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N-methylisatin-beta-thiosemicarbazone derivative (SCH 16) is an inhibitor of Japanese encephalitis virus infection in vitro and in vivo
Virology Journal volume 5, Article number: 64 (2008)
During the early and mid part of 20th century, several reports described the therapeutic effects of N-methylisatin-β-Thiosemicarbazone (MIBT) against pox viruses, Maloney leukemia viruses and recently against HIV. However, their ability to inhibit flavivirus replication has not been investigated. Hence the present study was designed to evaluate the antiviral activity of 14 MIBT derivatives against Flaviviruses that are prevalent in India such as Japanese Encephalitis Virus (JEV), Dengue-2 (Den-2) and West Nile viruses (WNV).
Amongst the fourteen Mannich bases of MIBT derivatives tested one compound – SCH 16 was able to completely inhibit in vitro Japanese encephalitis virus (JEV) and West Nile virus (WNV) replication. However no antiviral activity of SCH 16 was noted against Den-2 virus replication. This compound was able to inhibit 50% of the plaques (IC50) produced by JEV and WNV at a concentration of 16 μgm/ml (0.000025 μM) and 4 μgm/ml (0.000006 μM) respectively. Furthermore, SCH 16 at a concentration of 500 mg/kg body weight administered by oral route twice daily was able to completely (100%) prevent mortality in mice challenged with 50LD50 JEV by the peripheral route. Our experiments to understand the mechanism of action suggest that SCH 16 inhibited JEV replication at the level of early protein translation.
Only one of the 14 isatin derivatives -SCH 16 exhibited antiviral action on JEV and WNV virus infection in vitro. SCH 16 was also found to completely inhibit JEV replication in vivo in a mouse model challenged peripherally with 50LD50 of the virus. These results warrant further research and development on SCH 16 as a possible therapeutic agent.
Flaviviruses are considered to be important pathogens responsible for significant human morbidity and mortality. The World Health Organization estimated that more than 50 million Dengue viral infections and 50,000 cases of Japanese encephalitis occur annually worldwide . Severe manifestations of flavivirus disease include hemorrhagic fever, encephalitis and neurological sequelae. Despite the major clinical and public health impact of flaviviruses, there are no drugs available for chemoprophylaxis or chemotherapy of these infections. The advent of potent combination antiretroviral therapy has been an important breakthrough in the treatment of HIV-1 infection, resulting in marked reductions in HIV-1-related morbidity and mortality . This has rekindled interest in the search for antiviral agents for a variety of viral infections.
Earlier reports have described antiviral activity of some compounds against flaviviruses . However, only a few of them have described both in vitro and in vivo activity of antiviral agents against flaviviruses . Thiosemicarbazones were the first antiviral compounds recognized to have a broad-spectrum antiviral activity against a range of DNA and RNA viruses [4, 5]. The use of N-methylisatin-β-thiosemicarbazone (methisazone/marboran) as an effective antiviral drug in the chemoprophylaxis of small pox was demonstrated in human volunteers in South India as early as 1965 . In several trials during Indian epidemics methizasone proved its value by reducing the attack rates by 75 to 95% . Similarly, other studies have shown that Methyl isatin-β-diethylthiosemicarbazone inhibits replication of Moloney Leukemia Virus by interfering with the early phase of viral life cycle . However, the antiviral activity of isatin thiosemicarbazone derivatives has not been evaluated against flaviviruses. Therefore, this study was undertaken to investigate if any of the N-methylisatin-β-thiosemicarbazone derivatives could suppress common flavivirus infections encountered in South India such as Japanese Encephalitis, Dengue and West Nile viral infections. The aim was not to develop a clinical protocol for therapy of these infections but rather to investigate the possibility of identifying antiviral agents that could target flavivirus multiplication.
Antiviral screening of compounds in vitro by cytopathic inhibition assay
Initially, the 50% Cytotoxic Concentration (CC50) of the 14 MIBT derivatives and Ribavirin were determined on Porcine Stable kidney (PS) and Baby hamster kidney (BHK 21) cell lines and the results are depicted in Table 1. The antiviral activity of the 14 MIBT derivatives were initially evaluated against JEV, WNV and Den-2 using Cytopathic Effect (CPE) inhibition assay and it was observed that only SCH 16 showed inhibition of CPE. The structure of this MIBT derivative is depicted in Figure 1. Ribavarin, a known inhibitor of flavivirus was used as a control in all the experiments. Although there is no structural similarity between Ribavarin and SCH 16, we opted to use Ribavarin as a positive control in all experiments so that we have a reference value for comparing the results of SCH 16. These two compounds were then subjected to evaluation by the plaque reduction assay at non-cytotoxic concentrations (<CC50). It was noted that SCH 16 and Ribavirin exhibited a dose depended reduction of plaques formed by JEV and WNV (Figure 2, Panels A and B) with an IC50 of 16 μg/ml (0.000025 μM) and 4 ug/ml (0.000006 μM) for JEV and WNV respectively. On the contrary the IC50 of Ribavirin was 3.9 μg/ml (0.000016 μM) and 1.7 μg/ml (0.000007 μM) for JEV and WNV respectively. No antiviral activity of SCH 16 was noted against Den-2 although Ribavarin showed a dose dependent inhibition of Den-2 plaque formation (Figure 2, Panels C and D).
The specificity of the action of an antiviral compound is determined by calculating the Therapeutic Index (TI), which is the ratio of CC50 to IC50. The TI of SCH 16 was 5 and 19 for JEV and WNV respectively while for Ribavirin it was 13 and 29 respectively. This suggests that SCH 16 is moderately active against JEV and highly active against WNV.
