Multiplexed multicolor antiviral assay amenable for high-throughput research

被引:0
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作者
Li-Hsin Li
Winston Chiu
Yun-An Huang
Madina Rasulova
Thomas Vercruysse
Hendrik Jan Thibaut
Sebastiaan ter Horst
Joana Rocha-Pereira
Greet Vanhoof
Doortje Borrenberghs
Olivia Goethals
Suzanne J. F. Kaptein
Pieter Leyssen
Johan Neyts
Kai Dallmeier
机构
[1] Laboratory of Virology and Chemotherapy,KU Leuven Department of Microbiology, Immunology and Transplantation, Rega Institute
[2] Molecular Vaccinology and Vaccine Discovery group,KU Leuven Department of Neuroscience, Research Group Neurophysiology
[3] Laboratory for Circuit Neuroscience,Vlaams Instituut voor Biotechnologie
[4] Neuro-Electronics Research Flanders (NERF),KU Leuven Department of Microbiology, Immunology and Transplantation, Rega Institute, Laboratory of Virology and Chemotherapy
[5] Translational Platform Virology and Chemotherapy (TPVC),Janssen Therapeutics Discovery
[6] Janssen Pharmaceutica,Janssen Global Public Health
[7] Janssen Pharmaceutica,undefined
[8] AstriVax,undefined
[9] Cerba Research,undefined
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摘要
To curb viral epidemics and pandemics, antiviral drugs are needed with activity against entire genera or families of viruses. Here, we develop a cell-based multiplex antiviral assay for high-throughput screening against multiple viruses at once, as demonstrated by using three distantly related orthoflaviviruses: dengue, Japanese encephalitis and yellow fever virus. Each virus is tagged with a distinct fluorescent protein, enabling individual monitoring in cell culture through high-content imaging. Specific antisera and small-molecule inhibitors are employed to validate that multiplexing approach yields comparable inhibition profiles to single-virus infection assays. To facilitate downstream analysis, a kernel is developed to deconvolute and reduce the multidimensional quantitative data to three cartesian coordinates. The methodology is applicable to viruses from different families as exemplified by co-infections with chikungunya, parainfluenza and Bunyamwera viruses. The multiplex approach is expected to facilitate the discovery of broader-spectrum antivirals, as shown in a pilot screen of approximately 1200 drug-like small-molecules.
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