7,3ʹ-dimethyl ether, and 3,7-dihydroxy-3′,4ʹ-dimethoxyflavone, exhibited the highest binding affinity to HSV-1 glycoprotein gB at the surface site critical for gB–gH–gL interaction and gB-mediated membrane fusion, suggesting their involvement in inactivating virions. Therefore, A. argyi is an important source of antiviral drugs, and the AEE may be a potential novel antiviral agent against HSV-1 infection. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12985-023-01969-5. BioMed Central 2023-01-16 /pmc/articles/PMC9841929/ /pubmed/36647143 http://dx.doi.org/10.1186/s12985-023-01969-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Liu, Ping Zhong, Lishan Xiao, Ji Hu, Yuze Liu, Tao Ren, Zhe Wang, Yifei Zheng, Kai Ethanol extract from Artemisia argyi leaves inhibits HSV-1 infection by destroying the viral envelope |
title | Ethanol extract from Artemisia argyi leaves inhibits HSV-1 infection by destroying the viral envelope |
title_full | Ethanol extract from Artemisia argyi leaves inhibits HSV-1 infection by destroying the viral envelope |
title_fullStr | Ethanol extract from Artemisia argyi leaves inhibits HSV-1 infection by destroying the viral envelope |
title_full_unstemmed | Ethanol extract from Artemisia argyi leaves inhibits HSV-1 infection by destroying the viral envelope |
title_short | Ethanol extract from Artemisia argyi leaves inhibits HSV-1 infection by destroying the viral envelope |
title_sort | ethanol extract from artemisia argyi leaves inhibits hsv-1 infection by destroying the viral envelope |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9841929/ https://www.ncbi.nlm.nih.gov/pubmed/36647143 http://dx.doi.org/10.1186/s12985-023-01969-5 |
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