- Viral cytopathic effects can be studied with cytotoxicity/viability assays and used for the screening of virucidial drugs based on wild type viruses
- Using microplate readers for antiviral assays increases throughput and facilitates replicate measurements
- The study of viral cytopathic effects offers a fast and cheap method for early phase drug screening
The development of virucidal drugs requires the screening of compound libraries to assess their impact on viral cytopathic effects and viral replication1. Plaque counting remains the gold standard for evaluating the efﬁcacy of antiviral compounds, however, this process is very labour intensive and time consuming. Measuring a reduction in plaque formations is therefore only used to evaluate compounds that have already been identiﬁed as virus-speciﬁc inhibitors by other means such as their impact on the viral cytopathic effect2.
Here we describe the use of BMG LABTECH’s CLARIOstar® Plus microplate reader to carry out a high-throughput antiviral screen based on the inhibition of a viral cytopathic effect using commercially available cell-based assays such as the CellTiter-Glo® luminescent cell viability assay and CellTox™ Green ﬂuorescent cell cytotoxicity assay. Both CellTiter-Glo® and CellTox™ Green assays provide a very robust, easy to use assay platform for the high-throughput screening of viral cytopathic effects. Thereby, molecules with antiviral activity against viruses such as SARS-CoV-2 and RSV that cause a viral cytopathic effect in infected cells can be identiﬁed.
The CellTox™ Green cytotoxicity assay utilizes a cell membrane impermeable dye, which is only able to enter non-viable cells where it binds to DNA and becomes ﬂuorescent. This assay is not activity-based; the ﬂuorescent signal is proportional to the number of dead cells in culture and thereby to the viral cytopathic effect. CellTiter-Glo® is a viability assay based on the quantiﬁcation of ATP. Metabolically active cells provide ATP which is used to convert Luciferin to Oxyluciferin and light by the Ultra-Glo® Luciferase. Viral cytopathic effects can be assessed by the reduction of metabolic activity and decrease of the luminescence signal.
Materials & Methods
- NuncTM MicroWell™ 384 well, black, clear bottom (Thermo Fisher, # 142761), for FI
- 384 well, white, clear bottom, PS treated plates (Corning®#CLS3765), for Lumi
- Echo® 525 liquid handler (Labcyte)
- Vero-E6 cells
- RSV virus stock (2x107/mL)
- SARS-CoV-2 virus stock (1.5x107/mL)
- CellTiter-Glo® luminescent cell viability assay kit (Promega #G7570)
- CellTox™ Green ﬂuorescent cell cytotoxicity assay (Promega # G8741)
- CLARIOstar Plus microplate reader (BMG LABTECH)
For the viral cytopathic effect assay, 25 nL of each drug was spotted into 384 well plates using the Echo liquid handler and 50 µl of Vero-E6 cell suspension (3,000 cells per well) were added to obtain a ﬁnal drug concentration of 5 µM. DMSO was used as a control. Following a 24 h incubation the cells were infected with 5 µL of RSV or SARS-CoV-2 virus dilution which equals a multiplicity of infection (MOI) of 0.1. Infected cells were taken out of the incubator at 72 h post infection and were analysed for viral cytopathic effects by measuring cell cytotoxicity using CellTox™ Green or cell viability using CellTiter-Glo® on the CLARIOstar Plus plate reader.
|CellTox™ Green fluorescent cell cytotoxicity assay|
|Optic settings||Fluorescence, endpoint, bottom optic|
|General settings||Monochromator settings||Excitation 483-14 |
|Focal height||2.5 mm|
|Number of flashes per well||20|
|Settling time (S)||0.1|
|CellTiter-Glo® luminescent viability assay|
|Optic settings||Luminescence, endpoint, top optic|
|General settings||Filters No fi lter||No filter|
|Focal height||13.5 mm|
|Interval time (S)||0.25, normalised to 1|
Results & Discussion
The viral cytopathic effect of SARS-CoV-2 and RSV on Vero-E6 cell cultures was assessed with a CellToxTM Green and a CellTiter-Glo® assay, respectively, 72 h post infection. Fig. 3 shows the obtained data from the CellToxTM green assay performed on Vero-E6 cells infected with SARS-CoV-2. Drugs were classiﬁed as potential hits if they reduced the viral cytopathic effect below 90% (see green box) compared to the control samples, which were treated with DMSO and set to 1.
The graph below (ﬁg. 4) shows the results of the CellTiter-Glo® assay. In contrast to the CellToxTM Green assay, the luminescence signal represents cell viability and thus virucidal drugs are expected to lead to an increase in signal. Here, a viability of above 1.1 (=110%) in comparison to the DMSO control (set to 1) was deﬁned as a threshold to identify potential drugs inhibiting viral cytopathic effect.
The use of cytotoxicity/viability assays to study the impact of potential virucidal drugs on viral cytopathic effects offers several advantages. First, wild type viruses can be applied since the evaluation takes place indirectly through the assessment of viral cytopathic effect, thereby eliminating the need for additional labelling or modiﬁcation steps. Furthermore, running and evaluating luminescent and ﬂuorescent assays on microplate readers like the CLARIOstar Plus, enables large libraries to be screened in high throughput and in far less time compared to traditional applications.
Microplate readers offer the ideal measurement platform for the identiﬁcation of drugs, which effectively inhibit viral cytopathic effect allowing for the rapid elimination of 1000s of compounds which show no speciﬁc inhibition.
This approach has been used successfully by the University of Belfast to screen existing drugs and drug combinations.
1. Touret, F. et al. In vitro screening of a FDA approved chemical library reveals potential inhibitors of SARS-CoV-2 replication. Sci Rep. doi: 10.1038/s41598-020-70143-6 (2020).
2. Baer, A and Kehn-Hall, K. Viral concentration determination through plaque assays: using traditional and novel overlay systems. doi:10.3791/52065 (2014)