Cargando…
Antiviral activity and mechanism of the antifungal drug, anidulafungin, suggesting its potential to promote treatment of viral diseases
BACKGROUND: The severe fever with thrombocytopenia syndrome disease (SFTS), caused by the novel tick-borne SFTS virus (SFTSV), was listed among the top 10 priority infectious disease by World Health Organization due to the high fatality rate of 5–30% and the lack of effective antiviral drugs and vac...
Autores principales: | , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9585728/ https://www.ncbi.nlm.nih.gov/pubmed/36266654 http://dx.doi.org/10.1186/s12916-022-02558-z |
_version_ | 1784813554742853632 |
---|---|
author | Shen, Shu Zhang, Yaxian Yin, Zhiyun Zhu, Qiong Zhang, Jingyuan Wang, Tiantian Fang, Yaohui Wu, Xiaoli Bai, Yuan Dai, Shiyu Liu, Xijia Jin, Jiayin Tang, Shuang Liu, Jia Wang, Manli Guo, Yu Deng, Fei |
author_facet | Shen, Shu Zhang, Yaxian Yin, Zhiyun Zhu, Qiong Zhang, Jingyuan Wang, Tiantian Fang, Yaohui Wu, Xiaoli Bai, Yuan Dai, Shiyu Liu, Xijia Jin, Jiayin Tang, Shuang Liu, Jia Wang, Manli Guo, Yu Deng, Fei |
author_sort | Shen, Shu |
collection | PubMed |
description | BACKGROUND: The severe fever with thrombocytopenia syndrome disease (SFTS), caused by the novel tick-borne SFTS virus (SFTSV), was listed among the top 10 priority infectious disease by World Health Organization due to the high fatality rate of 5–30% and the lack of effective antiviral drugs and vaccines and therefore raised the urgent need to develop effective anti-SFTSV drugs to improve disease treatment. METHODS: The antiviral drugs to inhibit SFTSV infection were identified by screening the library containing 1340 FDA-approved drugs using the SFTSV infection assays in vitro. The inhibitory effect on virus entry and the process of clathrin-mediated endocytosis under different drug doses was evaluated based on infection assays by qRT-PCR to determine intracellular viral copies, by Western blot to characterize viral protein expression in cells, and by immunofluorescence assays (IFAs) to determine virus infection efficiencies. The therapeutic effect was investigated in type I interferon receptor defective A129 mice in vivo with SFTSV infection, from which lesions and infection in tissues caused by SFTSV infection were assessed by H&E staining and immunohistochemical analysis. RESULTS: Six drugs were identified as exerting inhibitory effects against SFTSV infection, of which anidulafungin, an antifungal drug of the echinocandin family, has a strong inhibitory effect on SFTSV entry. It suppresses SFTSV internalization by impairing the late endosome maturation and decreasing virus fusion with the membrane. SFTSV-infected A129 mice had relieving symptoms, reduced tissue lesions, and improved disease outcomes following anidulafungin treatment. Moreover, anidulafungin exerts an antiviral effect in inhibiting the entry of other viruses including SARS-CoV-2, SFTSV-related Guertu virus and Heartland virus, Crimean-Congo hemorrhagic fever virus, Zika virus, and Herpes simplex virus 1. CONCLUSIONS: The results demonstrated that the antifungal drug, anidulafungin, could effectively inhibit virus infection by interfering with virus entry, suggesting it may be utilized for the clinical treatment of infectious viral diseases, in addition to its FDA-approved use as an antifungal. The findings also suggested to further evaluate the anti-viral effects of echinocandins and their clinical importance for patients with infection of viruses, which may promote therapeutic strategies as well as treatments and improve outcomes pertaining to various viral and fungal diseases. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-022-02558-z. |
format | Online Article Text |
id | pubmed-9585728 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-95857282022-10-22 Antiviral activity and mechanism of the antifungal drug, anidulafungin, suggesting its potential to promote treatment of viral diseases Shen, Shu Zhang, Yaxian Yin, Zhiyun Zhu, Qiong Zhang, Jingyuan Wang, Tiantian Fang, Yaohui Wu, Xiaoli Bai, Yuan Dai, Shiyu Liu, Xijia Jin, Jiayin Tang, Shuang Liu, Jia Wang, Manli Guo, Yu Deng, Fei BMC Med Research Article BACKGROUND: The severe fever with thrombocytopenia syndrome disease (SFTS), caused by the novel tick-borne SFTS virus (SFTSV), was listed among the top 10 priority infectious disease by World Health Organization due to the high fatality rate of 5–30% and the lack of effective antiviral drugs and vaccines and therefore raised the urgent need to develop effective anti-SFTSV drugs to improve disease treatment. METHODS: The antiviral drugs to inhibit SFTSV infection were identified by screening the library containing 1340 FDA-approved drugs using the SFTSV infection assays in vitro. The inhibitory effect on virus entry and the process of clathrin-mediated endocytosis under different drug doses was evaluated based on infection assays by qRT-PCR to determine intracellular viral copies, by Western blot to characterize viral protein expression in cells, and by immunofluorescence assays (IFAs) to determine virus infection efficiencies. The therapeutic effect was investigated in type I interferon receptor defective A129 mice in vivo with SFTSV infection, from which lesions and infection in