- Open Access
MSP-1p42-specific antibodies affect growth and development of intra-erythrocytic parasites of Plasmodium falciparum
© Bergmann-Leitner et al; licensee BioMed Central Ltd. 2009
- Received: 8 May 2009
- Accepted: 3 August 2009
- Published: 3 August 2009
Antibodies are the main effector molecules in the defense against blood stages of the malaria parasite Plasmodium falciparum. Understanding the mechanisms by which vaccine-induced anti-blood stage antibodies work in protecting against malaria is essential for vaccine design and testing.
The effects of MSP-1p42-specific antibodies on the development of blood stage parasites were studied using microscopy, flow cytometry and the pLDH assay. To determine allele-specific effects, if present, allele-specific antibodies and the various parasite clones representative of these alleles of MSP-1 were employed.
The mode of action of anti-MSP-1p42 antibodies differs among the parasite clones tested: anti-MSP-1p42 sera act mainly through invasion-inhibitory mechanisms against FVO parasites, by either preventing schizonts from rupturing or agglutinating merozoites upon their release. The same antibodies do not prevent the rupture of 3D7 schizonts; instead they agglutinate merozoites and arrest the development of young parasites at the early trophozoite stage, thus acting through both invasion- and growth inhibitory mechanisms. The second key finding is that antibodies have access to the intra-erythrocytic parasite, as evidenced by the labeling of developing merozoites with fluorochrome-conjugated anti-MSP-1p42 antibodies. Access to the parasite through this route likely allows antibodies to exert their inhibitory activities on the maturing schizonts leading to their inability to rupture and be released as infectious merozoites.
The identification of various modes of action by which anti-MSP-1 antibodies function against the parasite during erythrocytic development emphasizes the importance of functional assays for evaluating malaria vaccines and may also open new avenues for immunotherapy and vaccine development.
- Immune Serum
- Parasitophorous Vacuole
- Immune Seron
- Parasite Culture
- Schizont Stage
Natural immunity against malaria is based on the presence of antibodies directed against the blood stage parasite, as demonstrated by passive transfer experiments of immunoglobulins [1–3]. The mode of action of blood stage-specific antibodies depends on their antigen-specificity: they can bind to merozoites, opsonize and target them towards phagocytic cells of the host , or prevent invasion of new erythrocytes . Once infected, antibodies against the asexual blood stage antigen Pf332 inhibit the intra-erythrocytic development of Plasmodium falciparum [6–8]. Furthermore, antibodies against free parasitic glycosylphosphatidylinositol (GPI) can control the severity of disease by neutralizing toxic components released from ruptured infected erythrocytes [9, 10].
The major merozoite surface protein -1 (MSP-1) was identified in immune complexes from merozoite lysates, which provided the rationale for developing vaccines against this antigen . MSP-1 undergoes two successive proteolytic cleavage events . The second processing event occurs immediately before invasion, resulting in the cleavage of the p42 molecule into a p33 and a p19 fragment. The p19 fragment remains attached to the merozoite surface through a GPI anchor  and is comprised of two epidermal growth factor (EGF)-like domains , which may have a role in the invading complex. Serological studies have provided significant evidence to suggest that immune responses directed against the C-terminus of MSP-1 (MSP-119 and MSP-142) are associated with immunity in preclinical models [15–18], as well as from individuals residing in endemic areas [16, 19].
In the course of characterizing immune responses induced by MSP-1 vaccines, it was recognized that: (1) proteins produced by various expression systems differ in their immunogenicity and ability to induce anti-parasite activities [20, 21]; (2) not all MSP-1-based vaccines induce protective immunity  and; (3) the degree of inhibition was dependent on the method chosen to measure invasion- and growth inhibition mediated by anti-MSP-1p42 and that only the methods that are based on cell viability and/or metabolic activity are able to accurately measure growth inhibition, while all the methods tested were equally able to detect invasion inhibition . Thus, selecting the appropriate method permits differentiation between the various mechanisms by which antibodies affect parasite development.
