Development of a Real-Time Cell Analysing (RTCA) method as a fast and accurate screen for the selection of chikungunya virus replication inhibitors

• Authors: Suria Marlina, University of Malaya; Meng-Hooi Shu, University of Malaya; Sazaly AbuBakar, University of Malaya; Keivan Zandi, Emory University
• Journal Title: Parasites and Vectors
• Volume: Volume 8, Number 1
• Publisher: BioMed Central | 2015-11-09, Pages 579-579
• Type of Work: Article | Final Publisher PDF
• Publisher DOI: http://doi.org/10.1186/s13071-015-1104-y
• Subjects: Biology, Microbiology; Health Sciences, Public Health
• Keywords: Science & Technology; Life Sciences & Biomedicine; Parasitology; Tropical Medicine; Real-time cell analysis; Cytopathogenicity; Antiviral screening; Chikungunya; Ribavirin; TECHNOLOGY

Abstract

Background: The xCELLigence real-time cell analysis (RTCA) system is an established electronic cell sensor array. This system uses microelectronic biosensor technology that is verified for real-time, label-free, dynamic and non-offensive monitoring of cellular features, including detection of viral cytopathic effect (CPE). Screening viral replication inhibitors based on presence of CPE has been applied for different viruses, including chikungunya virus (CHIKV). However, most CPE-based methods, including MTT and MTS assays, do not provide information on the initiation of CPE nor the changes in reaction rate of the virus propagation over time. Therefore, in this study we developed an RTCA method as an accurate and time-based screen for antiviral compounds against CHIKV. Methods: CHIKV-infected Vero cells were used as an in vitro model to establish the suitability of the RTCA system as a quantitative analysis method based on the induction of CPE. We also performed an MTS assay as a CPE-based conventional method. Experimental assays were carried out to evaluate the optimal seeding density of the Vero cells, cytotoxicity of the tested compounds, titration of CHIKV and the antiviral activity of ribavirin, which has been reported as an effective compound against CHIKV in vitro replication. Results: The optimal time point for viral inoculation was 18 h after seeding the cells. We determined that the maximum non-toxic dose (MNTD) of ribavirin was 200 μg/ml for Vero cells. Regarding the dynamic monitoring of Vero cell properties during antiviral assay, approximately 34 h post-infection, the normalised Cell Index (CI) values of CHIKV-infected Vero cells started to decrease, while the vehicle controls did not show any significant changes. We also successfully showed the dose dependent manner of ribavirin as an approved in vitro inhibitor for CHIKV through our RTCA experiment. Conclusion: RTCA technology could become the prevailing tool in antiviral research due to its accurate output and the opportunity to carry out quality control and technical optimisation.