- Open Access
Pitting of malaria parasites and spherocyte formation
© Anyona et al; licensee BioMed Central Ltd. 2006
- Received: 25 January 2006
- Accepted: 31 July 2006
- Published: 31 July 2006
A high prevalence of spherocytes was detected in blood smears of children enrolled in a case control study conducted in the malaria holoendemic Lake Victoria basin. It was speculated that the spherocytes reflect intraerythrocytic removal of malarial parasites with a concurrent removal of RBC membrane through a process analogous to pitting of intraerythrocytic inclusion bodies. Pitting and re-circulation of RBCs devoid of malaria parasites could be a host mechanism for parasite clearance while minimizing the anaemia that would occur were the entire parasitized RBC removed. The prior demonstration of RBCs containing ring-infected erythrocyte surface antigen (pf 155 or RESA) but no intracellular parasites, support the idea of pitting.
An in vitro model was developed to examine the phenomenon of pitting and spherocyte formation in Plasmodium falciparum infected RBCs (iRBC) co-incubated with human macrophages. In vivo application of this model was evaluated using blood specimens from patients attending Kisumu Ditrict Hospital. RBCs were probed with anti-RESA monoclonal antibody and a DNA stain (propidium iodide). Flow cytometry and fluorescent microscopy was used to compare RBCs containing both the antigen and the parasites to those that were only RESA positive.
Co-incubation of iRBC and tumor necrosis factor-alpha activated macrophages led to pitting (14% ± 1.31% macrophages with engulfed trophozoites) as opposed to erythrophagocytosis (5.33% ± 0.95%) (P < 0.01). Following the interaction, 26.9% ± 8.1% of the RBCs were spherocytes as determined by flow cytometric reduction in eosin-5-maleimide binding which detects RBC membrane band 3. The median of patient RBCs with pitted parasites (RESA+, PI-) was more than 3 times (95,275/μL) that of RESA+, PI+ RBCs (28,365/μL) (P < 0.01). RBCs with pitted parasites showed other morphological abnormalities, including spherocyte formation.
It is proposed that in malaria holoendemic areas where prevalence of asexual stage parasites approaches 100% in children, RBCs with pitted parasites are re-circulated and pitting may produce spherocytes.
- Malaria Parasite
- Hereditary Spherocytosis
- Thin Blood Smear
- Ring Stage
In the malaria holoendemic area of Lake Victoria basin, the estimated inoculation rate averages one infective bite daily and, as a consequence, prevalence rates of asexual stage malaria parasites in children is almost 100% . The persistent parasitaemia induces profound haematological abnormalities that include anaemia, platelet depletion, cytoadherence of infected red cells, leukocytic stimulation by released parasite antigens, induction of cytokines and splenomegaly, among others . In an attempt to contain these haematological aberrations, the macrophages of reticulo-endothelial system (RES) embark on clearance of parasites through mechanisms that are still not very clear .
Animal experiments conducted in late 60s suggested that the spleen can remove intraerythrocytic parasites while leaving the host erythrocyte intact, a process referred to as 'pitting' [4, 5]. This process is analogous to splenic removal of intraerythrocytic inclusion particles such as Heinz and Howell-Jolly bodies [4, 5]. Further evidence of pitting in patients with Plasmodium falciparum malaria [3, 6] has recently come from demonstration of circulating RBCs containing abundant ring-infected erythrocyte surface antigen (pf 155 or RESA) but no intracellular parasites [3, 6]. More recently, it has been demonstrated that, because of the rigidity that is associated with infected RBCs, trophozoites may be pitted out of infected erythrocyte by the shear pressure of the tight spleen capillary bed . Whether by action of macrophages or capillary bed pressure, the product of pitting is creation of surface area depleted RBCs  that are free of parasites. Such RBCs are referred to as spherocytes, a term that indicate cells that are spheroidal (less disc like) than normal RBCs. Depending on proportion of RBC membrane that has been lost, spherocytes can have normal sizes or smaller in which case they are referred to as microspherocytes.
