Open Access

Anti-malarial drugs: how effective are they against Plasmodium falciparum gametocytes?

  • Christopher L Peatey1, 2,
  • Didier Leroy3,
  • Donald L Gardiner1, 4 and
  • Katharine R Trenholme1, 5Email author
Contributed equally
Malaria Journal201211:34

https://doi.org/10.1186/1475-2875-11-34

Received: 10 October 2011

Accepted: 6 February 2012

Published: 6 February 2012

Abstract

Background

Recent renewed emphasis on the eradication of malaria has highlighted the need for more tools with which to achieve this ambitious goal. One high priority area is the need to determine the gametocytocidal activity of both currently used anti-malarial drugs and those in the development pipeline. However, testing the activity of compounds against Plasmodium falciparum gametocytes is technically challenging both in vivo and in vitro.

Methods

Here the use of a simple robust assay to screen a panel of currently used and experimental anti-malarial drugs against mature P. falciparum gametocytes is described.

Results

Eight of 44 compounds tested reduced gametocyte viability by at least 50% and three showed IC50 values in nM range.

Conclusions

There is a need to identify new compounds with activity against late stage gametocytes and the information provided by this in vitro assay is a valuable first step, which can guide future clinical studies.

Keywords

Plasmodium falciparum Gametocyte Anti-malarial drugs

Background

Gametocytes are the sexual stage of the malaria parasite, which develop in red blood cells and are essential for transmission to the mosquito vector. It has long been recognized that patients treated for malaria should be cleared of gametocytes in order to prevent them transmitting the infection to others [1]. This is particularly challenging in the case of Plasmodium falciparum infections as gametocytes of this species have a much longer lifespan than asexual stages. Late-stage gametocytes (stages IV-V) are more resistant to anti-malarial drugs and metabolic inhibitors [2] than early-stage gametocytes or asexual stage parasites. Primaquine is currently the only licensed anti-malarial drug that is effective against late stage P. falciparum gametocytes but has a number of drawbacks including its propensity to cause acute haemolysis in individuals with glucose-6-phosphate dehydrogenase (G6PD) deficiency.

With malaria eradication back on the global health agenda there is renewed emphasis on the identification of new and novel agents that can eliminate late-stage gametocytes in the patient's circulation and therefore block transmission of the parasite from its human host to the mosquito vector. However, evaluating the activity of promising anti-malarial drugs against Plasmodium gametocytes is difficult even in vitro. To this end a simple medium-high throughput assay suitable for assessing the potential of new and novel anti-gametocyte drugs has recently been described [3].

Here a modification of this innovative assay system is used to evaluate the activity of a panel of 44 compounds (comprising currently used and experimental anti-malarial drugs) against mature P. falciparum gametocytes.

Methods

Dixon et al. have previously reported the development of an assay utilizing a green fluorescent protein chimera of the early sexual blood stage protein Pfs16 as a marker for commitment to gametocytogenesis [4]. This reporter system allows accurate identification of gametocytes well before they are morphologically distinguishable from asexual parasites and allows for the isolation of large numbers of pure gametocytes.

Production of late stage gametocytes

Mature stage V gametocytes were obtained as described previously [3], briefly, 30 mL of synchronous ring stage cultures of the transgenic parasite line 3D7GFP16B were established at 1-2% parasitaemia. The parasites were grown under standard conditions [5] through one complete invasion cycle and gametocyte production induced by the addition of conditioned media to trophozoite stage parasites [6]. The parasites were grown through one further invasion cycle and gametocytes were separated from asexual parasites and uninfected red blood cells using a modified Percoll step gradient [7]. These gametocyte-enriched cultures were sorted and collected using a BD FACSAria II cell sorter (BD Biosciences). The gametocytes were sorted based on expression of the GFP reporter gene to give only stage I/II gametocytes which were matured to stage V in vitro under standard culture conditions. This maturation takes between 5 and 7 days and was monitored daily by examination of Giemsa stained thin smears.

Drug assay

Approximately 5,000 gametocytes were dispensed into each well of a 96-well plate. The test compounds were added to give a final volume of 100 μl and the plate incubated at 37°C for 24 hours under standard culture conditions. BacTiter-Glo reagents (Promega G8231) were added to a final volume of 200 μl and the assay read using a GloMax® 96 Microplate Luminometer [Cat.# E6501] with an integration constant of 0.5 seconds. BacTitre-Glo is a homogenous ATP-based bioluminescent assay for detecting and quantifying viable microbial cell numbers. The assay uses a single reagent to release and measure the ATP contained in the cells. The presence of ATP indicates live cells and when compared to a known standard can provide quantitative data on the gametocytocidal effect of compounds.