The current study was designed to investigate the effect of anti-MSP-1p42 antibodies on intra-erythrocytic parasite development and their consequences on parasite viability and infectivity. Depending on the parasite clone, anti-MSP-1p42 antibodies prevented schizont rupturing by stalling or arresting intra-erythrocytic parasite development likely through direct interactions with intra-erythrocytic parasites within the parasitophorous vacuole. The nature of the inhibitory effect was strongly affected not only by the parasite clone, but also by the fine-specificity of the antibodies. Only antibodies that bound the p19 subunit, but not the EGF-like domain 1 or 2 subunits, displayed growth inhibitory activities indicating that protective epitopes are dependent on the tertiary structure of the molecule.
Several important lessons can be gained from these findings: (1) various allele-specific effector mechanisms can develop to the same blood stage antigen; (2) while in vitro assays provide a useful tool to determine vaccine efficacy, such assays need to take into account the predominant antibody-mediated effector mechanisms against a particular clone; (3) inhibitory anti-MSP-1 specific antibodies map to epitopes formed through the "properly" folded p19 subunit and not to its sub-domains [24, 25]; (4) with the exclusion of potential effector cells, only macromolecules of a defined size have access to the intra-erythrocytic parasite either through the putative "parasitophorous duct" or through the "leaky" erythrocytic membrane [6, 26], and thus MSP-1-specific antibodies could be used as carriers and targeting moieties for anti-malarial drugs.
Complete media was prepared with RPMI 1640 (Invitrogen, Carlsbad, CA) containing 25 mM HEPES, 7.5% w/v NaHCO3 and 10% human pooled serum (bloodtype O+). Plasmodium falciparum clones 3D7, FVO and CAMP were maintained and synchronized by the temperature cycling method . Unless stated otherwise, cultures in the presence or absence of immune serum were set up at approximately six hours before rupture occurred (starting parasitaemia 0.3%, 1% haematocrit uninfected erythrocytes) in 96-well plates under static conditions.
Access of antibodies to the intra-erythrocytic parasite
To visualize the uptake of macromolecules, non-manipulated 3D7 and FVO cultures (2–3% parasitaemia at 4% haematocrit) were incubated at the late trophozoite/early schizont stage with either 2 μl of 1:100 diluted yellow-green fluorescent FluoSpheres beads (40 nm size, Molecular Probes, Eugene, OR), or diluent (BlockAid, Molecular Probes) or 1:50 diluted Alexa 488- (Molecular Probes) or PE-conjugated antisera for two hours. Samples were enriched for parasites by passing them through a column (MS+) (Miltenyi Biotech, Auburn, CA) inserted into a MiniMACS magnet (Miltenyi Biotech) at the end of the incubation time to avoid any stress related artifacts due to out-gassing.
Escherichia coli-expressed recombinant MSP-1p42(3D7) (FMP1, falciparum malaria protein 1), MSP-1p42(FVO) (FMP003) and the codon harmonized MSP1p42(FVO) (FMP010) were produced under GMP conditions as described elsewhere [15, 28, 29].
New Zealand White rabbits (n = 8/immunization group, Spring Valley Laboratories, Poolesville, MD) were immunized subcutaneously four times with either recombinant MSP-1p42 of the FVO clone (four immunizations with 36 μg)  or the 3D7 clone (prime with 225 μg and three boosts with 50 μg each)  emulsified in complete/incomplete Freund's adjuvant (CFA/IFA). Additional experimental groups were: rabbits (n = 4) immunized subcutaneously three times with 50 μg of codon harmonized MSP-1p42(FVO)  in CFA/IFA and Montanide ISA-720 (Seppic, Paris, France) and rabbits (n = 4) immunized subcutaneously three times with 50 μg of reduced/alkylated MSP-1p42 (3D7) and (FVO) in CFA/IFA (control sera) . Serum pools were aliquoted and stored frozen until analysis. Where indicated, immunoglobulins were purified from sera obtained after immunization with either reduced/alkylated MSP-1p42 (3D7 or FVO allele) emulsified in CFA/IFA. Immunoglobulins were purified using HiTrap Protein G columns (GE Healthcare, Piscataway, NJ) according to manufacturer's instructions and conjugated with fluorochromes following the manufacturer's instructions. Fluorochromes used were Alexa 488 or phycoerythrin (both purchased from Molecular Probes). Purified immunoglobulins were tested at concentrations normalized to the titers of the respective antisera. Both, antisera and purified immunoglobulins were tested in growth inhibition assays using recombinant MSP-1p42 antigen add-back (reversal of inhibition assay) to assure that the activity seen was antigen-specific.
