Title Anti-varicella-zoster virus activity of cephalotaxine esters in vitro
Author Jung-Eun Kim and Yoon-Jae Song*
Address Department of Life Science, Gachon University, Seongnam 13120, Republic of Korea
Bibliography Journal of Microbiology, 57(1),74–79, 2019,
DOI 10.1007/s12275-019-8514-z
Key Words varicella zoster virus, antiviral, harringtonine, homoharringtonine
Abstract Harringtonine (HT) and homoharringtonine (HHT), alkaloid esters isolated from the genus Cephalotaxus, exhibit antitumor activity. A semisynthetic HHT has been approved for treatment of chronic myelogenous leukemia. In addition to antileukemic activity, HT and HHT are reported to possess potent antiviral activity. In this study, we investigated the effects of HT and HHT on replication of varicella-zoster virus (VZV) in vitro. HT and HHT, but not their biologically inactive parental alkaloid cephalotaxine (CET), significantly inhibited replication of recombinant VZV-pOka luciferase. Furthermore, HT and HHT, but not CET, strongly induced down-regulation of VZV lytic genes and exerted potent antiviral effects against a VZV clinical isolate. The collective data support the utility of HT and HHT as effective antiviral candidates for treatment of VZV-associated diseases.