The kinetics of action of SCH 16 in relation to the replicative cycle of JEV in vitro
As a first step to understand JEV and SCH 16 interactions, experiments were designed to determine the kinetics of JEV replication in vitro. It was noted that the earliest appearance of JEV antigen in infected PS cells was at 10 hours post-adsorption as detected by IFA (data not presented). However, the first infectious progeny of virus was detected in the supernatant medium at 14 hours post-adsorption thereby suggesting that a single replicative cycle of JEV in vitro in PS cell line requires 14 hours for completion (data not presented).
The antiviral activity of SCH 16 was subsequently investigated in relation to the kinetics of JEV replication. Non-toxic concentration of SCH 16 was added at various time points following entry of JEV into PS cells and the experiments terminated following 48 hours incubation. The compound at a concentration of 76 μg/ml (0.00012 μM) was able to completely inhibit JEV replication when added to the infected monolayer at 2, 4, 6 and 8 hours post-infection evidenced by the absence of viral RNA, viral antigen and inhibition of virus yield (Figure 3, Panel A to C). However, addition of SCH 16 beyond 8 hours post infection did not completely inhibit JEV replication since JEV antigen, RNA and infectious virus were detected at subsequent time points (Figure 3, Panels A to C).
In order to determine the minimum contact period required for SCH 16 to exert its antiviral effect on JEV replication in vitro, a series of experiments were performed. SCH 16 was added to JEV infected cell cultures at '0' hour post-infection and removed at 4 hourly time points up to 14 hours and the monolayers were further incubated for 48 hours at 37°C under 5% CO2. It was observed that there was complete inhibition of virus replication when SCH 16 was allowed to be in contact with infected cultures for more than 8 hours post-infection. However, when SCH16 was withdrawn at earlier time points there was no inhibition of virus replication as confirmed by the detection of viral antigen, viral RNA and infectious virus yield (Figure 3, Panels D to F).
Effect of SCH 16 on viral translation
To understand the probable action of SCH 16 on the viral replicative cycle and to study the extent of damage caused by the compound on the viral RNA that might result in the inhibition of viral events such as protein synthesis (translation), an in vitro translation experiment was carried out as described in materials and methods. RNA was extracted from drug treated (4 hours and 10 hours post infection) and untreated monolayers of JEV infected cells and subjected to Real Time PCR analysis to confirm the presence of JEV RNA. Subsequently, the viral RNA was subjected to in vitro translation. It was observed that RNA extracted from JEV infected cells treated with SCH 16 for 4 hours failed to translate into JEV proteins in vitro. On the contrary, viral RNA extracted from infected cells treated with SCH 16 at 10 hours as well as RNA from infected cells that were not treated with SCH 16 showed the presence of JEV proteins (Figure 4).
In vivo evaluation of compounds against JEV using mouse model
After ascertaining the in vivo non-toxic concentrations in preliminary experiments, the therapeutic potential of SCH 16 was evaluated in mice using intracerebral and intraperitoneal challenge routes. In the intracerebral challenge model, mice that were treated with 100 and 200 mg/kg body weight of SCH 16 showed no protection. However, it was interesting to note that all the mice that were treated with SCH 16 remained healthy up to day 6 post-infection without showing any apparent symptoms of JEV infection (data not presented). The symptoms started appearing in these mice from day 7 post-infection. There was a gradual progression of the symptoms and death occurred on day 9. On the other hand, untreated mice appeared sick by day 3 and succumbed by day 5. This suggests that there was a prolonged survival time of 3 days between the treated and untreated mice.
The prolonged survival time observed in the intracerebral challenge experiments prompted us to make use of a peripheral challenge model (JEV 50LD50) using a multiple dosage regimen wherein 200, 400 and 500 mg/kg body weight of SCH 16 was administered by oral route. It was observed that, there was 25% protection in the group of mice administered with 200 mg/kg body weight of SCH 16, 50% protection observed in the group that received 400 mg/kg body weight and complete protection was observed in the group that were given with 500 mg/kg body weight of SCH 16 (Figure 5). Mice that survived the challenge post treatment were sacrificed; brains harvested and subjected to virus isolation, detection of viral antigen and viral RNA. Viable virus could not be isolated from the brain tissue of these mice. Further, no viral antigen could be demonstrated in the brain smears by immunofluorescent staining using monoclonal antibodies to JEV. However, the RT-PCR products amplified from the brain homogenate suggested that viral RNA was present in the brain of animals that survived JEV infection following treatment with 400 and 500 mg/kg body weight of SCH 16.
There is currently no specific antiviral treatment available for Japanese encephalitis, West Nile and Dengue virus infections. Recently there has been renewed interest in the search for antiviral compounds active against a variety of viral infections. For instance, there are several reports describing the in vitro inhibitory effect of compounds such as ribavirin, mycophenolic acid, imino sugars, inhibitors of serine protease, RNA interference and non-steroidal anti-inflammatory drugs against flaviviruses [8–13]. N-Methylisatin-β-thiosemicarbazone (MIBT) was one of the first antiviral compounds to be discovered. It exhibits antiviral activity against a variety of RNA and DNA viruses [14–17]. Recent studies have demonstrated that thiosemicarbazone and Mannich bases of thiosemicarbazone derivatives exhibit anti-HIV activity in vitro [18–22]. Therefore this study was designed to investigate the antiviral property of isatin β thiosemicarbazone derivatives against JEV, WNV and Den-2 viruses.
