Myrtus communis L. Essential Oil Exhibits Antiviral Activity against Coronaviruses

Author:

Li Dar-Yin1ORCID,Donadu Matthew G.23ORCID,Shue Taylor1,Dangas Georgios1ORCID,Athanasiadis Antonis1ORCID,Lan Shuiyun1,Wen Xin1,Battah Basem4,Zanetti Stefania5,Mazzarello Vittorio5ORCID,Sarafianos Stefan G.1,Ferrari Marco6ORCID,Michailidis Eleftherios1

Affiliation:

1. Laboratory of Biochemical Pharmacology, Department of Pediatrics, Center for ViroScience and Cure, Emory University School of Medicine, and Children’s Healthcare of Atlanta, 1750 Haygood Drive, Atlanta, GA 30322, USA

2. Scuola di Specializzazione in Farmacia Ospedaliera, Department of Medicine, Surgery and Pharmacy, University of Sassari, 07100 Sassari, Italy

3. Hospital Pharmacy, Giovanni Paolo II Hospital, ASL Gallura, 07026 Olbia, Italy

4. Department of Biochemistry and Microbiology, Antioch Syrian Private University, M5, Damascus 22734, Syria

5. Department of Biomedical Sciences, University of Sassari, 07100 Sassari, Italy

6. Institute for Maternal and Child Health, IRCCS Burlo Garofolo, Via dell’Istria, 65, 34137 Trieste, Italy

Abstract

Human coronaviruses are a continuous threat to the human population and have limited antiviral treatments, and the recent COVID-19 pandemic sparked interest in finding new antiviral strategies, such as natural products, to combat emerging coronaviruses. Rapid efforts in the scientific community to identify effective antiviral agents for coronaviruses remain a focus to minimize mortalities and global setbacks. In this study, an essential oil derived from Myrtus communis L. (MEO) is effective against HCoV-229E and HCoV-OC43 virus infections in comparison to two FDA-approved drugs, Remdesivir and Nirmatrelvir. Gas-chromatography and mass spectrometry were used to identify the chemical composition of MEO. Slight antioxidant activity was observed in MEO, indicating a role in oxidative stress. A dose–response curve measuring the EC50 indicates a high potency against HCoV-229E and HCoV-OC43 virus infections on Huh7.5 cells with low cytotoxicity using a PrestoBlue cell viability assay. Our findings demonstrate that MEO exhibits potent antiviral activity against HCoV-229E and HCoV-OC43 on Huh7.5 cells within a low-cytotoxicity range, but not on SARS-CoV-2. Artificial bacterial chromosome plasmids that expressed SARS-CoV-2 used for replicon—to determine viral replication and viral assembly/egress on HEK293T/17 cells—and virus-like particles on Huh7.5-AT cells—to determine viral entry and assembly/egress—showed no antiviral activity with MEO in comparison to Remdesivir. This study reveals the potential effectiveness of MEO as an alternative natural remedy to treat human coronaviruses and a potential antiviral agent for future coronavirus infections.

Publisher

MDPI AG

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