- Open Access
Variation in apoptosis mechanisms employed by malaria parasites: the roles of inducers, dose dependence and parasite stages
© Matthews et al.; licensee BioMed Central Ltd. 2012
- Received: 7 June 2012
- Accepted: 24 August 2012
- Published: 28 August 2012
Plasmodium berghei ookinetes exhibit an apoptotic phenotype when developing within the mosquito midgut lumen or when cultured in vitro. Markers of apoptosis increase when they are exposed to nitric oxide or reactive oxygen species but high concentrations of hydrogen peroxide cause death without observable signs of apoptosis. Chloroquine and other drugs have been used to induce apoptosis in erythrocytic stages of Plasmodium falciparum and to formulate a putative pathway involving cysteine protease activation and mitochondrial membrane permeabilization; initiated, at least in the case of chloroquine, after its accumulation in the digestive vacuole causes leakage of the vacuole contents. The lack of a digestive vacuole in ookinetes prompted the investigation of the effect of chloroquine and staurosporine on this stage of the life cycle. Finally, the suggestion that apoptosis may have evolved as a strategy employed by ookinetes to increase the fitness of surviving parasites was explored by determining whether increasing the ecological triggers parasite density and nutrient depletion induced apoptosis.
Ookinetes were grown in culture then either exposed to hydrogen peroxide, chloroquine or staurosporine, or incubated at different densities and in different media. The proportion of ookinetes displaying positive markers for apoptosis in treated samples was compared with controls and results were analyzed using analysis of variance followed by a Turkey’s test, or a Kruskal-Wallis test as appropriate.
Hydrogen peroxide below 50 μM triggered apoptosis but cell membranes were rapidly compromised by higher concentrations, and the mode of death could not be defined. Both chloroquine and staurosporine cause a significant increase in ookinetes with condensed chromatin, caspase-like activity and, in the case of chloroquine, phosphatidylserine translocation and DNA fragmentation (not investigated for staurosporine). However, mitochondrial membrane potential remained intact. No relationship between ookinete density and apoptosis was detected but nutrient depletion significantly increased the proportion of ookinetes with chromatin condensation in four hours.
It is proposed that both a mitochondrial and an amitochondrial apoptotic pathway may be involved, dependent upon the trigger that induces apoptosis, and that pathways may differ between erythrocytic stages and ookinetes, or between rodent and human malaria parasites.
- Plasmodium berghei
- Reactive oxygen species
Since Picot and colleagues first suggested that the crisis forms of cultured intra-erythrocytic stages of Plasmodium falciparum were undergoing apoptosis, acceptance of the putative existence of this form of programmed cell death, and discussion of the role it may be playing in the life history of the malaria parasite, has been growing[2–4]. A number of studies now report observations of morphological and biochemical markers of apoptosis (recently reviewed in). A few are contradictory, but it has been proposed that problems surrounding the use of differing parasite strains, induction with different drugs and drug doses and variation in life cycle stages, including sequential intra-erythrocytic stages, confound the ability to evaluate and compare studies. Almost all reports of an apoptosis-like phenotype (hitherto referred to as apoptosis) in Plasmodium spp. have been performed in vitro on intra-erythrocytic stages of P. falciparum. However, detailed studies have also been made, both in vitro and in vivo, of ookinetes of the rodent malaria, Plasmodium berghei[3, 6–8] and it was becoming clear that a more systematic examination of apoptosis inducers and markers needed to be made in an attempt to link reports concerning these different species and stages together. This was the aim of this study.
Classical biochemical markers, including loss of mitochondrial membrane potential (ΔΨm), DNA fragmentation and the activation of caspase-like proteases, have been observed in both species[6, 9–11]. Although alterations in the plasma membrane, such as externalization of phosphatidyl serine, cannot be detected in intra-erythrocytic stages of P. falciparum due to the various membranes surrounding the parasite, they have been reported in extracellular ookinetes (discussed in). Caspase-like activity has been detected in both intra-erythrocytic and ookinete stages but the nature of these caspases is unclear as, in common with other parasitic protozoan’s that exhibit markers of apoptosis, the Plasmodium genome does not contain classical caspases. However, both clan CD metacaspases and clan CA cysteine proteases have been implicated in P. falciparum apoptotic pathways[10, 11, 13, 14]. Recently genes orthologous to other components of apoptotic pathways in metazoan apoptosis have been identified using bioinformatics, but, so far, only in the P. falciparum genome. In addition to metacaspases, homologues of Tudor Staphylococcal Nuclease, ZEN1, a putative apoptotic DNase and AIF (apoptosis inducing factor) have been identified[15, 16]. Plasmodium falciparum apoptosis-related protein (Pf ARP) has been purified and localized to the cytosol but no role in apoptosis has yet been defined. However, disruption of the ClpQY protease machinery located in the mitochondria led to loss of ΔΨm and, one to two hours later, activation of a caspase-like cysteine proteases and DNA fragmentation.
The majority of studies of P. falciparum have used drug treatment to induce apoptosis[1, 9, 19–21], whereas studies of P. berghei ookinetes have been conducted without the application of toxic drugs[6, 7]. Triggers that occur naturally within the mosquito midgut, which have been shown to induce apoptosis in P. berghei ookinetes, include nitric oxide (NO) and reactive oxygen species (ROS). The ROS generator 3, 4-dihydroxy-L-phenylalanine (L-DOPA) acts in a dose- and time-dependent manner, whereas hydrogen peroxide (H2O2) caused death without detectable features of apoptosis. Death was defined as significant loss of cell membrane integrity. It occurred after one hour of exposure, even at the lowest concentration tested (100 μM). The conflicting results obtained when different donors of ROS were used in an attempt to induce ookinetes to undergo apoptosis may have been due to enhanced sensitivity to H2O2. This explanation has been tested here by exposing ookinetes to lower doses of H2O2 than had been used previously.
