Fig 1.
HCS screen of Apteeus TEElibrary for the identification of anti-SARS-CoV-2 compounds.
A, Workflow overview of the screening process. B, Dot-plot representations of all compounds tested based on their robust-Z-score for both the numbers of nuclei and the percentages of PI-positive nuclei. Dotted lines are indicative of the thresholds chosen for hit selectivity (within the green area). C, Dot-plot representation according to the molecular weight and the LogD of the compounds of interest. Dots are color-coded based on the ionization state at physiological pH.
Fig 2.
In vitro validation of the antiviral activity of clofoctol.
A, Clofoctol inhibits the genomic replication of SARS-CoV-2. Vero-81 and Vero-81-TMPRSS2 cells were infected for 6h at an MOI of 0.25 in the presence of increasing concentrations of clofoctol. Then, total RNA was extracted and viral RNA was quantified by RT-qPCR and normalized by the amount of total RNA. Results are presented as the percentage of the viral load of the control and represent the average of seven independent experiments performed in duplicates. Error bars represent the standard error of the mean (SEM). B, Clofoctol is not cytotoxic in cell culture at concentrations below 40 μM. Vero-81 cells and Calu-3 cells were cultured in the presence of given concentrations of clofoctol. Cell viability was monitored using the MTS-based viability assay after 24 hours of incubation. C, Clofoctol inhibits the production of progeny virions. Vero-81 and Vero-81-TMPRSS2 cells were infected with SARS-CoV-2 at a MOI of 0.25. After 1h, the inoculum was removed and the cells were washed with PBS prior treatment with clofoctol. Cells were then further incubated for 16h. Thereafter, supernatants were collected and the amounts of secreted infectious virus were quantified. The limit of detection was 1.5TCID50/mL. These data represent the average of three independent experiments (N = 3). Experiments were performed in duplicate for each condition. D, Clofoctol inhibits SARS-CoV-2 replication in Calu-3 cells. Calu-3 cells were infected at a MOI of 0.25 in the presence of increasing concentrations of clofoctol for 24h. Then, total cellular RNA was extracted and viral RNA was quantified by RT-qPCR. Results are presented as the percentage of the viral load of the control and represent the average of three independent experiments performed in duplicates. Error bars represent the standard error of the mean (SEM).
Fig 3.
Clofoctol targets the translation step of SARS-CoV-2 life cycle.
A, Clofoctol is mainly efficient at a post-entry step. Vero-81 cells were infected with SARS-CoV-2 at an MOI of 0.25. Clofoctol, remdesivir or CQ were present at a concentration of 15 μM either before infection, during virus entry, post-inoculation or throughout the steps as indicated on the schematic depiction of the experiment. Bars indicate when the drugs are present during the experiment for each condition. At 16h post-infection, cells were fixed with 4% paraformaldehyde and processed to detect the proportion of infected cells. Therefore, they were immunostained to allow for the detection of the viral double-stranded RNA and nuclei were detected by Hoechst staining to count the total number of cells. Results are presented as the percentage of infection inhibition and represent the average of five independent experiments. B, Time-of-addition experiment. Vero-81 cells were infected at an MOI of 0.5 for 1h. 15 μM of clofoctol, remdesivir or CQ were added every hour starting 1h before inoculation. Cells were lysed 8h after the end of the inoculation in Laemmli loading buffer and the amount of N protein was detected in immunoblot. Results are presented as the percentage of N protein expression relative to that in non-treated cells (CTL) and represent the average of three independent experiments. Error bars represent the standard error of the mean (SEM). C, Clofoctol does not inhibit SARS-CoV-2 entry. Huh-7 cells expressing ACE2 receptor were infected with SARS2pp or pseudoparticles containing the envelope glycoprotein of the vesicular stomatitis virus (VSV) used as a control (VSVpp) for 3 hours in the presence of increasing concentrations of clofoctol or CQ. At 48 hours post-infection, cells were lysed to quantify luciferase activity. The results are expressed in % of the controls of three independent experiments. The experiments were performed in triplicate (n = 3) in each condition. D, Clofoctol inhibits viral RNA translation. Schematic representation of the reporter construct expressing the Renilla luciferase placed between the 5’-UTR and the 3’-UTR of the SARS-CoV-2 genomic RNA and the control bicistronic construct containing the firefly luciferase sequence under the control of a cap structure, followed by the Renilla luciferase under the control of hepatitis C virus (HCV) IRES. Huh-7 or Vero-81 cells were electroporated with in vitro transcribed RNA. Cells were lysed after 8h and luciferase activities were recorded. The results are expressed in % of the controls of three independent experiments. The experiments were performed in quadruplicate (n = 4) in each condition. Two-way ANOVA followed by the Dunnett’s multiple comparisons test was performed for statistical analysis (*p < 0.05; **p < 0.01; ***p < 0.001).
