Abstract
Large-scale screening of antiviral compounds that target dengue virus life cycle requires a robust cell-based assay that is rapid, easy to conduct, and sensitive enough to be able to assess viral infectivity and cell viability so that antiviral efficacy can be measured. In this chapter we describe a method that uses high-content imaging to evaluate the in vitro antiviral efficacy in a modification to the cell-based flavivirus immunodetection (CFI) assay that was described previously in Wang et al. (Antimicrob Agents Chemother 53(5):1823–1831, 2009).
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Acknowledgements
This work was supported by the National Medical Research Council, Singapore (www.nmrc.gov.sg), under grant NMRC/1315/2011 to SGV and a Duke-NUS Graduate Medical School start-up grant to MK and SGV.
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Tan, K.H., Ki, K.C.W., Watanabe, S., Vasudevan, S.G., Krishnan, M. (2014). Cell-Based Flavivirus Infection (CFI) Assay for the Evaluation of Dengue Antiviral Candidates Using High-Content Imaging. In: Padmanabhan, R., Vasudevan, S. (eds) Dengue. Methods in Molecular Biology, vol 1138. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-0348-1_7
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DOI: https://doi.org/10.1007/978-1-4939-0348-1_7
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