Logo of plospathPLoS PathogensSubmit to PLoSGet E-mail AlertsContact UsPublic Library of Science (PLoS)View this Article
PLoS Pathog. Sep 2005; 1(1): e9.
Published online Sep 30, 2005. doi:  10.1371/journal.ppat.0010009
PMCID: PMC1238744

Exit of Plasmodium Sporozoites from Oocysts Is an Active Process That Involves the Circumsporozoite Protein

Kasturi Haldar, Editor

Abstract

Plasmodium sporozoites develop within oocysts residing in the mosquito midgut. Mature sporozoites exit the oocysts, enter the hemolymph, and invade the salivary glands. The circumsporozoite (CS) protein is the major surface protein of salivary gland and oocyst sporozoites. It is also found on the oocyst plasma membrane and on the inner surface of the oocyst capsule. CS protein contains a conserved motif of positively charged amino acids: region II-plus, which has been implicated in the initial stages of sporozoite invasion of hepatocytes. We investigated the function of region II-plus by generating mutant parasites in which the region had been substituted with alanines. Mutant parasites produced normal numbers of sporozoites in the oocysts, but the sporozoites were unable to exit the oocysts. In in vitro as well, there was a profound delay, upon trypsin treatment, in the release of mutant sporozoites from oocysts. We conclude that the exit of sporozoites from oocysts is an active process that involves the region II-plus of CS protein. In addition, the mutant sporozoites were not infective to young rats. These findings provide a new target for developing reagents that interfere with the transmission of malaria.

Synopsis

Malaria affects hundreds of millions of people, and kills at least 1 million children per year. The infective stages of the malaria parasites, named “sporozoites,” are found in the salivary gland of Anopheles mosquitoes, and are injected along with the saliva during blood feeding. From the skin, sporozoites enter the blood circulation and invade liver cells where the parasites multiply. When they exit the liver, these parasites infect blood cells and can cause severe symptoms. If ingested by mosquitoes, the blood-stage parasites continue their lifecycle in the insect stomach. Thousands of sporozoites are formed within a cyst-like structure (oocyst). The sporozoites come out of the oocyst and infect the salivary gland, where they remain until injected back into humans. Malaria parasites are increasingly resistant to drugs, mosquitoes are difficult to eliminate, and effective vaccines are not yet available. New tools to combat malaria are urgently needed. One exciting approach, although the application is in the distant future, is to release in endemic areas genetically modified mosquitoes that are resistant to parasite growth. This paper provides a new target for generating these “transmission-block” mosquitoes and shows that the exit of sporozoites from the oocysts is an active process that requires the enzymatic digestion of components of the oocyst wall. If these enzymes are inhibited in transgenic mosquitoes, sporozoites will never reach the salivary gland.

Introduction

The Plasmodium life cycle in the Anopheles mosquitoes begins with the ingestion of a blood meal containing Plasmodium gametocytes. After fertilization of the resulting gametes, the zygotes transform into motile ookinetes that traverse the midgut epithelium, reach the basal lamina, and then transform into oocysts. The young oocyst, surrounded by a capsule and by the basal lamina, undergoes multiple mitotic nuclear divisions and progressively enlarges in size without cytokinesis. At the same time, the cytoplasm is subdivided by membrane clefts forming structures named “sporoblasts.” Later, uninucleate sporozoites bud from the sporoblast membrane. The mature oocyst is about 50 μm in diameter and contains thousands of sporozoites. Sporozoites leave the oocysts asynchronously, enter the hemolymph, and then invade the salivary glands where they remain until they are injected, with the saliva, into the skin of the mammalian host [1,2].

In order to reach the flowing hemolymph, sporozoites must traverse two physical barriers: the oocyst capsule and the mosquito basal lamina. Because oocyst sporozoites display limited movement [3], their egress from oocysts is generally thought to be a passive process. Early ultrastructural observations reveal the presence of small openings in the capsule of mature oocysts and the basal lamina. Occasionally, sporozoites are found “penetrating” these openings and entering the hemolymph [4]. The oocyst capsule contains laminin of mosquito origin and displays trans-glutaminase activity probably of parasite origin [5,6]. In addition, the inner surface of the capsule is covered with the Plasmodium circumsporozoite (CS) protein [79].