In the present study, fourteen Mannich bases of MIBT derivatives were synthesized and evaluated for their ability to inhibit flaviviral replication. However, only one compound (SCH 16) showed antiviral activity against JEV and WNV in vitro with a therapeutic index of 5 and 16 respectively. This compound did not exhibit any virus inactivating property. SCH 16 (Figure 1) is a mannich base of N-Methylisatin-β-thiosemicarbazone possessing an isatin backbone with modifications made at the side chains. Chemically isatins are diketonic compounds. It has been earlier noted that, heteroaromatic thioamides containing N-substitution at more than one position per heterocyclic ring are worthy of investigation due to its increased antiviral property . It is therefore likely that the antiviral activity of SCH 16 may be due to the N substitution at the 8th position in the heterocyclic benzene ring and a NO2 group attached to the aromatic side chain.
Although SCH16 exhibited antiviral activity against WNV, we did not pursue further experiments with it since WNV is not a public health concern in India. In contrast, JEV is a major public health problem in India and hence we set about to investigate in detail the mechanism of antiviral activity of SCH 16 against JEV. Two crucial questions pertaining to the antiviral activity of SCH16 against JEV were addressed; (i) how long after virus infection can addition of drug be delayed in vitro in order to achieve inhibition of virus replication? and (ii) what is the minimum time required for SCH16 to exert its antiviral activity?. For this purpose we used an experimental approach similar to that described earlier by Baginiski et al and Lammarre et al [23, 24]. Our results showed that when the drug was added to infected cells at various time points post virus entry, neither viral antigen (Figure 3 Panel A & B) nor viral nucleic acid (Figure 3, Panel C) was detected up to 8 hours post infection. Beyond this time point however, viral antigen, nucleic acid and infectious virus was detectable in the cultures. Indeed viral antigen, viral RNA and virus yields were comparable to those obtained with untreated cells beyond the 8 hour time point thereby suggesting that SCH 16 did not inhibit normal cellular functions (Figure 3, Panels A to C). This suggests that the drug was not toxic to cells and did not inhibit the ability of cells to support virus replication at later time points. To ascertain the minimum time required for SCH16 to exert its antiviral activity, the compound was added at 2 hours post infection and removed at various time points post viral entry. The results revealed that, SCH 16 probably acted as an inhibitor of early protein synthesis. Had SCH 16 been an un-coating inhibitor or a polymerase inhibitor, the drug would have required a contact time of less than 4 hours to bring about its inhibitory effect. Similarly if it were a protease inhibitor the minimum contact period for SCH 16 to bring about inhibition of virus replication would have been greater than 8–10 hours. Since we observed that the minimum contact period of 8 hours was required for SCH16 to completely inhibit virus replication, it probably indicates that the drug is acting at the level of translation. Cooper et al  in an earlier study with vaccinia virus had demonstrated that the specific antiviral effect of MIBT was noted 6 hours post-infection thereby indicating inhibition of viral protein synthesis. In order to ascertain whether this was indeed also true for SCH 16 we adopted another approach to investigate the precise role of SCH 16 on translation events in JEV replication. We obtained RNA samples from the experiments that treated JEV infected monolayer's with SCH 16 for 4 hours and SCH 16 added at 10 hours post infection from infected cells treated with SCH 16 as well as cells that were untreated using identical extraction protocols. Subsequently we performed Real Time SYBR Green I PCR using JEV specific primers to confirm the presence of JEV RNA in samples obtained from both drug treated as well as untreated cells. The viral RNA thus obtained, was then subjected to in vitro translation experiments which clearly showed that there were no translation products obtained with RNA obtained from drug treated cells at 4 hours post infection (Figure 4, lane 3). On the contrary, RNA obtained from drug treated cells at 10 hours post infection (Figure 4, lane5) as well as RNA obtained from untreated cells at both 4 hours and 10 hours post infection (Figure 4, lanes 2 and 4). This result demonstrates that SCH16 is able to selectively suppress translation of JEV RNA at early time points in the life cycle. Similar observations have been made earlier by Ronen et al on other RNA virus  who investigated the inhibitory action of N-methyl isatin beta-diethylthiosemicarbazones on Moloney Leukemia virus replication.
The therapeutic potential of SCH 16 against JEV was evaluated in vivo in mice using the intracerebral and intraperitoneal challenge studies. The mice that were evaluated in the intracerebral challenge route did not show any protection although there was a delay in appearance of symptoms and death in drug treated mice. The lack of protection by this route may be due to (i) the direct introduction of large amount of infectious virus (50LD50) into the CNS which might have compromised the inhibitory action of SCH 16 and/or (ii) inability to achieve therapeutic concentrations of the drug in the brain either due to delay in the compound reaching the brain from the intraperitoneal compartment or poor penetration of the drug into the brain parenchyma. On the contrary, the drug treated mice challenged by the intraperitoneal route showed a dose dependent reduction in mortality, whilst all the untreated mice succumbed to the challenge with 50LD50 of JEV by day seven (Figure 5). Furthermore, neither viable virus nor viral antigen could be demonstrated in the brains of the mice that survived the challenge. However, viral RNA was detected by real-time RT-PCR in all the brain tissues. Since flavivirus RNA dependent RNA polymerases are active within three hours of viral entry this is not a surprise finding . Because, SCH 16 is primarily an early translation inhibitor, it appears that this drug does not interfere with RNA polymerization resulting in accumulation of viral RNA in the brains of drug treated mice that survived the challenge. Alternatively, SCH 16 treatment could have curtailed JEV replication in the periphery resulting in a very small amount of JEV entering the brain. Consequently the virus was unable to establish a productive infection in the brain and the presence of viral RNA could be as a result of residual virus in brains of mice that survived the challenge. In an experimental rat model, with post-encephalitic Parkinsonism induced by JEV infections [28, 29] it was observed that, administration of isatin improved the motor neuron activities significantly. Indeed, they attributed that the improvement in the motor weakness was probably due to the MAO inhibitory activity of isatin and suggested that isatin could possibly serve as a new therapeutic agent for Parkinsonism. However, these studies were not designed to address the antiviral action of isatin against JEV but aimed at investigating the neurotransmitter inhibitory effect. It may be argued therefore that the in vivo effect of SCH 16 against JEV noted in this study may also be attributed to the immunomodulating or neuroprotective property of SCH 16.
