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The CO Extract (Ze 339) Blocks SARS-CoV-2 Replication In Vitro

Overview
Journal Viruses
Publisher MDPI
Specialty Microbiology
Date 2022 Jan 22
PMID 35062310
Authors
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Abstract

The coronavirus disease 2019 (COVID-19), caused by a novel coronavirus (SARS-CoV-2), has spread worldwide, affecting over 250 million people and resulting in over five million deaths. Antivirals that are effective are still limited. The antiviral activities of the CO extract Ze 339 were previously reported. Thus, to assess the anti-SARS-CoV-2 activity of Ze 339 as well as isopetasin and neopetasin as major active compounds, a CPE and plaque reduction assay in Vero E6 cells was used for viral output. Antiviral effects were tested using the original virus (Wuhan) and the Delta variant of SARS-CoV-2. The antiviral drug remdesivir was used as control. Pre-treatment with Ze 339 in SARS-CoV-2-infected Vero E6 cells with either virus variant significantly inhibited virus replication with IC values of 0.10 and 0.40 μg/mL, respectively. The IC values obtained for isopetasin ranged between 0.37 and 0.88 μM for both virus variants, and that of remdesivir ranged between 1.53 and 2.37 μM. In conclusion, Ze 339 as well as the petasins potently inhibited SARS-CoV-2 replication in vitro of the Wuhan and Delta variants. Since time is of essence in finding effective treatments, clinical studies will have to demonstrate if Ze339 can become a therapeutic option to treat SARS-CoV-2 infections.

Citing Articles

Bioactive natural products in COVID-19 therapy.

Wang Z, Wang N, Yang L, Song X Front Pharmacol. 2022; 13:926507.

PMID: 36059994 PMC: 9438897. DOI: 10.3389/fphar.2022.926507.

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