key: cord-0001321-xkqxawj2
authors: Fang, Jin'e; Sun, Leqiang; Peng, Guiqing; Xu, Jia; Zhou, Rui; Cao, Shengbo; Chen, Huanchun; Song, Yunfeng
title: Identification of Three Antiviral Inhibitors against Japanese Encephalitis Virus from Library of Pharmacologically Active Compounds 1280
date: 2013-11-04
journal: PLoS One
DOI: 10.1371/journal.pone.0078425
sha: 2c5983eedfe4431e007a45dcf0103176ed1d9ff8
doc_id: 1321
cord_uid: xkqxawj2

Japanese encephalitis virus (JEV) can cause severe central nervous disease with a high mortality rate. There is no antiviral drug available for JEV-specific treatment. In this study, a cytopathic-effect-based, high-throughput screening assay was developed and applied to screen JEV inhibitors from Library of Pharmacologically Active Compounds 1280. The antiviral effects of three hit compounds including FGIN-1-27, cilnidipine, and niclosamide were evaluated in cells by western blotting, indirect immunofluorescence assay, and plaque reduction assay. A time-of-addition assay proved that all three compounds inhibited JEV at the stage of replication. The EC50s of FGIN-1-27, cilnidipine, and niclosamide were 3.21, 6.52, and 5.80 µM, respectively, while the selectivity indexes were 38.79, 30.67, and 7.49. FGIN-1-27 and cilnidipine have high efficiency and selectivity against JEV. This study provided two JEV antiviral inhibitors as candidates for treatment of JEV infection.

Japanese encephalitis virus (JEV), a member of the genus Flavivirus in the family Flaviviridae, is a mosquito-transmitted and zoonotic pathogen that causes 50,000 cases and 10,000 deaths per year [1] . There are .70 arboviruses in the genus Flavivirus including JEV, dengue virus (DENV), West Nile virus (WNV), and yellow fever virus [2] . JEV can cause severe central nervous disorders such as poliomyelitis-like paralysis, aseptic meningitis, and encephalitis in humans. The fatality rate caused by JEV is 10-50% and half of the survivors have severe neurological sequelae, including persistent motor defects and severe cognitive and language impairments [3] . The geographic range of JEV is still expanding with an enhanced threat, and JEV infections have been reported in Australia [4, 5] , Pakistan [6] , and Saipan [7] in the past 30 years. Therefore, JEV is still an important pathogen that has global health significance.

Inactivated and live-attenuated vaccines have been used for prevention of JEV infection for many years [8, 9] . Although vaccines have reduced the incidence of JE in some countries, they seem not to be effective against all the clinical isolates [10] . In August 2006, there was an outbreak of JEV in Shanxi Province, China, which caused 66 cases and 19 deaths [11] . There is an urgent need for antiviral agents that can reduce the death toll and neurological sequelae of JEV infection [12] . Two anti-hepatitis C virus drugs targeting viral protease, telaprevir VX-950 (developed by Vertex) and boceprevir SCH503034 (developed by Merck), won approval in 2011 [13] . Various effective inhibitors against DENV and WNV have also been identified as drug candidates [14, 15] . In recent studies, some agents were found to have good antiviral effects against JEV. Indirubin, derived from Isatis indigotica extract, was proved to have inhibitory effects on JEV in vitro with less cytotoxicity [16] . Dehydroepiandrosterone (DHEA) suppressed the replication and virus-induced apoptosis in neuroblastoma cells by acting on the extracellular signal-regulated protein kinase [17] . N-nonyl-deoxynojirimycin affected the interaction between calnexin (endoplasmic reticulum chaperone) and JEV glycoproteins (premembrane, envelope, and non-structural protein 1), and thus had anti-JEV effects both in vitro and in vivo [18] . SCH 16, a derivative of N-methylisatin-b-thiosemicarbazone, inhibited 50% of the plaques produced by JEV at a concentration of 16 mg/ mL (0.000025 mM) [19] . However, there are currently only a small number of JEV inhibitors available for drug development.

In this study, a cytopathic-effect-(CPE)-based, high-throughput screening (HTS) assay was developed for discovery of JEV antiviral inhibitors. It was used to screen 1280 pharmacologically active compounds and three compounds were identified to have antiviral effects against JEV.