An intriguing observation in this study was the differential ability of SCH 16 to suppress JEV, WNV and Den-2 multiplication in vitro. It is difficult to hypothesize the differential antiviral property of SCH 16 noted against JEV and WNV in this study as they are structurally similar and we have used the same cell system (PS cells) for evaluating the drug. On the contrary, we used BHK 21 cells for assaying the antiviral activity of SCH 16 against Den-2 virus, which could have contributed to the lack of anti-Dengue activity of SCH 16. Protein synthesis consists of an intricate series of events requiring components that are too numerous to be encoded by viral genomes [30, 31]. It has been observed that Den-2 and other flaviviruses, such as WNV, yellow fever, JEV, and Kunjin viruses, are presumed to undergo cap-dependent translation [32, 33]. However, evidence exists that under certain conditions that inhibit cap dependent translation, Den-2 viruses can switch to more efficient cap independent translation. Further, mammalian cellular stress response and immune functions, such as the interferon antiviral response [34, 35], may compel viral translation by one mechanism over the other. Since we used PS cells for evaluation of JEV and WNV and BHK 21 cells for Den-2 it is possible that the translation pathway adopted by Den-2 against SCH 16 may be due to the presence of certain BHK 21 cell specific factors. However, strong experimental evidence is needed to support this hypothesis and it would be interesting to investigate whether SCH 16 is indeed a cap dependent translation inhibitor.
In conclusion, the findings of this study unequivocally demonstrate that SCH 16 has antiviral activity against JEV and WNV in vitro. Furthermore, SCH 16 was also found to completely inhibit JEV replication in vivo in a mouse model challenged peripherally with 50LD50 of the virus in a dose dependent manner. This necessitates further investigation into the pharmacokinetcis of the compound. Its moderate therapeutic index (TI = 5) may be a concern. However, further investigation on structure – activity relationships and appropriate modification in the aryl ring of the isatin moiety could provide more effective JEV-inhibitors with improved efficacy in future.
Materials and methods
Standard strains of JEV (P20778), Den-2 virus (P23085) and WNV (G22886) were obtained from National Institute of Virology (NIV), Pune, India.
Cells and animals
Aedes albopictus (C6/36) mosquito cell line and Porcine Stable kidney (PS) cells were maintained in Minimum Essential Medium (MEM) with 10% fetal calf serum while Baby Hamster Kidney (BHK-21) cells were maintained in Dulbecco's MEM with 10% fetal calf serum (NCCS, Pune, India). Random bred Swiss albino mice (4–5 week old) were obtained from Central Animal Research Facility, NIMHANS, Bangalore, India, and used for the in vivo evaluation. All animal experiments were conducted after obtaining permission from Institutional Animal Ethics Committee.
N-Methylisatinisatin-β-Thiosemicarbazone (MIBT) derivatives
Fourteen mannich bases of isatin-β-thiosemicarbazone derivatives (Table 1) were obtained from Dr. Sriram, Birla Institute of Technology and Science (BITS), Pilani, India. The compounds were synthesized by Schiff reaction. N, N-diethyl thiosemicarbazide was condensed with isatin in the presence of glacial acetic acid to form 1H-indole-2, 3-dione -3-N, N-diethyl thiosemicarbazone (Schiff base). The N-Mannich bases were further condensed using acidic imino group along with formaldehyde and various secondary amines to obtain isatin thiosemicarbazone derivatives. Ribavirin, which is a known inhibitor of flavivirus replication, was obtained from commercial sources (Sigma, USA) and used as a control drug in this study.
Cytotoxicity of Ribavirin and MIBT derivatives
Cytotoxicity of the antiviral compounds was evaluated using the Trypan blue exclusion assay . Briefly, PS and or BHK-21 cells grown to semi-confluence in 24-well plates were exposed to different concentrations of the compounds for 4 days at 37°C. Following this, the cells were harvested by trypsinization and re-suspended in 0.5 ml of MEM containing 10% FCS. A 100 μl of the cell suspension was mixed with 50 μl of 2.5% Trypan blue and the number of viable cells was enumerated using a hemocytometer. The concentration of compound that reduced cell growth by 50% was estimated as the 50% cytotoxic concentration (CC50). The effect of the compounds on cellular proliferation was also studied. Briefly, the drug treated cells and untreated cells were seeded at a rate of 2 × 104 cells per well into 24-well plates and allowed to proliferate for 3 days in MEM, containing 10% FCS. The proliferations of cells were monitored every day microscopically by recording signs of toxicity such as altered morphology presence or absence of vacuoles and/or dead cells.