The growth of P. falciparum in the RBC leads to membrane insertion of parasite antigens such as RESA and P. falciparum erythrocyte membrane protein-1 (Pf EMP-1), and also induces profound modifications to the erythrocyte integral membrane proteins such as Band 3, which then becomes the sites for deposition of immunoglobulins or complement . All these alterations of RBC surface are signals to macrophage attack and destroy these RBCs by erythrophagocytosis or perhaps lysis. Certainly the removal of large numbers of infected RBCs (iRBCs) and modified non-infected RBC is one of the mechanisms that contribute to development of malaria anaemia in children living in conditions of intense malaria transmission [10–12]. A competing mechanism of parasite clearance through the process of pitting with RBC salvage has been suggested as a host mechanism of attenuating anaemia . The trigger mechanisms for RBC salvage as opposed to destruction are unknown.
This paper reports on high prevalence of spherocytes in children that are constantly exposed to malaria and provides evidence that this may be caused by pitting of malaria parasites. An in vitro model system of studying the process of pitting in an environment that is devoid of host factors is also described. This model may provide a method of identifying RBC membrane changes that trigger macrophages to engage iRBCs and, thereby, initiate the pitting process. The in vivo relevance of this model was evaluated using blood specimens from patients attending Kisumu Ditrict Hospital.
Giemsa-stained thin blood smears were made from patients enrolled in a case control study whose details have been described earlier [11, 12]. Briefly, the case control study comprised three groups: cases of severe malarial anaemia (SA) defined as children with asexual P. falciparum parasitaemia and a haemoglobin level of ≤ 5 g/dL, and two controls, a symptomatic control (SC) and asymptomatic control (AC), each matched by age and gender to a case. SC were children with asexual P. falciparum parasitaemia and haemoglobin greater than 5 g/dL. AC were healthy children recruited from the same village as the cases. From each group, 25 thin blood films were examined by microscopy for abnormal RBC morphology. The haematologist slide's examiner had no prior information on the clinical status of the children. Blood specimens were also obtained from another group of 25 patients who were recruited in a case control study at Kisumu Ditrict Hospital. In this study, cases as defined above were matched with symptomatic controls of similar age and gender (± 2 months). In both studies, the protocols were approved by the Ethical Review Committee of the Kenya Medical Research Institute (KEMRI).
Culture and synchronization of parasites
A laboratory strain of P. falciparum, NF54, was cultured in normal O+ RBC from healthy donors and maintained in vitro using continuous culture conditions . Parasites at an initial parasitaemia of 2% were enriched for ring stages using D-sorbitol . Briefly, 6 mLs of culture at 2% parasitaemia of mainly young rings (10–12 h post invasion) were spun at 600 g and the pellet re-suspended in 6 mL 5% D-sorbitol. After 10 min incubation at room temperature, the cells were washed twice in malaria culture medium, diluted to 5% haematocrit and cultured as described above. This treatment was repeated every 48 hours until all the parasites were at ring stage as confirmed by microscopy. At 8% trophozoite parasitaemia, the iRBC were harvested by Percoll gradient purification method. Briefly, Percoll gradients were prepared by adding 10 mL of 90% Percoll to the bottom of a 45 mL Oakridge tube. Subsequent 5 mL layers of the 80%, 70% and 40% gradients were added consecutively. Parasites were suspended in 5 mL of RPMI 1640 and layered on top of the 40% gradient. This preparation was centrifuged in a SS34 fixed angle rotor (RC-5C Sorvall instruments, Du Pont, Maryland) at 10,000 rpm for 20 minutes, at 20°C. Trophozoite infected erythrocytes were removed from the second interphase and washed twice in RPMI 1640 containing 0.5% bovine serum albumin.
Culture of monocytes
THP-1 cells were obtained from American Type Culture Collection (ATCC., Manassas, VA, USA) and were maintained in RPMI 1640 medium supplemented with 10% foetal bovine serum, 0.05 mM 2-mercaptoethanol, 100 U/mL penicillin, 100 μg/mL streptomycin, 1.0 mM sodium pyruvate, 2.5 g/L D (+) glucose and 2 g/L sodium bicarbonate at cell densities of 3 × 105 cells/mL in a humidified incubator at 37°C, 5% CO2.