Inhibition of the activity of NO synthase in the mosquito significantly reduced the number of ookinetes with activated caspase-like molecules in their cytoplasm at 15 hr post-infection and increased the intensity of oocyst infection 12 days post-infection. However, although in vitro incubation with the NO donor sodium Nitroprusside resulted in a significant increase in nuclear chromatin condensation, PS translocation and caspase-like activity, it did not induce the loss of ΔΨm, indicating that there may be more than one apoptotic pathway operating in ookinetes.
Using micromolar concentrations of chloroquine (CQ) and staurosporine (ST) to induce several features of apoptosis in P. falciparum trophozoite stages, Ch’ng and co-workers[10, 22] have begun to delineate a putative cell death pathway in this species and life cycle stage. They suggest that, following CQ exposure, activation of cysteine proteases results in mitochondrial outer membrane permeabilization (MOMP). Importantly, following accumulation of CQ in the digestive vacuole, destabilization of the membrane was recognized as the initial downstream event that released Ca2+ and cysteine proteases into the parasite cytosol. They propose that both this damage to the diges-tive vacuole, the resultant MOMP and subsequent amplification of cytoplasmic cysteine protease activity resulted in DNA fragmentation and death and conclude that cysteine proteases are acting both up- and down-stream of MOMP. Inhibitor studies suggested the cysteine proteases belonged to clan CA, rather than CD.
There are several discrepancies between observations of apoptosis features pertaining to putative pathways in ookinetes of P. berghei and those of the trophozoite stages of P. falciparum outlined above. In P. berghei, apoptosis can be inhibited by cyclohexamine (suggesting some part of the process relies on protein synthesis) and also by clan CD cysteine protease inhibitors, including the general caspase inhibitors, Z-VAD.fmk and boc-ASP as well as the more specific caspase-3 inhibitor, Z-DEVD.fmk, but not by clan CA cysteine protease inhibitors E64d and K11777. These differences may result, in part, from differences in morphology. Notably, although ookinetes contain haemazoin crystals as a legacy from macro gametocytes, they do not feed by using a phagosome and lack a digestive vacuole that could accumulate CQ or initiate the pathway that has been proposed for intra-erythrocytic stages. As an initial step towards ascertaining whether multiple PCD pathways may exist in different Plasmodium spp., and/or at different stages in the life cycle, ookinetes were exposed to CQ and to ST and monitored for several markers of apoptosis to determine whether these drugs initiated apoptosis.
It is becoming clear that there are several triggers that induce features of apoptosis in Plasmodium. In addition to drug treatments, NO derivatives and oxidative stress[8, 20], high parasite density has been implicated. In order for density to be a trigger that initiates apoptosis in protozoan parasites, a mechanism to sense the presence of conspecifics must be present. It has been suggested that protozoan parasites form communities in which individuals may communicate with each other in a manner similar to the quorum sensing seen in bacteria[16, 24, 25]. At times of nutrient stress this communication may be advantageous if it results in the altruistic suicide of some parasites, thus reducing competition for nutrients or limiting host/vector damage. Indeed, nutrient stress itself may be an inducer of apoptosis and this concept has been explored here. As well as exposure to drug treatment, ookinetes were cultured at different densities and in different nutrient conditions so that the effect of parasite density and nutrient depletion could be investigated. Thus, the objective of this study was to further the understanding of the process of apoptotic cell death in malaria parasites by integrating recent reports on the process in intra-erythrocytic stages with observations made on the extracellular ookinete stage. Although CQ and ST were also found to act as inducers of apoptosis in ookinetes, the effect of chemical and ecological triggers on various morphological and biochemical markers support the view that more than one apoptotic pathway may exist in ookinetes.
Products were purchased from Sigma Aldridge Company Ltd (Dorset, England, UK) unless otherwise stated. All animals were handled in strict accordance with good animal practice as defined by the UK Animal (Scientific Procedures) Act 1986 and approved by the UK Home Office, license number PPL 40/2997. Work was also approved by the University of Keele Animal Care and Ethical Review Committee. All incubations with reagents were carried out at 19°C (a temperature appropriate for P. berghei ookinetes).
Parasite culture and harvesting
Plasmodium berghei ANKA 2.34 was maintained by passage in Charles River-derived mice (CD1). Blood containing exflagellating gametocytes collected by cardiac puncture and then incubated in RPMI 1640 medium, supplemented with foetal bovine serum, sodium bicarbonate, hypoxanthine and antibiotics (ookinete medium), for 18–22 hr to allow for the formation of ookinetes. To harvest ookinetes from this culture, erythrocytes were lyses by incubation on ice with 0.17 M ammonium chloride (1:50 vol/vol) for 20–30 min. The remnants of the red blood cells were removed by washing twice with cold phosphate buffered saline (PBS). Ookinetes were pelleted by centrifugation at 800 g for 5 min and resuspended in 1 ml PBS or ookinete medium for counting.
In order to determine whether the anti-malarial drug CQ and the apoptosis inducer ST act as triggers of apoptosis in the ookinete stage, as well as the intra-erythrocytic stage, parasites were incubated in the presence of these drugs. Chloroquine diphosphate was dissolved to a concentration of 1 mM in RPMI or ookinete medium. Solutions were prepared fresh and stored in the dark prior to use. Two different protocols were used to test the effect of CQ on ookinetes. Initially, a range of dilutions was prepared from the stock CQ/RPMI solution and a 200 μl aliquot of ookinetes, resuspended in PBS, was added to 1 ml of each dilution and incubated for 2 hr. Controls were incubated in RPMI medium alone. Thereafter, ookinetes were resuspended directly in 1 ml of 1 mM chloroquine/ookinete medium and incubated for 2 hr. Controls for each replicate were incubated in ookinete medium alone.
