- Open Access
Parasitostatic effect of maslinic acid. I. Growth arrest of Plasmodium falciparum intraerythrocytic stages
© Moneriz et al; licensee BioMed Central Ltd. 2011
- Received: 1 January 2011
- Accepted: 10 April 2011
- Published: 10 April 2011
Natural products have played an important role as leads for the development of new drugs against malaria. Recent studies have shown that maslinic acid (MA), a natural triterpene obtained from olive pomace, which displays multiple biological and antimicrobial activities, also exerts inhibitory effects on the development of some Apicomplexan, including Eimeria, Toxoplasma and Neospora. To ascertain if MA displays anti-malarial activity, the main objective of this study was to asses the effect of MA on Plasmodium falciparum-infected erythrocytes in vitro.
Synchronized P. falciparum-infected erythrocyte cultures were incubated under different conditions with MA, and compared to chloroquine and atovaquone treated cultures. The effects on parasite growth were determined by monitoring the parasitaemia and the accumulation of the different infective stages visualized in thin blood smears.
MA inhibits the growth of P. falciparum Dd2 and 3D7 strains in infected erythrocytes in, dose-dependent manner, leading to the accumulation of immature forms at IC50 concentrations, while higher doses produced non-viable parasite cells. MA-treated infected-erythrocyte cultures were compared to those treated with chloroquine or atovaquone, showing significant differences in the pattern of accumulation of parasitic stages. Transient MA treatment at different parasite stages showed that the compound targeted intra-erythrocytic processes from early-ring to schizont stage. These results indicate that MA has a parasitostatic effect, which does not inactivate permanently P. falciparum, as the removal of the compound allowed the infection to continue
MA displays anti-malarial activity at multiple intraerythrocytic stages of the parasite and, depending on the dose and incubation time, behaves as a plasmodial parasitostatic compound. This novel parasitostatic effect appears to be unrelated to previous mechanisms proposed for current anti-malarial drugs, and may be relevant to uncover new prospective plasmodial targets and opens novel possibilities of therapies associated to host immune response.
- Infected Erythrocyte
- Thin Blood Smear
- Schizont Stage
Despite the increasing number of synthetic and natural compounds which are reported to inhibit the infective cycle of the malaria-related Plasmodium species [1–5] only a few of them have been found to be useful in the treatment and prevention of the disease . Current anti-malarial drugs have an effect on a limited selection of plasmodial targets: inhibition of the conversion of toxic haem to haemozoin in the vacuole (chloroquine, quinine, mefloquine and other alkaloids), the inhibition of synthesis of parasite nucleic acids by hindering of the dihydrofolate pathway (pyrimethamine, sulphadoxine, proguanil), the triggering of oxidative stress (artemisinin and derivatives, primaquine) or inhibition of the mitochondrial electron transport chain (atovaquone). Some drugs may affect multiple processes, like chloroquine, which may also cause oxidative damage at the erythrocytic stage . The widespread use of the most effective and affordable drugs, such as chloroquine and the anti-folate combination pyrimetamine-sulphadoxine, has favoured the appearance of resistant Plasmodium variants making the control of the disease more difficult in endemic areas . Resistance to artemisinin has been also recently reported [9, 10]. Alternative existing medications are, on the other hand, virtually unaffordable in the countries most seriously affected, or their efficacy may be compromised in the near future by the emergence of new resistant variants. Hence, the search of new synthetic or natural compounds targeting novel biochemical pathways or cell functions is still an imperative need.