Fig 4.
Clofoctol inhibits other SARS-CoV-2 variants as well as HCoV-229E.
A, Vero-81 cells were infected either with SARS-CoV-2 of lineage B1 containing the D614G mutation (SARS-CoV-2/human/FRA/Lille_Vero-TMPRSS2/2020) or with SARS-CoV-2 of lineage B1.1.7 (GISAID accession number EPI_ISL_1653931) or lineage B.1.351 (GISAID accession number EPI_ISL_1653932) or lineage B.1.617.2 (GISAID accession number EPI_ISL_2143633). Viral genomes were quantified by RT-qPCR and normalized by the amount of total RNA. Results are presented as the percentage of the viral load of the control and represent the average of three independent experiments performed in duplicates. Error bars represent the standard error of the mean (SEM). B, Clofoctol is not cytotoxic in cell culture at concentrations below 40 μM. Huh-7 cells were cultured in the presence of given concentrations of clofoctol. Cell viability was monitored using the MTS-based viability assay after 24 hours of incubation. C, Huh-7 cells were infected with HCoV-229E-Rluc in presence of different concentrations of clofoctol or remdesivir. At 7h post-infection, cells were lysed and luciferase activities were quantified. Results are presented as the percentages of the control and represent an average of three independent experiments performed in triplicates. Errors bars represent the standard error of the mean (SEM).
Fig 5.
Pharmacokinetics and antiviral properties of clofoctol in a mouse model of COVID-19.
A, Pharmacokinetics characterization of clofoctol in mice. Left panel, 8–10 week-old female C57BL/6J mice were treated i.p. with a single dose of clofoctol (62.5mg/kg) and were sacrificed at different time points thereafter. Right panel, Clofoctol was inoculated twice daily during two days and mice were sacrificed 1h after the last injection. Clofoctol concentrations in lungs (n = 3/time point, 3 samples/lung) and plasma (n = 3/time point, 2 technical replicates) are depicted. B-D, Effects of clofoctol treatment on SARS-CoV-2 infection in K18-hACE2 transgenic C57BL/6J mice. B, Left panel, Scheme of the experimental design in which the effect of clofoctol was assessed in mice. Mice were treated i.p. with clofoctol (62.5mg/kg) or vehicle 1h and 8h after i.n. inoculation of SARS-CoV-2 (5x102 TCID50 per mouse) and treated again twice at day 1 post-infection. Animals were sacrificed at day 2 and day 4 post-infection. Right panel, Body weight curves are shown. C,The viral load was determined by titration on Vero-E6 cells (middle panel) and by RT-qPCR (right panel) (day 2 post-infection). D, mRNA copy numbers of genes were quantified by RT-qPCR. Data are expressed as fold change over average gene expression in mock-treated (uninfected) animals (day 2 post-infection). E, Lung sections were analyzed at day 4 post-infection. Shown are representative lungs (hematoxylin and eosin staining). Lower panels, enlarged views of the area circled in black in upper panels. F, Blinded sections were scored for levels of pathological severity. The inflammatory score is depicted. B-C, Results are expressed as the mean ± SD (n = 13 for panels B and D and n = 6–7 for panel E and F). Significant differences were determined using the Mann-Whitney U test (**p < 0.01; ***p < 0.001).