The development of sporozoites in oocysts is CS dependent. When the CS gene is deleted, the oocysts are devoid of mature parasites [10]. To investigate the mechanisms leading to this developmental arrest, we have generated Plasmodium berghei parasites bearing different mutations in the CS coding region. In one of the P. berghei CS mutants, we substituted the positively charged amino acids of the conserved region II-plus with alanines. Region II-plus is located at the 5′ end of the thrombospondin type 1 repeat (TSR) domain of CS protein. Several in vitro observations strongly suggest that region II-plus participates in the initial steps of sporozoite attachment and invasion of the host's hepatocytes via interaction with heparan sulfate proteoglycan (HSPGs) on the host cells [11,12]. Here we show for the first time that the mutation in region II-plus of CS protein prevents the exit of sporozoites from oocysts and progression of the Plasmodium lifecycle. In addition, the mutant sporozoites are unable to infect rats.

Results/Discussion

Construction of CS-RIImut and CS-WT

A P. berghei clone with mutated region II-plus of CS protein (R290A, K291A, R292A, and K293A) was obtained by homologous recombination. In order to avoid any potential defects in the locus associated with the recombination event, a control clone, CS-WT, which produces wild-type CS protein, was generated by the same method (pRCS-WT and pRCS-RIImut, Figure 1A and and1B).1B). A PstI site was introduced in pRCS-RIImut in order to detect the presence of mutations by PCR and Southern blot analysis [13]. The schematic structure of CS and the sequence of region II-plus of wild-type and mutant CS are shown in Figure 1C.

Figure 1
Gene Targeting at the CS Locus of P. berghei

Genomic DNA from WT, CS-WT, and CS-RIImut were digested with XbaI and PstI, and subjected to Southern blot hybridization. WT displays a 7.9-kb band, whereas CS-WT displays a 5.5-kb band and CS-RIImut a 2.2-kb band, indicating that the CS-RIImut and CS-WT have a correct recombination locus (Figure 1D). This was confirmed by PCR amplification specific for recombinants (Figure 1E and and1F),1F), subsequent PstI digestion (Figure 1E), and by sequencing of PCR products. The sequences of coding regions of wild-type and mutant CS are as expected.

We cannot exclude the possibility that the substitution of the four positively charged amino acids of region II-plus led to secondary changes in the structure of CS protein.

CS-RIImut Sporozoites Do Not Exit from Oocysts

Groups of Anopheles stephensi mosquitoes were infected with CS-WT, a clone of wild-type P. berghei NK65 strain (WT), and two independent clones of CS-RIImut. CS-WT and WT are identical; therefore, CS-WT was used as a wild type control in all experiments. The numbers of oocysts and oocyst sporozoites at 14 d after blood meal (post-infection [PI]) were very similar in CS-WT and in the two mutant clones (Table 1). However, profound differences were observed at later time points. At day 16 and 18 PI, mutant infected mosquitoes contained many more oocyst sporozoites compared to wild-type infected ones (Figure 2A). In two other independent feeding experiments, similar results were obtained at day 16 PI: 50,000 and 96,000 oocyst sporozoites/mosquito for CS-RIImut, versus 35,000 and 75,000 oocyst sporozoites/mosquito for CS-WT, respectively. By contrast, the hemolymph of mosquitoes infected with CS-WT parasites contained many more sporozoites compared to mosquitoes infected with mutant parasites. CS-WT sporozoites entered the hemolymph beginning at day 12 PI, and the peak numbers were reached around day 18 PI. In contrast, even at 28 days PI, only minimal numbers of CS-RIImut sporozoites were found in the hemolymph (Figure 2B and and2C).2C). Thus, the observed increase in the numbers of CS-RIImut oocyst sporozoites between days 14 and 18 is most likely a consequence of their inability to be released in to the hemolymph.

Figure 2
CS-RIImut Oocyst Sporozoites Are Not Released from the Midguts
Table 1
Parasite Development in Mosquitoes

