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Ebola virus causes sporadic outbreaks of lethal hemorrhagic fever in humans, but there is no currently approved therapy. Cells take up Ebola virus by macropinocytosis, followed by trafficking through endosomal vesicles. However, few factors controlling endosomal virus movement are known. Here we find that Ebola virus entry into host cells requires the endosomal calcium channels called two-pore channels (TPCs). Disrupting TPC function by gene knockout, small interfering RNAs, or small-molecule inhibitors halted virus trafficking and prevented infection. Tetrandrine, the most potent small molecule that we tested, inhibited infection of human macrophages, the primary target of Ebola virus in vivo, and also showed therapeutic efficacy in mice. Therefore, TPC proteins play a key role in Ebola virus infection and may be effective targets for antiviral therapy.

Original publication

DOI

10.1126/science.1258758

Type

Journal article

Journal

Science

Publication Date

27/02/2015

Volume

347

Pages

995 - 998

Keywords

Animals, Antiviral Agents, BALB 3T3 Cells, Benzylisoquinolines, Calcium Channel Blockers, Calcium Channels, Ebolavirus, Female, Gene Knockout Techniques, HeLa Cells, Hemorrhagic Fever, Ebola, Humans, Macrophages, Mice, Molecular Targeted Therapy, NADP, RNA Interference, Signal Transduction, Verapamil, Virus Internalization, Two-Pore Channels