Co-incubation of iRBC and monocytes
Three triplicate THP-1 cultures were grown overnight (17–19 hours) in sterile 15 mL polypropylene tubes at a concentration of 3 × 106/mL in 6 mL medium containing TNF-α at a final concentration 4 ng/mL. This treatment did not affect cell viability as determined by trypan blue exclusion. Activated monocytes were washed once in RPMI and co-incubated with 1 × 106 trophozoite iRBCs in a water bath for 1 hour at 37°C. The cells were washed twice by centrifugation and the resulting pellet resuspended in 80 μL of RPMI. Giemsa-stained thin smears were made using 10 μL of the cell suspension. Thereafter, the smears were examined by microscopy to identify: 1) pitted malaria parasites, 2) spherocytes and 3) the number of RBCs with and without the parasites.
Eosin-5-maleimide (EMA) labeling of RBC
The EMA dye binds quantitatively to the RBC integral membrane protein Band 3 and can be used to reveal RBC membrane loss . EMA preparation and storage was done as recommended by King et al . Following co-incubation of iRBC and the monocytes, the cell mixture was washed, pelleted by centrifugation and resuspended in 50 μL of RPMI containing 0.5 mg/mL EMA (Eugene, Oregon USA). The procedure was used to stain patient RBCs. The mixture was incubated with intermittent mixing in the dark for one hour at room temperature. EMA stained cells were washed thrice and the pellet re-suspended in 500 μL of RPMI containing 0.5% bovine serum albumin. Acquisition and analysis were done immediately thereafter using a FACScan (Becton Dickinson, CA. USA) loaded with WinFCM and EXPO software (Applied Cytometry Systems, Sheffield UK). RBCs were gated on the basis of their logarithmic forward and side scatter characteristics. The level of EMA median logarithmic FL-1 channel fluorescence was determined for 15,000 events.
Probing of patient RBC with anti-RESA monoclonal antibody and propidium iodide
For flow cytometry, patient RBCs (1 × 106) were washed in PBS containing 1% BSA. The cells were then incubated with 1 mL 0.05% glutaldehyde for 30 minutes at room temperature. The glutaldehyde fixed cells were washed and permeabilized with 500 μL 1% Saponin in PBS for 5 minutes at room temperature. After two washes the cells were either resuspended in PBS containing 1 μg/mL RESA Mab, clone 28/2 (a gift from Robin F. Anders, Department of Biochemistry, La Trobe University, Bundoora, Victoria, Australia) and or in PBS containing 50 μg/mL propidium iodide and incubated at room temperature for 30 minutes. The cells were then washed twice with PBS and a FITC conjugated goat anti-mouse IgG-Fab fragment (Sigma-Aldrich Inc. St Luis, USA) added and cells incubated for 30 minutes at room temperature. RBCs were gated on the basis of their logarithmic forward and side scatter characteristics. 10,000 events were acquired and the proportions of RBCs that were RESA positive detected in the FL1 channel and those that were PI positive in the FL3 channel.
For fluorescent microscopy, thin blood smears were prepared and fixed with absolute ethanol for 3 minutes and air-dried. The slides were frozen at -20°C until used. Following removal from the freezer, the slides were washed gently in PBS and air dried for 5 minutes. The slides were then flooded with PBS containing either 1 μg/mL RESA Mab, and or 50 μg/mL propidium iodide and incubated for 30 minutes at room temperature. The slides were then washed twice with PBS and a FITC conjugated goat anti-mouse IgG-Fab fragment (Sigma-Aldrich Inc. St Luis, USA) added and the slides incubated as above. The slides were washed twice with PBS and examined using a BX40 fluorescent microscope (Olympus, Melville, NY), equipped with a Magnafire digital camera.
Welch corrected t test was used to compare the number of monocytes with engulfed parasites against those with engulfed iRBCs from a set of six experiments. Results are given as mean and standard error of the mean (SEM). For detection of proportion of RBCs that were both RESA+ and PI- and those that were RESA+ and PI+, the % RBCs population identified by flow cytometry was multiplied by total RBC count in each sample as determined by Coulter. The Mann-Whitney test was then used to compare proportion of RBCs that were both RESA+ and PI- and those that were RESA+ and PI+. Dye binding results are expressed as median channel fluorescence (MCF) and SEM. The Kruskal-Wallis test was used to compare the dye binding results for the un-interacted iRBCs, interacted normal RBC and interacted iRBC.