Staurosporine (ST) was dissolved in 1 ml dimethylsulphoxide (DMSO) to make a 2.14 mM stock solution and stored at 2-8°C. The stock solution (7 μl) was added directly to 1 ml of ookinetes suspended in ookinete medium to give a final concentration of 15 μM and ookinetes were incubated in 1 ml of this for 30 min. Preliminary experiments had established that DMSO at this concentration did not cause ookinetes to die and informed the dose and incubation time used in this experiment (unpublished data). Ookinetes incubated in ookinete medium alone served as controls for each replicate experiment.
Hydrogen peroxide was diluted to 1 mM with PBS and stored for no more than 1 week. RPMI 1640 was used to prepare a range of concentrations from this stock solution and 1 ml added to ookinetes resuspended in 200 μl PBS and incubated for 1 hr. For each replicate experiment, controls were incubated in ookinete medium only.
Following treatment with each inducer, ookinetes were washed two to three times with cold PBS and immediately assayed for apoptotic activity.
The effect of ookinete density and incubation medium on the proportion of ookinetes undergoing apoptosis
To determine whether the ecological triggers, high parasite density or nutrient depletion, acted to induce apoptosis, ookinetes were washed, counted and incubated further for 4 hr in RPMI medium supplemented with 10% foetal bovine serum, RPMI medium alone or PBS, at densities of 1, 2 and 4 x 107 ookinetes/ml. Ookinetes were immediately assayed for signs of condensed chromatin (at least two replicates of counts of 50 ookinetes) and experiments were repeated three times. In a further experiment, ookinetes were incubated in PBS for 4, 6 and 24 hr before assaying for condensed chromatin.
Markers of apoptosis
Following treatment, ookinetes were assayed for morphological markers of apoptosis using techniques adapted from those used for metazoans. Ookinetes stained with fluorochrome markers of apoptosis were viewed under oil immersion (x1,000) using a Leica DM IRB inverted microscope. Low parasite yield and time constraints restricted the use of all the markers in some experiments.
Chromatin condensation was detected using acridine orange, a fluorescent cationic dye that stains nuclear material. Three μl of acridine orange (final concentration 2.5 μg/ml PBS) was added to ookinetes suspended in an equal volume of PBS on a microscope slide. Vectashield mounting medium (0.5 μl) (Vector Laboratories Inc) was added and the samples were viewed immediately. Live ookinetes stained uniformly green, nuclei with condensed chromatin were stained an intensified green.
An annexin V-FITC Apoptosis Detection Kit was used to detect translocation of phosphatidylserine (PS) to the external leaflet of the plasma membrane according to the manufacturer’s instructions, except that incubations were performed for 12 min followed by the addition of 1 μl of propidium iodide (PI), followed by a further 3 min incubation. Ookinetes were mounted with Vectashield (0.5 μl) containing 4’, 6-diamidino-2-phenylindole (DAPI) (Vector Laboratories Inc) prior to examination. Ookinetes staining PS positive/PI negative were regarded as apoptotic.
The activation of caspase-like molecules was detected using CaspaTagTM Pan-Caspase In Situ Assay Kit (Chemicon International, USA). The assay is based on fl uorochrome i nhibitors of ca spases (FLICA) that bind covalently to activated caspases. This kit contains the carboxyfluorescein-labelled fluoromethyl ketone peptide inhibitor of caspases (FAM-VAD-FMK). The assay was carried out following the manufacturer’s instructions except that 250 μM PI was used in some of these assays to detect cells with compromised membranes. Samples were mounted with Vectashield or Vectashield containing DAPI or PI (as indicated in the results) (Vector Laboratories Inc) and viewed immediately. Staining of activated caspases was taken as a marker for apoptotic cells. PI staining is indicative of a compromised membrane which could be due to necrotic cell death or a late stage of apoptotic cell death.
Collapse of ΔΨm resulting in mitochondrial outer membrane permeabilization (MOMP) was detected using the JC-1 assay kit (Invitrogen) according to manufacturer’s instructions. This is regarded as a reliable fluorescent probe for use with intact cells and has been used with appropriate controls in previous studies as a marker of apoptosis. Samples were mounted with Vectashield containing DAPI prior to examination. In live cells, the presence of a negative charge established by an intact mitochondrial membrane potential allows the cationic, lipophilic dye to accumulate in the mitochondria, forming orange JC-1 aggregates. Mitochondrial depolarization and loss of mitochondrial membrane potential is indicated by loss of these aggregates leaving only green fluorescent staining throughout the cytoplasm.
The In Situ Death Detection Kit, Fluorescein (Roche) was used to detect DNA fragmentation. During apoptosis DNA strands break leaving the strand termini exposed. In this reaction the enzyme terminal deoxynucleotidyl transferase is used to catalyze the addition of fluorescently labeled nucleotides to free 3’-OH termini (TUNEL-reaction). The TUNEL assay was completed in accordance with the manufacturer’s instructions with a few modifications. Briefly, ookinetes were fixed onto positively charged SuperfrostPlus slides (Thermo Scientific) using neutral buffered 10% formalin solution, washed twice with PBS and stored at −20°C until further processing. Once thawed, ookinetes were permeabilized for 5 min at room temperature using 40 mM sodium citrate and 1% Titron X-100 (BDH Chemicals). One slide, which served as the positive control, was then incubated with 3U/ml DNAase 1 recombinant for 10 min to induce the breakage of DNA strands. All slides, apart from the negative control, were incubated with the TUNEL reaction mixture (freshly prepared) at 37°C for 75 min. The negative control was incubated with labeling solution only. Subsequent to staining, the slides were washed with PBS, air dried and mounted in Vectashield containing DAPI. In this study, ookinetes with stained nuclei were considered apoptotic whilst ookinetes with unstained nuclei were recorded as live. Although it is recognized that DNA fragmentation can occur during the process of necrosis, this assay was used in conjunction with other markers of apoptosis to confirm the apoptotic phenotype.