The search of natural products showing anti-malarial activity for its direct use or as leads for new drugs is one of the alternatives which are currently explored . Maslinic acid (2α,3β-dihydroxyolean-12-en-28-oic acid) (MA) is natural olenane-type pentacyclic triterpene found in the olive fruit and can be readily obtained from olive pomace oils . Several pharmacological activities have been reported for this compound, such as anti-tumor [13, 14], anti-oxidant [15, 16], HIV protease inhibitor , antimicrobial , vasorelaxation , and anti-diabetic action mediated by inhibition of glycogen phosphorylase [20, 21] and protein tyrosine phosphatase 1B . In addition, it has been shown that MA displays low toxicity on non-tumoral cells [23, 24] indicating that it should be safe for use in humans. Several lines of evidence point to a possible anti-malarial activity of MA. HIV protease inhibitors have been recently shown to hinder the pre-erythrocytic stages of Plasmodium . Anti-parasitic activities of MA were also identified against other Apicomplexans . It has been also proposed that the observed growth inhibition of Toxoplasma gondii cultures treated with maslinic acid may be related to inhibition of protease activity, leading to defects in gliding motility and ultrastructural alterations of the parasite . Such a possibility suggests a potential activity of maslinic acid, or structurally related molecules, on parasitic processes different from those targeted by current anti-malarial drugs. In addition, other triterpenoid molecules structurally related to MA display very different cytotoxic and antiparasitic activities. Thus, cucurbitane-type triterpenoids have been recently shown to display anti-malarial activity , while ursane-type urosolic acid was reported to inhibit growth of Trypanosoma cruzi showing in contrast low anti-plasmodial activity . However, hybrid molecules consisting on ursolic acid bound to pharmacophores showed enhanced inhibitory activity on Plasmodium, presumably by facilitating the access of the bound pharmacophore to haem . Maslinic acid has also been used as core compound to synthesize modified derivatives displaying new activities: binding of heterocyclic rings at MA C-2 and C-3 positions increase significantly the inhibitory activity upon human protein tyrosine phosphatase 1B , while attachment of hydrophobic groups at C-28 increase inhibition of human glycogen phosphorylase . Coupling of amino acids or dipeptides at C-28 allowed to retain the anti HIV-1 activity while lowering alongside the cytotoxicity . Should MA show significant anti-malarial activity, it would be feasible to use this molecule as a lead compound for the development of a new family of highly active and low toxic anti-plasmodial drugs.
To explore the suitability of maslinic acid as anti-malarial agent, the activity of this triterpene on cultures of P. falciparum 3D7 and the chloroquine-resistant Dd2 strains has been tested. As none of the currently used anti-malarial drugs targets plasmodial proteases, MA activity was compared to those of chloroquine and atovaquone as examples of effective drugs which interfere the intra-erythrocytic stage of the parasitic cycle.
Drugs and inhibitors
Maslinic acid (MA) was obtained from pressed fruits of olive (Olea europaea) by a method previously published . Chloroquine diphosphate salt was purchased from Sigma-Aldrich. Atovaquone was kindly provided by Glaxo-SmithKline. Stock solutions of atovaquone 30 mM and MA 300 mM were prepared in 100% dimethyl sulfoxide (DMSO). Chloroquine was dissolved in distilled water at 100 mM. All compounds were stored at -20°C until use. For the drug assays, serial dilutions were made in culture medium and added to 96-well culture plates. Control cultures were treated with equivalent amounts of DMSO diluted in culture medium.
In vitro cultures of Plasmodium falciparum
Plasmodium falciparum strains Dd2 (clone MRA-150) and 3D7 (clone MRA-102) obtained from the MR4  were used for this study. Erythrocytes were obtained from type A+ human healthy local donor and collected in tubes with citrate-phosphate-dextrose anticoagulant (Vacuette®). The culture media consisted of standard RPMI 1640 (Sigma-Aldrich) supplemented with 0.5 % Albumax I (Gibco), 100 μM hypoxanthine (Sigma-Aldrich), 25 mM HEPES (Sigma-Aldrich), 12.5 μg/mL gentamicine (Sigma-Aldrich) and 25 mM NaHCO3 (Sigma-Aldrich). Each culture was started by mixing uninfected and infected erythrocytes to achieve a 1 % haematocrit and incubated in 5% CO2 at 37°C in tissue culture flasks (Iwaki). The progress of growth in the culture was determined by microscopy in thin blood smears stained with Wright's eosin methylene blue solution (Merck), using the freely available Plasmoscore software  to monitor the parasitaemia. The detailed description of the culture and synchronization methods used have been reported previously .
