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咖啡叶抗 SARS-CoV-2 感染的前景。

Prospects of Coffee Leaf against SARS-CoV-2 Infection.

机构信息

Graduate Institute of Biomedical Sciences, China Medical University, Taichung 406040, Taiwan.

Department of Cosmeceutics, China Medical University, Taichung 406040, Taiwan.

出版信息

Int J Biol Sci. 2022 Jul 11;18(12):4677-4689. doi: 10.7150/ijbs.76058. eCollection 2022.

DOI:10.7150/ijbs.76058
PMID:35874948
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9305275/
Abstract

In the current climate, many countries are in dire need of effective preventive methods to curb the Severe Acute Respiratory Syndrome Coronavirus Type 2 (SARS-CoV-2) pandemic. The purpose of this research is to screen and explore natural plant extracts that have the potential to against SARS-CoV-2 and provide alternative options for SARS-CoV-2 prevention and hand sanitizer or spray-like disinfectants. We first used Spike-ACE2 ELISA and TMPRSS2 fluorescence resonance energy transfer (FRET) assays to screen extracts from agricultural by-products from Taiwan with the potential to impede SARS-CoV-2 infection. Next, the SARS-CoV-2 pseudo-particles (Vpp) infection assay was tested to validate the effectiveness. We identified an extract from coffee leaf (), a natural plant that effectively inhibited wild-type SARS-CoV-2, and five Variants of Concern (Alpha, Beta, Gamma, Delta, and Omicron strain) from entering host cells. In an attempt to apply coffee leaf extract for hand sanitizer or spray-like disinfectants, we designed a skin-like gelatin membrane experiment. We showed that the high concentration of coffee leaf extract on the skin surface could block SARS-CoV-2 into cells more potently than 75% Ethanol, a standard disinfectant to inactivate SARS-CoV-2. Finally, LC-HRMS analysis was used to identify compounds such as caffeine, chlorogenic acid (CGA), quinic acid, and mangiferin that are associated with an anti-SARS-CoV-2 activity. Our results demonstrated that coffee leaf extract, an agricultural by-product effectively inhibits SARS-CoV-2 Vpp infection through an ACE2-dependent mechanism and may be utilized to develop products against SARS-CoV-2 infection.

摘要

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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1675/9305275/0405bde6e65c/ijbsv18p4677g006.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1675/9305275/0405bde6e65c/ijbsv18p4677g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1675/9305275/849f750577a7/ijbsv18p4677g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1675/9305275/bb8938af6116/ijbsv18p4677g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1675/9305275/186838f638ed/ijbsv18p4677g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1675/9305275/0405bde6e65c/ijbsv18p4677g006.jpg

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Int J Biol Sci. 2022 Feb 14;18(5):1865-1877. doi: 10.7150/ijbs.66369. eCollection 2022.
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Altered TMPRSS2 usage by SARS-CoV-2 Omicron impacts infectivity and fusogenicity.
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