Data were analyzed using Minitab® software (version 16) or Microsoft excel. The Anderson-Darling test was used to test for normality and normally distributed data analyzed using one- way or two-way ANOVA with a general linear model for two parameters. When significant differences were found, this was followed by a Turkey’s test for paired comparisons. If data were not normally distributed they were arcsine transformed prior to performance of a one-way ANOVA. If the arcsine-transformed data were not normal they were log transformed prior to analysis. If data was not normal after both data transformations, a non-parametric, Kruskal-Wallis test was carried out on the original data.
The dose dependent effect of chloroquine on the induction of apoptosis in Plasmodium berghei ookinetes
Staurosporine induces markers of apoptosis in Plasmodium berghei ookinetes
The dose-dependent effect of hydrogen peroxide on markers of apoptosis in Plasmodium berghei ookinetes
The effect of incubation medium and density on the induction of apoptosis in Plasmodium berghei ookinetes
The occurrence, semantics, function and evolutionary origin of cell death modalities in unicellular eukaryotes have been discussed at length[5, 12, 15, 16, 26, 29] and will not be addressed further in this paper. Suffice to state that the detection of markers for apoptosis in protozoan parasites relies upon assays developed for metazoans, all of which have constraints associated with them and none by themselves is conclusive. Thus, where possible, several assays were used to corroborate observations in this work. The investigation of chemical and ecological inducers of apoptosis found that the anti-malaria drug, CQ, caused a significant increase in the proportion of ookinetes with condensed chromatin, translocation of PS, caspase-like activity and DNA fragmentation, but did cause a loss of ΔΨm. Staurosporine also induced chromatin condensation and caspase-like activity to increase without loss of ΔΨm. and incubation with low doses of H2O2 resulted in a significant increase in two early markers of apoptosis, chromatin condensation and PS translocation; caspase-like activity and DNA fragmentation were not investigated. Finally, no effect of parasite density was observed, but withdrawal of nutrients also induced ookinetes to exhibit chromatin condensation although plasma membranes were intact. Although it is time consuming, cytofluorometry on a cell-by-cell basis is the most convenient method to detect features of apoptosis in the relatively small samples of ookinetes that could be collected for each experiment. Unfortunately, parasite yields and handling times precluded the use of all markers of apoptosis in every experiment, particularly those involving several chemical doses, parasite densities or incubation times.
The previous suggestion that exposure to low concentrations of H2O2 would induce markers of apoptosis was confirmed as the proportion of parasites displaying signs of chromatin condensation or PS translocation increased significantly at concentrations of 50 μM or below; whilst the plasma membrane remained intact. However, as shown previously, higher concentrations resulted in rapid death, detected as the proportion of PI positive ookinetes, with no detectable signs or features of apoptosis. Although death may have occurred by means other than apoptosis, a very rapid progression to late stage apoptosis at these higher concentrations cannot be ruled out, as discussed in.
The malaria ookinete is very susceptible to oxidative stress, as are the intra-erythrocytic stages. Of four effective selenium compounds tested against CQ-resistant P. falciparum, three generated ROS and caused a collapse of ΔΨm and DNA fragmentation, whereas one compound induced a similar apoptosis pathway without the production of ROS. Unconjugated Bilirubin also induces oxidative stress in intra-erythrocytic stages and inhibits growth in culture, apparently because the parasites are undergoing apoptosis. In that study, induction of oxidative stress was associated with loss of ΔΨm and up-regulation of Pf ARP expression, (a molecule that has the highest homology with TFAR-19, a mammalian TF-1 cell apoptosis-related gene). It also causes a six-fold activation of caspase-3-like proteases, which could be prevented with an inhibitor of caspase-3 activity, and condensation of nuclear chromatin was observed. Kumar and colleagues suggested that oxidative stress occurred as a result of Bilirubin-inhibited haemozoin formation, although other routes for the generation of ROS were not ruled out.
Ookinetes develop in vivo in a complex redox-active environment. It has been suggested that haem and haematin, released as the blood meal is digested, could react with iron and oxygen in the blood bolus to produce ROS. Additionally, the midgut epithelial cells of infected mosquitoes are themselves a source of ROS (as discussed in). Dual oxidase (Duox), a transmembrane protein present on the midgut epithelium, generates hydrogen peroxide and mediates an antimicrobial response to dietary bacteria and yeast in Drosophila. However, it has recently been shown that in anopheline mosquitoes, Duox, together with immunomodulatory peroxidase (IMPer), makes the insect more susceptible to Plasmodium infection by forming a di-tyrosine network that inhibits activation of the epithelial immune system when bacteria or malaria parasites are present. The role of epithelium-generated ROS in the induction of apoptosis in ookinetes in the midgut lumen is therefore uncertain.
In addition to extrinsic sources, it is possible that damaged mitochondria may themselves act as a major source of ROS that could initiate an apoptotic programmed. Indeed, ookinetes exhibiting loss of ΔΨm caused by a mitochondrial membrane potential disrupter were shown to display an apoptosis phenotype. Loss of ΔΨm is also associated with the display of other markers of apoptosis, exhibited by an increasing proportion of ookinetes as the length of time they are incubated in PBS or ookinete medium increases[8, 23]. These findings point to a role for mitochondria in a putative apoptosis pathway in P. berghei ookinetes, however, findings presented here, and elsewhere, suggest that an amitochondrial pathway also exists.
