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    Competency of Anopheles stephensi mysorensis strain for Plasmodium vivax and the role of inhibitory carbohydrates to block its sporogonic cycle

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    <p>Abstract</p> <p>Background</p> <p>Despite the abundance of studies conducted on the role of mosquitoes in malaria transmission, the biology and interaction of <it>Plasmodium </it>with its insect host still holds many mysteries. This paper provides the first study to follow the sporogonic cycle of <it>Plasmodium vivax </it>in a wild insecticide-resistant mysorensis strain of <it>Anopheles stephensi</it>, a major vector of vivax malaria in south-eastern Iran. The study subsequently demonstrates that host-parasite sugar binding interactions are critical to the development of this parasite in the salivary glands of its mosquito host. The identity of the receptors or sugars involved was revealed by a receptor "pre-saturation" strategy in which sugars fed to the mosquitoes inhibited normal host-parasite interactions.</p> <p>Methods</p> <p><it>Anopheles stephensi </it>mysorensis mosquitoes were artificially infected with <it>P. vivax </it>by feeding on the blood of gametocytaemic volunteers reporting to local malaria clinics in the Sistan-Baluchistan province of south-eastern Iran. In order to determine the inhibitory effect of carbohydrates on sporogonic development, vector mosquitoes were allowed to ingest blood meals containing both gametocytes and added carbohydrates. The carbohydrates tested were GlcNAc, GalNAc, arabinose, fucose, mannose, lactose, glucose and galactose. Sporogonic development was assessed by survival of the parasite at both the oocyst and sporozoite stages.</p> <p>Results</p> <p>Oocyst development was observed among nearly 6% of the fed control mosquitoes but the overall number of mosquitoes exhibiting sporozoite invasion of the salivary glands was 47.5% lower than the number supporting oocysts in their midgut. Of the tested carbohydrates, only arabinose and fucose slightly perturbed the development of <it>P. vivax </it>oocysts at the basal side of the mosquito midgut, and the remaining sugars caused no reductions in oocyst development. Strikingly however, sporozoites were completely absent from the salivary glands of mosquitoes treated with mannose, GalNAc, and lactose.</p> <p>Conclusion</p> <p>The study indicates that <it>An. stephensi </it>in southern Iran has the potential to survive long enough to be re-infected and transmit vivax malaria several times, based on the average adult female longevity (about 30 days) and its gonotrophic cycle (2–3 days) during the malaria transmission season. Certain sugar binding interactions are important for the development of <it>P. vivax </it>sporozoites, and this information may be instrumental for the development of transmission blocking strategies.</p

    Competency of mysorensis strain for and the role of inhibitory carbohydrates to block its sporogonic cycle-0

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    Staining.<p><b>Copyright information:</b></p><p>Taken from "Competency of mysorensis strain for and the role of inhibitory carbohydrates to block its sporogonic cycle"</p><p>http://www.malariajournal.com/content/7/1/131</p><p>Malaria Journal 2008;7():131-131.</p><p>Published online 15 Jul 2008</p><p>PMCID:PMC2500038.</p><p></p

    Competency of mysorensis strain for and the role of inhibitory carbohydrates to block its sporogonic cycle-1

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    as the mean of three independent experiments. For each of the three developmental stages, the number of insects containing parasites in each treatment group was statistically compared with the corresponding control using the Chi Squared test (* P < 0.05). Numbers in parentheses refer to the sample size (n), i.e. total number of engorged insects.<p><b>Copyright information:</b></p><p>Taken from "Competency of mysorensis strain for and the role of inhibitory carbohydrates to block its sporogonic cycle"</p><p>http://www.malariajournal.com/content/7/1/131</p><p>Malaria Journal 2008;7():131-131.</p><p>Published online 15 Jul 2008</p><p>PMCID:PMC2500038.</p><p></p
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