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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...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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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. |
format | Online Article Text |
id | pubmed-8404181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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