Fluorimetric assays for anti-malarial drug activity
A PicoGreen® microfluorimetric DNA-based assay was used to monitor parasite growth inhibition at different drug concentrations . PicoGreen® (P7589) was purchased to Invitrogen and diluted as indicated by the manufacturer in TE buffer (10 mM Tris-HCl, 1 mM EDTA, pH 7.5). Synchronized rings from stock cultures were used to test 200 μM to 0.1 μM serial dilutions of maslinic acid in 96-well culture microplates. Thus, 150 μL of parasites at 2% haematocrit and 1% parasitaemia were allowed to grow for 48-hour in 5% CO2 at 37°C. The parasites were then centrifuged at 600 × g for 10 minutes and re-suspended in saponin (0.15%, w/v in phosphate-buffered saline) to lyse the erythrocytes and release the malaria parasites. To eliminate all traces of haemoglobin the pellet was washed by the addition of 200 μL of PBS followed by centrifugation at 600 × g. The washing step was repeated twice to ensure complete removal of haemoglobin. Finally, pellets were re-suspended in 100 μL of PBS. 100 μL of PicoGreen® diluted in TE were added to each well. Plates were incubated for 30-60 minutes in the dark and the fluorescence intensity was measured at 485 nm excitation and 528 nm emission. Growth inhibition was calculated as previously described .
Assay for haem polymerization
The effect of drugs on haem polymerization was tested in vitro as described previously . Briefly, a mixture containing 50 μL of 0.5 mg/ml haem (ferriprotoporphyrin IX chloride from Fluka, HPLC purity > 98%, dissolved in dimethylsulphoxide), 100 μL of 0.5 M sodium acetate buffer pH 4.4 and 50 μL of drug solution or solvent (for control), was incubated in a flat bottom 96-well plate (Costar 3799) at 37°C for 48 h. Microplates were then centrifuged at 3300 × g for 15 min. The supernatant was discarded and the remaining pellet was resuspended with 200 μL DMSO to remove unreacted haemin. The microplate was then centrifuged once again and the supernatant eliminated. The pellet consisting of β-haematin was dissolved in 200 μL of 0.1 M NaOH for spectroscopic quantification at 405 nm. The data were expressed as the percentage of inhibition of haem polymerization calculated by the following equation: % inhibition = 100 × (O.D. control - O.D. drug) / (O.D. control).
Effect of maslinic acid, chloroquine and atovaquone on P. falciparum cultures
Synchronized mature rings (22 h) of P. falciparum Dd2 at 1% parasitaemia were incubated for 48 hours to complete an infective cycle in the presence of different concentrations of the drugs, and parasite morphology was evaluated by microscopic analysis of Wright's -stained thin blood smears. Smears from drug-free cultures were used as control.
Viability of P. falciparum cultures after treatment with maslinic acid
Synchronous ring, trophozoite, or schizont-stage P. falciparum 3D7-infected erythrocytes at 10% parasitaemia were incubated with 100 μM MA for 12 hr. All cultures were started using a single synchronized culture from which aliquots were taken at 12 h (young rings), 24 h (trophozoites) and 36 h (schizonts) and treated with MA for 12 hours, followed by MA removal by multiple washes. Untreated cultures and cultures grown in the presence of MA throughout the whole experiment were run in parallel as controls. Stage-specific development was assessed by examining a minimum of 1,000 parasitized cells on each smear, for differential counting of rings, trophozoites, schizonts, and pyknotic forms whose developmental stage could not be established. The fraction of each group was calculated as a percentage of the total parasitized cells. Parasitaemia was measured by counting 1,000 red cells and is reported as the percent of parasitized erythrocytes. Parasite replication was evaluated from successive parasitaemia measurements at the beginning of each new asexual cycle. Smears were made each 12 h and stained. The cultures were monitored for at least 90 hours, corresponding to approximately two cycles of P. falciparum.
