Identification of inositol monophosphatase as a broad‐spectrum antiviral target of ivermectin

Author:

Jitobaom Kunlakanya1,Peerapen Paleerath2,Boonyuen Usa3,Meewan Ittipat4,Boonarkart Chompunuch1,Sirihongthong Thanyaporn1,Thongon Songkran1,Thongboonkerd Visith2ORCID,Auewarakul Prasert1ORCID

Affiliation:

1. Department of Microbiology, Faculty of Medicine Siriraj Hospital Mahidol University Bangkok Thailand

2. Medical Proteomics Unit, Research Department, Faculty of Medicine Siriraj Hospital Mahidol University Bangkok Thailand

3. Department of Molecular Tropical Medicine and Genetics, Faculty of Tropical Medicine Mahidol University Bangkok Thailand

4. Institute of Molecular Biosciences Mahidol University Nakhon Pathom Thailand

Abstract

AbstractIvermectin has broad‐spectrum antiviral activities. Despite the failure in clinical application of COVID‐19, it can serve as a lead compound for the development of more effective broad‐spectrum antivirals, for which a better understanding of its antiviral mechanisms is essential. We thus searched for potential novel targets of ivermectin in host cells by label‐free thermal proteomic profiling using Huh‐7 cells. Inositol monophosphatase (IMPase) was found among the proteins with shifted thermal stability by ivermectin. Ivermectin could inhibit IMPase activity and reduce cellular myo‐inositol and phosphatidylinositol‐4‐phosphate levels. On the other hand, inositol could impair the antiviral activity of ivermectin and lithium, an IMPase inhibitor with known antiviral activity. As phosphatidylinositol phosphate is crucial for the replication of many RNA viruses, inhibition of cellular myo‐inositol biosynthesis may be an important antiviral mechanism of ivermectin. Hence, inhibition of IMPase could serve as a potential target for broad‐spectrum antiviral development.

Funder

Faculty of Medicine Siriraj Hospital, Mahidol University

Publisher

Wiley

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