Open Access

The microneme proteins CTRP and SOAP are not essential for Plasmodium berghei ookinete to oocyst transformation in vitro in a cell free system

Malaria Journal20087:82

https://doi.org/10.1186/1475-2875-7-82

Received: 02 January 2008

Accepted: 19 May 2008

Published: 19 May 2008

Abstract

Background

Two Plasmodium berghei ookinete micronemal proteins, circumsporozoite and TRAP related protein (CTRP) and secreted ookinete adhesive protein (SOAP) both interact with the basal lamina component laminin. Following gene disruption studies it has been proposed that, apart from their role in motility, these proteins may be required for interactions leading to ookinete-to-oocyst transformation.

Methods

CTRP and SOAP null mutant P. berghei ookinetes were compared to P. berghei ANKA wild-type for their ability to transform and grow in vitro. To confirm in vitro findings for P. berghei CTRP-KO ookinetes were injected into the haemocoel of An opheles gambiae female mosquitoes.

Results

Transformation, growth, and viability were comparable for the gene disrupted and wild-type parasites. P. berghei CTRP-KO ookinetes were able to transform into oocysts in the haemocoel of An. gambiae mosquitoes.

Conclusion

Neither CTRP nor SOAP is required for parasite transformation in vitro. By-passing the midgut lumen allows for the transformation of P. berghei CTRP-KO ookinetes suggesting that it is not required for transformation in vivo.

Background

Ever since the early 1900s, an appreciation of the role that anopheline mosquitoes play in the transmission of malaria [1] has directed disease control efforts towards the vectors. Many campaigns relied upon insecticide usage and, latterly, the use of insecticide treated bed nets is proving effective [2]. However, attendant concerns regarding the development of insecticide resistance [2, 3] make it imperative that new tools are developed to inhibit malaria transmission. This will be best achieved by gaining and applying a better understanding of vector-parasite interactions.

The sporogonic stages which occur in the mosquito vector begin when a mosquito ingests infected blood containing gametocytes. Within approximately 18 hours, gametogenesis, fertilization, and the transformation of the zygote to a motile ookinete have occurred. Ookinetes migrate out of the blood bolus, through the peritrophic matrix and invade and transit through the midgut epithelium cells, transforming into oocysts beneath the basal lamina 20–30 hours post-bloodfeeding. The initial period post-infection is critical for the malaria parasites as losses of up to 100,000 fold occur, dependant upon parasite/vector combinations [48].

Within recent years, knowledge of the ookinete at the molecular level has burgeoned and many proteins have been shown to be involved in midgut invasion. These include several with functions associated with motility and/or invasion, such as the major surface proteins P25/P28 [911], secreted ookinete adhesive protein (SOAP) [12], von Willebrand Factor A Domain-related protein (WARP) [13], circumsporozoite and TRAP-related protein (CTRP) [1419], cell-traversal protein (CelTOS) [20], calcium-dependent protein kinase 3 (CDPK3) [21, 22], the guanylate cyclase, PbGCβ [23], membrane-attack ookinete protein (MOAP) [24, 25], and Plasmodium perforin-like proteins [26]. The rodent malaria, Plasmodium berghei, has proven to be a useful model with which to investigate the function of these proteins and targeted gene disruption has assisted these studies.

The micronemal protein CTRP, first described in Plasmodium falciparum by Trottein et al [17], has structural homologues in P. berghei [14, 18], Plasmodium vivax, Plasmodium knowlesi, Plasmodium gallinaceum, and Plasmodium yoelii [27]. CTRP contains two types of adhesive domains (von Willebrand factor type A-related and thrombospondin type 1-related) and belongs to a family of proteins located in the micronemes of several genera of apicomplexan parasites [14, 28]. It is expressed in P. berghei ookinetes from 10 hours post-fertilization and expression continues for at least 24 hours [18]. Using immuno-electron microscopy, Limviroj and colleagues [15] localized PbCTRP to the ookinete micronemes and detected it at the site of contact with the basal lamina; suggesting that the junction so formed may induce the ookinete to stop and begin to transform into an oocyst.

Targeted disruption of CTRP has demonstrated that, although ookinetes form, transgenic parasites fail to develop into oocyst in vivo, consequently blocking mosquito transmission of these parasites [14, 16, 19]. These studies further demonstrated that CTRP is involved in ookinete locomotion [14]. CTRP has also been shown to bind to laminin and collagen IV, major components of the basal lamina, prompting further suggestions of a putative role in the transformation of ookinete to oocyst via involvement in a signal transduction pathway [29, 30].

