An improved method for the in vitro differentiation of Plasmodium falciparum gametocytes into ookinetes
© Ghosh et al. 2010
Received: 8 May 2010
Accepted: 8 July 2010
Published: 8 July 2010
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© Ghosh et al. 2010
Received: 8 May 2010
Accepted: 8 July 2010
Published: 8 July 2010
Ookinete is the form of the malaria parasite that invades the mosquito midgut epithelium to initiate sporogony. Differentiation of ingested gametocytes into ookinetes in the mosquito midgut lumen and subsequent interaction with the lumenal surface of the midgut epithelium in preparation for invasion is a complex and multi-stepped process. To facilitate the study of these events in detail it is necessary to produce sufficient numbers of pure, fully mature and functional ookinetes. However, production of even a small number of Plasmodium falciparum ookinetes in vitro has proven to be a daunting task. Consequently, over the past four decades our collective understanding of the biology of this parasite form remains sorely deficient. This article reports on investigations of five different ookinete media, in an effort to improve the in vitro transformation efficiency of P. falciparum gametocytes into mature ookinetes and their infectivity of the mosquito midgut.
Five different ookinete media were evaluated for their ability to support the differentiation of gametocytes into gametes and further into mature stage V ookinetes. Moreover, infectivity of the in vitro-transformed ookinetes was evaluated by feeding them to vector mosquitoes and measuring their ability to traverse the midgut and form oocysts.
One of the five media (medium E) was clearly superior in that the cultured ookinetes produced the largest number of oocysts when fed to mosquitoes. Key components were additions of human serum, human red blood cell lysate and mosquito pupal extract, resulting in the production of larger numbers of ookinetes able to develop into oocysts when fed to mosquitoes.
This simple and practical improvement over the prevailing methodology will facilitate the investigation of how this important human malaria parasite initiates its development in the mosquito and will contribute to the understanding of its transmission biology.
Plasmodium, the causative agent of malaria, infects an estimated 500 million people every year and has the highest health impact on women and young children in sub-Saharan Africa . Parasite resistance to available drugs and vector mosquito resistance to insecticides have hampered the fight of this devastating disease. Moreover, despite massive efforts, an effective vaccine has not yet been developed. New strategies need to be developed. One approach is to interrupt parasite transmission by the mosquito vector, an approach that requires in depth understanding of parasite development in the mosquito.
Soon after the mosquito ingests an infected blood meal, gametocytes differentiate into gametes that mate to form zygotes and later motile ookinetes. To exit the mosquito midgut lumen, ookinetes traverse the midgut epithelium and lodge beneath the basal lamina where they differentiate into oocysts. Upon maturation, each oocyst releases several thousand sporozoites into the haemocoel from where they invade the salivary glands. At this point, the sporozoites are ready to be transmitted when the mosquito takes a blood meal from another vertebrate host . Little is known about the developmental processes that operate during the differentiation of gametocytes into ookinetes .
While gametocytes can be easily obtained from an in vitro Plasmodium falciparum culture, current methods for the transformation of gametocytes into ookinetes are poor with a reported transformation efficiency of only 0.002% (0.2 mature ookinetes per 10,000 red blood cells (RBCs)) . Moreover, the ability of these ookinetes to develop into oocysts in the mosquito has not been determined . This is in contrast with the in vitro differentiation of the rodent parasite Plasmodium berghei, which is efficient and yields about 106 ookinetes from a single infected mouse . The lack of an efficient P. falciparum differentiation protocol has hampered the study of ookinete differentiation and its interactions with the mosquito vector.
In the work presented here, a culture medium was established that supports the efficient development and differentiation into mature P. falciparum ookinetes. The medium described by Carter et al  was modified by replacing 20% foetal bovine serum (FBS) with O-positive human serum (medium A). Four additional media (media B-E) were created by addition of various supplements and functional integrity of the resulting ookinetes was verified by measuring their infectivity to mosquitoes.
RPMI 1640 (Invitrogen), Schneiders medium (Invitrogen), Waymouth medium (Invitrogen), O-positive human serum (Interstate Blood Bank), xanthurenic acid (Sigma), hypoxanthine (Sigma), anti-Pfs25 mouse monoclonal antibody (obtained from the Malaria Research and Reference Reagent Resource Center (MR4)), mouse monoclonal anti-P. falciparum chitinase antibody (a gift from Dr. Joseph Vinetz), goat anti-mouse IgG labeled with Texas Red (Invitrogen), antibody labeling Kit (Pierce).
The colony of Anopheles gambiae (Keele strain) was obtained from Drs. Hilary Hurd and Paul Eggleston at Keele University. Larvae were reared on dry cat food. Adults were maintained on 10% sucrose solution at 27 ± 1°C and 80 ± 5% relative humidity with a 14 h/10 h light/dark cycle. About 5- to 6-day-old An. gambiae mosquitoes were starved overnight and selected by placing a bottle with water at 37~40°C next to the cage (touching a meshed side of a cage or the side of an ice cream container). Host-seeking mosquitoes that are attracted to the heat were transferred by aspiration to separate 16 oz. feeder cups.