CS-RIImut Sporozoites Display Normal Morphology and Motility

The morphology of CS-RIImut sporozoites was analyzed by immunofluorescence assays (Figure 3A), transmission electron microscopy, and immuno-electron microscopy using monoclonal antibodies (3D11) to the repeats of the CS protein. (Figure 3B–3F). CS-RIImut did not display any abnormalities in the sporozoite morphology during development (Figure 3B). The detailed structure of the mutant sporozoite surface is shown Figure 3C and and3D.3D. The structures of the trimembrane pellicle (plasma membrane and inner membrane complex) and subpellicular microtubules are indistinguishable from those of wild type. Patterns of CS protein labeling in CS-WT and CS-RIImut sporozoites were indistinguishable. In the mutants, very similar to wild type, CS protein was detected on the surface of budding or fully developed sporozoites (Figure 3A and and3E),3E), and on the inner surface of the capsule (Figure 3E and and3F)3F) [2,14]. To compare the amounts of CS protein in mutant and CS-WT parasites, extracts of CS-WT and CS-RIImut oocyst sporozoites were analyzed by Western blot (Figure 3G). The intensity of both precursor (54 kDa) and mature (44 kDa) forms of CS [15], was very similar in the WT and the mutant. The two bands appear slightly smaller in the mutant as a result of the replacement of four basic residues (R290, K291, R292, and K293) with alanines. As a control we analyzed levels of TRAP (thrombospondin-related anonymous protein), another sporozoite surface protein [16], and found that it was not affected in the CS mutant (Figure 3G). We conclude that the recombination event and mutations did not grossly affect CS protein expression or stability.

Figure 3
Ultrastructure and CS Localization of CS-WT and CS-RIImut

It could be argued that the sporozoite exit from oocysts requires sporozoite motility and that the motility is impaired in the mutants. In fact, previous studies have shown that sporozoite motility is neither required nor does it ensure the exit of sporozoites from oocysts [14,17]. In contrast to the circular gliding observed in salivary gland sporozoites, movements of oocyst sporozoites are mostly limited to stretching and back-and-forth gliding [3]. We observed that approximately 3% CS-RIImut oocyst sporozoites display discontinuous gliding motility, and approximately 10%–15% display stretching and bending. The numbers are very similar to those of CS-WT.

CS-RIImut Oocysts Are More Resistant to Proteolytic Activity

Although CS-WT and CS-RIImut are morphologically indistinguishable, develop equally well in mosquitoes, move similarly, and contain equal levels of CS protein, sporozoite egress from mutant oocyst is profoundly defective. Little is known of the process of sporozoite exit from oocysts, but some information can be obtained from the erythrocytic stages of the parasite. During development in the red blood cells, malaria parasites reside inside a parasitophorous vacuole. Merozoite egress requires the rupture of the parasitophorous vacuole and the membrane of the red blood cells. Release of merozoites from infected erythrocytes requires proteases and is inhibited by inhibitors of proteolytic enzymes [1820]. Plasmodium falciparum falcipain-2 (a cysteine protease) cleaves erythrocyte membrane skeletal proteins at late stages of parasite development [21], facilitating the merozoite egress.

To examine the possible role of a proteolytic event in the release of sporozoites from oocysts, we treated isolated midguts from CS-WT– or CS-RIImut–infected mosquitoes (14 days PI) with trypsin and measured the number of released sporozoites (Figure 4). The lower temperature (25 °C) was chosen to mimic natural conditions of oocyst development in the mosquito midguts. In the absence of trypsin, very few sporozoites were released from either CS-WT– or CS-RIImut–infected midguts even after 3 h of incubation. Treatment with trypsin for 40 min leads to a significant increase in the number of sporozoites released from CS-WT, but not from CS-RIImut. Release of sporozoites from CS-RIImut oocysts was achieved only after extended treatment with trypsin. In Figure 4 we show the release at 14 d PI, but identical results were observed with 18-d oocysts (data not shown). This effect is trypsin specific, because the release of sporozoites was abolished when the soybean trypsin inhibitor was included in the incubation (data not shown).

Figure 4
In Vitro Oocyst Sporozoite Release Assay

These results indicated that the sporozoite egress from oocysts is a protease-dependent process and that CS-RIImut oocysts are more resistant to the trypsin treatment. CS is detected on the inner surface of the oocyst capsule [79]. Therefore, on their way out from the oocysts, sporozoites have to first traverse the CS protein layer beneath the capsule. The positively charged residues, arginines and lysines, of region II-plus are preferred substrates for certain cysteine proteases and serine proteases, such as trypsin. Therefore, it is possible that proteolysis of the CS protein layer underneath the capsule is required for sporozoite egress and is abolished in the mutant in which region II-plus has been substituted. Thus, a possible explanation for the defect of the mutant sporozoite is that the substitutions made in the region II-plus render CS protein more resistant to the putative protease. Trypsin treatment of the oocysts most likely cleaved the CS protein in many places, not only in region II-plus, since lysines and arginines are very abundant in the CS domains outside the repeats. Nevertheless, the subtle mutations introduced in CS region II-plus resulted in a clear difference in the kinetics of sporozoite release after treatment with the enzyme.

