Multicolor bioluminescence boosts malaria research: Quantitative dual-color assay and single-cell imaging in Plasmodium falciparum parasites: Quantitative dual-color assay and single-cell imaging in Plasmodium falciparum parasites

  • Luca Cevenini
  • , Grazia Camarda
  • , Elisa Michelini
  • , Giulia Siciliano
  • , Maria Maddalena Calabretta
  • , Roberta Bona
  • , T. R.Santha Kumar
  • , Andrea Cara
  • , Bruce R. Branchini
  • , David A. Fidock
  • , Aldo Roda
  • , Pietro Alano

Research output: Contribution to journalArticlepeer-review

53 Citations (Scopus)

Abstract

New reliable and cost-effective antimalarial drug screening assays are urgently needed to identify drugs acting on different stages of the parasite Plasmodium falciparum, and particularly those responsible for human-to-mosquito transmission, that is, the P. falciparum gametocytes. Low Z′ factors, narrow dynamic ranges, and/or extended assay times are commonly reported in current gametocyte assays measuring gametocyte-expressed fluorescent or luciferase reporters, endogenous ATP levels, activity of gametocyte enzymes, or redox-dependent dye fluorescence. We hereby report on a dual-luciferase gametocyte assay with immature and mature P. falciparum gametocyte stages expressing red and green-emitting luciferases from Pyrophorus plagiophthalamus under the control of the parasite sexual stage-specific pfs16 gene promoter. The assay was validated with reference antimalarial drugs and allowed to quantitatively and simultaneously measure stage-specific drug effects on parasites at different developmental stages. The optimized assay, requiring only 48 h incubation with drugs and using a cost-effective luminogenic substrate, significantly reduces assay cost and time in comparison to state-of-the-art analogous assays. The assay had a Z′ factor of 0.71 ± 0.03, and it is suitable for implementation in 96- and 384-well microplate formats. Moreover, the use of a nonlysing d-luciferin substrate significantly improved the reliability of the assay and allowed one to perform, for the first time, P. falciparum bioluminescence imaging at single-cell level.
Original languageEnglish
Pages (from-to)8814-8821
Number of pages8
JournalAnalytical Chemistry
Volume86
Issue number17
DOIs
Publication statusPublished - 2 Sept 2014

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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