Screening for inhibition of virus induced cytopathic effect in vitro
The antiviral activity assay of the Ribavarin and MIBT derivatives against JEV, Den-2 virus or WNV were screened in vitro using the cytopathic effect (CPE) inhibition assay carried out in a 96 well plate. Briefly, monolayers of PS and/or BHK-21 were inoculated with 100 μl of appropriate virus suspension containing 1 MOI of virus and adsorbed for two hours at 37°C. At the end of incubation period, the virus (JEV, Den-2 or WNV) was removed and the monolayers were rinsed with MEM to remove unbound virus. Doubling dilutions of different concentrations of Ribavirin and MIBT derivatives (beginning with CC50) were prepared in MEM, added to the monolayer (100 μl) and incubated at 37°C for 3 days under 5% CO2. The experiment was terminated when the virus control showed maximum CPE. The presence or absence of CPE was recorded microscopically every day and the plates were stained using crystal violet at the termination of experiment and compared with the untreated virus controls and drug controls. All the experiments were run in triplicates to ensure reproducibility.
Confirmation of antiviral activity by plaque reduction assay
The compounds that showed inhibition of virus replication in the CPE inhibition assay were further evaluated using plaque-reduction assay. Briefly, PS (4 × 104 cells/well) cells were grown to a confluent monolayer in a 24 well plate and infected with 100 μl of virus suspension containing 1 MOI of JEV and incubation was carried out for 2 hours at 37°C. At the end of adsorption, monolayers were rinsed with sterile PBS and 100 μl MEM containing varying concentrations of the compounds were added. The monolayer was then overlaid with maintenance medium containing 0.2% molten agarose (Sigma-Aldrich, USA). Appropriate controls were included in each run of the assay. Incubation was carried out at 37°C for 3 days. At the end of incubation period monolayers were fixed in 10% formal saline, the agarose was gently removed and the cells were stained using 1% crystal violet. Two independent observers counted the plaques using a hand lens. All the experiments were run in triplicates. Percentage inhibitions of plaques were determined using the formula given below.
The antiviral activity was expressed as 50% inhibitory concentration (IC50) of the compound, which is the concentration of the compound required to inhibit viral plaques by 50% as compared to virus control. The therapeutic potential and specificity of action was determined by calculating the Therapeutic Index (TI), which is the ratio of CC50 to IC50 (CC50/IC50) .
Understanding the mechanism of action of SCH 16 in relation to JEV replication
To understand the possible mechanism of action in relation to the replicative cycle of JEV, the compounds that showed 100% inhibition of viral plaques were evaluated by in vitro experiments detailed below.
Determining kinetics of JEV replication in PS cells
A 24 well plate containing sterile cover slips in each well was seeded with 4 × 104 cells/well and incubated at 37°C overnight. When the cells were a confluent monolayer, they were infected with JEV (MOI = 1) for 1 hour at 37°C. The monolayer was rinsed thoroughly with sterile PBS and replenished with medium containing 1% FCS. This time point was considered as '0' hour post-infection. Subsequently at 2, 4, 6, 8, 10, 12, 14, 16 and 24 hours post-infection, the medium was harvested to determine the amount of extracellular virus released into the supernatant. At each time point, the cover slip containing cells was also removed, fixed in chilled acetone and stained by Immunofluorescent Assay (IFA) using a monoclonal antibody to envelope protein of JEV to detect the cell bound antigen .
Understanding the kinetics of the antiviral activity of SCH 16
A 24 well plate was seeded with 4 × 104 cells/well and incubated at 37°C overnight. To this monolayer JEV was added (MOI = 1) and incubated for 1 hour at 37°C. At the end of adsorption, the virus was removed, the monolayer was rinsed 3 – 4 times using sterile PBS and replenished with MEM containing 1% FCS. This time point was considered as 0 hour post-infection. Starting from 0 hour time point, 76 ug/ml (IC50) of the compound was added at 2, 4, 6, 8, 10, 12, 14, 16, and 24 hours post-infection and incubated at 37°C. The supernatant fluid was harvested from the respective wells at 48 hours post-infection. The fluid was divided into two parts. One part was used to determine the virus yield in the supernatant fluid (TCID50/ml) and the second part of the fluid was used to detect the presence of soluble JEV antigen using an antigen capture ELISA described elsewhere . In order to detect cell bound antigen the cover slip cultures were fixed in chilled acetone for 30 minutes at 4°C and stained using monoclonal antibody to JEV (Clone F2C2) and anti-mouse IgG FITC conjugate by indirect IFA as described earlier. The cells in each well were treated with 750 μl of TRIzol (Invitrogen, USA) for RNA extraction and reverse transcription was carried out using cDNA archive kit (Applied Biosystems, USA) as described below.
Real Time PCR using Syber Green I chemistry
Detection of viral RNA was carried out by Real Time PCR using Syber Green I chemistry as described by Shu et al  with minor modifications. Briefly, a 120 base pair product of the PreM gene of JEV was amplified using the forward primer F1 (gga gcc atg aag ttg tca aat ttc) and reverse primer R1 (ttg ccc gga ccc aac at) based on the prototype standard strain of JEV (P20778) Gen Bank Ac.No.7080251.