The exit of sporozoites from oocysts is most likely a stepwise process aimed at the sequential disruption of the capsule and the mosquito-derived basal lamina. In P. falciparum, PfCCp2 or PfCCp3, two secreted multidomain putative adhesive proteins, play an essential role in sporozoite release—in the absence of either protein, sporozoites were not released from the oocysts—but their localization and mechanism of action are unknown [22]. Our observations suggest that proteolysis of CS protein that lies beneath the capsule is likely to be an early event in sporozoite egress. Our hypothesis is supported by a recent finding that a papain-like cysteine protease egress cysteine protease 1 (ECP1) is required for sporozoite egress from oocysts [23]. Members of the papain family of cysteine proteases, similar to trypsin, consistently attack peptide bonds formed by lysine and arginine. We presume that ECP1 is only active when oocysts are “mature” and the sporozoites are ready to enter the hemolymph. At that particular time, only the CS protein that is beneath the capsule, but not CS on the sporozoite surface, is cleaved by ECP1, facilitating the egress of sporozoites from the oocysts. A possible explanation for this selectivity is that the enzyme that cleaves the capsule CS protein is also part of the capsule. We cannot exclude the possibility that the egress of sporozoites from oocysts is preceded by a proteolytic cascade and that ECP1 is only one of the participants.

CS-RIImut Oocysts Sporozoites Are Not Infective to Mammalian Hosts

As mentioned earlier, in vitro experiments strongly suggest that the region II-plus of CS protein plays an important role in the initial stages of sporozoite invasion of hepatocytes. Initial studies demonstrated that CS protein binds specifically to HSPGs in sections of human liver and that this binding is region II-plus dependent [24,25]. Synthetic peptides representing region II-plus specifically inhibit CS protein binding and sporozoite adhesion of HepG2 cells, the reference cell line that allows sporozoites to develop into mature exo-erythrocytic forms [26]. This inhibition is dependant on the downstream positively charged residues of region II-plus [26]. These and other findings (reviewed in [11,12]) give evidence that it is likely that the lysines and arginines (highly conserved in Plasmodium species) of region II-plus form ionic bonds with the negatively charged sulfate molecules of the HSPG glycosaminoglycan chains (GAGs). Our region II-plus mutant provided an opportunity to confirm the in vitro studies using a genetic approach. The wild-type and mutant sporozoites obtained by mechanical disruption of the midguts were incubated briefly with HepG2 cells to compare their binding to host cells. The sporozoites were obtained at a time when they are fully developed but not yet egressing from oocysts. There was a significant difference (~40%) in the binding of wild-type and mutant sporozoites (Figure 5). We emphasize that this assay was performed under static condition. The shear force generated by circulating blood in vivo should lead to more dramatic decrease in adhesion of mutant sporozoites to cells, as shown previously in vitro when the attachment assay was performed under rotating conditions [12]. Indeed, this is what we observed when we compared the infectivity of oocyst sporozoites from CS-WT and CS-RIImut to rats. The CS-WT and CS-RIImut sporozoites were injected intravenously into rats, and the pre-patent period of infection (time until the proportion of infected erythrocytes is less than 0.01%) measured. In two independent experiments, there was no infection in rats injected with 1–9 million CS-RIImut oocyst sporozoites (Table 2). In contrast, blood-stage parasites were detected in all rats injected with as few as 100,000 CS-WT oocyst sporozoites or 2,000 CS-WT salivary gland sporozoites [27].

Figure 5
Region II-plus is Important for Sporozoite Adhesion to HepG2 Cells
Table 2
Infectivity of Sporozoites

Tewari et al. [28] also investigated the function of CS regions II-plus. In their study, the mutation was introduced in a P. berghei line in which the endogenous CS (PbCS) had been replaced by P. falciparum CS (PfCS), leading to a substantial decrease in parasite infectivity [29,30]. In their studies, Tewari et al. deleted the entire region II-plus of CS protein, including two of the four cysteines of the CS thrombospondin domain, and noted that the mutants did not enter the salivary glands. However, they did not measure the number of parasites in the mosquito hemocoel. It is possible therefore that the Tewari's mutant has the same phenotype as ours.

