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Epigallocatechin gallate from green tea effectively blocks infection of SARS-CoV-2 and new variants by inhibiting spike binding to ACE2 receptor

BACKGROUND: As the COVID-19 pandemic rages on, the new SARS-CoV-2 variants have emerged in the different regions of the world. These newly emerged variants have mutations in their spike (S) protein that may confer resistance to vaccine-elicited immunity and existing neutralizing antibody therapeutic...

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Autores principales: Liu, Jinbiao, Bodnar, Brittany H., Meng, Fengzhen, Khan, Adil I., Wang, Xu, Saribas, Sami, Wang, Tao, Lohani, Saroj Chandra, Wang, Peng, Wei, Zhengyu, Luo, Jinjun, Zhou, Lina, Wu, Jianguo, Luo, Guangxiang, Li, Qingsheng, Hu, Wenhui, Ho, Wenzhe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8404181/
https://www.ncbi.nlm.nih.gov/pubmed/34461999
http://dx.doi.org/10.1186/s13578-021-00680-8
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author Liu, Jinbiao
Bodnar, Brittany H.
Meng, Fengzhen
Khan, Adil I.
Wang, Xu
Saribas, Sami
Wang, Tao
Lohani, Saroj Chandra
Wang, Peng
Wei, Zhengyu
Luo, Jinjun
Zhou, Lina
Wu, Jianguo
Luo, Guangxiang
Li, Qingsheng
Hu, Wenhui
Ho, Wenzhe
author_facet Liu, Jinbiao
Bodnar, Brittany H.
Meng, Fengzhen
Khan, Adil I.
Wang, Xu
Saribas, Sami
Wang, Tao
Lohani, Saroj Chandra
Wang, Peng
Wei, Zhengyu
Luo, Jinjun
Zhou, Lina
Wu, Jianguo
Luo, Guangxiang
Li, Qingsheng
Hu, Wenhui
Ho, Wenzhe
author_sort Liu, Jinbiao
collection PubMed
description BACKGROUND: As the COVID-19 pandemic rages on, the new SARS-CoV-2 variants have emerged in the different regions of the world. These newly emerged variants have mutations in their spike (S) protein that may confer resistance to vaccine-elicited immunity and existing neutralizing antibody therapeutics. Therefore, there is still an urgent need of safe, effective, and affordable agents for prevention/treatment of SARS-CoV-2 and its variant infection. RESULTS: We demonstrated that green tea beverage (GTB) or its major ingredient, epigallocatechin gallate (EGCG), were highly effective in inhibiting infection of live SARS-CoV-2 and human coronavirus (HCoV OC43). In addition, infection of the pseudoviruses with spikes of the new variants (UK-B.1.1.7, SA-B.1.351, and CA-B.1.429) was efficiently blocked by GTB or EGCG. Among the 4 active green tea catechins at noncytotoxic doses, EGCG was the most potent in the action against the viruses. The highest inhibitory activity was observed when the viruses or the cells were pre-incubated with EGCG prior to the infection. Mechanistic studies revealed that EGCG blocked infection at the entry step through interfering with the engagement of the receptor binding domain (RBD) of the viral spikes to angiotensin-converting enzyme 2 (ACE2) receptor of the host cells. CONCLUSIONS: These data support further clinical evaluation and development of EGCG as a novel, safe, and cost-effective natural product for prevention/treatment of SARS-CoV-2 transmission and infection. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13578-021-00680-8.
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spelling pubmed-84041812021-08-30 Epigallocatechin gallate from green tea effectively blocks infection of SARS-CoV-2 and new variants by inhibiting spike binding to ACE2 receptor Liu, Jinbiao Bodnar, Brittany H. Meng, Fengzhen Khan, Adil I. Wang, Xu Saribas, Sami Wang, Tao Lohani, Saroj Chandra Wang, Peng Wei, Zhengyu Luo, Jinjun Zhou, Lina Wu, Jianguo Luo, Guangxiang Li, Qingsheng Hu, Wenhui Ho, Wenzhe Cell Biosci Research BACKGROUND: As the COVID-19 pandemic rages on, the new SARS-CoV-2 variants have emerged in the different regions of the world. These newly emerged variants have mutations in their spike (S) protein that may confer resistance to vaccine-elicited immunity and existing neutralizing antibody therapeutics. Therefore, there is still an urgent need of safe, effective, and affordable agents for prevention/treatment of SARS-CoV-2 and its variant infection. RESULTS: We demonstrated that green tea beverage (GTB) or its major ingredient, epigallocatechin gallate (EGCG), were highly effective in inhibiting infection of live SARS-CoV-2 and human coronavirus (HCoV OC43). In addition, infection of the pseudoviruses with spikes of the new variants (UK-B.1.1.7, SA-B.1.351, and CA-B.1.429) was efficiently blocked by GTB or EGCG. Among the 4 active green tea catechins at noncytotoxic doses, EGCG was the most potent in the action against the viruses. The highest inhibitory activity was observed when the viruses or the cells were pre-incubated with EGCG prior to the infection. Mechanistic studies revealed that EGCG blocked infection at the entry step through interfering with the engagement of the receptor binding domain (RBD) of the viral spikes to angiotensin-converting enzyme 2 (ACE2) receptor of the host cells. CONCLUSIONS: These data support further clinical evaluation and development of EGCG as a novel, safe, and cost-effective natural product for prevention/treatment of SARS-CoV-2 transmission and infection. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13578-021-00680-8. BioMed Central 2021-08-30 /pmc/articles/PMC8404181/ /pubmed/34461999 http://dx.doi.org/10.1186/s13578-021-00680-8 Text en © The Author(s) 2021 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, Jinbiao
Bodnar, Brittany H.
Meng, Fengzhen
Khan, Adil I.
Wang, Xu
Saribas, Sami
Wang, Tao
Lohani, Saroj Chandra
Wang, Peng
Wei, Zhengyu
Luo, Jinjun
Zhou, Lina
Wu, Jianguo
Luo, Guangxiang
Li, Qingsheng
Hu, Wenhui
Ho, Wenzhe
Epigallocatechin gallate from green tea effectively blocks infection of SARS-CoV-2 and new variants by inhibiting spike binding to ACE2 receptor
title Epigallocatechin gallate from green tea effectively blocks infection of SARS-CoV-2 and new variants by inhibiting spike binding to ACE2 receptor
title_full Epigallocatechin gallate from green tea effectively blocks infection of SARS-CoV-2 and new variants by inhibiting spike binding to ACE2 receptor
title_fullStr Epigallocatechin gallate from green tea effectively blocks infection of SARS-CoV-2 and new variants by inhibiting spike binding to ACE2 receptor
title_full_unstemmed Epigallocatechin gallate from green tea effectively blocks infection of SARS-CoV-2 and new variants by inhibiting spike binding to ACE2 receptor
title_short Epigallocatechin gallate from green tea effectively blocks infection of SARS-CoV-2 and new variants by inhibiting spike binding to ACE2 receptor
title_sort epigallocatechin gallate from green tea effectively blocks infection of sars-cov-2 and new variants by inhibiting spike binding to ace2 receptor
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8404181/
https://www.ncbi.nlm.nih.gov/pubmed/34461999
http://dx.doi.org/10.1186/s13578-021-00680-8
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