SOAP, another microneme protein, is unique to the genus Plasmodium. It is expressed in ookinetes and young oocysts and asexual stages but has not been reported in gametocytes of P. berghei and thus has a similar transcriptional pattern in the mosquito to PbCTRP [12, 31]. It is a cysteine-rich, secreted protein not present on the parasite surface. Dessens and colleagues [12] showed that disrupting the SOAP gene resulted in null mutant parasites that were impaired in their ability to invade the mosquito midgut wall and form oocysts. They further showed that this 21-kDa protein also interacts with laminin in a yeast two-hybrid system and suggested that EGF-like domains of laminin gamma 1 interact with SOAP sequence domains that are homologous to laminin EGF-like domains [12]. SOAP was thus thought to play an important role during ookinete-to-oocyst development in mosquitoes [12]. Interestingly, they also showed that PbSOAP-KO ookinetes invaded co-cultured mosquito cells and transformed into oocysts therein at a more efficient rate than wild-type ookinetes; a finding that is at odds with their identification of SOAP as a key molecule for ookinete-to-oocyst differentiation in the mosquito [12].

PbCRTP and PbSOAP null mutants, grown in an axenic culture system [32], were used to determine the role, if any, of these microneme proteins in the transformation of ookinetes into oocysts. Ookinetes were cultured in the presence or absence of a basal lamina substitute. The results show that neither microneme protein is essential for transformation as ookinetes from both parasite null mutants are able to transform into oocysts via the transitional took stage recently described by Carter et al [32].

Methods

Parasites and ookinete cultures

Experiments were performed using approved protocols in accordance with the UK. Animals (Scientific Procedures) Act 1986. Male CD mice were treated with phenylhydrazine two days prior to infection with either P. berghei ANKA (clone 2.34; wild-type), P. berghei CTRP-KO [14], or P. berghei SOAP-KO [12] by the inoculation of parasites obtained from a donor mouse between the 2nd and 6th passage from cryopreserved stock.

Blood from infected mice was collected by cardiac puncture into a heparinized syringe two days post-infection, after the confirmation of an infection by Giemsa staining of thin blood smears. Blood was diluted 1:10 into RPMI-1640 medium containing 10% foetal calf serum (FCS), 14.7 mM sodium bicarbonate, 0.367 mM hypoxanthine, 1000 U/ml penicillin, and 1 mg/ml streptomycin (pH 8.4) prior to incubation for 18 h at 19°C as detailed in [33, 34].

Ookinetes were harvested using a MidiMacs LS magnetic column as described previously [32, 35]. Briefly, following centrifugation at 648 g for 5 min all but 20% of the medium was removed and the blood mixture was passed through a magnetic column. Following several column washes, ookinetes were eluted with 3 ml of oocyst medium (supplemented Schneider's insect cell culture medium).

Plasmodium berghei wild-type (WT), PbCTRP-KO or PbSOAP-KO ookinetes were immediately seeded into 8-well LabTek™ chamber slides at a density of approximately 1 × 104 in 400 μl of oocyst medium (see [32] for medium details). For each experiment, ookinetes were seeded in chamber slides either previously coated with 80 μl Matrigel™ or with no coating. In order to minimize parasite loss from the wells, medium was not removed during culture. However, to counter the effect of evaporation, 100 μl of fresh medium was added to each well every 48 or 72 h post-culture. Triplicate wells were assessed at each time point and the experiment was repeated three times.

Demonstration of morphological changes during transformation

The presence of a transitional stage between ookinete and oocyst in P. berghei ANKA WT, called the took, was recently reported [32]. To demonstrate clearly the presence of a took stage during the development of oocysts of the null mutants, cultures were collected 21 h post-culture in oocyst medium. Parasites were fixed in 1:1 methanol: acetone, washed and labelled with an anti-P28 monoclonal antibody derived from a hybridoma cell line maintained in the laboratory. Following a 30 min incubation the slides were washed and incubated for 30 min with a goat anti-mouse fluorescein isothiocyanate-conjugated secondary antibody [32]. The slides were washed and mounted in VectaShield (Vector Laboratories) containing 4', 6-diamidino-2-phenyl indole (DAPI) before viewing samples with a Leica DM IRB Fluorescence Microscope (DAPI excitation/emission: 340–380 nm/425 nm; FITC: 450–490 nm/535 nm). Appropriate controls were included for each experiment.

Assessment of parasite transformation and growth

Ookinetes have a propensity to clump together in culture, so well contents were mixed vigorously by pipetting to ensure even distribution within the well prior to counting ookinetes/oocysts. Measurements and counts were conducted on days 1, 3 and 5 post-culture for wells that were not coated and day 1 for wells coated in Matrigel. Parasites were counted in alternate fields of view along a cross representing two diameters of the well, at a magnification of 630×, viewed under phase contrast. In all, 30 fields of view were examined per well (3.58% of the whole well). In order to assess transformation of ookinetes to oocysts, the proportion of P. berghei WT, PbCTRP-KO or PbSOAP-KO ookinetes, tooks and oocysts was calculated for each culture condition at each time point. Only parasites that were fully rounded, translucent, with pigment visible and a diameter greater than 5 micrometers were regarded as having transformed into oocysts [32].

