4.7 Article

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

Journal

PHYTOTHERAPY RESEARCH
Volume 36, Issue 8, Pages 3232-3247

Publisher

WILEY
DOI: 10.1002/ptr.7452

Keywords

antivirals; HIV-1; SARS-CoVs; Spatholobus suberectus Dunn

Funding

  1. Guangxi Science and Technology Key Research and Development Program [AB16450012]

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The percolation extract of Spatholobus suberectus Dunn (SSP) was found to have broad-spectrum viral entry inhibitory activity against SARS-CoV-1/2 and other enveloped viruses. In vivo studies showed no abnormal toxicity or behavior in long-term SSP treatment. These findings suggest that SSP has the potential to be developed as a drug candidate for preventing and treating COVID-19 and other emerging enveloped viruses.
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-1(ADA and HXB2), and H5N1. SSP effectively inhibited viral entry and with EC50 values ranging from 3.6 to 5.1 mu g/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 mu g/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.

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