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Methylene blue is a potent and broad-spectrum inhibitor against Zika virus in vitro and in vivo
Many flaviviruses including the Dengue virus (DENV), Zika virus (ZIKV), West Nile virus, Yellow Fever virus, and Japanese encephalitis virus are significant human pathogens, unfortunately without any specific therapy. Here, we demonstrate that methylene blue, an FDA-approved drug, is a broad-spectru...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7646565/ https://www.ncbi.nlm.nih.gov/pubmed/33078696 http://dx.doi.org/10.1080/22221751.2020.1838954 |
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author | Li, Zhong Lang, Yuekun Sakamuru, Srilatha Samrat, Subodh Trudeau, Nicole Kuo, Lili Rugenstein, Natasha Tharappel, Anil D'Brant, Lianna Koetzner, Cheri A. Hu, Saiyang Zhang, Jing Huang, Ruili Kramer, Laura D. Butler, David Xia, Menghang Li, Hongmin |
author_facet | Li, Zhong Lang, Yuekun Sakamuru, Srilatha Samrat, Subodh Trudeau, Nicole Kuo, Lili Rugenstein, Natasha Tharappel, Anil D'Brant, Lianna Koetzner, Cheri A. Hu, Saiyang Zhang, Jing Huang, Ruili Kramer, Laura D. Butler, David Xia, Menghang Li, Hongmin |
author_sort | Li, Zhong |
collection | PubMed |
description | Many flaviviruses including the Dengue virus (DENV), Zika virus (ZIKV), West Nile virus, Yellow Fever virus, and Japanese encephalitis virus are significant human pathogens, unfortunately without any specific therapy. Here, we demonstrate that methylene blue, an FDA-approved drug, is a broad-spectrum and potent antiviral against Zika virus and Dengue virus both in vitro and in vivo. We found that methylene blue can considerably inhibit the interactions between viral protease NS3 and its NS2B co-factor, inhibit viral protease activity, inhibit viral growth, protect 3D mini-brain organoids from ZIKV infection, and reduce viremia in a mouse model. Mechanistic studies confirmed that methylene blue works in both entry and post entry steps, reduces virus production in replicon cells and inhibited production of processed NS3 protein. Overall, we have shown that methylene blue is a potent antiviral for management of flavivirus infections, particularly for Zika virus. As an FDA-approved drug, methylene blue is well-tolerated for human use. Therefore, methylene blue represents a promising and easily developed therapy for management of infections by ZIKV and other flaviviruses. |
format | Online Article Text |
id | pubmed-7646565 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-76465652020-11-17 Methylene blue is a potent and broad-spectrum inhibitor against Zika virus in vitro and in vivo Li, Zhong Lang, Yuekun Sakamuru, Srilatha Samrat, Subodh Trudeau, Nicole Kuo, Lili Rugenstein, Natasha Tharappel, Anil D'Brant, Lianna Koetzner, Cheri A. Hu, Saiyang Zhang, Jing Huang, Ruili Kramer, Laura D. Butler, David Xia, Menghang Li, Hongmin Emerg Microbes Infect Research Article Many flaviviruses including the Dengue virus (DENV), Zika virus (ZIKV), West Nile virus, Yellow Fever virus, and Japanese encephalitis virus are significant human pathogens, unfortunately without any specific therapy. Here, we demonstrate that methylene blue, an FDA-approved drug, is a broad-spectrum and potent antiviral against Zika virus and Dengue virus both in vitro and in vivo. We found that methylene blue can considerably inhibit the interactions between viral protease NS3 and its NS2B co-factor, inhibit viral protease activity, inhibit viral growth, protect 3D mini-brain organoids from ZIKV infection, and reduce viremia in a mouse model. Mechanistic studies confirmed that methylene blue works in both entry and post entry steps, reduces virus production in replicon cells and inhibited production of processed NS3 protein. Overall, we have shown that methylene blue is a potent antiviral for management of flavivirus infections, particularly for Zika virus. As an FDA-approved drug, methylene blue is well-tolerated for human use. Therefore, methylene blue represents a promising and easily developed therapy for management of infections by ZIKV and other flaviviruses. Taylor & Francis 2020-11-03 /pmc/articles/PMC7646565/ /pubmed/33078696 http://dx.doi.org/10.1080/22221751.2020.1838954 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group, on behalf of Shanghai Shangyixun Cultural Communication Co., Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Li, Zhong Lang, Yuekun Sakamuru, Srilatha Samrat, Subodh Trudeau, Nicole Kuo, Lili Rugenstein, Natasha Tharappel, Anil D'Brant, Lianna Koetzner, Cheri A. Hu, Saiyang Zhang, Jing Huang, Ruili Kramer, Laura D. Butler, David Xia, Menghang Li, Hongmin Methylene blue is a potent and broad-spectrum inhibitor against Zika virus in vitro and in vivo |
title | Methylene blue is a potent and broad-spectrum inhibitor against Zika virus in vitro and in vivo |
title_full | Methylene blue is a potent and broad-spectrum inhibitor against Zika virus in vitro and in vivo |
title_fullStr | Methylene blue is a potent and broad-spectrum inhibitor against Zika virus in vitro and in vivo |
title_full_unstemmed | Methylene blue is a potent and broad-spectrum inhibitor against Zika virus in vitro and in vivo |
title_short | Methylene blue is a potent and broad-spectrum inhibitor against Zika virus in vitro and in vivo |
title_sort | methylene blue is a potent and broad-spectrum inhibitor against zika virus in vitro and in vivo |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7646565/ https://www.ncbi.nlm.nih.gov/pubmed/33078696 http://dx.doi.org/10.1080/22221751.2020.1838954 |
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