We conclude that the same CS protein motif participates in two different stages of the sporozoite lifecycle. Region II-plus is first required for sporozoite egress from oocysts. Later it is required for the invasion of the mammalian hepatocytes. It is tempting to speculate that receptors for region II-plus are identical in the mammalian host liver and in the oocysts capsule/basal lamina in the mosquito midgut, i.e., they are HSPGs. The presence of HSPGs has been documented in Drosophila [31], and HSPG core proteins are represented in the Anopheles genome (http://www.ensembl.org) but have not yet been characterized biochemically. Perhaps capsule/basal lamina HSPGs interact with the positively charged stretch of amino acids of CS region II-plus, and the disruption of those peptide bonds by the newly identified cysteine protease (ECP1), or other participating proteases in the same proteolytic cascade, is an early and necessary step for sporozoite egress from oocysts.

Materials and Methods

Parasite.

The parasite is a wild-type pyrimethamine-sensitive, gametocyte-producing clone of the P. berghei NK65 strain.

DNA construct and mutagenesis.

pQWCS-WT contains pUC19 backbone and 2.8 kb of CS cassette [32] cloned into XbaI and XhoI sites. Mutations were introduced into the CS coding region by using QuikChange Site-Directed Mutagenesis Kit (Stratagene, La Jolla, California, United States). Primer1 (sense, 5′-GGTATAAGAGTTGCTGCAGCAGCAGGTTCAAATAAGAAAGC-3′) and its reverse and complement primer2 were used to mutate R290, K291, R292, and K293 to alanines. The resulting construct is named “pQWCS-RIImut.”

Targeting construct.

pMD205GFP is used as a backbone to generate targeting constructs, pRCS-WT and pRCS-RIImut. pMD205GFP contains the mutated copy of P. berghei DHFR-TS gene that confers resistance to pyrimethamine [33] and an Aequorea victoria green-fluorescent protein open reading frame (ORF) [34], and 2.2 kb and 0.55 kb of 5′- and 3′UTRs of P. berghei DHFR-TS. pQWCS-WT was digested with KpnI and XhoI to release the 2.1-kb fragment containing the CS cassette (0.6 kb of 5′UTR, 1-kb CS protein ORF and 0.5-kb 3′UTR). Subsequently, this fragment was cloned into pMD205GFP treated with same restriction enzymes to generate the intermediate construct pCS-WT. Targeting construct pRCS-WT was constructed by cloning a 0.6-kb BamHI-NotI fragment of CS 3′UTR (500–1,100 base pairs downstream of the stop codon) into the pCS-WT treated with the same restriction enzymes. Targeting construct pRCS-RIImut was constructed in the same way as pRCS-WT.

Parasite transfection and genotype analysis.

Schizonts were collected for transfection, and targeting constructs were introduced by electroporation as previous described [33]. Southern blotting was performed with the entire CS ORF and 0.6-kb 5′UTR as a probe. The probe was labeled with DIG-ddUTP by random priming, and the chemiluminescence was detected using CSPD (Roche, Basel, Switzerland). Specific amplification of the 5′ recombinant locus was preformed with a forward primer CS1 (sense: 5′-CTTTTTCACCCTCAAGTTGGG-3′, which hybridizes to the CS 5′UTR missing in the pRCS-WT/pRCS-RIImut), and a reverse primer PB103 (sense, 5′-TAATTATATGTTATTTTATTTCCAC-3′, which hybridizes to the 5′UTR of DHFR-TS). Specific amplification of the 3′ recombinant locus was preformed with a forward primer PB106 (sense, 5′-TGTGCATGCACATGCATGTA-3′, which hybridizes to the 3′UTR of DHFR-TS), and a reverse primer CS4 (sense, 5′-CGAAATAAGTTACTATTCGTGCCC-3′, which hybridizes to the CS 3′UTR missing in the pRCS-WT/pRCS-RIImut).

Mosquito infection and analysis of parasite development.

A. stephensi mosquitoes were fed on infected young Sprague-Dawley rats and dissected at various days PI. Midgut and salivary gland sporozoite populations were prepared from the various mosquito compartments and analyzed as previous described [27]. Hemolymph from each mosquito was perfused from the hemocoel with RPMI medium via air displacement from a micro-inoculation capillary inserted through the neck membrane and into the hemocoel. A small drop was made in the distal abdominal wall by gently removing the last two segments. The first three drops of perfusate (hemolymph and medium) from each mosquito were collected. Perfusate from at least 20 mosquitoes was collected. The number of sporozoites was determined using a haemocytometer.

Indirect immunofluorescence assays.

Oocyst sporozoites were collected at day 18 PI, centrifuged onto glass slides, and fixed with 4% paraformaldehyde for 20 min at room temperature. Sporozoites then were pre-incubated in PBS-3% BSA for 1 h at 37 °C followed by incubation of various anti-CS antibodies for 1 h at 37 °C. Bound anti-CS was detected with FITC-conjugated anti-mouse IgG.