Oocyst viability

Parasites were collected by centrifugation for 1.5 min at 2,000 g. The pellet was resuspended in 5 μl of PBS to which 5 μl of 0.1% Erythrosin B was added to assess parasite viability. This was immediately spotted onto a microscope slide, a coverslip applied and a minimum of 100 oocysts and any remaining ookinetes and tooks were examined at magnification of 400× and scored as viable or having a compromised membrane. Three repeat experiments were performed in which triplicate wells were assessed on each of the days chosen for observation.

Injection of Anopheles gambiae mosquitoes with P. berghei CTRP KO ookinetes

Unlike PbSOAP-KO, for which it has been reported that between 15–40% of ookinetes transform into oocysts in vivo [12], no PbCTRP-KO oocysts have been observed in vivo [14, 16, 19]. In order to confirm the lack of a role of CTRP in transformation, in vitro ookinete cultures were injected into the haemocoel of 4 day old An. gambiae KIL mosquitoes. The preparation and injection protocols were adapted from Paskewtiz and Shi [36]. Briefly, PbCTRP-KO ookinetes were cultured for 18 h at 19°C in ookinete medium. Cultures were centrifuged at 648 g for 5 min at 4°C. The majority of red blood cells were removed by resuspending the culture pellet in 20 volumes of 0.17 M ammonium chloride and incubating for 10 min on ice. All subsequent steps were performed at 4°C. An equal volume of PBS was added to stop red blood cell lysis and cultures were immediately centrifuged. The pellet was washed once in 40 volumes of PBS, resuspended in 1 ml of PBS and counted on a haemocytometer.

Fifty ookinetes in 69 nl of PBS were injected per mosquito with a Nanoject II automatic nanoliter injector (Drummond Scientific Company, USA). A total of 50 mosquitoes were injected and maintained at 20°C for seven days prior to dissection. Mosquitoes were dissected in PBS and the contents of the abdomen were immediately stained in 0.05% mercurochrome. Tissue was viewed on a Leica DM IRB inverted microscope and images were acquired with a Leica DC 300F digital camera (Leica Microsystems, Germany).

Statistical analysis

All data sets were analysed using the statistical software package Minitab® Release 14 (Minitab, Inc.). Where necessary, data were normalized with an arcsine transformation prior to analysis with a General Linear Model (GLM).

Results and discussion

Transformation of CTRP- and SOAP-KO ookinetes to oocysts

It has been proposed that SOAP and CTRP may play a role in ookinete-to-oocyst transformation in vivo as the null mutants for either gene produce very few, or no oocysts respectively [12, 14, 19]. Moreover, both of these molecules have been reported to bind to laminin and it has been proposed that interactions between SOAP and/or CTRP with the basal lamina, and laminin in particular, may trigger transformation [12, 30]. However, it was found that when P. berghei CTRP- and SOAP-KO ookinetes were cultured in vitro, plus or minus Matrigel (a source of laminin), the same proportion transformed to oocysts as did the wild-type. Furthermore, transformation proceeded via a took stage (Figure 1) as recently described by Carter et al [32].
Figure 1

Transformation of P. berghei CTRP-KO ookinetes via a took stage. Ookinetes were cultured in oocyst medium for 21 h and labelled for the major ookinete surface protein, P28, by indirect immunofluoresence assay. A) mature ookinete; (B, C) tooks; (D) oocyst.

The percentage of transformed ookinetes (i.e. oocysts) was calculated on days 1, 3, and 5 post-culture after counting the number of ookinetes, tooks and oocysts per well. Over all conditions, a mean of 93% (SE ± 1.33) of ookinetes had transformed into oocysts by day 1. There was no significant difference in the percentage of ookinete to oocyst transformations between parasites lines (GLM, F(2,1,2,2)= 1.64, P = 0.213) or the presence or absence of a basal lamina substitute (GLM, F(2,1,2,2)= 0.60, P = 0.446) (Table 1). As the majority of parasites had transformed by day 1 and no differences were observed between culture conditions, data for day 3 and 5 was only collected from wells that were not coated with Matrigel. For all parasite genotypes, nearly 100% of ookinetes had transformed by day 5 (Table 1).
Table 1

Ookinete to oocyst transformation of P. berghei WT, PbCTRP-KO, and PbSOAP-KO parasites.

