Multiplexed multicolor antiviral assay amenable for high-throughput research

被引:2
作者
Li, Li-Hsin [1 ,2 ]
Chiu, Winston [1 ]
Huang, Yun-An [3 ,4 ]
Rasulova, Madina [5 ]
Vercruysse, Thomas [5 ,6 ,8 ]
Thibaut, Hendrik Jan [5 ]
ter Horst, Sebastiaan [1 ,7 ,9 ]
Rocha-Pereira, Joana [1 ]
Vanhoof, Greet
Borrenberghs, Doortje
Goethals, Olivia
Kaptein, Suzanne J. F. [1 ]
Leyssen, Pieter [1 ]
Neyts, Johan [1 ]
Dallmeier, Kai [1 ,2 ]
机构
[1] Katholieke Univ Leuven, Dept Microbiol Immunol & Transplantat, Lab Virol & Chemotherapy, Rega Inst, Leuven, Belgium
[2] Mol Vaccinol & Vaccine Discovery Grp, Leuven, Belgium
[3] Katholieke Univ Leuven, Lab Circuit Neurosci, Res Grp Neurophysiol, Dept Neurosci, Leuven, Belgium
[4] Vlaams Inst Biotechnol, Neuroelect Res Flanders NERF, Leuven, Belgium
[5] Katholieke Univ Leuven, Translat Platform Virol & Chemotherapy TPVC, Lab Virol & Chemotherapy, Dept Microbiol Immunol & Transplantat,Rega Inst, Leuven, Belgium
[6] Janssen Pharmaceut, Janssen Therapeut Discovery, Nv Beerse, Belgium
[7] Janssen Pharmaceut, Janssen Global Publ Hlth, Nv Beerse, Belgium
[8] AstriVax, Heverlee, Belgium
[9] Cerba Res, Rotterdam, Netherlands
关键词
SUPERINFECTION EXCLUSION; VIRUS-REPLICATION; FLUORESCENT PROTEINS; SELECTIVE INHIBITOR; DENGUE VIRUS; ZIKA; STRATEGIES; INFECTION; FUSION; SCREEN;
D O I
10.1038/s41467-023-44339-z
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
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.
引用
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页数:15
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