Spherocytosis and hypochromia is prevalent in all the clinical groups
Number of patients with spherocytes, hypochromia and parasitaemia in the three clinical groups. Details of these patients have been described earlier [11-12]
Severe anaemia N = 25
Symptomatic controls N = 24
Asymptomatic controls N = 24
Optimization of conditions for pitting
The success of pitting experiment was dependent on the ability to: 1) identify pitted malaria parasites from intact iRBCs co-incubated with the monocytes, and 2) detect increase in the number of uninfected RBCs as a result of this interaction. This required having a stage of malaria parasite that does not rupture during experimental manipulation and having a near 100% purified iRBCs before the interaction. The preferred method of preparing different stages of malaria parasites is by Percoll gradient. It was technically impossible to separate non-infected RBCs from ring stage iRBCs. But, while it was possible to obtain pure preparation of schizonts iRBCs by Percoll, during the 1 hour co-incubation with monocytes, many were found to have ruptured and it was, therefore, difficult to tell whether the engulfed schizonts were extracted from iRBCs or were from already ruptured parasites. Pure preparation of trophozoites iRBCs was easy to obtain by Percoll separation and they remained intact during the period of interaction with monocytes as confirmed by light microscopy. Therefore, all the experiments were conducted using trophozoites iRBCs.
The average number of pitted or erythrophagocytosed iRBCs was one, although multiple pitting and erythrophagocytosis were occasionally detected (Figure 1B and 1C, respectively). The number of RBCs devoid of trophozoites before and after interaction with the monocytes were enumerated. A 5% ± 1.5% increase in the number of un-parasitized RBCs was detected following the interaction (results not shown). The disparity between the reduction in parasitaemia and the number of monocytes with ingested naked parasites is probably due to lysis of damaged RBCs following the pitting process. RBCs devoid of parasites were smaller, globular and lacked a central hollow (Figure 1D) that is typical of normal human RBC.
Detection of spherocytes by flow cytometry
EMA staining did not reveal presence of spherocytes in the RBCs of the 25 patients attending Kisumu District Hospital (results not shown).
The proportion of parasite with pitted RBCs is higher than RBCs with parasites
A retrospective examination of blood films made from children with malaria revealed high prevalence of spherocytes regardless of their clinical status or parasitaemia (Table 1). It is not clear what the genesis of such high prevalence of spherocytes (79%) is, but it was speculated that the spherocytes reflect the pitting of malaria parasites from infected RBCs with a con-current removal of RBC membrane. Other studies have reported the phenomenon of pitting [3, 6, 7, 16–20] and was recently shown to happen when the spleen traps the parasitized RBCs and pits out the parasites . The study reported here is the first attempt to link pitting and occurrence of spherocytes in malaria. Spherocyte formation could have been enhanced by presence of activated macrophages and splenic enlargement is one of the indicators of macrophage activation. Indeed, splenomegaly was greater in SA (mean 3.6 ± 1.8 cm) than controls (SC = 0.8 ± 1.3 cm, AC = 0.1 ± 0.5 cm, P < 0.01) . These findings prompted experiments to determine whether spherocytes could have been created by pitting of malaria parasites.
Model human monocytes (THP-1) were used to demonstrate removal of intra-erythrocytic malaria parasites (Figure 1). Pitting of trophozoites (Figure 1) was associated with loss of RBC membrane, as indicated by reduction of EMA binding (Figure 2). The EMA binding is known to quantitatively detect the RBC integral membrane protein, Band 3, and the reduction of Band 3 has been used as a screening test for hereditary spherocytosis [15, 17]. It could be argued that the change in EMA staining that was observed after interaction with monocytes is due to dye loss from the interaction of RBCs with the monocytes with no real changes in membrane area. Indeed, some changes in EMA staining occurred when uninfected RBC were interacted with monocytes (Figure 2, panel B) but, the change in EMA staining was always much more pronounced when the interaction was carried with infected RBCs.
In an in vitro study, Kumaratilake et al interacted human peripheral leukocytes with cultured P. falciparum and showed that extraction of intraerythrocytic malarial parasites was preferred to ingestion of infected erythrocytes . However, they did not comment on the formation of spherocytes after the parasites had been removed. In the current study, RBCs from patients were stained with EMA but the presence of spherocytes could not be revealed by this method. When interpreting this data, it is important to realize that some spherocytes have normal sizes and EMA will only reveal microspherocytes that result from removal of considerable proportion of RBC surface. In malaria, it is the circulating ring stage parasites that are pitted, unlike in the in vitro set up where macrophages were interacted with the much bigger trophozoite stages. It is conceivable that unlike in the trophozoite stages, pitting of the small ring stages would not involve removal of sizeable RBC membrane. Another explanation is that EMA is not sensitive enough to detect the small numbers of spherocytic cells that emanate from pitting. Fluorescent microscopy did however identify RESA+, P. falciparum negative RBCs that were spherocytic (Figure 4D). EMA would work best in situations whereby large numbers of spherocytes are created for example in hereditary spherocytosis [15, 17].