The reports that CQ causes a significant decline in the proportion of P. falciparum trophozoites with functional ΔΨm[9, 10] are at odds with these findings for P. berghei ookinetes. Despite finding a significant increase in the proportion of parasites with condensed chromatin, caspase-like activity, PS translocation and fragmented DNA, loss of ΔΨm following a 2-h incubation with 1 mM CQ could not be detected. Interestingly, Srivastava et al. found that CQ was unable to disrupt the mitochondrial membrane potential of another species of rodent malaria, Plasmodium yoelii, at concentrations up to 10-3 M, whereas the broad spectrum anti-malarial drug, Atovaquone, caused loss of ΔΨm at far lower doses.
Similar to findings for CQ exposure, ookinetes incubated with ST did not loose ΔΨm, although there was a significant increase in the proportion with condensed chromatin and activated cysteine proteases. This is also in contrast to its effect on trophozoites, where it did cause loss of ΔΨm. In the latter study, ST treatment significantly increased CaspaTag binding, but this was not inhibited by the cysteine protease inhibitor zVAD, although binding induced by CQ was. This suggests that different cysteine proteases may be involved in the pathways induced by these drugs in P. falciparum trophozoites and in P. berghei, but pathways in ookinetes clearly need more investigation before any conclusions can be drawn.
One possible explanation for the apparent differences in the role of mitochondria in CQ-induced apoptosis in malaria parasites is the timing of exposure to CQ. Ch’ng and co-workers incubated trophozoites for 4–6 hr before detecting apoptosis markers. Monitoring this length of drug exposure is difficult as, when maintained in ookinete medium, the proportion of ookinetes that display features of apoptosis increases with time, even when no apoptosis-inducer is added to the medium[6, 7]. However, as several markers of apoptosis increase significantly following just 2-hr exposure to CQ, these differences are not attributed to the need for longer exposure time. It is likely that CQ induces apoptosis via a pathway that does not involve mitochondria in ookinetes. As the pathway for the action of CQ that Ch’ng et al. propose could not occur in ookinetes, due to the absence of a digestive vacuole, the drug may initially accumulate somewhere else, act directly in the cytoplasm to activate cysteine proteases, or work via another route. Chloroquine is known to be cytotoxic to mammalian cells and molecular mechanisms including MOMP, the induction of NO synthesis, glutathione depletion and cellular redox changes have been implicated[37, 38]. Of note here is the observation that, at the specific time investigated, more ookinetes have condensed chromatin than caspase-like activity and fewer still had fragmented DNA. This may have some bearing on the timing of the pathway by which the apoptotic phenotypes are manifested. The elucidation of apoptotic pathways occurring in ookinetes will also shed light on CQ action.
The finding that micromolar concentrations of CQ induce ookinetes to undergo apoptosis could have implications for their survival in vivo. The effect of the administration of CQ to vertebrate hosts on malaria transmission has been widely investigated in the laboratory and the field. Conflicting findings have been reported, but enhanced transmission has often been associated with CQ-resistant Plasmodium compared to susceptible ones and it has been suggested that selection for these parasites may be due to increased survival of gametocytes or sporogonic stages when under CQ pressure (reviewed in). However, it is probable that blood meals taken following CQ treatment may not contain sufficiently high concentrations of CQ to induce apoptosis in zygotes and ookinetes. In the study reported herein, 416 μM CQ was the lowest concentration that induced a significant increase in apoptotic ookinetes. This is considerably higher than the treatment with nanomolar concentrations of CQ that causes accumulation in the digestive vacuole, alteration of haemozoin polymerization and trophozoite killing, and even the 3 μM concentration that induces permeabilization of the digestive vacuole and triggers apoptosis, as discussed by Ch’ng and colleagues. These authors reviewed various clinical trials involving dose escalation that may have resulted in micromolar levels of CQ in the blood. They also discuss the feasibility of redeploying CQ, using regimes/formulations that that may induce programmed cell death in the parasite. The likelihood of such regimes producing sustained blood concentrations high enough to be active upon mosquito stages of Plasmodium is remote but, as an apoptosis inducer that is active in vitro, CQ has a role to play in future investigations of the pathways involved in apoptosis in ookinetes.
The apoptosis triggers discussed so far result from a toxic external environment that may, or may not, be influenced by the presence of other ookinetes. Several authors have proposed that protozoan parasites may undergo apoptosis in a density dependent manner[26, 41]. Reece and colleagues, review previous proposals that the removal, by suicide, of a proportion of the population could benefit the remaining parasites by preventing premature host death, by avoiding the stimulation of a density related immune response or removal of less fit members[42, 43]; all of these scenarios are density dependent. Studies of the population dynamics of early sporogony have demonstrated losses at all transitional stages within the mosquito midgut (reviewed in) and recently Sinden and colleagues found negative density-dependence operating for densities greater than 355 ookinetes per Anopheles stephensi and speculated that factors such as a density-dependent, parasite-killing mechanism or competition for resources may be operating in the mosquito. The ookinete densities used here (starting at 10,000 per μl) were far greater than those calculated to initiate a density dependent effect in vivo. Although no density-dependent induction of apoptosis was demonstrated, this might be due to factors associated with experimental design such as the developmental stage investigated (for example, signaling molecules produced earlier may have been removed during ookinete harvesting) or the limited period of incubation at high density. In view of the proposed function of density-driven apoptosis as a method of improving the fitness of a clonal population of ookinetes, further investigation using different experimental approaches, additional assays for apoptosis and, in particular, experiments in vivo, need to be performed before density can be completely ruled out as a trigger for apoptosis.