A second set of experiments was designed to estimate the minimum time required for the compound to bring about complete inhibition of JEV replication. A 24 well plate was seeded with 4 × 104 cells/well in quadruplicates and incubated at 37°C overnight. Confluent PS monolayers were infected with JEV (MOI = 1) and adsorbed for 1 hour at 37°C. Following this, the monolayer was rinsed with sterile PBS and replenished with plain medium containing non-toxic concentration of SCH16. Control wells received plain medium. This time point was considered as '0' hour post-infection. Starting from 0 hour time point, medium containing the compound was removed at 0, 4, 8, 12, and 14 hours post-infection and replenished with MEM containing 1% FCS. At the end of 48 hours incubation, the fluid harvested from one of the quadruplicate set of wells, was evaluated for presence of extracellular virus by titration while soluble antigen was detected using an antigen capture ELISA described earlier. Cells in a second set of wells were trypsinised, re-suspended in maintenance medium and subjected to three freeze thaw cycles to release intracellular virus, which was quantitated by titration. Cells from the third set of wells were stained by an IFA to detect cell bound antigen. The cells in the fourth set of wells were treated with 750 μl of TRIzol (Invitrogen, USA) for RNA extraction and reverse transcription was carried out using cDNA archive kit (Applied Biosystems, USA).
Effect of SCH 16 on the translation of JEV
In order to understand the probable action of SCH 16 on the events of viral replication, an in vitro translation experiment was carried out using commercially available Transcend™ non-radioactive translation detection system and rabbit reticulocyte lysate kit (Promega, USA). A 24 well plate was seeded with PS cells (4 × 104/ml), incubated at 37°C for 18 to 24 hrs and the monolayer formed was adsorbed with JEV (MOI = 1) for 1 hour. The infected monolayer was rinsed with sterile PBS to remove the unbound virus. To one set of JEV infected monolayer cultures, SCH 16 at non-toxic concentration was added at '0' hour and incubated for 4 hours. Medium containing SCH 16 was removed at 4 post-infection and replenished. To a second set of monolayer cultures, SCH 16 at the same concentration was added at 10 hours post adsorption. The plates were further incubated for 48 hours at 37°C. Appropriate virus and cell controls were included in parallel to the test. At the end of incubation, the cells were treated with 750 μl of TRIzol and the viral RNA was extracted as described earlier. The viral RNA thus obtained, was divided in to two equal parts. One part was subjected to RT-PCR using JEV specific primers to confirm the presence of JEV RNA. The second part was subjected to in vitro translation carried out using a commercial kit (Promega, USA) and manufacturer's guidelines. Briefly, a 50 μl reaction containing 35 μl of rabbit reticulocyte lysate, 10 μl of nuclease free water, 1 μl of RNasin (40 U/μl), 1 μl of complete amino acid mixture (1 mM), 1 μl of Transcend ™ tRNA and 2 μl of RNA template was set up at 30°C and incubated for 60 minutes. After the completion of translation reaction, 1 ul of the product was subjected to SDS – PAGE, electroblotted on to a PVDF membrane, blocked with skimmed milk powder solution, reacted with JEV specific monoclonal antibody to visualize the bands.
In vivo evaluation of SCH 16 against JEV
Evaluation of non-toxic concentration of the compounds in mice
In order to determine the in vivo non-toxic concentrations, the compound SCH 16 (100, 200, 400 and 500 mg/kg body weight) were administered either per orally, or intraperitoneally into four different groups of 4 – 5 weeks old Swiss albino mice (n = 4). Two groups of mice served as normal controls that received plain medium per orally or intraperitoneally. All mice were observed for a period of 45 days for loss or gain in weight, and other evidences of toxicity as compared to the untreated normal mice.
In vivo evaluation of SCH 16 by intracerebral challenge
To determine the in vivo antiviral potential of SCH 16, three groups of mice (4 mice per group) were injected intracerebrally with 30 μl of virus suspension containing 50 LD50 of JEV. This was followed by intraperitoneal administration of SCH16 (100 and 200 mg/Kg body weight) into two groups of mice twice daily for 10 days. A third group of mice served as control animals that received virus intracerebrally and plain MEM intraperitoneally. Animals were monitored for the appearance of symptoms for JEV infections such as paralysis and death.
In vivo evaluation of SCH 16 by peripheral challenge
The therapeutic potential of SCH 16 was also evaluated using a peripheral challenge model wherein JEV (50LD50) was injected (200 μl) intraperitoneally into four groups of 4–5 weeks old mice (n = 4). Two hours later, each group received 30 μl of 1% sterile starch intracerebrally to facilitate virus entry into the brain. This was followed by oral administration of SCH 16 in a dose of 200, 400 or 500 mg/kg body weight twice daily into the three respective groups for 12 days. A fourth group of mice (n = 4) served as 'no drug controls' which received virus intraperitoneally, starch intracerebrally and plain MEM orally while a fifth group of mice (n = 4) served as sham controls and received MEM intraperitoneally and starch intracerebrally. Mice were observed every day for 20 days post-infection for the appearance of symptoms and death. At the end of the observation period the mice that survived the infection were sacrificed, brains harvested and subjected to JEV antigen detection by IFA, JEV nucleic acid detection by real-time PCR and virus isolation using shell vial method .
Ray Shi: Recent advances in Flavivirus Antiviral Drug Discovery and Vaccine Development. Recent Patents on Anti-Infective Drug Discovery 2006, 1: 45-55. 10.2174/157489106775244055
Simon Ho: HIV dynamics in vivo: implications for therapy. Nature Review Microbiology 2003, 13: 181-190. 10.1038/nrmicro772
Shi PY: Strategies for the identification of inhibitors of West Nile virus and other flaviviruses. Current Opinion in Investigational Drugs 2002, 3: 1567-1573.
Bauer DJ, Sadler PW: The structural activity relationships of the antiviral chemotherapeutic activity of isatin β-thiosemicarbazone. British Journal of Pharmacology 1960, 15: 101-110.