 

Mean % transformation

 

Day 1

Day 3

Day 5

WT -MAT

92.68 (± 1.51)

99.73 (± 0.17)

99.94 (± 0.06)

WT +MAT

96.27 (± 0.86)

  

CTRP-KO -MAT

96.76 (± 0.78)

99.70 (± 0.22)

100.00 (± 0.00)

CTRP-KO +MAT

98.85 (± 0.45)

  

SOAP-KO -MAT

87.05 (± 5.38)

99.13 (± 0.43)

100.00 (± 0.00)

SOAP-KO +MAT

89.21 (± 4.89)

  

Ookinetes from each of the clones were seeded in the absence of Matrigel (-MAT) or with Matrigel (+MAT). Transformation was assessed on days 1, 3, and 5 post-culture. The figures show the mean percentage of transformed ookinetes (± standard error of the mean).

The large percentage of ookinete-to-oocyst conversion in these experiments was surprising as it has previously been reported that over 30% of ookinetes cultured in vitro are dying by an apoptosis-like mechanism by 24 h post-culture [37]. This suggests that ookinetes harvested at 18 h post-culture and immediately placed in oocyst medium, which supports transformation and growth (see [32]), may be rescued from triggers that induce cell death. It was previously observed that the proportion of ookinetes displaying markers typical of apoptotic cells was under 10% after 12 h in culture [37]. Current findings confirm this observation, but also show that the proportion of dying or dead ookinetes varies considerably between cultures, possibly as a result of factors from the murine host (Hurd, Ali and Arambage, personal observations).

Of the 50 mosquitoes injected with P. berghei CTRP-KO ookinetes only four survived to day 7 post-injection. P. berghei CTRP-KO oocysts were observed in all four mosquitoes. Thus PbCTRP-KO ookinetes are able to transform into oocysts when injected into the haemocoel of 4-day old female An. gambiae KIL mosquitoes. Qualitative observations were made of the infections as it is difficult to quantify oocysts as they can develop anywhere in the haemocoel [36]. Upon dissection the majority of oocysts recovered were observed to be floating in the haemolymph. However, oocysts were also found bound to the midgut (Figure 2) and the Malpighian tubules.
Figure 2

Transformation of PbCTRP-KO ookinetes in Anopheles gambiae. Phase contrast image of a PbCTRP-KO oocyst (arrow) attached to the midgut of An. gambiae KIL mosquito. The trachea (arrow heads) and Malpighian tubules (MT) are also shown. Plasmodium berghei CTRP-KO ookinetes were injected 18 h post-culture into the haemocoel of 4-day old An. gambiae KIL females and allowed to develop for 7 days prior to mosquito dissection.

These findings confirmed suggestions that both PbCTRP and PbSOAP null mutants have retained their full potential to develop into oocysts. Both microneme proteins have been implicated in ookinete motility [12, 14, 16, 19, 27, 38] and findings presented here suggest that the barrier to further development in vivo must be caused by the necessity to migrate out of the blood bolus, traverse the peritrophic matrix and invade the midgut epithelium. Dessens et al [12] also observed the transformation of PbSOAP-KO parasites in vitro, but surprisingly, in their system ookinetes invaded and developed inside Aedes aegypti Mos20 cells. The axenic culture system used here also shows that cell invasion is not a prerequisite for transformation. Interestingly, Hirai et al [23] recently reported that disruption of the gene encoding PbGCβ also resulted in normal ookinetes that do not produce oocysts in vivo. Here too these transgenic ookinetes transformed into oocysts in an in vitro system based on Al-Olayan et al [37] and ookinete motility was shown to be defective.

Interactions with the basal lamina

Transformation rates of null mutants and wild-type P. berghei were the same in the presence or absence of Matrigel in this study (Table 1). These results suggest that the binding of either one of these micronemal proteins to basal lamina components is not a requirement for transformation. Indeed, the study also confirms that interactions between basal lamina components and any ookinete molecule are unnecessary to initiate conversion to oocysts [32]. It has been suggested that the mosquito midgut basal lamina plays an essential role in the development of Plasmodium oocysts [39]. Gene silencing technology resulting in the depletion of mosquito laminin greatly reduced oocyst numbers developing in vivo [39] and interactions between laminin and microneme and/or surface proteins support this suggestion [12, 29]. If this idea is correct then, as it is clearly not involved in triggering transformation or supporting very early growth, it may perform a function as a protective coat, disguising the oocyst from the mosquito defence system [39, 40] or just serve to bind the ookinete in place between the midgut basolateral plasma membrane and the basal lamina, thus preventing the ookinetes from migrating into the haemocoel, as do most insect parasites.