BHK-21 cells were cultured in Dulbecco's Modified Eagle's Medium (Sigma-Aldrich, St. Louis, MO, USA) supplemented with 10% fetal calf serum (FCS) (Invitrogen, Grand Island, NY, USA), 100 U/mL penicillin (Sigma-Aldrich), and 100 mg/mL streptomycin (Sigma-Aldrich). JEV (P3 strain, Genbank accession no. U47032.1) was propagated in BHK-21 cells with maintenance medium containing 1% FCS, 100 U/mL penicillin, and 100 mg/ mL streptomycin.

Cell viability was evaluated by Celltiter-Glo Luminescent Cell Viability Assay reagent (Promega, Madison, WI, USA) following the manufacturer's protocol. An equal volume of Celltiter-Glo reagents was added to the cells in 96-well white plates (Corning, Tewksbury, MA, USA) and mixed for 2 min on an orbital shaker and incubated for a further 10 min at room temperature. The luminescence of each well was measured by a 1450 MicroBeta TriLux (Perkin Elmer, Waltham, MA, USA). Percentage of cell viability was calculated as follows: Percentage of cell viability 

The cell density, assay endpoint, and infective dose in the HTS assay were optimized. BHK-21 cells at different densities (5,000-25,000 cells per well) were infected with JEV at various multiplicity of infections (MOIs) (0.64-0.0025). Cell viability was detected at different times (72-120 h) after JEV inoculation. The suitable cell density, assay endpoint, and infective dose for HTS assay were selected by comparing cell growth, S/B ratio, and Z9 value in different conditions. The Z9 value and S/B ratio were calculated as previously described [20] .

BHK-21 cells were seeded onto 96-well plates at 10,000 cells per well. After 12 h incubation, the culture supernatant was replaced with maintenance medium. One microliter of each compound was added to 99 mL maintenance medium in the first well, followed by twofold serial dilutions for two wells. After full mixing in the third well, 50 mL medium was discarded. Then, 50 mL maintenance medium containing 0.02 MOI JEV was added to each well. The plates were subjected to 30 s horizontal shaking to achieve thorough mixing. Three wells of mock-infected cells as well as three wells of JEV-infected cells containing 1% DMSO were set on each plate as controls. After 120 h incubation, the percentage of CPE inhibition was calculated as previously described [21] : Percentage of inhibition = (luminescence of experimental group -average luminescence of virus control) / (average luminescence of cell control -average luminescence of virus control) 6100. Each concentration was assayed in triplicate. Forty-eight hours post-infection, the viruses in each group were harvested by freezing/thawing three times and mixed in a tube. Then, 50 mL virus suspension was inoculated into BHK-21 cells in 12-well plates for the plaque assay, as previously described [23] .

The antiviral mechanism of compounds was evaluated by timeof-addition assay as previously described [24] . BHK-21 cells were seeded in 96-well white plates at 10,000 cells per well, and then infected with JEV at MOI 0.01 after 12 h incubation. The test compounds at10 mM were added to cells at 1 h pre-infection 

BHK-21 cells were seeded in 96-well white plates at 10,000 cells per well. Twelve hours later, the growth medium was replaced with maintenance medium containing 0.01 MOI JEV as well as different concentrations of compounds. Cell incubation was continued for 120 h, and the percentage of inhibition was measured as described above. The EC50 values were calculated by nonlinear regression analysis.

BHK-21 cells were seeded in 96-well white plates at 10,000 cells per well. After 12 h incubation for cell attachment, different concentrations of compounds were added to the cells. Cell viability was tested as described above after 120 h incubation. The 50% cytotoxicity concentration (CC50) was calculated by nonlinear regression analysis.

The HTS assay conditions including seeding cell density, infective dose, and assay endpoint were optimized by comparing the Z9 values and S/B ratios under different conditions. Finally, we chose 10,000 cells per well as the optimized cell density, 0.01 MOI as the optimized infective dose, and 120 h post-inoculation as the endpoint of the HTS. Under the optimized conditions, three independent assays were performed to validate the robustness and reproducibility of the HTS assay. The Z9 values in the three repeats were 0.92, 0.93, and 0.97, respectively, and the average was 0.9460.015. The S/B values were 10.82, 9.65, and 10.94, respectively, and the average was 10.4760.41. The average coefficient variation (CV) in mock-infected and JEV-infected cells was 1.2660.45% and 5.7260.23%, respectively. All the results fitted well with the standard parameters of HTS, which demonstrated that the assay was robust and suitable for largescale compound screening.