Western blotting analysis of sporozoite lysates.

Protein samples were analyzed by SDS-PAGE and electrophoretically transferred to polyvinylidene difluoride membrane. CS-WT and CS-RIImut oocyst sporozoites on day 14 and 18 PI were collected, resuspended in SDS sample buffer, and incubated for 5 min at 70 °C prior to loading. The migrating bands were revealed with antibodies to P. berghei TRAP and CS protein, followed by horseradish peroxidase–coupled donkey anti-rabbit, and sheep anti-mouse IgG respectively, and visualized with enhanced chemiluminescence (ECL; Amersham Bioscience, Little Chalfont, United Kingdom).

Analysis of sporozoite infectivity.

To analyze sporozoite motility, sporozoites were incubated in 3% BSA-RPMI 1640 medium for 3 h prior to microscopic examination [3]. To determine the infectivity of sporozoites in vivo, young Sprague/Dawley rats were injected intravenously with sporozoite suspensions in RPMI 1640. The parasitemia of inoculated rodents was checked daily by a 10-min examination of a Giemsa-stained blood smear.

Sporozoite attachment assay.

A total of 100,000 midgut sporozoites were added and centrifuged down to confluent HepG2 cells. After 5-min incubation at 37 °C, cells were washed twice with PBS, and fixed with 4% formaldehyde. Adherent sporozoites were stained with a combination of anti-CS 3D11 and goat anti-mouse FITC antibodies. For each well, 25 microscopic fields were counted in duplicate using a 400× magnification.

In vitro assay of oocyst sporozoite release.

Intact midguts were dissected from either CS-WT– or CS-RIImut–infected mosquitoes. For each experiment, 10 midguts were incubated at 25 °C in 200-μl RPMI medium with or without trypsin (50 μg/ml; Sigma, St. Louis, Missouri, United States). At different time points, 10 μl was taken out after gentle shaking the tubes, and sporozoites were counted. At the end of the experiment, the midguts were ground in order to determine the mean number of remaining oocyst sporozoites per mosquito.

Transmission electron microscopy.

P. berghei (CS-WT and CS-RIImut) oocysts within mosquito midguts were fixed with 2.5% glutaraldehyde in 0.05 M phosphate buffer (pH 7.4) with 4% sucrose for 2 h. and then post-fixed in 1% osmium tetroxide for 1 h. After a 30-min en bloc stain with 1% aqueous uranyl acetate, the cells were dehydrated in ascending concentrations of ethanol and embedded in Epon 812. Ultrathin sections were stained with 2% uranyl acetate in 50% methanol and with lead citrate, and then examined in a Zeiss CEM902 electron microscope.

Immunoelectron microscopy.

P. berghei oocysts within mosquito midguts were fixed with 3% paraformaldehyde, 0.25% glutaraldehyde in 0.1 M phosphate buffer (pH 7.4). Fixed samples were washed, dehydrated, and embedded in LR White resin (Polysciences, Warrington, Pennsylvania, United States) as described previously [7]. Thin sections were blocked in PBS containing 0.01% (v/v) Tween-20 and 5% (w/v) nonfat dry milk (PBTM). Grids were then incubated for 2 h at room temperature with the primary mouse anti-CS monoclonal antibody 3D11, and diluted 1:500 in PBTM. Normal mouse serum or PBTM were used as negative controls. After washing, grids were incubated for 1 h with 15-nm gold-conjugated goat anti-mouse IgG (Amersham Life Sciences), diluted 1:20 in PBS containing 1% (w/v) BSA and 0.01% (v/v) Tween-20, rinsed with Tween-20, and fixed with glutaraldehyde to stabilize the gold particles. Samples were stained with uranyl acetate and lead citrate, and then examined in a Zeiss CEM902 electron microscope.

Acknowledgments

This work was supported by a grant from the National Institutes of Health to Victor Nussenzweig. The authors wish to thank Dr. Elizabeth H. Nardin, Dr. Purnima Bhanot, and Dr. Jayne Raper for valuable comments on the manuscript. We also wish to thank Dr. Robert E. Sinden, Dr. Vandana Thathy, Dr. Purnima Bhanot, and members of Dr. Victor Nussenzweig's lab for discussions.

