Antiviral Activity of Lanatoside C Against Dengue Virus Infection
Overview
Affiliations
Dengue infection poses a serious threat globally due to its recent rapid spread and rise in incidence. Currently, there is no approved vaccine or effective antiviral drug for dengue virus infection. In response to the urgent need for the development of an effective antiviral for dengue virus, the US Drug Collection library was screened in this study to identify compounds with anti-dengue activities. Lanatoside C, an FDA approved cardiac glycoside was identified as a candidate anti-dengue compound. Our data revealed that lanatoside C has an IC50 of 0.19μM for dengue virus infection in HuH-7 cells. Dose-dependent reduction in dengue viral RNA and viral proteins synthesis were also observed upon treatment with increasing concentrations of lanatoside C. Time of addition study indicated that lanatoside C inhibits the early processes of the dengue virus replication cycle. Furthermore, lanatoside C can effectively inhibit all four serotypes of dengue virus, flavivirus Kunjin, alphavirus Chikungunya and Sindbis virus as well as the human enterovirus 71. These findings suggest that lanatoside C possesses broad spectrum antiviral activity against several groups of positive-sense RNA viruses.
A Comprehensive Review of the Development and Therapeutic Use of Antivirals in Flavivirus Infection.
Tripathi A, Chauhan S, Khasa R Viruses. 2025; 17(1).
PMID: 39861863 PMC: 11769230. DOI: 10.3390/v17010074.
Cardiac glycosides inhibit early and late vaccinia virus protein expression.
Samolej J, White I, Strang B, Mercer J J Gen Virol. 2024; 105(3).
PMID: 38546099 PMC: 10995631. DOI: 10.1099/jgv.0.001971.
Vector-Transmitted Flaviviruses: An Antiviral Molecules Overview.
Diani E, Lagni A, Lotti V, Tonon E, Cecchetto R, Gibellini D Microorganisms. 2023; 11(10).
PMID: 37894085 PMC: 10608811. DOI: 10.3390/microorganisms11102427.
The Antiviral Activity of Varenicline against Dengue Virus Replication during the Post-Entry Stage.
Lin C, Kiu Y, Kan J, Chang Y, Hung P, Lu C Biomedicines. 2023; 11(10).
PMID: 37893127 PMC: 10604274. DOI: 10.3390/biomedicines11102754.
Cheminformatics-Based Study Identifies Potential Ebola VP40 Inhibitors.
Broni E, Ashley C, Adams J, Manu H, Aikins E, Okom M Int J Mol Sci. 2023; 24(7).
PMID: 37047270 PMC: 10094735. DOI: 10.3390/ijms24076298.