The CPE-based HTS assay was used to screen JEV inhibitors from the Library of Pharmacologically Active Compounds 1280. We obtained an average Z9 value of 0.9160.02, average S/B ratio of 11.960.55, and average CV of 1.9561.76% in mock-infected controls and 7.9860.99% in JEV-infected cells in this HTS assay.

The inhibition rate of each compound at different concentrations was calculated at the end of the assay and plotted in Figure 1A -C. There were 3, 12, and 3 compounds identified to have .50% inhibition at concentrations of 50, 25, and 12.5 mM, respectively. In these compounds, seven compounds were selected for a second screening according three criterions: (1) the compounds had an inhibition rate at about 50%; (2) the compounds showed inhibitory effect to JEV in at least two concentrations; (3) there had normal cells without cytopathic-changes observed by microcopy. After the second screening, four compounds were confirmed to have about 50% CPE inhibition at two concentrations ( Figure 1D ). The antiviral effects of three commercial available compounds, cilnidipine, FGIN-1-27 (N,N-dihexyl-2-(4-fluorophenyl)indole-3acetamide), and niclosamide, were identified by western blotting, IFA, plaque reduction assay, and time-of-addition assays in the subsequent studies. Figure 4D ). In the FGIN-1-27-treated group, the number of plaques was also ,20 (,400 PFU/mL) when the compound concentration was 10 mM ( Figure 4A ). As a control, the virus titer in the untreated group was 2.7610 6 PFU/mL (data not show).

The compounds were added to JEV-infected cells at 21, 0, and +1 h post-infection, and the percentage inhibition was evaluated after 120 h incubation. No inhibition of infection was detectable when the compounds were added before or during JEV attachment. However, the anti-JEV activities of these compounds were all observed in the post-infection groups ( Figure 5A-C) . Thus, all three compounds might inhibit JEV at the stage of viral replication.

To quantify the antiviral effect, the inhibition rates of the three compounds at different concentrations were determined and EC50 was calculated by nonlinear regression. The inhibitory effects of all three compounds showed dose-dependent patterns. The EC50s of FGIN-1-27, cilnidipine and niclosamide were 3.21, 6.52, and 5.80 mM, respectively ( Figure 6A , C and E). To assess cytotoxicity, cell viability with different concentrations of compounds was tested and CC50s of FGIN-1-27, cilnidipine and niclosamide were determined to be 124.5, 200, and 43.26 mM ( Figure 6B, D and F) . So, the selectivity indexes of FGIN-1-27, cilnidipine and niclosamide were 38.79, 30.67 and 7.49, respectively.

To acquire complete CPE induced by JEV, the endpoint of HTS assay was optimized at 120 h post-inoculation. Such a long incubation period posed a real challenge to the robustness and repetitiveness of the HTS assay. After the optimization of cell density and infective dose, this CPE-based HTS showed a high reproducibility including an average Z9 value over 0.9, and a suitable S/B ratio around 10.0. Variations from cell control (1.2660.45%) and virus infected control (5.7260.23%) were no more than 10%. In addition, the similar Z9, S/B, and CV values were obtained in the HTS of 1280 compounds, which demonstrated that this assay was reliable for large scale screening of antiviral inhibitors. Meanwhile, this CPE-based assay could also be used to determine the EC50 of compound on JEV, or quantify the cytopathic effect caused by JEV.

The potential cytotoxicity and inhibition concentration of compounds in a library might be quite different. So in a HTS, to choose one suitable concentration for all compounds is not possible. In the present study, we evaluated the inhibitory effects of each compound in three concentrations (50, 25 and 12.5 mM), and some compounds were found to have higher inhibition rate at 25 mM than 50 mM. The compound in high concentration might influence the cell viability and thus exhibited a lower inhibition rate. Especially in the CC50 analysis, the three tested compounds were proven to have more or less cytotoxicity at 50 mM to cells (Fig. 6B, D and F) . So it is not difficult to understand why the inhibition rate of some compounds at 50 mM is lower than that at 25 mM.