Abbreviations

CS
circumsporozoite
ECP1
egress cysteine protease 1
HSPG
heparan sulfate proteoglycan
ORF
open reading frame
PI
postinfection
TSR
thrombospondin type I repeats

Footnotes

Competing interests. The authors have declared that no competing interests exist.

Author contributions. QW and VN conceived and designed the experiments. QW and HF performed the experiments. QW, HF, and VN analyzed the data. QW and VN wrote the paper.

Citation: Wang Q, Fujioka H, Nussenzweig V (2005) Exit of Plasmodium sporozoites from oocysts is an active process that involves the circumsporozoite protein. PLoS Pathog 1(1): e9.

References

  • Vanderberg J, Rhodin J. Differentiation of nuclear and cytoplasmic fine structure during sporogonic development of Plasmodium berghei. J Cell Biol. 1967;32:C7–C10. [PMC free article] [PubMed]
  • Sinden RE. Molecular interactions between Plasmodium and its insect vectors. Cell Microbiol. 2002;4:713–724. [PubMed]
  • Vanderberg JP. Studies on the motility of Plasmodium sporozoites. J Protozool. 1974;21:527–537. [PubMed]
  • Sinden RE. Excystment by sporozoites of malaria parasites. Nature. 1974;252:314. [PubMed]
  • Adini A, Krugliak M, Ginsburg H, Li L, Lavie L, et al. Transglutaminase in Plasmodium parasites: Activity and putative role in oocysts and blood stages. Mol Biochem Parasitol. 2001;117:161–168. [PubMed]
  • Adini A, Warburg A. Interaction of Plasmodium gallinaceum ookinetes and oocysts with extracellular matrix proteins. Parasitology. 1999;119:331–336. [PubMed]
  • Aikawa M, Atkinson CT, Beaudoin LM, Sedegah M, Charoenvit Y, et al. Localization of CS and non-CS antigens in the sporogonic stages of Plasmodium yoelii. Bull World Health Organ. 1990;68((Suppl)):165–171. [PMC free article] [PubMed]
  • Posthuma G, Meis JF, Verhave JP, Hollingdale MR, Ponnudurai T, et al. Immunogold localization of circumsporozoite protein of the malaria parasite Plasmodium falciparum during sporogony in Anopheles stephensi midguts. Eur J Cell Biol. 1988;46:18–24. [PubMed]
  • Hamilton AJ, Suhrbier A, Nicholas J, Sinden RE. Immunoelectron microscopic localization of circumsporozoite antigen in the differentiating exoerythrocytic trophozoite of Plasmodium berghei. Cell Biol Int Rep. 1988;12:123–129. [PubMed]
  • Menard R, Sultan AA, Cortes C, Altszuler R, van Dijk MR, et al. Circumsporozoite protein is required for development of malaria sporozoites in mosquitoes. Nature. 1997;385:336–340. [PubMed]
  • Kappe SH, Buscaglia CA, Nussenzweig V. Plasmodium sporozoite molecular cell biology. Annu Rev Cell Dev Biol. 2004;20:29–59. [PubMed]
  • Pinzon-Ortiz C, Friedman J, Esko J, Sinnis P. The binding of the circumsporozoite protein to cell surface heparan sulfate proteoglycans is required for Plasmodium sporozoite attachment to target cells. J Biol Chem. 2001;276:26784–26791. [PMC free article] [PubMed]
  • Nunes A, Thathy V, Bruderer T, Sultan AA, Nussenzweig RS, et al. Subtle mutagenesis by ends-in recombination in malaria parasites. Mol Cell Biol. 1999;19:2895–2902. [PMC free article] [PubMed]
  • Thathy V, Fujioka H, Gantt S, Nussenzweig R, Nussenzweig V, et al. Levels of circumsporozoite protein in the Plasmodium oocyst determine sporozoite morphology. EMBO J. 2002;21:1586–1596. [PMC free article] [PubMed]
  • Yoshida N, Potocnjak P, Nussenzweig V, Nussenzweig RS. Biosynthesis of Pb44, the protective antigen of sporozoites of Plasmodium berghei. J Exp Med. 1981;154:1225–1236. [PMC free article] [PubMed]
  • Sultan AA, Thathy V, Frevert U, Robson KJ, Crisanti A, et al. TRAP is necessary for gliding motility and infectivity of plasmodium sporozoites. Cell. 1997;90:511–522. [PubMed]
  • Sultan AA, Briones MR, Gerwin N, Carroll MC, Nussenzweig V. Sporozoites of Plasmodium yoelii infect mice with targeted deletions in ICAM-1 and ICAM-2 or complement components C3 and C4. Mol Biochem Parasitol. 1997;88:263–266. [PubMed]