The identification of the molecular composition of the mosquito midgut is rapidly advancing. The major components of the basal lamina, collagen IV and laminin, have been characterized in An. gambiae [41, 42], as has beta integrin, a receptor for laminin and collagen IV[43]. The latter has been implicated in ookinete invasion of the midgut and may have a role in facilitating putative interactions between ookinetes and laminin or vice versa [43]. However, it now appears that these molecules are more likely to be involved in later phases of oocyst development such as growth, maturation, and sporozoites formation.

Growth and viability

In addition to transforming into oocysts, PbCRTP-KO and PbSOAP-KO parasites were able to grow in culture at a comparable rate to P. berghei WT and, here too, no significant differences were found between the presence and absence of the basal lamina substitute (Figure 3). Over the five day period there were significant increases in parasite sizes. Tukey's pairwise comparison day 1 vs day 3 (T = 4.946, P < 0.001), and day 3 and 5 (T = 3.195, P < 0.01) (Figure 3). However a significant decrease in the number of viable oocysts between each of the time points was observed (GLM: F(2,1,2,2) = 117.32, P < 0.001), but with no significant difference between parasite genotype (GLM: F(2,1,2,2) = 0.70, P = 0.497) or the presence or absence of Matrigel (GLM: F(2,1,2,2) = 1.85, P = 0.175) (Figure 4). Although not statistically significant, fewer parasites were viable when incubated with Matrigel at day 5. This could be caused by additional gentamycin, present in Matrigel as well as in the oocyst culture medium.
Figure 3

The effect of basal lamina components on the growth of P. berghei wild-type, PbCTRP-KO, and PbSOAP-KO oocysts. Three clones of Plasmodium berghei were cultured in the presence or absence of Matrigel. -MAT = no Matrigel; +MAT = with Matrigel; WT = P. berghei ANKA clone 2.34; CTRP-KO = P. berghei CTRP-KO; SOAP-KO = P. berghei SOAP-KO. No differences were observed in the mean size of oocysts cultured in the presence or absence of Matrigel or between parasite clones.

Figure 4

The effect of basal lamina components on the viability of P. berghei wild-type, PbCTRP-KO, and PbSOAP-KO oocysts. Three clones of Plasmodium berghei were cultured in the presence or absence of Matrigel. -MAT = no Matrigel; +MAT = with Matrigel; WT = P. berghei ANKA clone 2.34; CTRP-KO = P. berghei CTRP-KO; SOAP-KO = P. berghei SOAP-KO. There was a significant reduction in the number of viable oocysts with increasing time of culture (GLM: F(2,1,2,2) = 117.32, P < 0.001).

Conclusion

The microneme proteins SOAP and CTRP are not involved in ookinete to oocyst transformation or early growth in vitro. Furthermore, by by-passing the need to invade the midgut, PbCTRP-KO ookinetes are capable of transforming into oocysts in the haemocoel of An. gambiae mosquitoes. These results suggest that the role of these micronemal proteins may be restricted to motility and/or invasion.

In order to find adequate targets for transmission blocking strategies it is necessary to gain a better understanding of the proteins expressed during the malaria parasite sporogonic stages and their influence on parasite development. The technique of gene disruption is an extremely useful tool in this quest and it is suggested that, in additional to in vivo studies to determine gene function, an in vitro culture system will facilitate these investigations.

Declarations

Acknowledgements

Thanks are extended to T. Hall (WRAIR, USA) for the provision of the EW62A hybridoma cell line, J.T. Dessens for the provision of the CTRP- and SOAP-KO parasites and an anonymous referee for the suggestion that in vivo experiments be performed. Funding for this project was provided by The Wellcome Trust (069128/Z/02/Z and 069162/Z/02/Z).

Authors’ Affiliations

(1)
Centre for Applied Entomology and Parasitology, Institute of Science and Technology in Medicine, School of Life Sciences, Keele University

