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Activity of clinically relevant antimalarial drugs on Plasmodium falciparum mature gametocytes in an ATP bioluminescence “transmission blocking”assay
Malaria Journalvolume 11, Article number: P7 (2012)
Current anti-malarial drugs have been selected on the basis of their activity against the symptom-causing asexual blood stage of the parasite. How many of these drugs also target gametocytes, the sexual stage responsible for disease transmission, remains unknown. Blocking transmission is one of the main strategies in the eradication agenda and implies the identification of new molecules active against gametocytes. However, so far, the main limitation for measuring the effect of molecules against mature gametocytes on a large scale is the lack of a standardized and reliable method. Here we provide an efficient method to produce and purify mature gametocytes in vitro. Based on this new procedure, we developed a robust, affordable and sensitive ATP bioluminescence-based assay. We then assessed the activity of 17 gold-standard anti-malarial drugs on Plasmodium late stage gametocytes.
Materials and methods
Difficulties in producing large amounts of gametocytes have limited progress in the development of malaria transmission blocking assays. We improved the method established by Ifediba and Vanderberg to obtain viable, mature gametocytes en masse. We designed an assay to determine the activity of antimalarial drugs based on the intracellular ATP content of purified stage IV-V gametocytes after 48h of drug exposure in 96/384-well microplates. Measurement of drug activity on asexual stages and cytotoxicity on HepG2 cells were also obtained to estimate the specificity of the active drugs. The methodology is fully described at Lelièvre et al.
The assay was validated by comparing traditional microscopy examination with the ATP bioluminescence assay using a set of 6 anti-plasmodial drugs. We obtained comparable IC50 values with both methods.
After validation, 16 clinically relevant antimalarial drugs presenting different mechanism of action were tested. Only epoxomicin (0.42 nM) and methylen blue (0.49 µM) showed IC50 values in the range of nanomolar.
Epoxomicin is an inhibitor of proteasome activity, exerting a toxic effect on the parasite, but as this function is also essential in mammalian cells its cytotoxicity is of concern.
Primaquine has been reported to destroy the inner structure of P.falciparum mitochondria. It is assumed that primaquine activity depends on the formation of metabolites, more active than the parent compound. This 8-aminoquinoline has long been known to reduce the prevalence of circulating gametocytes in the peripheral bloodstream of patients. Due to the absence of the active metabolites involved in its mechanism of action, primaquine remains inactive in vitro (20.9 µM). Methylene blue (MB) was identified as a specific inhibitor of P. falciparum glutathione reductase, blocking heme polymerization within the food vacuole. Our study evaluated for the first time the IC50 of MB on stage IV-V gametocytes and HepG2 cell line (6.52 µM), founding a good activity but quite high cytotoxicity.
The work described represents another significant step  towards determination of activity of new molecules on mature gametocytes with an automated assay suitable for medium/high-throughput screening. Considering that the biology of the sexual stages is very different from asexual forms, screening of compound libraries would allow us to discover novel anti-malarial drugs to target gametocyte-specific metabolic pathways.
Lelievre J, Almela MJ, Lozano S, Miguel C, Franco V, Leroy D, Herreros E: Activity of clinically relevant antimalarial drugs on Plasmodium falciparum mature gametocytes in an ATP bioluminescence “transmission blocking” assay. PLoS One. 7: e35019-
Adjalley SH, Johnston GL, Li T, Eastman RT, Ekland EH, Eappen AG, Richman A, Sim BK, Lee MC, Hoffman SL, Fidock DA: Quantitative assessment of Plasmodium falciparum sexual development reveals potent transmission-blocking activity by methylene blue. Proc Natl Acad Sci U S A. 2011, 108: E1214-1223. 10.1073/pnas.1112037108.
Joël Lelièvre, Maria Jesus Almela contributed equally to this work.