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- Publisher Website: 10.1002/ptr.7452
- WOS: WOS:000838795500013
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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
Title | Broad‐spectrum antiviral activity of Spatholobus suberectus Dunn against SARS‐CoV ‐2, SARS‐CoV ‐1, H5N1, and other enveloped viruses |
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Authors | |
Issue Date | 2022 |
Citation | Phytotherapy Research, 2022, v. 36, p. 3232-3247 How to Cite? |
Abstract | The 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 Identifier | http://hdl.handle.net/10722/315657 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | LIU, Q | - |
dc.contributor.author | Kwan, KYH | - |
dc.contributor.author | Cao, T | - |
dc.contributor.author | Yan, B | - |
dc.contributor.author | KUMAR, M | - |
dc.contributor.author | Jia, L | - |
dc.contributor.author | ZHANG, F | - |
dc.contributor.author | LIM, CYH | - |
dc.contributor.author | WU, Y | - |
dc.contributor.author | Feng, Y | - |
dc.contributor.author | Chen, Z | - |
dc.contributor.author | Liu, L | - |
dc.contributor.author | Chen, J | - |
dc.date.accessioned | 2022-08-19T09:01:59Z | - |
dc.date.available | 2022-08-19T09:01:59Z | - |
dc.date.issued | 2022 | - |
dc.identifier.citation | Phytotherapy Research, 2022, v. 36, p. 3232-3247 | - |
dc.identifier.uri | http://hdl.handle.net/10722/315657 | - |
dc.description.abstract | The 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.language | eng | - |
dc.relation.ispartof | Phytotherapy Research | - |
dc.title | Broad‐spectrum antiviral activity of Spatholobus suberectus Dunn against SARS‐CoV ‐2, SARS‐CoV ‐1, H5N1, and other enveloped viruses | - |
dc.type | Article | - |
dc.identifier.email | Kwan, KYH: hallieky@hku.hk | - |
dc.identifier.email | Yan, B: ybp1205@hku.hk | - |
dc.identifier.email | Feng, Y: yfeng@hku.hk | - |
dc.identifier.email | Chen, Z: zchenai@hku.hk | - |
dc.identifier.email | Liu, L: liuli71@hkucc.hku.hk | - |
dc.identifier.email | Chen, J: abchen@hkucc.hku.hk | - |
dc.identifier.authority | Feng, Y=rp00466 | - |
dc.identifier.authority | Chen, Z=rp00243 | - |
dc.identifier.authority | Liu, L=rp00268 | - |
dc.identifier.authority | Chen, J=rp01316 | - |
dc.identifier.doi | 10.1002/ptr.7452 | - |
dc.identifier.hkuros | 336038 | - |
dc.identifier.volume | 36 | - |
dc.identifier.spage | 3232 | - |
dc.identifier.epage | 3247 | - |
dc.identifier.isi | WOS:000838795500013 | - |