Plasmodium falciparum NF54 parasites (0.5% parasitemia) were maintained at 5% haematocrit in P. falciparum culture medium (RPMI 1640 medium containing L-glutamine supplemented with 0.2% sodium bicarbonate and 10% v/v O-positive human serum) in a 37°C chamber with 'malaria gas mixture' (5% CO2, 5% O2 and 90% nitrogen) [6, 7].
Gametocytogenesis was induced by stopping addition of human RBCs and by changing 'the medium daily until day 18. On alternate days about 10 μl of the culture was smeared on a slide, fixed with methanol and stained in Giemsa stain (1:40 dilution) to count the gametocytes and the male:female ratio.
About 500 An. gambiae pupae were collected, washed with sterile distilled water several times and after a final wash in PBS they were stored at -80°C until use. Frozen pupae were thawed, resuspended in 500 μl of PBS and transferred to a glass homogenizer. Homogenization was done on ice with 10 to 12 strokes and the homogenate was centrifuged at 14,500 g for 10 min at 4°C. The clarified supernatant was transferred to a clean tube, heated at 60°C for 1 h and after cooling to room temperature it was centrifuged at 14,500 g for 30 min at 4°C. The clarified supernatant was aliquoted and stored at -80°C until use.
O-positive human RBCs were washed (about 0.5 ml of packed volume) in sterile PBS. RBCs were lysed by adding 900 μl of sterile distilled water and swirled for 30 sec for lysis to occur. Immediately following lysis, 100 μl of 10× PBS was added to the tube to make it isotonic. The lysate was centrifuged at 14,500 g for 30 min at 4°C. The supernatant was aliquoted and stored at -80°C until use.
Composition of five ookinete differentiation media
RPMI 1640, 20% Human group A serum, Hypoxanthine (50 μg/ml), Sodium bicarbonateb (2 g/l).
RPMI1640 and Waymouth medium (1:1) Remaining components are the same.
RPMI 1640, Waymouth, and Schneider's Drosophila Medium (1:1:1). Remaining components are the same.
Same as medium C with 0.2 μM xanthurenic acid.
Same as medium C with pupal extract and human blood lysate.
About 100 μl of the gametocyte culture was sampled on day 18 and centrifuged at 650 g for 5 min followed by resuspension of the packed cells in the same volume of ookinete medium. A drop (4-6 μl) of the resuspended gametocytes was placed on a slide. After breathing on a cover slip, it was placed over the droplet, followed by incubation at room temperature (22°C) to induce exflagellation. After 10 min the slides were observed with differential interference contrast (DIC) optics to count exflagellation events at five positions of the cover slip (4 corners and the center of the cover slip, all together 25 fields; the average value was used) using a 40× objective. If no exflagellation events were observed at 10 min, slides were checked every 2 min until exflagellation was observed.
After checking gametocytaemia, about 3 ml of the gametocyte culture was transferred into a conical 15 ml COSTAR tube and centrifuged at 650 g for 5 min at 37°C. The cell pellet was washed three times with incomplete medium (RPMI 1640 medium only, no serum). After the final wash, packed cells were resuspended in 250 μl of each of the five ookinete culture media (Table 1). Cells were gently resuspended in each medium, transferred into a well of a 24-well tissue culture plate and incubated at 24 ± 2°C on a shaker (50 revolutions per min) for 24 h.
About 100 μl of the ookinete culture was centrifuged at 650 g for 5 min and the supernatant was discarded. Packed cells were resuspended in 20 μl of human serum by flicking the tube and the suspended cells were used to make a thin smear on 2~4 slides, followed by methanol fixation for 3 min at room temperature. Slides were air-dried and stored at room temperature for subsequent histological analysis after Giemsa staining. Different stages of ookinete differentiation were counted by microscopic examination of the Giemsa-stained slides using a 100× oil-immersion objective and images were recorded. Total number of each ookinete stage per 10,000 RBCs was determined. For immunostaining slides were fixed with 4% paraformaldehyde (Fisher Scientific) for 1 h at 4°C. The slides were washed with PBS and stored at -80°C for later use.
Slides containing paraformaldehyde-fixed cells (see above) were thawed and air-dried at room temperature and blocked in blocking solution (PBS with 4% BSA, pH 7.4) for 1 h. Slides were incubated with anti-Pfs25 monoclonal antibody (diluted 1:1000 in blocking solution) for 1 h at room-temperature and washed several times at 5 min intervals with PBS. Slides were blocked in blocking solution as described above and incubated for 45 min at room temperature and in the dark with Texas Red-labeled anti-mouse IgG (1:2000 dilutions in blocking solution). Slides were washed several times with PBS, mounted in Slowfade ProLong Gold antifade reagent with DAPI (Invitrogen) mounting medium, overlaid with a coverslip and sealed with nail varnish. Slides were kept in the dark at 4°C until image acquisition.