References

  1. Ross R: On some peculiar pigmented cells found in two mosquitoes fed on malaria blood. BMJ. 1897, 18: 1789-1788.Google Scholar
  2. Takken W: Do insecticide-treated bednets have an effect on malaria vectors?. Trop Med Int Health. 2002, 7 (12): 1022-1030. 10.1046/j.1365-3156.2002.00983.x.View ArticlePubMedGoogle Scholar
  3. Guyatt HL, Snow RW: The cost of not treating bednets. Trends Parasitol. 2002, 18 (1): 12-14. 10.1016/S1471-4922(01)02143-2.View ArticlePubMedGoogle Scholar
  4. Alavi Y, Arai M, Mendoza J, Tufet-Bayona M, Sinha R, Fowler K, Billker O, Franke-Fayard B, Janse CJ, Waters AP, Sinden RE: The dynamics of interactions between Plasmodium and the mosquito: a study of the infectivity of Plasmodium berghei and Plasmodium gallinaceum, and their transmission by Anopheles stephensi, Anopheles gambiae and Aedes aegypti. Int J Parasitol. 2003, 33 (9): 933-943. 10.1016/S0020-7519(03)00112-7.View ArticlePubMedGoogle Scholar
  5. Vaughan JA, Hensley L, Beier JC: Sporogonic development of Plasmodium yoelii in five anopheline species. J Parasitol. 1994, 80 (5): 674-681. 10.2307/3283245.View ArticlePubMedGoogle Scholar
  6. Vaughan JA, Noden BH, Beier JC: Population dynamics of Plasmodium falciparum sporogony in laboratory-infected Anopheles gambiae. J Parasitol. 1992, 78 (4): 716-724. 10.2307/3283550.View ArticleGoogle Scholar
  7. Vaughan JA, Noden BH, Beier JC: Sporogonic development of cultured Plasmodium falciparum in six species of laboratory-reared Anopheles mosquitoes. Am J Trop Med Hyg. 1994, 51 (2): 233-243.PubMedGoogle Scholar
  8. Zollner GE, Ponsa N, Garman GW, Poudel S, Bell JA, Sattabongkot J, Coleman RE, Vaughan JA: Population dynamics of sporogony for Plasmodium vivax parasites from western Thailand developing within three species of colonized Anopheles mosquitoes. Malar J. 2006, 5: 68-10.1186/1475-2875-5-68.PubMed CentralView ArticlePubMedGoogle Scholar
  9. Sidén-Kiamos I, Vlachou D, Margos G, Beetsma AL, Waters AP, Sinden RE, Louis C: Distinct roles for Pbs21 and Pbs25 in the in vitro ookinete to oocyst transformation of Plasmodium berghei. J Cell Sci. 2000, 113: 3419-3426.PubMedGoogle Scholar
  10. Tomas AM, Margos G, Dimopoulos G, van Lin LHM, de Koning-Ward TF, Sinha R, Lupetti P, Beetsma AL, Rodriguez MC, Karras M, Hager A, Mendoza J, Butcher GA, Kafatos F, Janse CJ, Waters AP, Sinden RE: P25 and P28 proteins of the malaria ookinete surface have multiple and partially redundant functions. EMBO J. 2001, 20 (15): 3975-3983. 10.1093/emboj/20.15.3975.PubMed CentralView ArticlePubMedGoogle Scholar
  11. Tsuboi T, Cao YM, Hitsumoto Y, Yanagi T, Kanbara H, Torii M: Two antigens on zygotes and ookinetes of Plasmodium yoelii and Plasmodium berghei that are distinct targets of transmission-blocking immunity. Infect Immun. 1997, 65 (6): 2260-2264.PubMed CentralGoogle Scholar
  12. Dessens JT, Siden-Kiamos I, Mendoza J, Mahairaki V, Khater E, Vlachou D, Xu XJ, Kafatos FC, Louis C, Dimopoulos G, Sinden RE: SOAP, a novel malaria ookinete protein involved in mosquito midgut invasion and oocyst development. Mol Microbiol. 2003, 49 (2): 319-329. 10.1046/j.1365-2958.2003.03566.x.View ArticlePubMedGoogle Scholar
  13. Yuda M, Yano K, Tsuboi T, Torii M, Chinzei Y: von Willebrand Factor A Domain-related Protein, a novel microneme protein of the malaria ookinete highly conserved throughout the Plasmodium parasites. Mol Biochem Parasitol. 2001, 116: 65-72. 10.1016/S0166-6851(01)00304-8.View ArticlePubMedGoogle Scholar
  14. Dessens JT, Beetsma AL, Dimopoulos G, Wengenlik K, Crisanti A, Kafatos F, Sinden RE: CTRP is essential for mosquito infection by malaria ookinetes. EMBO J. 1999, 18 (22): 6221-6227. 10.1093/emboj/18.22.6221.PubMed CentralView ArticlePubMedGoogle Scholar