Activity of maslinic acid on Plasmodium-infected erythrocyte cultures
Effect of MA in the viability of Plasmodium intra-erythrocytic cycle
In addition to the broad range of biological activities previously reported for maslinic acid, this compound displays also a significant inhibitory activity on the erythrocytic cycle of P. falciparum. Evaluation of IC50 for MA by inhibition of DNA replication in vitro yields a value in the range of 30 μM. This value is even lower than the 54 μM IC50 previously reported for MA on T. gondii. The accumulation of rings observed in cultures incubated with this concentration of MA for 48 hours suggest a delay in the progress of the parasite maturation. However, incubation of infected erythrocyte cells with 100 μM MA for 48 hours led to the appearance of non-viable cells. Maslinic acid at concentrations approaching the IC50 appears therefore to slowdown the erythrocytic cycle of P. falciparum, while higher doses may induce parasite cell death. In contrast, infected cultures treated with IC50 concentrations of chloroquine or atovaquone led to different parasite stage profiles. Chloroquine 0.2 μM-treated cultures consisted almost exclusively of ring-stage parasites, which may correspond to cell-cycle delayed cells, similarly to the dose-dependent delay recently reported for mefloquine-treated 3D7, W2 and FCB strains . Treatment with atovaquone at 1 nM yields predominantly schizonts. The proposed plasmodial target for atovaquone, an ubiquinone analog, is the mitochondrial bc1 cytochrome complex which, once inactivated, leads to mitochondrial membrane depolarization and ultimately, inhibition of DNA synthesis . Such mechanism of action may explain the accumulation of mature forms of the parasite.
Further evidence of the difference between MA and chloroquine inhibitory mechanisms was obtained as MA does not inhibit the accumulation of haematin, thus discarding a possible inhibition of the synthesis haemozoin. In addition the chloroquine-resistant Dd2 strain did not show relevant differences in survival to MA. The resistance to chloroquine has been associated to the acquisition of a mutant transporter PfCRT that is capable of reducing intracellular exposure to the drug . The minor differences observed in the response of Dd2 and 3D7 to MA suggests that PfCRT polymorphisms yielding resistance to chloroquine do not affect the activity of maslinic acid.
The incubation of P. falciparum synchronized cultures with MA at different stages of the intra-erythrocytic cycle revealed that the presence of 100 μM MA completely prevents the increase in parasitaemia, leading to parasite cell death if the compound is present up to 86 hours. Remarkably, even at such high concentration, the removal of MA after 12 hour incubation led to the recovery of parasite growth independently of the parasitic stage at treatment, indicating that the effect of this compound on the cell cycle is reversible, although cultures treated with MA at schizont stage showed the slowest rate of recovery to normal parasitaemia. This result is compatible with the possible inhibition of schizont-specific processes. However, the distribution of parasitic stages observed after the removal of MA at different times suggests a more complex picture. Exposure to MA at ring-stage generates accumulation of ring forms and the delay of appearance of trophozoites suggesting that MA inhibition takes place as soon as ring stage. A comparable accumulation of trophozoite and schizont forms are observed after treatments at trophozoite and schizont stages, respectively. Two possible situations may explain this behavior of MA on the infection: either the putative target for MA is a process which takes place along the whole erythrocytic cycle or, alternatively, the compound may display a multiple-target activity, affecting sequentially processes occurring at ring-trophozoite and schizont stages. While ring-trophozoite stages are characterized by massive hemoglobin ingestion, intake of nutrients from the surrounding medium and formation of organelles, schizonts are characterized by DNA replication and the beginning of maturation of merozoite cells with the appearance of merozoite organelles, such as rhoptry and dense granules. Genes expressed preferentially at ring-trophozoite or schizont stages have been identified  and may constitute potential targets for the observed activity of MA. Hence, it can be hypothesized that the observed hindering of plasmodial infection progress may be explained as a consequence of proteases and/or phosphatases inhibition, in accordance with previous activities reported for MA and other related triterpenoid molecules [17, 22, 24, 42]. Other possible targets, such as plasmodial topoisomerases  or the inhibition of isoprenoid biosynthesis, reported for various terpenes , can not be discarded as they may be essential in the processes leading to the development of merozoites.
