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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.
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.
  • Liu J; Department of Pathology and Laboratory Medicine, Center for Metabolic Disease Research, and Department of Neurology, Temple University Lewis Katz School of Medicine, Philadelphia, PA, 19140, USA.
  • Bodnar BH; Guangdong Key Laboratory of Virology, Institute of Medical Microbiology, Jinan University, Guangzhou, 510632, China.
  • Meng F; Department of Pathology and Laboratory Medicine, Center for Metabolic Disease Research, and Department of Neurology, Temple University Lewis Katz School of Medicine, Philadelphia, PA, 19140, USA.
  • Khan AI; Department of Pathology and Laboratory Medicine, Center for Metabolic Disease Research, and Department of Neurology, Temple University Lewis Katz School of Medicine, Philadelphia, PA, 19140, USA.
  • Wang X; Department of Pathology and Laboratory Medicine, Center for Metabolic Disease Research, and Department of Neurology, Temple University Lewis Katz School of Medicine, Philadelphia, PA, 19140, USA.
  • Saribas S; Department of Pathology and Laboratory Medicine, Center for Metabolic Disease Research, and Department of Neurology, Temple University Lewis Katz School of Medicine, Philadelphia, PA, 19140, USA.
  • Wang T; Department of Pathology and Laboratory Medicine, Center for Metabolic Disease Research, and Department of Neurology, Temple University Lewis Katz School of Medicine, Philadelphia, PA, 19140, USA.
  • Lohani SC; Nebraska Center for Virology, School of Biological Sciences, University of Nebraska-Lincoln, Lincoln, NE, 68583-0900, USA.
  • Wang P; Nebraska Center for Virology, School of Biological Sciences, University of Nebraska-Lincoln, Lincoln, NE, 68583-0900, USA.
  • Wei Z; Department of Pathology and Laboratory Medicine, Center for Metabolic Disease Research, and Department of Neurology, Temple University Lewis Katz School of Medicine, Philadelphia, PA, 19140, USA.
  • Luo J; Department of Pathology and Laboratory Medicine, Center for Metabolic Disease Research, and Department of Neurology, Temple University Lewis Katz School of Medicine, Philadelphia, PA, 19140, USA.
  • Zhou L; Department of Pathology and Laboratory Medicine, Center for Metabolic Disease Research, and Department of Neurology, Temple University Lewis Katz School of Medicine, Philadelphia, PA, 19140, USA.
  • Wu J; Department of Pathology and Laboratory Medicine, Center for Metabolic Disease Research, and Department of Neurology, Temple University Lewis Katz School of Medicine, Philadelphia, PA, 19140, USA.
  • Luo G; Guangdong Key Laboratory of Virology, Institute of Medical Microbiology, Jinan University, Guangzhou, 510632, China.
  • Li Q; Department of Microbiology, University of Alabama At Birmingham School of Medicine, Birmingham, AL, 35294, USA. gluo@uab.edu.
  • Hu W; Nebraska Center for Virology, School of Biological Sciences, University of Nebraska-Lincoln, Lincoln, NE, 68583-0900, USA. qli@unl.edu.
  • Ho W; Department of Pathology and Laboratory Medicine, Center for Metabolic Disease Research, and Department of Neurology, Temple University Lewis Katz School of Medicine, Philadelphia, PA, 19140, USA. whu@temple.edu.
Cell Biosci ; 11(1): 168, 2021 Aug 30.
Article in English | MEDLINE | ID: covidwho-1379800
Preprint
This scientific journal article is probably based on a previously available preprint. It has been identified through a machine matching algorithm, human confirmation is still pending.
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ABSTRACT

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.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies / Prognostic study Topics: Vaccines / Variants Language: English Journal: Cell Biosci Year: 2021 Document Type: Article Affiliation country: S13578-021-00680-8

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies / Prognostic study Topics: Vaccines / Variants Language: English Journal: Cell Biosci Year: 2021 Document Type: Article Affiliation country: S13578-021-00680-8