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. Author manuscript; available in PMC: 2020 Nov 25.
Published in final edited form as: Nat Microbiol. 2020 May 25;5(9):1069–1078. doi: 10.1038/s41564-020-0727-8

Extended Data Fig. 2.

Extended Data Fig. 2

Miglustat inhibition of gradient-purified naked and quasi-enveloped hepatovirus infection.

a. (top) Schematic showing the organization of the HM175/18f-NLuc virus genome, and (bottom) distribution of viral RNA associated with naked and quasi-enveloped eHAV 18f-NLuc virions from supernatant fluids of infected cells in fractions of an isopycnic iodixanol gradient. b. Miglustat inhibition of naked 18f-NLuc virus replication. Data shown are mean NLuc expression in Huh-7.5 cells pre-treated with miglustat for 72 hrs prior to infection, and lysed and assayed for NLuc activity 18 hrs after infection. n= 3 technical replicates. The estimated 50% inhibitory concentration (IC50) was 44.5 μM (95% CI = 29.8–66.0) using a four-parameter, variable slope nonlinear regression model (R=0.900). c. NLuc activity expressed by Huh-7.5 cells 18 hrs after infection with naked (nHAV) or quasi-enveloped (eHAV) virus. Cells were treated with the indicated concentration of miglustat beginning 72 hrs prior to infection. Data shown are means of 3 technical replicates. d. ATP assay for viability of Huh7.5 cells treated with indicated concentrations of miglustat for 72 hrs (CellTiter-Glo, Promega). Data shown are means of 4 technical replicates.