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Article: Broad‐spectrum antiviral activity of Spatholobus suberectus Dunn against SARS‐CoV ‐2, SARS‐CoV ‐1, H5N1, and other enveloped viruses

TitleBroad‐spectrum antiviral activity of Spatholobus suberectus Dunn against SARS‐CoV ‐2, SARS‐CoV ‐1, H5N1, and other enveloped viruses
Authors
Issue Date2022
Citation
Phytotherapy Research, 2022, v. 36, p. 3232-3247 How to Cite?
AbstractThe current COVID-19 pandemic caused by SARS-Cov-2 is responsible for more than 6 million deaths globally. The development of broad-spectrum and cost-effective antivirals is urgently needed. Medicinal plants are renowned as a complementary approach in which antiviral natural products have been established as safe and effective drugs. Here, we report that the percolation extract of Spatholobus suberectus Dunn (SSP) is a broad-spectrum viral entry inhibitor against SARS-CoV-1/2 and other enveloped viruses. The viral inhibitory activities of the SSP were evaluated by using pseudotyped SARS-CoV-1 and 2, HIV-1ADA and HXB2 , and H5N1. SSP effectively inhibited viral entry and with EC50 values ranging from 3.6 to 5.1 μg/ml. Pre-treatment of pseudovirus or target cells with SSP showed consistent inhibitory activities with the respective EC50 value of 2.3 or 2.1 μg/ml. SSP blocked both SARS-CoV-2 spike glycoprotein and the host ACE2 receptor. In vivo studies indicated that there was no abnormal toxicity and behavior in long-term SSP treatment. Based on these findings, we concluded that SSP has the potential to be developed as a drug candidate for preventing and treating COVID-19 and other emerging enveloped viruses.
Persistent Identifierhttp://hdl.handle.net/10722/315657
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLIU, Q-
dc.contributor.authorKwan, KYH-
dc.contributor.authorCao, T-
dc.contributor.authorYan, B-
dc.contributor.authorKUMAR, M-
dc.contributor.authorJia, L-
dc.contributor.authorZHANG, F-
dc.contributor.authorLIM, CYH-
dc.contributor.authorWU, Y-
dc.contributor.authorFeng, Y-
dc.contributor.authorChen, Z-
dc.contributor.authorLiu, L-
dc.contributor.authorChen, J-
dc.date.accessioned2022-08-19T09:01:59Z-
dc.date.available2022-08-19T09:01:59Z-
dc.date.issued2022-
dc.identifier.citationPhytotherapy Research, 2022, v. 36, p. 3232-3247-
dc.identifier.urihttp://hdl.handle.net/10722/315657-
dc.description.abstractThe current COVID-19 pandemic caused by SARS-Cov-2 is responsible for more than 6 million deaths globally. The development of broad-spectrum and cost-effective antivirals is urgently needed. Medicinal plants are renowned as a complementary approach in which antiviral natural products have been established as safe and effective drugs. Here, we report that the percolation extract of Spatholobus suberectus Dunn (SSP) is a broad-spectrum viral entry inhibitor against SARS-CoV-1/2 and other enveloped viruses. The viral inhibitory activities of the SSP were evaluated by using pseudotyped SARS-CoV-1 and 2, HIV-1ADA and HXB2 , and H5N1. SSP effectively inhibited viral entry and with EC50 values ranging from 3.6 to 5.1 μg/ml. Pre-treatment of pseudovirus or target cells with SSP showed consistent inhibitory activities with the respective EC50 value of 2.3 or 2.1 μg/ml. SSP blocked both SARS-CoV-2 spike glycoprotein and the host ACE2 receptor. In vivo studies indicated that there was no abnormal toxicity and behavior in long-term SSP treatment. Based on these findings, we concluded that SSP has the potential to be developed as a drug candidate for preventing and treating COVID-19 and other emerging enveloped viruses.-
dc.languageeng-
dc.relation.ispartofPhytotherapy Research-
dc.titleBroad‐spectrum antiviral activity of Spatholobus suberectus Dunn against SARS‐CoV ‐2, SARS‐CoV ‐1, H5N1, and other enveloped viruses-
dc.typeArticle-
dc.identifier.emailKwan, KYH: hallieky@hku.hk-
dc.identifier.emailYan, B: ybp1205@hku.hk-
dc.identifier.emailFeng, Y: yfeng@hku.hk-
dc.identifier.emailChen, Z: zchenai@hku.hk-
dc.identifier.emailLiu, L: liuli71@hkucc.hku.hk-
dc.identifier.emailChen, J: abchen@hkucc.hku.hk-
dc.identifier.authorityFeng, Y=rp00466-
dc.identifier.authorityChen, Z=rp00243-
dc.identifier.authorityLiu, L=rp00268-
dc.identifier.authorityChen, J=rp01316-
dc.identifier.doi10.1002/ptr.7452-
dc.identifier.hkuros336038-
dc.identifier.volume36-
dc.identifier.spage3232-
dc.identifier.epage3247-
dc.identifier.isiWOS:000838795500013-

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