  15. Limviroj W, Yano K, Yuda M, Ando K, Chinzei Y: Immuno-electron microscopic observations of Plasmodium berghei CTRP localisation in the midgut of the vector mosquito Anopheles stephensi. J Parasitol. 2002, 88 (4): 664-672.View ArticlePubMedGoogle Scholar
  16. Templeton TJ, Kaslow DC, Fidock DA: Developmental arrest of the human malaria parasite Plasmodium falciparum within the mosquito midgut via CTRP gene disruption. Mol Microbiol. 2000, 36 (1): 1-9. 10.1046/j.1365-2958.2000.01821.x.View ArticlePubMedGoogle Scholar
  17. Trottein F, Triglia T, Cowman AF: Molecular cloning of a gene from Plasmodium falciparum that codes for a protein sharing motifs found in adhesive molecules from mammals and plasmodia. Mol Biochem Parasitol. 1995, 74 (2): 129-141. 10.1016/0166-6851(95)02489-1.View ArticlePubMedGoogle Scholar
  18. Yuda M, Sawai T, Chinzei Y: Structure and expression of an adhesive protein-like molecule of mosquito invasive-stage malarial parasite. J Exp Med. 1999, 189 (12): 1947-1952. 10.1084/jem.189.12.1947.PubMed CentralView ArticlePubMedGoogle Scholar
  19. Yuda M, Shakaida H, Chinzei Y: Targeted disruption of the Plasmodium berghei CTRP gene reveals its essential role malaria infection of the vector mosquito. J Exp Med. 1999, 190 (11): 1711-1715. 10.1084/jem.190.11.1711.PubMed CentralView ArticlePubMedGoogle Scholar
  20. Kariu T, Ishino T, Yano K, Chinzei Y, Yuda M: CelTOS, a novel malarial protein that mediates transmission to mosquito and vertebrate hosts. Mol Microbiol. 2006, 59 (5): 1369-1379. 10.1111/j.1365-2958.2005.05024.x.View ArticlePubMedGoogle Scholar
  21. Ishino T, Orito Y, Chinzei Y, Yuda M: A calcium-dependent protein kinase regulates Plasmodium ookinete access to the midgut epithelial cell. Mol Microbiol. 2006, 59 (4): 1175-1184. 10.1111/j.1365-2958.2005.05014.x.View ArticleGoogle Scholar
  22. Sidén-Kiamos I, Ecker A, Nyback S, Louis C, Sinden RE, Billker O: Plasmodium berghei calcium-dependent protein kinase 3 is required for ookinete gliding motility and mosquito midgut invasion. Mol Microbiol. 2006, 60 (6): 1355-1363. 10.1111/j.1365-2958.2006.05189.x.PubMed CentralView ArticlePubMedGoogle Scholar
  23. Hirai M, Arai M, Kawai S, Matsuoka H: PbGCbeta is essential for Plasmodium ookinete motility to invade midgut cell and for successful completion of parasite life cycle in mosquitoes. J Biochem. 2006, 140 (5): 747-757. 10.1093/jb/mvj205.View ArticlePubMedGoogle Scholar
  24. Kadota K, Ishino T, Matsuyama T, Chinzei Y, Yuda M: Essential role of membrane-attack protein in malarial transmission to mosquito host. Proc Natl Acad Sci USA. 2004, 101 (46): 16310-16315. 10.1073/pnas.0406187101.PubMed CentralView ArticlePubMedGoogle Scholar
  25. Kaiser K, Camargo N, Coppens I, Morrisey JM, Vaidya AB, Kappe SH: A member of a conserved Plasmodium protein family with membrane-attack complex/perforin (MACPF)-like domains localizes to the micronemes of sporozoites. Mol Biochem Parasitol. 2004, 133 (1): 15-26. 10.1016/j.molbiopara.2003.08.009.View ArticlePubMedGoogle Scholar
  26. Ecker A, Pinto SB, Baker KW, Kafatos FC, Sinden RE: Plasmodium berghei: Plasmodium perforin-like protein 5 is required for mosquito midgut invasion in Anopheles stephensi. Exp Parasitol. 2007, 116 (4): 504-508. 10.1016/j.exppara.2007.01.015.PubMed CentralView ArticleGoogle Scholar
  27. Kaneko O, Templeton TJ, Iriko H, Tachibana M, Otsuki H, Takeo S, Sattabongkot J, Torii M, Tsuboi T: The Plasmodium vivax homolog of the ookinete adhesive micronemal protein, CTRP. Parasitol Int. 2006, 55 (3): 227-231. 10.1016/j.parint.2006.04.003.View ArticlePubMedGoogle Scholar
  28. Naitza S, Spano F, Robson KJ, Crisanti A: The Thrombospondin-related Protein Family of Apicomplexan Parasites: The Gears of the Cell Invasion Machinery. Parasitol Today. 1998, 14 (12): 479-484. 10.1016/S0169-4758(98)01346-5.View ArticlePubMedGoogle Scholar