ELISA assays were performed as previously described in detail .
Affinity purification of MSP-1 subunit specific antibodies
GSH resin was coated with 2.5 mg/ml protein (GST-MSP-1p19 and GST-p19 EGF-domain 1 or 2 of either the 3D7 or the FVO allele ). Pooled sera from five or eight rabbits, respectively, immunized with either MSP-1p42(3D7)/FA or MSP-1p42(FVO)/FA were incubated with protein-coated GSH resin (GE Healthcare) for 1 hr at RT. Resin was washed and the bound antibodies were eluted by washing the resin three times with 75 mM glycine (pH = 3.0) and followed by two times with 0.5 M NaCl. Eluted antibodies were analysed by SDS gel electrophoresis using 4–20% SDS-PAGE gels (Invitrogen, Carlsbad, CA).
Cultures were harvested at various time points as indicated and blood smears were made from each well. Blood smears were fixed in methanol and stained in a 10% Giemsa solution (Sigma, St. Louis, MO) for 10 min. Slides were washed in water and allowed to air dry before analysis. Evaluation was performed at 1,000× magnification (oil-immersion) using a Nikon E400 Eclipse microscope and photographs were taken with an Olympus BX-50 microscope with digital camera (Magnafire Software). Three slides per group were evaluated by counting 2000 erythrocytes (RBC) or 100 parasitized erythrocytes (pRBCs)/slide in a blinded fashion.
Confocal images were taken on a Nikon E800 microscope and the laser confocal system, BioRad Radiance 2100. Thirty layers at a spacing of 0.5 μm were scanned for each image and then z-stacked (performing 3D Blind Deconvolution on the stack (AutoDeblur deconvolution software, AutoQuant Imaging Inc, Watervliet, NY)). Images were analysed at 3% laser power.
Evaluation of invasion-/growth inhibition
Cultures for growth inhibition assays were set up at the schizont stage and cultured for one cycle as described . For pLDH detection, cells were harvested, washed and frozen at -30°C until analysis. pLDH was detected and measured as described previously [31, 32]. For flow cytometric analysis of growth- and invasion inhibition, 50 μl culture aliquots were stained with hydroethidine (HE) (Polysciences, Warrington, PA) or Syto-16 (Molecular Probes, Eugene, OR). Stock solutions of HE were prepared at 10 mg/ml dissolved in DMSO (Sigma) and stored at -30°C. Samples were stained by adding 500 μl of freshly diluted HE (diluted 1:200 in warm (37°C) phosphate buffered saline (PBS) (Biowhittaker, Walkersville, MD)) to the parasite suspensions and incubating for 20 min at 37°C. Syto-16 was diluted to 200 nM with PBS; a 500 ml aliquot was added to the parasite suspensions and incubated for 30 min at 37°C. Staining was stopped by transferring the samples to ice (which allowed stabilization of the staining for up to two hours) and diluted with 1 ml PBS prior to analysis. The data were acquired on a FACSCalibur flow cytometer (Becton Dickinson, San Jose, CA) using CellQuest software for acquisition and analysis.
Immune rabbit sera raised against various MSP-1p42 proteins are growth/invasion inhibitory against homologous and heterologous clones of P. falciparum
MSP-1p42 specific antibodies cause morphological changes to parasite in in vitro cultures
Quantitative analysis of Giemsa-stained blood smears of cultures incubated with various antisera.
(A) 6 hrs post invasion
Antisera tested a
Proportion of phenotype [%] b
(B) 12 hrs post invasion
Antisera tested a
Proportion of phenotype [%] b
Macromolecules and antibodies have access to the intra-erythrocytic parasite
The observation that antibodies can mediate growth retardation including the stalling of schizonts indicates that antibodies can access intra-erythrocytic parasite. Previous findings suggested that the membranes of infected-erythrocytes become "leaky" prior to rupture , providing a route through which antibodies could enter the infected RBC. An alternative explanation is that the site of invasion on the erythrocyte membrane never completely closes, leaving a pore and a small duct extending into the parasitophorous vacuole . This parasitophorous duct is used for transporting macromolecules into the parasitophorous vacuole bypassing the erythrocyte membrane [26, 33].