Clearly nutrients are not limiting when incubation is in RPMI, but incubation for 4 hr in PBS alone resulted in a large increase in ookinetes with condensed chromatin, although no density effect was noted. As multiple markers for apoptosis were not examined for this experiment, the conclusion that nutrient depletion resulted in an apoptotic phenotype rather than autophagy should be viewed with caution.
These, and previous results, strongly suggest that ookinetes respond to adverse conditions such as redox stress or drug treatment; orchestrating their own death and exhibiting a phenotype akin to metazoan apoptosis. Multiple mechanisms may exist as there appears to be both a mitochondrial and an amitochondrial pathway involved, and pathways may differ between erythrocytic stages and ookinetes, or between rodent and human malaria parasites. So far, there is more experimental evidence to support the view that apoptosis is a way to die when subjected to factors that may be of host origin, rather than a strategy employed by ookinetes to increase the fitness of surviving parasites (discussed in). However, further investigations are required, particularly in vivo and with mixed clones of Plasmodium, before a direct role for density-dependent mechanisms is dismissed, as relatedness is also essential if apoptosis is to be regarded as a beneficial trait. This apoptotic trait has probabilistic expression as a proportion of ookinetes survive the expression of apoptotic triggers; understanding what governs this, and the pathways operating in Plasmodium ookinetes may inform novel transmission-blocking strategies if the knowledge can be used to cause all ookinetes to commit suicide in the midgut lumen.
The authors are grateful to Anthony Polwart for advice on statistical analysis. VC and AU were supported by The Wellcome Trust (WT 084582/MA) and MA received a travel award from Ain Shams University, Egypt. Thanks also go to Sarah Reece for comments that enabled the improvement of the manuscript.
- Picot S, Burnod J, Bracchi V, Chumpitazi BF, Ambroise-Thomas P: Apoptosis related to chloroquine sensitivity of the human malaria parasite Plasmodium falciparum. Trans R Soc Trop Med Hyg. 1997, 91: 590-591. 10.1016/S0035-9203(97)90039-0.View ArticlePubMedGoogle Scholar
- Hurd H, Carter V, Nacer A: Interactions between malaria and mosquitoes: the role of apoptosis in parasite establishment and vector response to infection. Curr Top Microbiol Immunol. 2005, 289: 185-217. 10.1007/3-540-27320-4_9.PubMedGoogle Scholar
- Pollitt LC, Colegrave N, Khan SM, Sajid M, Reece SE: Investigating the evolution of apoptosis in malaria parasites: the importance of ecology. Parasit Vectors. 2010, 3: 105-10.1186/1756-3305-3-105.PubMed CentralView ArticlePubMedGoogle Scholar
- Reece SE, Pollitt LC, Colegrave N, Gardner A: The meaning of death: evolution and ecology of apoptosis in protozoan parasites. PLoS Pathog. 2011, 7: e1002320-10.1371/journal.ppat.1002320.PubMed CentralView ArticlePubMedGoogle Scholar
- Engelbrecht D, Durand PM, Coetzer TL: On programmed cell death in Plasmodium falciparum: status quo. J Trop Med. 2012, 2012: 646534-PubMed CentralView ArticlePubMedGoogle Scholar
- Al-Olayan EM, Williams GT, Hurd H: Apoptosis in the malaria protozoan, Plasmodium berghei: a possible mechanism for limiting intensity of infection in the mosquito. Int J Parasitol. 2002, 32: 1133-1143. 10.1016/S0020-7519(02)00087-5.View ArticlePubMedGoogle Scholar
- Arambage SC, Grant KM, Pardo I, Ranford-Cartwright L, Hurd H: Malaria ookinetes exhibit multiple markers for apoptosis-like programmed cell death in vitro. Parasit Vectors. 2009, 2: 32-10.1186/1756-3305-2-32.PubMed CentralView ArticlePubMedGoogle Scholar
- Ali M, Al-Olayan EM, Lewis S, Matthews H, Hurd H: Naturally occurring triggers that induce apoptosis-like programmed cell death in Plasmodium berghei ookinetes. PLoS One. 2010, 5: 12634-10.1371/journal.pone.0012634.View ArticleGoogle Scholar
- Meslin B, Barnadas C, Boni V, Latour C, De Monbrison F, Kaiser K, Picot S: Features of apoptosis in Plasmodium falciparum erythrocytic stage through a putative role of PfMCA1 metacaspase-like protein. J Infect Dis. 2007, 195: 1852-1859. 10.1086/518253.View ArticlePubMedGoogle Scholar
- Ch'ng JH, Kotturi SR, Chong AG, Lear MJ, Tan KS: A programmed cell death pathway in the malaria parasite Plasmodium falciparum has general features of mammalian apoptosis but is mediated by clan CA cysteine proteases. Cell Death Dis. 2010, 1: e26-10.1038/cddis.2010.2.PubMed CentralView ArticlePubMedGoogle Scholar