  29. Arrighi RBG, Hurd H: The role of Plasmodium berghei ookinete proteins in binding to basal lamina components and transformation into oocysts. Int J Parasitol. 2002, 32: 91-98. 10.1016/S0020-7519(01)00298-3.View ArticlePubMedGoogle Scholar
  30. Mahairaki V, Voyatzi T, Siden-Kiamos I, Louis C: The Anopheles gambiae gamma1 laminin directly binds the Plasmodium berghei circumsporozoite- and TRAP-related protein (CTRP). Mol Biochem Parasitol. 2005, 140 (1): 119-121. 10.1016/j.molbiopara.2004.11.012.View ArticlePubMedGoogle Scholar
  31. Oakley MS, Kumar S, Anantharaman V, Zheng H, Mahajan B, Haynes JD, Moch JK, Fairhurst R, McCutchan TF, Aravind L: Molecular factors and biochemical pathways induced by febrile temperature in intraerythrocytic Plasmodium falciparum parasites. Infect Immun. 2007, 75 (4): 2012-2025. 10.1128/IAI.01236-06.PubMed CentralView ArticlePubMedGoogle Scholar
  32. Carter V, Nacer A, Underhill BA, Sinden RE, Hurd H: Minimum requirements for ookinete to oocyst transformation in Plasmodium. Int J Parasitol. 2007, 37 (11): 1221-1232. 10.1016/j.ijpara.2007.03.005.PubMed CentralView ArticlePubMedGoogle Scholar
  33. Al-Olayan E, Beetsma AL, Butcher G, Sinden RE, Hurd H: Complete development of the mosquito phases of the malaria parasite in vitro. Science. 2002, 295: 677-679. 10.1126/science.1067159.View ArticlePubMedGoogle Scholar
  34. Sinden RE: Infection of mosquitoes with rodent malaria. The Molecular Biology of Insect Disease Vectors. Edited by: Crampton JM, Beard CB, Louis C. 1997, London , Chapman and Hall, 67-92.View ArticleGoogle Scholar
  35. Carter V, Cable HC, Underhill BA, Williams J, Hurd H: Isolation of Plasmodium berghei ookinetes in culture using Nycodenz density gradient columns and magnetic isolation. Malar J. 2003, 2 (1): 35-10.1186/1475-2875-2-35.PubMed CentralView ArticlePubMedGoogle Scholar
  36. Paskewitz SM, Shi L: Bypassing the midgut results in development of Plasmodium berghei oocysts in refractory strain of Anopheles gambiae (Diptera: Culicidae). J Med Entomol. 2005, 42 (4): 712-715. 10.1603/0022-2585(2005)042[0712:BTMRID]2.0.CO;2.View ArticlePubMedGoogle Scholar
  37. 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 (9): 1133-1143. 10.1016/S0020-7519(02)00087-5.View ArticlePubMedGoogle Scholar
  38. Vlachou D, Schlegelmilch T, Runn E, Mendes A, Kafatos FC: The developmental migration of Plasmodium in mosquitoes. Curr Opin Genet Dev. 2006, 16 (4): 384-391. 10.1016/j.gde.2006.06.012.View ArticlePubMedGoogle Scholar
  39. Arrighi RBG, Lycett G, Mahairaki V, Siden-Kiamos I, Louis C: Laminin and the malaria parasite's journey through the mosquito midgut. J Exp Biol. 2005, 208 (13): 2497-2502. 10.1242/jeb.01664.View ArticlePubMedGoogle Scholar
  40. Warburg A, Shtern A, Cohen N, Dahan N: Laminin and a Plasmodium ookinete surface protein inhibit melanotic encapsulation of Sephadex beads in the hemocoel of mosquitoes. Microbes Infect. 2007, 9 (2): 192-199. 10.1016/j.micinf.2006.11.006.View ArticlePubMedGoogle Scholar
  41. Gare DC, Piertney SB, Billingsley PF: Anopheles gambiae collagen IV genes: cloning, phylogeny and midgut expression associated with blood feeding and Plasmodium infection. Int J Parasitol. 2003, 33 (7): 681-690. 10.1016/S0020-7519(03)00055-9.View ArticlePubMedGoogle Scholar
  42. Vlachou D, Lycett G, Siden-Kiamos I, Blass C, Sinden RE, Louis C: Anopheles gambiae laminin interacts with the P25 surface protein of Plasmodium berghei ookinetes. Mol Biochem Parasitol. 2001, 112 (2): 229-237. 10.1016/S0166-6851(00)00371-6.View ArticlePubMedGoogle Scholar
  43. Mahairaki V, Lycett G, Siden-Kiamos I, Sinden RE, Louis C: Close association of invading Plasmodium berghei and beta integrin in the Anopheles gambiae midgut. Arch Insect Biochem Physiol. 2005, 60 (1): 13-19. 10.1002/arch.20077.View ArticlePubMedGoogle Scholar

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