All compounds were dissolved in DMSO and tested in triplicate on three separate occasions at a final concentration of 10 μM (1% DMSO). The assay included a positive control for gametocytocidal effect that consisted of gametocytes lysed with H2O2 and a negative control made of standard culture media with 1% DMSO (final concentration of solvent in all samples tested).

Data analysis

Read-outs from drug-treated wells were compared to those of control wells and percentage inhibition calculated. IC50 values were determined using Graphpad Prism.

Results

A panel of 44 compounds, provided by the Medicines for Malaria Venture, was made up of both currently used and experimental anti-malarial drugs. All compounds were tested at a single concentration of 10 μM in a blinded study for activity against late stage P. falciparum gametocytes. Compounds were unblinded following data analysis (Figure 1A).
Figure 1

A: The activity of a panel of currently used and experimental anti-malarial drugs against late stage Plasmodium falciparum gametocytes. Bars with diagonal lines indicate compounds which resulted in a greater than 50% reduction in ATP production as compared to the control. All drugs were tested at a concentration of 10 μM. B: IC50 values were determined for compounds which demonstrated a greater than 50% reduction in ATP production.

Of the 44 compounds tested eight demonstrated a reduction in ATP production greater than 50%, indicating that these compounds reduced gametocyte viability by at least 50%. Methylene blue was the most active compound, giving an 88% reduction in ATP production compared to controls; a further seven compounds showed inhibition of ATP production ranging from 57% (hydroxychloroquine) to 66% (pyronaridine). Of the remaining 39 compounds, several showed no inhibition of ATP production, indicating they have no activity against mature gametocytes; these include the currently used anti-malarial drugs chloroquine, doxycyclin and quinine.

Compounds which demonstrated a greater than 50% reduction in ATP production also underwent dose response testing in an 11-point dilution curve at concentrations ranging from 5 μM to 0.5 nM. IC50 values were determined using Graphpad Prism and are shown in Figure 1B. Thiostrepton was excluded from this analysis due to insufficient compound for testing at a range of concentrations.

Three compounds had IC50 values in the nM range; methylene blue had the lowest at IC50 value at 12 nM, and was followed by pyronaridine (280 nM) and pentamidine (404 nM).

Discussion

Ideal drugs and combination therapies for malaria eradication campaigns should clear asexual parasitaemia, reducing clinical symptoms as quickly as possible and prevent transmission of the sexual stages. However, gametocytes are refractory to most currently used anti-malarials and this lack of drugs with activity against late-stage P. falciparum gametocytes makes identification of new compounds with such activity a high priority. Indeed, the malERA Consultative Group on Drugs [8] recently identified the need to determine the gametocytocidal activity of both currently used anti-malarial drugs and those in the development pipeline as a high priority, alongside the need to develop new drugs with the ability to kill or prevent development of gametocytes.

Here a simple, rapid in vitro assay is used to undertake a comprehensive study into the effect of currently used and experimental anti-malarial drugs on late stage gametocytes. Eight out of 44 compounds tested reduced gametocyte viability by at least 50%. Three of these were currently used anti-malarial drugs, hydroxychloroquine, artesunate, pyronaridine and three were anti-malarial drugs currently in the development pipeline: NPC1161B, OZ277 and methylene blue. Two additional compounds, pentamidine: an anti-microbial effective in treatment of leishmaniasis and Trypanosoma brucei, and thiostrepton, a complex natural product derived from Streptomyces and mainly used in veterinary medicine, are unlikely to be suitable for mass use as anti-gametocyte agents. The finding, that artesunate has demonstrated activity against mature stage gametocytes, confirms the findings of other groups but this does not appear to translate into a significant clinical effect against mature stage gametocytes in patients [9]. The most likely explanation is that in vitro testing cannot take into account in vivo pharmacokinetics, and artesunate has a relatively short half-life in vivo [10]. However, the in vitro activity of methylene blue has been shown to translate into strong gametocytocidal activity against P. falciparum in vivo [11]. Primaquine has been reported to kill mature-stage gametocytes, however, in this study primaquine showed a 43% inhibition in ATP production but the in vivo effect is likely to be much greater as it is thought that one or more metabolites of primaquine are responsible for its observed gametocytocidal activity in vivo [12]

Testing the activity of compounds against P. falciparum gametocytes is difficult both in vivo and in vitro. An advantage of the in vitro testing described here is that it allows compounds to be assessed in the absence of confounding host factors but has the disadvantage that it is not suitable for testing anti-folate drugs such as sulphadoxine and proguanil, because the transgenic parasite clone used in the study has altered sensitivity to folate antagonists [4]. Pyrimethamine was tested as part of this blinded study and as expected no reduction in ATP production was seen. However, the creation of transgenic parasite lines with alternative drug selection cassettes is possible and would overcome this limitation. It is also feasible that some compounds may inhibit the detection of ATP, resulting in false positives, so as with all such assays additional orthogonal screening is still recommended.

