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Multiplexed multicolor antiviral assay amenable for high-throughput research.

Li-Hsin LiWinston ChiuYun-An HuangMadina RasulovaThomas VercruysseHendrik-Jan ThibautSebastiaan Ter HorstJoana Rocha-PereiraGreet VanhoofDoortje BorrenberghsOlivia GoethalsSuzanne J F KapteinPieter LeyssenJohan NeytsKai Dallmeier
Published in: Nature communications (2024)
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.
Keyphrases
  • high throughput
  • single cell
  • small molecule
  • zika virus
  • high resolution
  • protein protein
  • dengue virus
  • genetic diversity
  • randomized controlled trial
  • cell therapy
  • drug induced
  • clinical trial
  • artificial intelligence