- Mutai BK, Waitumbi JN: Apoptosis stalks Plasmodium falciparum maintained in continuous culture condition. Malar J. 2010, 9 (Suppl 3): S6-10.1186/1475-2875-9-S3-S6.PubMed CentralView ArticlePubMedGoogle Scholar
- Jimenez-Ruiz A, Alzate JF, MacLeod ET, Luder CGK, Fasel N, Hurd H: Apoptotic markers in protozoan parasites. Parasit Vectors. 2010, 3: 104-10.1186/1756-3305-3-104.PubMed CentralView ArticlePubMedGoogle Scholar
- Meslin B, Beavogui AH, Fasel N, Picot S: Plasmodium falciparum metacaspase PfMCA-1 triggers a z-VAD-fmk inhibitable protease to promote cell death. PLoS One. 2011, 6: e23867-10.1371/journal.pone.0023867.PubMed CentralView ArticlePubMedGoogle Scholar
- Meslin B, Zalila H, Fasel N, Picot S, Bienvenu AL: Are protozoan metacaspases potential parasite killers?. Parasit Vectors. 2011, 4: 26-10.1186/1756-3305-4-26.PubMed CentralView ArticlePubMedGoogle Scholar
- Nedelcu AM: Comparative genomics of phylogenetically diverse unicellular Eukaryotes provide new insights into the genetic basis for the evolution of the programmed cell death machinery. J MolEvol. 2009, 68: 256-268.Google Scholar
- Kaczanowski S, Sajid M, Reece SE: Evolution of apoptosis-like programmed cell death in unicellular protozoan parasites. Parasit Vects. 2011, 4: 44-10.1186/1756-3305-4-44.View ArticleGoogle Scholar
- Guha M, Choubey V, Maity P, Kumar S, Shrivastava K, Puri SK, Bandyopadhyay U: Overexpression, purification and localization of apoptosis related protein from Plasmodium falciparum. Protein Expr Purif. 2007, 52: 363-372. 10.1016/j.pep.2006.11.004.View ArticlePubMedGoogle Scholar
- Rathore S, Jain S, Sinha D, Gupta M, Asad M, Srivastava A, Narayanan MS, Ramasamy G, Chauhan VS, Gupta D, Mohmmed A: Disruption of a mitochondrial protease machinery in Plasmodium falciparum is an intrinsic signal for parasite cell death. Cell Death Dis. 2011, 2: e231-10.1038/cddis.2011.118.PubMed CentralView ArticlePubMedGoogle Scholar
- Sharma N, Mohanakrishnan D, Shard A, Sharma A, Sinha AK, Sahal D, Saima: Stilbene-chalcone hybrids: design, synthesis, and evaluation as a new class of antimalarial scaffolds that trigger cell death through stage specific apoptosis. J Med Chem. 2012, 55: 297-311.View ArticlePubMedGoogle Scholar
- Kumar S, Guha M, Choubey V, Maity P, Srivastava K, Puri SK, Bandyopadhyay U: Bilirubin inhibits Plasmodium falciparum growth through the generation of reactive oxygen species. Free Radic Biol Med. 2008, 44: 602-613. 10.1016/j.freeradbiomed.2007.10.057.View ArticlePubMedGoogle Scholar
- Suradji EW, Hatabu T, Kobayashi K, Yamazaki C, Abdulah R, Nakazawa M, Nakajima-Shimada J, Koyama H: Selenium-induced apoptosis-like cell death in Plasmodium falciparum. Parasitology. 2011, 138: 1-11.View ArticleGoogle Scholar
- Ch'ng JH, Liew K, Goh AS, Sidhartha E, Tan KS: Drug-induced permeabilization of parasite's digestive vacuole is a key trigger of programmed cell death in Plasmodium falciparum. Cell Death Dis. 2011, 2: e216-10.1038/cddis.2011.97.PubMed CentralView ArticlePubMedGoogle Scholar
- Arambage SC: An in vitro study of apoptosis-like cell death in Plasmodium berghei. 2008, Institute for Science and Technology in Medicine: Keele UniversityGoogle Scholar
- James ER, Green DR: Manipulation of apoptosis in the host-parasite interaction. Trends Parasitol. 2004, 20: 280-287. 10.1016/j.pt.2004.04.004.View ArticlePubMedGoogle Scholar
- Mideo N, Reece SE: Plasticity in parasite phenotypes: evolutionary and ecological implications for disease. Future Microbiol. 2012, 7: 17-24. 10.2217/fmb.11.134.View ArticlePubMedGoogle Scholar
- Hurd H, Carter V: The role of programmed cell death in Plasmodium-mosquito interactions. Int J Parasitol. 2004, 34: 1459-1472. 10.1016/j.ijpara.2004.10.002.View ArticlePubMedGoogle Scholar
- Carter V, Nacer AM, Underhill A, Sinden RE, Hurd H: Minimum requirements for ookinete to oocyst transformation in Plasmodium. Int J Parasitol. 2007, 37: 1221-1232. 10.1016/j.ijpara.2007.03.005.PubMed CentralView ArticlePubMedGoogle Scholar
- Salvioli S, Ardizzoni A, Franceschi C, Cossarizza A: JC-1, but not DiOC(6)(3) or rhodamine 123, is a reliable fluorescent probe to assess Delta Psi changes in intact cells: Implications for studies on mitochondrial functionality during apoptosis. FEBS Lett. 1997, 411: 77-82. 10.1016/S0014-5793(97)00669-8.View ArticlePubMedGoogle Scholar
- van Zandbergen G, Luder CGK, Heussler V, Duszenko M: Programmed cell death in unicellular parasites: a prerequisite for sustained infection?. Trends Parasitol. 2010, 26: 477-483. 10.1016/j.pt.2010.06.008.View ArticlePubMedGoogle Scholar