The relatively small number of compounds shown to have significant anti-gametocyte activity in this study highlights the lack of compounds with activity against this important parasite life cycle stage and emphasizes the need for continued research in this area.

Conclusion

This study reports the use of a novel in vitro assay to test the activity of a panel of currently used and experimental anti-malarial drugs against late stage P. falciparum gametocytes. Only eight out of 44 compounds tested reduced gametocyte viability by at least 50%, highlighting the need to develop novel compounds with activity against this key life cycle stage. When used as part of a screening programme the information provided by this assay is a valuable first step, which can guide future clinical studies.

Notes

Declarations

Acknowledgements

This work was supported by an Australian Postgraduate Award to CLP, and Australian National Health and Medical Research Council Career Development Fellowship (NHMRC 496700) to DLG.

Authors’ Affiliations

(1)
Malaria Biology Laboratory, Queensland Institute of Medical Research
(2)
School of Molecular and Microbial Sciences University of Queensland
(3)
Medicines for Malaria Venture
(4)
School of Biomolecular and Physical Sciences, Griffith University
(5)
School of Medicine, University of Queensland

References

  1. Darling ST: Studies in relation to malaria. Isthmanian Canal Commission 1910. 1910, Washington D.C.: Laboratory of the Board of Health, Istmanian Canal Commission, 3-38.Google Scholar
  2. Lang-Unnasch N, Murphy AD: Metabolic changes of the malaria parasite during the transition from the human to the mosquito host. Ann Rev Microbiol. 1998, 52: 561-590. 10.1146/annurev.micro.52.1.561.View ArticleGoogle Scholar
  3. Peatey CL, Spicer T, Hodder PS, Trenholme KR, Gardiner DL: A high-throughput assay for the identification of drugs against late-stage Plasmodium falciparum gametocytes. Mol Biochem Parasitol. 2011, 180: 127-131. 10.1016/j.molbiopara.2011.09.002.View ArticlePubMedGoogle Scholar
  4. Dixon MWA, Peatey CL, Gardiner DL, Trenholme KR: A green fluorescent protein-based assay for determining gametocyte production in Plasmodium falciparum. Mol Biochem Parasitol. 2009, 163: 123-126. 10.1016/j.molbiopara.2008.10.004.View ArticlePubMedGoogle Scholar
  5. Trager W, Jensen JB: Human malaria parasites in continuous culture. Science. 1976, 193: 673-675. 10.1126/science.781840.View ArticlePubMedGoogle Scholar
  6. Williams JL: Stimulation of Plasmodium falciparu gametocytogenesis by conditioned medium from parasite cultures. Am J Trop Med Hyg. 1999, 60: 7-13.PubMedGoogle Scholar
  7. Kariuki MM, Kiaira JK, Mulaa FK, Mwangi JK, Wasunna MK, Martin SK: Plasmodium falciparum: purification of the various gametocyte developmental stages from in vitro-cultivated parasites. Am J Trop Med Hyg. 1998, 59: 505-508.PubMedGoogle Scholar
  8. The malERA Consultative Group on Drugs: A research agenda to underpin malaria eradication. PLoS Med. 2011, 8: e10003978-View ArticleGoogle Scholar
  9. Kiszewski AE: Blocking Plasmodium falciparum malaria transmission with drugs. Pharmaceutical. 2011, 4: 44-68.Google Scholar
  10. Karbwang J, Na-Bangchang K, Congpoung K, Thanavibul A, Harinasuta T: Pharmacokinetics of oral artesunate in thai patients with uncomplicated falciparum malaria. Clin Drug Investig. 1998, 15: 37-43. 10.2165/00044011-199815010-00005.View ArticlePubMedGoogle Scholar
  11. Coulibaly B, Zoungrana A, Mockenhaupt FP, Schirmer RH, Klose C, Mansmann U, Meissner PE, Muller O: Strong gametocytocidal effect of methylene blue-based combination therapy against falciparum malaria: a randomized controlled trial. PLOS One. 2009, 4: e5318-10.1371/journal.pone.0005318.PubMed CentralView ArticlePubMedGoogle Scholar
  12. Bates MD, Meshnick SR, Sigler CI, Leland P: In vitr effects of primaquine and primaquine metabolites on exoerythrocytic stages of Plasmodium berghe. Am J Trop Med Hyg. 1990, 42: 532-327.PubMedGoogle Scholar

Copyright

© Peatey et al; licensee BioMed Central Ltd. 2012

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.

Advertisement