Anti-MSP-1p42 specific antibodies retard the development of intra-erythrocytic parasites
MSP-1p42 and p19-specific antibodies are responsible for the functional activity in immune sera
There is significant data in the literature supporting the development of MSP-1p42 as a blood-stage vaccine candidate primarily as antibodies directed against this antigen have been shown to protect against homologous challenge in Aotus monkey studies, albeit using strong adjuvants like complete Freund's/incomplete Freund's , as well as shown to correlate with reduced parasite burden and clinical disease from human sero-epidemiological studies (reviewed in ). Thus, it is crucial to understand the potential mechanisms underlying the anti-parasitic activities for this target antigen in order to design MSP-1-based vaccines with maximal vaccine efficacy. In two recent studies which compare various MSP-1-based vaccine candidates with regards to their immunogenicity and ability to induce antibodies that mediate anti-parasitic activity [20, 21], the differences observed in antibody binding and functional activities induced were attributed to either the immunogens ability to induce more "biologically" relevant activities against the parasite or from the effects on the immunogens conformation as a result of the expression or purification systems utilized. This is not surprising as the quality of the immune response induced may be influenced by the quality of the protein produced. To avoid issues of expression and purification process differences, the recombinant MSP-1p42 molecules used as immunogens in the current study were all expressed similarly from E. coli and purified as soluble proteins [15, 28, 29]. Where directly comparable, no apparent differences were observed in the anti-parasitic activities induced by either the single codon mutated MSP-1p42 (FMP003) and full gene codon harmonized MSP-1p42 (FMP010) in FA or Montanide ISA 720 as adjuvant. Therefore, for at least the two adjuvants tested, the mode of action of the functional activities induced in rabbits was not adjuvant-dependent.
The present study demonstrates that antibodies directed against MSP-1p42 play a complex role during invasion and intra-erythrocytic maturation (growth) of parasites. Using comparative studies of P. falciparum FVO, CAMP/FUP and 3D7 parasite cultures, we made several observations: first, that the quality of the response of MSP-1p42 specific antibodies is independent of the immunogen and adjuvant used (Figure 1); second, that the "type" of response against the parasite, whether invasion or growth inhibitory, was dependent on the assay clone, for instance, invasion- and growth inhibition was observed for 3D7 and CAMP/FUP parasites while only invasion inhibition was observed for FVO parasites (Figures 1, 6); third, that only antibodies raised against MSP-1p42 or affinity-purified using either the 3D7 or FVO p19 fragments had any inhibitory activity, while antibodies affinity-purified using either the EGF-like domain 1 or 2 did not (Figure 6); fourth, that the MSP-1p19 specific antibodies component exhibited homologous allele-specific inhibitory activities that were not observed for antibodies to the total MSP-1p42; and finally, that antibodies were able to enter viable infected erythrocytes and bind to intra-erythrocytic parasites, and that likely through this action, inhibit either further development or prevent rupture of maturing schizonts (Figures 2, 5, 6).
The present study revealed various reaction patterns of blood stage parasites in response to MSP-1p42 specific antibodies: invasion inhibition mediated by preventing schizont maturation ("stalled schizonts"), schizont rupturing and agglutination of merozoites prior to or upon their release (Figure 2). The observation that anti-MSP-1p42 specific antibodies cannot prevent the rupture of 3D7 schizonts (Figure 2) is not due to a general inability of the schizonts to be stalled as anti-AMA-1 specific antibodies induced this phenotype as well (Bergmann-Leitner, unpublished observations). Preventing schizonts from rupturing permanently affected the schizonts, as no spike in parasitaemia at any later time points could be detected suggesting that the observed effect was likely not due to a transient phenotype. Growth inhibition or retardation becomes evident by progressive losses in the ability to stain DNA with HE and reductions in the levels of pLDH measured in the cultures in the presence of immune serum. Moreover, growth retardation was observed when pRBC cultures treated with either control or immune serum were compared for their DNA content as a measurement of parasite maturation (Figure 5). As suggested by the HE-staining, 3D7 parasites were more affected by the phenomenon of growth retardation than were FVO parasites. However, measuring the DNA content as a marker for maturation does not necessarily indicate that the effect of immune antibodies is persistent, i.e., even though the maturation is slowed these cultures retained similar multiplication rates as control cultures. Thus currently, the only feasible measures of growth inhibition are those methods that are based on parasite viability such as HE-staining of DNA and measurement of pLDH .