Glover V, Bhattacharya SK, Sandler M: Isatin – A new biological factor. Indian Journal of Experimental Biology 1991, 29: 1-5.
Bauer DJ: Clinical experience with the antiviral drug marboran (1-methylisatin3-thiosemicarbazone). Annals of New York Academy of Sciences 1965, 130: 110-117. 10.1111/j.1749-6632.1965.tb12545.x
Ronen D, Nir E, Teitz Y: Effect of N-methylisatin-β-4': 4'-diethylthiosemicarbazones on intracellular Moloney Leukemia virus constituents. Antiviral Research 1985, 5: 249-254. 10.1016/0166-3542(85)90029-4
Leyssen P, Balzarini J, De Clercq E, Neyts J: The predominant mechanism by which ribavirin exerts its antiviral activity in vitro against flaviviruses and paramyxoviruses is mediated by inhibition of IMP dehydrogenase. Journal of Virology 2005, 79: 1943-1947. 10.1128/JVI.79.3.1943-1947.2005
Diamond MS, Zachariah M, Harris E: Mycophenolic acid inhibits Dengue virus infection by preventing replication of viral RNA. Virology 2002, 304: 211-221. 10.1006/viro.2002.1685
Wu SF, Lee CJ, Lia CL, Dwek RA, Zitzmann N, Lin YL: Antiviral effects of an iminosugar derivative on flavivirus infections. Journal of Virology 2002, 76: 3596-3604. 10.1128/JVI.76.8.3596-3604.2002
Genesh VK, Muller N, Judge K, Luan CH, Padmanabhan R, Murthy KH: Identification and characterization of non-substrate based on inhibitors of the essential dengue and West Nile virus proteases. Bioorganic Medicinal Chemistry 2005, 13: 257-264. 10.1016/j.bmc.2004.09.036
Geiss BJ, Peirson TC, Diamond MS: Actively replicating West Nile Virus is resistant to cytoplasmic delivery of SiRNA. Virology Journal 2005, 2: 53. 10.1186/1743-422X-2-53
Chen CJ, Raung SL, Kuo MD, Wang Y-M: Suppression of Japanese encephalitis virus infection by non-steroidal anti-inflammatory drugs. Journal of General Virology 2002, 83: 1897-1905.
Logan JC, Fox MP, Morgan JH, Makohon AM, Pfau CJ: Arenavirus inactivation on contact with N-substituted isatin beta-thiosemicarbazones and certain cations. Journal of General Virology 1975, 28: 271-83.
Teiz Y, Ronnen D, Vansover A, Stematsky T, Riggs JL: Inhibition of human immunodeficiency virus by N-Methyl isatin β4':4' diethyl thiosemicarbazone and N-allyl isatin β4':4' diallylthiosemicarbzone. Antiviral Research 1994, 24: 305-314. 10.1016/0166-3542(94)90077-9
Levinson W, Woodson B, Jackson J: Inactivation of Rous sarcoma virus on contact with N-Ethyl Isatin beta thiosemicarbazone. Nature new biology 1971, 232: 116-118. 10.1038/232116a0
Woodson B, Joklik WK: The inhibition of Vaccinia virus multiplication by Isatin-beta-thiosemicarbazone. Proceedings of National Academy of Sciences USA 1965, 54: 946-953. 10.1073/pnas.54.3.946
Pandeya SN, Yogeeswari P, Sriram D, de Clercq E, Pannecouque C, Witvrouw M: Synthesis and screening for anti-HIV activity of some N-Mannich bases of isatinderivatives. Chemotherapy 1999, 4: 192-6. 10.1159/000007182
Sriram D, Yogeeswari P, Srichakravarty N, Bal TR: Synthesis of stavudine amino acid ester prodrugs with broad-spectrum chemotherapeutic properties for the effective treatment of HIV/AIDS. Bioorganic Medicinal Chemistry Letters 2004,8,14(5):1085-1087. 10.1016/j.bmcl.2004.01.007
Sriram D, Bal TR, Yogeeswari P: Aminopyrimidinimino isatin analogues: Design of novel nonnucleoside HIV-1 reverse transcriptase inhibitors with broadspectrum chemotherapeutic properties. Journal of Pharmacy and Pharmaceutical Sciences 2005, 8: 565-577.
Sriram D, Yogeeswari P, Meena K: Synthesis of anti-HIV and anti-tubercular activities of isatin derivatives. Pharamzie 2006, 61: 274-277.
Bal TR, Anand B, Yogeeshawri P, Sriram D: Synthesis and evaluation of anti-HIV activity of isatin β-thiosemicarbazone derivatives. Bioorganic Medicinal Chemistry Letters 2005, 15: 4451-4455. 10.1016/j.bmcl.2005.07.046
Baginiski SB, Pavear DC, Seipel M, Chang Sun SC, Benetatos CA, Chunduru SK, Rice CM, Collett MS: Mechanism of action of a Pestivirus antiviral compound. Proceedings of National Academy of Sciences 2000, 97: 7981-7986. 10.1073/pnas.140220397
Lamarre D, Croteau G, Wardrop E, Bourgon L, Thibeault D, Clouette C, Vaillancourt M, Cohen E, Pargelis C, Yoakim C, Anderson PC: Antiviral properties of Palinavir, a potent inhibitor of the Human Immunodeficiency virus type-1 protease. Antimicrobial Agents Chemotherapy 1997, 41: 965-971.
