Effect of fluorescent dyes on in vitro-differentiated, late-stage Plasmodium falciparum gametocytes
- PMID: 25267675
- PMCID: PMC4249569
- DOI: 10.1128/AAC.03772-14
Effect of fluorescent dyes on in vitro-differentiated, late-stage Plasmodium falciparum gametocytes
Abstract
Plasmodium falciparum gametocytes are not associated with clinical symptoms, but they are responsible for transmitting the pathogen to mosquitoes. Therefore, gametocytocidal interventions are important for malaria control and resistance containment. Currently available drugs and vaccines are not well suited for that purpose. Several dyes have potent antimicrobial activity, but their use against gametocytes has not been investigated systematically. The gametocytocidal activity of nine synthetic dyes and four control compounds was tested against stage V gametocytes of the laboratory strain 3D7 and three clinical isolates of P. falciparum with a bioluminescence assay. Five of the fluorescent dyes had submicromolar 50% inhibitory concentration (IC50) values against mature gametocytes. Three mitochondrial dyes, MitoRed, dihexyloxacarbocyanine iodide (DiOC6), and rhodamine B, were highly active (IC(50)s < 200 nM). MitoRed showed the highest activity against gametocytes, with IC(50)s of 70 nM against 3D7 and 120 to 210 nM against clinical isolates. All compounds were more active against the laboratory strain 3D7 than against clinical isolates. In particular, the endoperoxides artesunate and dihydroartemisinin showed a 10-fold higher activity against 3D7 than against clinical isolates. In contrast to all clinically used antimalarials, several fluorescent dyes had surprisingly high in vitro activity against late-stage gametocytes. Since they also act against asexual blood stages, they shall be considered starting points for the development of new antimalarial lead compounds.
Copyright © 2014, American Society for Microbiology. All Rights Reserved.
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References
-
- WHO. 2013. World malaria report. WHO Global Malaria Programme, Geneva, Switzerland: http://www.who.int/iris/bitstream/10665/97008/1/9789241564694_eng.pdf Accessed 20 March 2014.
-
- Aguilar R, Magallon-Tejada A, Achtman AH, Moraleda C, Joice R, Cistero P, Li Wai Suen CS, Nhabomba A, Macete E, Mueller I, Marti M, Alonso PL, Menendez C, Schofield L, Mayor A. 2014. Molecular evidence for the localization of Plasmodium falciparum immature gametocytes in bone marrow. Blood 123:959–966. 10.1182/blood-2013-08-520767. - DOI - PMC - PubMed
-
- Gates B. 2007. Malaria Forum keynote address. http://www.gatesfoundation.org/media-center/speeches/2007/10/melinda-fre... Accessed 20 March 2014.
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