tissues caused by SFTSV infection were assessed by H&E staining and immunohistochemical analysis. RESULTS: Six drugs were identified as exerting inhibitory effects against SFTSV infection, of which anidulafungin, an antifungal drug of the echinocandin family, has a strong inhibitory effect on SFTSV entry. It suppresses SFTSV internalization by impairing the late endosome maturation and decreasing virus fusion with the membrane. SFTSV-infected A129 mice had relieving symptoms, reduced tissue lesions, and improved disease outcomes following anidulafungin treatment. Moreover, anidulafungin exerts an antiviral effect in inhibiting the entry of other viruses including SARS-CoV-2, SFTSV-related Guertu virus and Heartland virus, Crimean-Congo hemorrhagic fever virus, Zika virus, and Herpes simplex virus 1. CONCLUSIONS: The results demonstrated that the antifungal drug, anidulafungin, could effectively inhibit virus infection by interfering with virus entry, suggesting it may be utilized for the clinical treatment of infectious viral diseases, in addition to its FDA-approved use as an antifungal. The findings also suggested to further evaluate the anti-viral effects of echinocandins and their clinical importance for patients with infection of viruses, which may promote therapeutic strategies as well as treatments and improve outcomes pertaining to various viral and fungal diseases. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-022-02558-z. BioMed Central 2022-10-21 /pmc/articles/PMC9585728/ /pubmed/36266654 http://dx.doi.org/10.1186/s12916-022-02558-z Text en © The Author(s) 2022 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 Article Shen, Shu Zhang, Yaxian Yin, Zhiyun Zhu, Qiong Zhang, Jingyuan Wang, Tiantian Fang, Yaohui Wu, Xiaoli Bai, Yuan Dai, Shiyu Liu, Xijia Jin, Jiayin Tang, Shuang Liu, Jia Wang, Manli Guo, Yu Deng, Fei Antiviral activity and mechanism of the antifungal drug, anidulafungin, suggesting its potential to promote treatment of viral diseases |
title | Antiviral activity and mechanism of the antifungal drug, anidulafungin, suggesting its potential to promote treatment of viral diseases |
title_full | Antiviral activity and mechanism of the antifungal drug, anidulafungin, suggesting its potential to promote treatment of viral diseases |
title_fullStr | Antiviral activity and mechanism of the antifungal drug, anidulafungin, suggesting its potential to promote treatment of viral diseases |
title_full_unstemmed | Antiviral activity and mechanism of the antifungal drug, anidulafungin, suggesting its potential to promote treatment of viral diseases |
title_short | Antiviral activity and mechanism of the antifungal drug, anidulafungin, suggesting its potential to promote treatment of viral diseases |
title_sort | antiviral activity and mechanism of the antifungal drug, anidulafungin, suggesting its potential to promote treatment of viral diseases |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9585728/ https://www.ncbi.nlm.nih.gov/pubmed/36266654 http://dx.doi.org/10.1186/s12916-022-02558-z |
work_keys_str_mv | AT shenshu antiviralactivityandmechanismoftheantifungaldruganidulafunginsuggestingitspotentialtopromotetreatmentofviraldiseases AT zhangyaxian antiviralactivityandmechanismoftheantifungaldruganidulafunginsuggestingitspotentialtopromotetreatmentofviraldiseases AT yinzhiyun antiviralactivityandmechanismoftheantifungaldruganidulafunginsuggestingitspotentialtopromotetreatmentofviraldiseases AT zhuqiong antiviralactivityandmechanismoftheantifungaldruganidulafunginsuggestingitspotentialtopromotetreatmentofviraldiseases AT zhangjingyuan antiviralactivityandmechanismoftheantifungaldruganidulafunginsuggestingitspotentialtopromotetreatmentofviraldiseases AT wangtiantian antiviralactivityandmechanismoftheantifungaldruganidulafunginsuggestingitspotentialtopromotetreatmentofviraldiseases AT fangyaohui antiviralactivityandmechanismoftheantifungaldruganidulafunginsuggestingitspotentialtopromotetreatmentofviraldiseases AT wuxiaoli antiviralactivityandmechanismoftheantifungaldruganidulafunginsuggestingitspotentialtopromotetreatmentofviraldiseases AT baiyuan antiviralactivityandmechanismoftheantifungaldruganidulafunginsuggestingitspotentialtopromotetreatmentofviraldiseases AT daishiyu antiviralactivityandmechanismoftheantifungaldruganidulafunginsuggestingitspotentialtopromotetreatmentofviraldiseases AT liuxijia antiviralactivityandmechanismoftheantifungaldruganidulafunginsuggestingitspotentialtopromotetreatmentofviraldiseases AT jinjiayin antiviralactivityandmechanismoftheantifungaldruganidulafunginsuggestingitspotentialtopromotetreatmentofviraldiseases AT tangshuang antiviralactivityandmechanismoftheantifungaldruganidulafunginsuggestingitspotentialtopromotetreatmentofviraldiseases AT liujia antiviralactivityandmechanismoftheantifungaldruganidulafunginsuggestingitspotentialtopromotetreatmentofviraldiseases AT wangmanli antiviralactivityandmechanismoftheantifungaldruganidulafunginsuggestingitspotentialtopromotetreatmentofviraldiseases AT guoyu antiviralactivityandmechanismoftheantifungaldruganidulafunginsuggestingitspotentialtopromotetreatmentofviraldiseases AT dengfei antiviralactivityandmechanismoftheantifungaldruganidulafunginsuggestingitspotentialtopromotetreatmentofviraldiseases |