Cooper JA, Moss B, Katz E: Inhibition of Vaccinia virus late protein synthesis by isatin thiosemicarbazone: characterization and in vitro translation of viral mRNA. Journal of Virology 1979, 96: 381-392. 10.1016/0042-6822(79)90096-5
Ronen DL, Sherman S, Bar-nun , Teitz Y: N-Methyl-β-4',4'-diethylthiosemicarbazone, an inhibitor of Moloney Leukemia Virus protein production: Characterization and in vitro translation of viral mRNA. Antimicrobial Agents Chemotherapy 1987, 31: 1798-1802.
Gubler DJ, Kuno G, Markoff L: Flaviviruses. In Fields Virology. 5th edition. Philadelphia: Lippincot Willims and Wilkins; 2007:1153-1225.
Ogata A, Hamaue N, Terado M, Minami M, Nagashima K, Tashiro K: Isatin, an endogenous MAO inhibitor, improves bradykinesia and Dopamine levels in rat model of Parkinson's disease induced by Japanese encephalitis virus. Journal of Neurological Sciences 2003, 206: 79-83. 10.1016/S0022-510X(02)00342-8
Hamaue N, Minami M, Terado m, Hirafuji M, Endo T, Machida M, Heroshige T, Ogata A, Tashiro K, Saito H, Parvez SH: Comparative study of the effects of isatin, an endogenous MAO-inhibitor, and seleginine on bradykinasia and dopamine levels in a rat model Parkinson's disease induced by the Japanese encephalitis virus. Neurotoxicology 2004, 25: 205-213. 10.1016/S0161-813X(03)00100-1
Brown DM, Kauder SE, Cornell CT, Jang GM, Racaniello VR, Semler BL: Cell-dependent role for the poliovirus 3' noncoding region in positive-strand RNA synthesis. Journal of Virology 2004, 78: 1344-1351. 10.1128/JVI.78.3.1344-1351.2004
Dobrikova E, Florez P, Bradrick S, Gromeier M: Activity of a type 1 picornavirus internal ribosomal entry site is determined by sequences within the 3' nontranslated region. Proceedings of National Academy of Sciences, USA 2003, 100: 15125-15130. 10.1073/pnas.2436464100
Edgil DM, Diamond S, Holden KL, Paranjape SM, Harris E: Differences in cellular infection among dengue virus type 2 strains correlate with efficiency of translation. Virology 2003, 317: 275-290. 10.1016/j.virol.2003.08.012
Edgil D, Polaecek C, Harris E: Dengue viruses utilize a novel strategy for translation initiaition when cap-dependent translation is inhibited. Journal of Viology 2006, 80: 2976-2986. 10.1128/JVI.80.6.2976-2986.2006
Gil J, Alcami J, Esteban M: Induction of apoptosis by double stranded-RNA-dependent protein kinase (PKR) involves the alpha subunit of eukaryotic translation initiation factor 2 and NF-κ-B. Molecular Cell Biology 1999, 19: 4653-4663.
Egloff MP, Benarroch D, Selisko B, Romette JL, Canard B: An RNA cap (nucleoside-2_-O-)-methyltransferase in the flavivirus RNA polymerase NS5: crystal structure and functional characterization. EMBO Journal 2002, 21: 2757-2768. 10.1093/emboj/21.11.2757
Crance JM, Scarmozzino N, Jouan A, Garin D: Interferon, Ribavirin, 6-Azauridine and Glycyrrhizin: antiviral compounds active against pathogenic flavivirus. Antiviral Research 2003, 57: 73-79. 10.1016/S0166-3542(02)00185-7
Briolant S, Garin D, Scaramozzino N, Jouan A, Crance JM: In vitro inhibition of Chikungunya and Semliki forest virus replication by antiviral compounds: Synergistic effect of interferon-α and ribavirin combination. Antiviral Research 2004, 61: 111-117. 10.1016/j.antiviral.2003.09.005
Desai A, Ravi V, Guru SC, Shankar SK, Kaliaperumal VG, Chandramuki A, Gourie-Devi M: Detection of autoantibodies to neural antigens in the CSF of Japanese encephalitis patients and co-relation of findings with the outcome. Journal of Neurological Sciences 1994, 51: 1-8.
Whitby K, Pierson TC, Geiss B, Lane K, Engle M, Zhou Y, Doms RW, Diamond MS: Castanospermine, a potent inhibitor of dengue virus infection in vitro and in vivo . Journal of Virology 2005, 79: 8698-706. 10.1128/JVI.79.14.8698-8706.2005
Shu PY, Chang SF, Kuo YC, Yueh YY, Chien LJ, Sue CL, Lin TH, Huang JH: Development of group and serotype specific one-step Syber Green-I based real time reverse transcription PCR assay for Dengue virus. Journal of Clinical Microbiology 2003, 41: 2408-2416. 10.1128/JCM.41.6.2408-2416.2003
Rafique A, Tahir , Goyal SM: Rapid detection of pseudorabies virus by shell vial technique. Journal of veterinary diagnostic investigation 1995, 7: 173-176.
The authors thank Mr. Sunil Gowekar, research scholar, Department of Neurovirology, NIMHANS, Bangalore, for making the computer generated structure of SCH 16
The authors declare that they have no competing interests.
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Sebastian, L., Desai, A., Shampur, M.N. et al. N-methylisatin-beta-thiosemicarbazone derivative (SCH 16) is an inhibitor of Japanese encephalitis virus infection in vitro and in vivo. Virol J 5, 64 (2008) doi:10.1186/1743-422X-5-64
- Antiviral Activity
- West Nile Virus
- Japanese Encephalitis Virus
- Mannich Base
- Japanese Encephalitis Virus