- Kroemer G, Galluzzi L, Vandenabeele P, Abrams J, Alnemri ES, Baehrecke EH, Blagosklonny MV, El-Deiry WS, Golstein P, Green DR, Hengartner M, Knight RA, Kumar S, Lipton SA, Malorni W, Nuňez G, Peter ME, Tschopp J, Yuan J, Piacentini M, Zhivotovsky B, Melino G: Classification of cell death: recommendations of the Nomenclature Committee on Cell Death 2009. Cell Death Differ. 2009, 16: 3-11. 10.1038/cdd.2008.150.PubMed CentralView ArticlePubMedGoogle Scholar
- Galluzzi L, Aaronson SA, Abrams J, Alnemri ES, Andrews DW, Baehrecke EH, Bazan NG, Blagosklonny MV, Blomgren K, Borner C, Bredesen DE, Brenner C, Castedo M, Cidlowski JA, Ciechanover A, Cohen GM, De Laurenzi V, De Maria R, Deshmukh M, Dynlacht BD, El-Deiry WS, Flavell RA, Fulda S, Garrido C, Golstein P, Gougeon ML, Green DR, Gronemeyer H, Hajnoczky G, Hardwick JM, Hengartner MO, Ichijo H, Jaattela M, Kepp O, Kimchi A, Klionsky DJ, Knight RA, Kornbluth S, Kumar S, Levine B, Lipton SA, Lugli E, Madeo F, Malorni W, Marine JCW, Martin SJ, Medema JP, Mehlen P, Melino G, Moll UM, Morselli E, Nagata S, Nicholson DW, Nicotera P, Nunez G, Oren M, Penninger J, Pervaiz S, Peter ME, Piacentini M, Prehn JHM, Puthalakath H, Rabinovich GA, Rizzuto R, Rodrigues CMP, Rubinsztein DC, Rudel T, Scorrano L, Simon HU, Steller H, Tschopp J, Tsujimoto Y, Vandenabeele P, Vitale I, Vousden KH, Youle RJ, Yuan J, Zhivotovsky B, Kroemer G: Guidelines for the use and interpretation of assays for monitoring cell death in highereukaryotes. Cell Death Differ. 2009, 16: 1093-1107. 10.1038/cdd.2009.44.PubMed CentralView ArticlePubMedGoogle Scholar
- Lanz-Mendoza H, Hernandez-Martinez S, Ku-Lopez M, Rodriguez Mdel C, Herrera-Ortiz A, Rodriguez MH: Superoxide anion in Anopheles albimanus hemolymph and midgut is toxic to Plasmodium berghei ookinetes. J Parasitol. 2002, 88: 702-706.View ArticlePubMedGoogle Scholar
- Peterson TM, Gow AJ, Luckhart S: Nitric oxide metabolites induced in Anopheles stephensi control malaria parasite infection. Free Radic Biol Med. 2007, 42: 132-142. 10.1016/j.freeradbiomed.2006.10.037.PubMed CentralView ArticlePubMedGoogle Scholar
- Ha EM, Oh CT, Bae YS, Lee WJ: A direct role for dual oxidase in Drosophila gut immunity. Science. 2005, 310: 847-850. 10.1126/science.1117311.View ArticlePubMedGoogle Scholar
- Kumar S, Molina-Cruz A, Gupta L, Rodrigues J, Barillas-Mury C: A peroxidase/dual oxidase system modulates midgut epithelial immunity in Anopheles gambiae. Science. 2010, 327: 1644-1648. 10.1126/science.1184008.PubMed CentralView ArticlePubMedGoogle Scholar
- Srivastava IK, Rottenberg H, Vaidya AB: Atovaquone, a broad spectrum antiparasitic drug, collapses mitochondrial membrane potential in a malarial parasite. J Biol Chem. 1997, 272: 3961-3966. 10.1074/jbc.272.7.3961.View ArticlePubMedGoogle Scholar
- Park BC, Park SH, Paek SH, Park SY, Kwak MK, Choi HG, Yong CS, Yoo BK, Kim JA: Chloroquine-induced nitric oxide increase and cell death is dependent on cellular GSH depletion in A172 human glioblastoma cells. Toxicol Lett. 2008, 178: 52-60. 10.1016/j.toxlet.2008.02.003.View ArticlePubMedGoogle Scholar
- Jiang PD, Zhao YL, Shi W, Deng XQ, Xie G, Mao YQ, Li ZG, Zheng YZ, Yang SY, Wei YQ: Cell growth inhibition, G2/M cell cycle arrest, and apoptosis induced by chloroquine in human breast cancer cell line Bcap-37. Cell Physiol Biochem. 2008, 22: 431-440. 10.1159/000185488.View ArticlePubMedGoogle Scholar
- Butcher GA: Antimalarial drugs and the mosquito transmission of Plasmodium. Int J Parasitol. 1997, 27: 975-987. 10.1016/S0020-7519(97)00079-9.View ArticlePubMedGoogle Scholar
- Ch'ng JH, Renia L, Nosten F, Tan KS: Can we teach an old drug new tricks?. Trends Parasitol. 2012, 28: 220-224. 10.1016/j.pt.2012.02.005.View ArticlePubMedGoogle Scholar
- Welburn SC, Maudlin I: Control of Trypanosoma brucei brucei infections in tsetse, Glossina morsitans. Med Vet Entomol. 1997, 11: 286-289. 10.1111/j.1365-2915.1997.tb00408.x.View ArticlePubMedGoogle Scholar
- Duszenko M, Figarella K, Macleod ET, Welburn SC: Death of a trypanosome: a selfish altruism. Trends Parasitol. 2006, 22: 536-542. 10.1016/j.pt.2006.08.010.View ArticlePubMedGoogle Scholar
- Hurd H, Grant KM, Arambage SC: Apoptosis-like death as a feature of malaria infection in mosquitoes. Parasitology. 2006, 132 (Suppl): S33-47.View ArticlePubMedGoogle Scholar
- Vaughan JA: Population dynamics of Plasmodium sporogony. Trends Parasitol. 2007, 23: 63-70. 10.1016/j.pt.2006.12.009.View ArticlePubMedGoogle Scholar
- Sinden RE, Dawes EJ, Alavi Y, Waldock J, Finney O, Mendoza J, Butcher GA, Andrews L, Hill AV, Gilbert SC, Basanez MG: Progression of Plasmodium berghei through Anopheles stephensi is density-dependent. PLoS Pathog. 2007, 3: e195-10.1371/journal.ppat.0030195.PubMed CentralView ArticlePubMedGoogle Scholar
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