Anti-Pfs25 antibodies were conjugated with FITC using the Pierce antibody labeling kit and following the manufacturer's protocol. Slides containing paraformaldehyde-fixed cells were thawed, air-dried and permeabilized with blocking buffer containing 0.1% Triton X-100 (Sigma) for 1 h at room temperature. Slides were incubated with anti-Pf chitinase mouse monoclonal antibody (1:200 dilutions) for 1 h at room temperature. Slides were washed in PBS and blocked again followed by incubation for 45 min at room temperature and in the dark with Texas Red-labeled anti-mouse IgG (1:2000 dilution in blocking solution). Slides were washed in PBS and blocked again followed by incubation with the FITC-labeled anti-Pfs25 monoclonal antibody (see above; 1:100 dilution in blocking solution). The slides were washed several times with PBS and mounted in Slowfade ProLong Gold antifade reagent with DAPI (Invitrogen). All images were acquired and processed equally with Photoshop, using the same parameters.
Clean membrane glass feeders were connected with 4 inch-long tubing in a row (maximum six feeders) and the tubing was connected to the outlet manifold of an immersion circulating water bath that had been set to 40 ± 2°C. Just before adding cultures to the feeders, a piece of Parafilm (1 square inch) was taken and stretched across the open bell-shaped end of the feeder, to make a shallow feeding chamber. Ookinete culture was introduced into the chamber making sure that the culture covered the entire feeding surface. Each feeder was placed over a container with mosquitoes that had been starved overnight at 27 ± 1°C and 80 ± 5% relative humidity and mosquitoes were allowed to feed for 15 min.
Human blood (RBCs) was washed three times with human serum and resuspended to the original volume with human serum kept at 37°C. Gametocyte culture was centrifuged at 650 g for 5 min at 37°C and the supernatant was removed. The packed cell volume of the pellet was measured and washed RBCs were added using a ratio 1:3 (vol/vol), mixed well and the mixture was kept in a 37°C water bath until feeding.
Mature ookinetes (24-hour culture) were centrifuged at 650 g for 5 min at room temperature. The packed cell volume of the pellet was measured and the pellet was resuspended with washed human RBCs (prepared as above) using a ratio 1:3 (vol/vol), mixed well and the suspension was kept at room temperature until feeding using membrane feeders as described earlier. Mosquitoes were allowed to feed for 15 min in the dark.
Unfed mosquitoes were removed at ~24 h after feeding and the fed mosquitoes were kept for 8 d with 10% sucrose solution in an incubator at 27 ± 1°C and 80 ± 5% humidity. On day 8 post-feeding mosquitoes were dissected and incubated with 0.2% mercurochrome (Sigma) in sterile distilled water; for 10-20 min. Midguts were washed in PBS and mounted on a slide with PBS. The number of stained oocysts in each gut was counted at 20× or 40× magnification.
Images were captured using a CCD camera and Spot 3 software using a 100× oil immersion objective. Images were merged using Adobe Photoshop 7.
Several procedures have been employed to induce gametocyte formation, but the most reproducible and convenient one is to stop adding fresh RBCs while changing media daily. This was routinely used to obtain mature gametocytes on day 18. These cultures typically had 2~3% gametocytaemia and provided the starting material for the experiments reported below.
In vitro induction of exflagellation is normally accomplished by lowering of the temperature and addition of xanthurenic acid . Media A-C contain only basic components and no specific gamete-inducing factors, therefore exflagellation was likely induced by the drop in temperature from 37°C to 22°C. The high exflagellation values achieved by medium D was likely due to the added xanthurenic acid  and for medium E due to the presence of xanthurenic acid in the pupal extract .
This work sought to reproduce in vitro two essential steps of parasite development. The first occurs in the vertebrate host and involves differentiation of asexually dividing parasites into male and female gametocytes. The second occurs in the mosquito midgut and involves gametogenesis, fertilization and development into functional stage V ookinetes. This report focuses mostly on the second step. Modification of the existing procedures resulted in a dramatic improvement (about 75-fold) over the originally published procedure . Key factors may include a slightly higher initial gametocyte yield, a slightly lower temperature (24 ± 2°C instead of 25-27°C) for the ookinete differentiation step and replacement of Fetal Bovine Serum by human serum in this study. Infectivity of in vitro-generated ookinetes to mosquitoes has not been measured previously. The experiments of Figures 5 and 6 illustrate the importance of this type of assessment: number of morphologically mature looking ookinetes is not a direct indication of success of mosquito infection. Factor(s) contained in the pupal extract and/or RBC lysate may be crucial for promoting functional viability.
Taken together, the data presented in this study showed that use of human serum together with the combined addition of pupal extract and human RBC lysate in medium E enhances the full development of male and female gametocytes into mature ookinetes. Importantly, the in vitro differentiated ookinetes efficiently produced oocysts when fed to mosquitoes.
Malaria Research and Reference Reagent Resource Center
red blood cell
fetal bovine serum
differential interference contrast
phosphate buffered saline
We thank the Johns Hopkins Malaria Research Institute mosquito and Plasmodium core facilities. Chris Kizito provided An. gambiae mosquitoes and Ms. Yessika Vasquez P. falciparum cultures (NF54 isolate obtained from Sanaria Inc.). This work was supported by grants from the National Institutes of Health, by the Johns Hopkins Malaria Research Institute and the Bloomberg Family Foundation.
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.