The antiviral mechanism of the three hit compounds was explored in this study. All three compounds showed inhibitory effects at the post-infection stage, using the time-of-addition assay ( Figure 5) . Therefore, these compounds should inhibit virus in the process of replication. The essential viral proteins related to replication include NS3 protease, NS3 helicase, methyltransferase (MTase) and RNA-dependent RNA polymerase (RdRp) [25] . In our study, the inhibitory effects of the compounds on JEV NS3 protease and helicase were tested by fluorescence resonance energy transfer (FRET) respectively, as previously described [26, 27] , but the compounds did not inhibit these two proteins (unpublished data). Then the potential antiviral targets may be the MTase, RdRp or other cellular enzymes. How the compounds inhibit JEV replication was under further investigation.

Cilnidipine is a dual blocker of L-and N-type calcium channels in vascular smooth muscle or sympathetic nerve terminals that supply blood vessels [28] . It is effective for treatment of essential hypertension and has been approved in Japan [29] . The toxicity of cilnidipine is low (MLD50 .5 g/kg) and has a low incidence of unfavorable side effects in humans [30] . In the present study, cilnidipine also showed effective inhibition of JEV. The replication of JEV was almost completely inhibited by 20 or 15 mM cilnidipine. So, cilnidipine might be a candidate anti-JEV drug.

FGIN-1-27 is an anxiolytic drug acting on the peripheral benzodiazepine receptor, producing anxiolytic effects by stimulating steroidogenesis of neuroactive steroids such as allopregnanolone [31] . In the present study, FGIN-1-27 showed ideal antiviral effects at concentrations of 5-20 mM. The high selectivity index (38.78) illustrated that FGIN-1-27 could inhibit JEV with high specificity. A previous study showed that FGIN-1-27 had the ability to enter the brain [32] . Therefore, FGIN-1-27 might inhibit JEV in brain cells, and could be a potential drug for treatment of encephalitis caused by JEV.

Japanese encephalitis virus

A structural perspective of the flavivirus life cycle

Emerging flaviviruses: the spread and resurgence of Japanese encephalitis, West Nile and dengue viruses

Japanese encephalitis in north Queensland

Japanese encephalitis as an emerging virus: the emergence and spread of Japanese encephalitis virus in Australasia

Detection of west Nile and Japanese encephalitis viral genome sequences in cerebrospinal fluid from acute encephalitis cases in Karachi

Japanese encephalitis on Saipan: a survey of suspected mosquito vectors

Protection against Japanese encephalitis by inactivated vaccines

Safety of a live-attenuated Japanese encephalitis virus vaccine (SA14-14-2) for children

Homologous and heterologous neutralization antibody responses after immunization with Japanese encephalitis vaccine among Taiwan children

Japanese Encephalitis Outbreak

Does antiviral therapy have a role in the control of Japanese encephalitis?

First specific drugs raise hopes for hepatitis C

Strategies for the identification of inhibitors of West Nile virus and other flaviviruses

Strategies for development of Dengue virus inhibitors

Antiviral activity of Isatis indigotica extract and its derived indirubin against Japanese encephalitis virus

Antiviral effect of dehydroepiandrosterone on Japanese encephalitis virus infection

Antiviral effects of an iminosugar derivative on flavivirus infections

Nmethylisatin-beta-thiosemicarbazone derivative (SCH 16) is an inhibitor of Japanese encephalitis virus infection in vitro and in vivo

The development, optimization and validation of an assay for high throughput antiviral drug screening against Dengue virus

Development and validation of a high-throughput screen for inhibitors of SARS CoV and its application in screening of a 100,000-compound library

Monoclonal antibodies against NS3 and NS5 proteins of Japanese encephalitis virus

A model to study neurotropism and persistency of Japanese encephalitis virus infection in human neuroblastoma cells and leukocytes

Identification of a small-molecule entry inhibitor for filoviruses

Novel approaches to flavivirus drug discovery

Enzymatic analysis of recombinant Japanese encephalitis virus NS2B(H)-NS3pro protease with fluorogenic model peptide substrates

Direct fluorometric measurement of hepatitis C virus helicase activity

L/T-type and L/ N-type calcium-channel blockers attenuate cardiac sympathetic nerve activity in patients with hypertension

Renal and vascular protective effects of Cilnidipine in patients with essential hypertension

The efficacy and safety of cilnidipine on mild to moderate essential hypertension: a systematic review and meta-analysis of randomized controlled trials in Chinese patients

Stimulation of brain steroidogenesis by 2-aryl-indole-3-acetamide derivatives acting at the mitochondrial diazepam-binding inhibitor receptor complex

2-Aryl-3-indoleacetamides (FGIN-1): a new class of potent and specific ligands for the mitochondrial DBI receptor (MDR)