Maslinic acid displays dose-dependent effect on Plasmodium. Long incubations (48 h) with MA at IC50 range, or short incubations (12 h) with 3X IC50 concentrations lead to the growth arrest of the parasite, while long incubations, even at 1.7X IC50, yield non-viable cells. Unlike antibiotics inhibiting protein synthesis or DNA gyrase activity, which do not lead to phenotypic effects at the end of the first cycle but cause a delayed effect by rendering nonfunctional apicoplasts and schizont arrest in the progeny [45–48], MA appears to exert a non-delayed inhibition of maturation on first-cycle parasites, suggesting different MA-targets to those reported for slow-action antibiotics. The in vitro parasitostatic effect of MA was reproduced in vivo using a murine malaria model (Moneriz et al, accompanying paper). The use of parasitostatic drugs have not been explored sufficiently as a potential anti-malarial treatment. The interruption of the parasite cycle during the erythrocytic phase should enhance the development of a protective response in the host by extension of the time in which the antigens are exposed to the immune system. Such enhanced acquisition of immunity in mice treated with MA is shown in the accompanying report by Moneriz et al. Thus, anti-malarial drugs which specifically interrupt the parasite development maintaining the exposure of antigens may, therefore, become a kind of combined treatment-vaccination approach by using a single compound.
From the results reported in this work, it can be proposed that maslinic acid may be a valuable lead compound to develop a new class of drugs targeting unexploited plasmodial pathways. Following a reverse approach, these molecules would allow to identify and test novel targets for drug development. By comparison of the structures and the activities exhibited by maslinic acid and related molecules, it would be feasible to identify the structural characteristics essential for their anti-parasitic activity and, subsequently, use the natural products as lead compounds for the synthesis of new drugs.
Maslinic acid emerges as a novel Plasmodium parasitostatic natural compound, affecting the whole process of parasite maturation throughout the intraerythrocytic cycle and inhibiting merozoite egression at the IC50 range. The growth arrest can be released by elimination of the compound from the culture medium, allowing the parasite to proceed through the subsequent infective stages. Taking into account the parasitostatic effect observed from ring to schizont stages, a multiple-target action on P. falciparum is proposed for MA, likely including the inhibition of protease activities essential for growth. The use of parasitostatic agents alone or in combination with other anti-malarial compounds may fuel the development of new therapeutic strategies encompassing the presentation of parasite antigens to the host immune system.
AGG is listed as inventor on a patent owned by the University of Granada related to the use of maslinic acid as antiparasitic agent (date of filing: March 29, 2007; Patent Number: WO/2007/034009). The other authors declare no competing financial interests
This work was supported by grants from the Spanish Ministry of Science and Innovation (BIO2007-67885 and BIO2010-17039), the Research Teams Consolidation Programme of the UCM (Research Team 920267-Comunidad de Madrid) and the Iberoamerican CYTED network No. 210RT0398. CM is supported by the Universidad de Cartagena (Colombia) and the Alban Programme of High Level Scholarships for Latin America, fellowship E07D400516CO. PMG is supported by a postdoctoral fellowship from the Spanish Ministry of Education and Science. We thank Glaxo SmithKline for providing atovaquone. The excellent technical help of Susana Pérez-Benavente is also aknowledged.
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