In an effort to better understand how MSP-1p42 specific antibodies affect intra-erythrocytic parasite development, such that schizonts can no longer rupture, it was first corroborated that antibodies, regardless of their specificity, can enter infected RBCs (Figure 4), as shown previously for other macromolecules, such as beads having diameters up to 80 nm [26, 33], iron chelators , antisense oligonucleotides , plasmids  and antibodies . In the case where these antibodies are unable to prevent invasion of erythrocytes, antibodies that are bound to parasites may be dragged into the newly invaded RBC and remain bound to the ring stage parasite during the early phases of development immediately after invasion (unpublished observation, and ). A recent report demonstrates that the p19 fragment of MSP-1 may be involved in the formation of the food vacuole . It needs to be determined how antibody binding to p19 during and after invasion affects the role of the molecule during this crucial developmental step. In the later development it is possible that the antibody-bound MSP-1 on intra-erythrocytic parasites interferes with the ability to cause the phenotypic changes on FVO and CAMP/FUP schizonts that lead to rupture. Finally, this study addressed the question of anti-MSP-1p42 specific antibodies fine specificities and their role in mediating the various phenotypes of invasion and growth inhibition that were detected. To this end, antibodies were affinity-purified using either recombinant MSP-1p19 or the EGF-like domain 1 or 2 (representative of the 3D7 or FVO allele) contained within the p19 fragment (Figure 6). Flow cytometric analysis of parasite cultures treated with the various antibody preparations derived from rabbit immune serum revealed that only antibodies raised against the MSP-1p42 or affinity purified antibodies specific for MSP-1p19 had any inhibitory activity. These results are consistent with the findings obtained from naturally-exposed Western Kenyan adults' immune sera where using transgenic P. falciparum expressing MSP-1-p19 orthologs, the majority of the inhibitory activity was directed to the MSP-1p19 portion of the molecule [19, 35]. Affinity purified anti-MSP-1 antibodies using EGF-like domain 1 and 2 proteins did not capture antibodies that had any inhibitory function indicating that the crucial epitopes are formed by both domains or that the epitope is larger than just one of the domains alone. This finding is in agreement with epitope mapping studies for the growth inhibitory mAb, namely 12.10 , where both domains were required for mAb binding [25, 43]. Interestingly, MSP-1p19-purified antibodies appeared to be more allele-specific with regard to invasion inhibition than the total MSP-1p42 antibody population as MSP-1p19 (3D7) antibodies were only able to inhibit 3D7 parasites and to a lesser extent CAMP/FUP parasites and not FVO parasites. Similarly, MSP-1p19 (FVO)-purified antibodies only inhibited invasion of FVO parasites, while the effect on 3D7 and CAMP/FUP parasites was solely growth-inhibitory. Thus the mechanism of invasion inhibition may be more allele-specific than the mechanism of growth inhibition.
The findings from pre-clinical studies in rabbits provide new insights into the possible mode of action of anti-MSP-1p42 specific antibodies and their broader effect on intra-erythrocytic stage parasite development and thus solicit similar characterizations of antibodies directed against other blood stage antigens. Likewise, affinity purification of MSP-1p42 specific antibodies isolated from "protected" individuals residing in endemic regions may further support and define the relevance of these findings and lead to a better understanding of the role and modes of action of these antibody activities.
The authors declare that they have no competing interests.
Research was conducted in compliance with the Animal Welfare Act and other federal statutes and regulations relating to animals and experiments involving animals and adheres to principles stated in the Guide for the Care and Use of Laboratory Animals, NRC Publication, 1996 edition.
The authors' views are private and are not to be construed as official policy of the Department of Defense or the U.S. Army.
The authors would like to thank Dr. Michael Zidanic (WRAIR, Silver Spring, MD) for the confocal microscopy analysis and Dr. Mark Wilson (NIH, Bethesda, MD) for critically reviewing and editing the manuscript. The work was initiated under the guidance of Dr. Jeffrey A. Lyon.
This work was supported by the United States Agency for International Development, Project Number 936-6001, Award Number AAG-P-00-98-00006, Award Number AAG-P-00-98-00005, and by the United States Army Medical Research and Materiel Command.
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