The growth of P. falciparum induces profound modifications to the erythrocyte membrane. It causes oxidative damage to proteins such as Band 3 while intraerythrocytic parasite growth causes insertion into the membrane of antigens such as RESA and Pf EMP 1 [6, 9, 20, 22]. In vivo, these alterations, particularly the haemichrome-mediated oxidation of Band 3, are thought to mark the iRBCs for immunoglobulin and complement deposition and subsequent erythrophagocytosis . Although pitting was the dominant phenomenon in the in vitro model, erythrophagocytosis also occurred (Figure 1B) indicating that host factors do not have to be present for erythrophagocytosis to take place. Crucial to either pitting or erythrophagocytosis was activation of the THP-1 monocytes by TNF-α. Unstimulated monocytes did not engage in either of the two processes (results not shown). TNF-α was used to activate the monocytes because it is a major pro-inflammatory cytokine produced by macrophages of RES in children with malaria .
Patient RBCs were probed for "footprint" of previous parasitization using anti-RESA Mab. The proportion of previously parasitized RBC was consistently higher than that of RBCs with patent infection as determined by flow-ctytometry (Figure 3) and immunofluorescence (Figure 4). This is consistent with the estimated survival period for RESA positive, P. falciparum negative RBCs that are longer than that of parasitized RBCs .
In conclusion, in vitro data from this study indicate that pitting of malaria parasites can produce spherocytes. Taken together with other studies that indicate that pitting of malaria parasites is common [18, 19], and indeed preferred to phagocytosis of infected RBC , it is proposed that, in malaria holoendemic areas where the prevalence of asexual stage malaria parasites approaches 100% in children , the day-in-day-out pitting of malaria parasites produces high spherocytic rates. Of course, spherocyte formation may be a consequence of the pitting of intraerythrocytic inclusion bodies like Howell-Jolly bodies or the Heinz bodies produced in conditions associated with RBC oxidant stress such as glucose-6-phosphate dehydrogenase (G6PD) deficiency. G6PD deficiency is common in malaria endemic areas . It could be argued that pitting of parasites and returning surface area depleted RBC to the circulation is biologically preferable to erythrophagocytosis. Erythrophagocytosis results in removal of the entire iRBC and, thus, contributes to the clinically important anaemia. In contrast, pitting restores a red cell, albeit damaged, to the circulation. The damage is complex consisting of a loss of surface area and produces a spherocyte that can no longer undergo the full elliptical deformation required to traverse the microcirculation . The neoantigens present on the damaged RBC membrane lead to deposition of immunoglobulins and complement, all of which are signals for macrophagic attack. Nevertheless, despite its relatively shortened survival, the damaged red cell may perform useful oxygen carrying functions.
Finally, the in vitro model described here may prove useful in dissecting out those RBC membrane changes that trigger macrophages to engage iRBCs and thereby initiate the pitting or erythrophagocytosis process.
This work is published with the permission of the Director, Kenya Medical Research Institute. We thank Jose Stoute of Department of Cellular Injury, Walter Reed Army Institute of Research for providing the Giemsa stained slides. We are grateful to Ronald Taylor of Department of Biochemistry and Molecular Genetics, University of Virginia, Charlottesville for training in the use of fluorescent microscope. We thank Professor Robin F Anders, Department of Biochemistry, La Trobe University, Victoria, Australia for providing us with RESA monoclonal antibodies. This study was supported in part by a grant from the US Army Medical Research and Materiel Command. The BX40 fluorescent microscope was obtained with funds from The Ellison Medical Foundation. Samuel Anyona was a graduate student in Kenyatta University, Nairobi Kenya.
Disclaimer: The views of the authors do not purport to reflect the position of the Department of the Army or the Department of Defense. The U.S. Government has the right to retain a nonexclusive, royalty-free license in and to any copyright covering this paper.
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