  • Wickham ME, Culvenor JG, Cowman AF. Selective inhibition of a two-step egress of malaria parasites from the host erythrocyte. J Biol Chem. 2003;278:37658–37663. [PubMed]
  • Salmon BL, Oksman A, Goldberg DE. Malaria parasite exit from the host erythrocyte: A two-step process requiring extraerythrocytic proteolysis. Proc Natl Acad Sci U S A. 2001;98:271–276. [PMC free article] [PubMed]
  • Rosenthal PJ. Cysteine proteases of malaria parasites. Int J Parasitol. 2004;34:1489–1499. [PubMed]
  • Hanspal M, Dua M, Takakuwa Y, Chishti AH, Mizuno A. Plasmodium falciparum cysteine protease falcipain-2 cleaves erythrocyte membrane skeletal proteins at late stages of parasite development. Blood. 2002;100:1048–1054. [PubMed]
  • Pradel G, Hayton K, Aravind L, Iyer LM, Abrahamsen MS, et al. A multidomain adhesion protein family expressed in Plasmodium falciparum is essential for transmission to the mosquito. J Exp Med. 2004;199:1533–1544. [PMC free article] [PubMed]
  • Aly AS, Matuschewski K. A malarial cysteine protease is necessary for Plasmodium sporozoite egress from oocysts. J Exp Med. 2005;202:225–230. [PMC free article] [PubMed]
  • Cerami C, Frevert U, Sinnis P, Takacs B, Clavijo P, et al. The basolateral domain of the hepatocyte plasma membrane bears receptors for the circumsporozoite protein of Plasmodium falciparum sporozoites. Cell. 1992;70:1021–1033. [PubMed]
  • Frevert U, Sinnis P, Cerami C, Shreffler W, Takacs B, et al. Malaria circumsporozoite protein binds to heparan sulfate proteoglycans associated with the surface membrane of hepatocytes. J Exp Med. 1993;177:1287–1298. [PMC free article] [PubMed]
  • Sinnis P, Clavijo P, Fenyo D, Chait BT, Cerami C, et al. Structural and functional properties of region II-plus of the malaria circumsporozoite protein. J Exp Med. 1994;180:297–306. [PMC free article] [PubMed]
  • Vanderberg JP. Development of infectivity by the Plasmodium berghei sporozoite. J Parasitol. 1975;61:43–50. [PubMed]
  • Tewari R, Spaccapelo R, Bistoni F, Holder AA, Crisanti A. Function of region I and II adhesive motifs of Plasmodium falciparum circumsporozoite protein in sporozoite motility and infectivity. J Biol Chem. 2002;277:47613–47618. [PubMed]
  • Nussenzweig V, Menard R. Analysis of a malaria sporozoite protein family required for gliding motility and cell invasion. Trends Microbiol. 2000;8:94–97. [PubMed]
  • Matuschewski K, Nunes AC, Nussenzweig V, Menard R. Plasmodium sporozoite invasion into insect and mammalian cells is directed by the same dual binding system. EMBO J. 2002;21:1597–1606. [PMC free article] [PubMed]
  • Princivalle M, de Agostini A. Developmental roles of heparan sulfate proteoglycans: A comparative review in Drosophila, mouse and human. Int J Dev Biol. 2002;46:267–278. [PubMed]
  • Eichinger DJ, Arnot DE, Tam JP, Nussenzweig V, Enea V. Circumsporozoite protein of Plasmodium berghei: Gene cloning and identification of the immunodominant epitopes. Mol Cell Biol. 1986;6:3965–3972. [PMC free article] [PubMed]
  • de Koning-Ward TF, Fidock DA, Thathy V, Menard R, van Spaendonk RM, et al. The selectable marker human dihydrofolate reductase enables sequential genetic manipulation of the Plasmodium berghei genome. Mol Biochem Parasitol. 2000;106:199–212. [PubMed]
  • Sultan AA, Thathy V, Nussenzweig V, Menard R. Green fluorescent protein as a marker in Plasmodium berghei transformation. Infect Immun. 1999;67:2602–2606. [PMC free article] [PubMed]

Articles from PLoS Pathogens are provided here courtesy of Public Library of Science
PubReader format: click here to try

Formats:

Related citations in PubMed

See reviews...See all...

Cited by other articles in PMC

See all...

Links

Recent Activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...