Transmission of malaria from one human to another is solely dependent upon the successful sporogonic development of the parasite in vector mosquitoes. If a mosquito does not allow the development, the parasite dies and the transmission of malaria is blocked. Interference with parasite development in vector mosquitoes is, therefore, a proposed strategy to block the spread of malaria. To design such strategies, however, an understanding of the parasite development in vector mosquitoes is essential. Development of the malaria parasite in the mosquito is complex. After being ingested by a susceptible mosquito, the parasite undergoes elaborate changes. Expression of stage-specific parasite genes, and interaction of the parasite with various tissues and molecules in the mosquito, accompany these morphologic changes. The development in the mosquito, therefore, is a challenge to the parasite. In fact, most ingested parasites fail to develop successfully, even in a most successful vector. Interruption of the natural course of development in the mosquito would block malaria transmission.In the mosquito, most of the developmental changes occur to parasites while they are associated with the midgut. The majority of parasites die in the midgut. It can be hypothesized that molecules involved with the parasite/mosquito midgut interaction would be crucial determinants of the sporogonic development of the parasite. Therefore it is important to investigate the ookinete interaction with the midgut epithelium and the survival of the parasite in the vector. The information obtained through these studies may lead to development of novel strategies to control malaria. - Mosquito, malaria, vector, disease, transmission, transmission-blocking, parasite

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Intramural Research (Z01)
Project #
1Z01AI000811-03
Application #
6288993
Study Section
Special Emphasis Panel (LPD)
Project Start
Project End
Budget Start
Budget End
Support Year
3
Fiscal Year
1999
Total Cost
Indirect Cost
City
State
Country
United States
Zip Code
Shahabuddin, Mohammed (2002) Do Plasmodium ookinetes invade a specific cell type in the mosquito midgut? Trends Parasitol 18:157-61
Silva-Neto, Mario A C; Atella, Georgia C; Shahabuddin, Mohammed (2002) Inhibition of Ca2+/calmodulin-dependent protein kinase blocks morphological differentiation of plasmodium gallinaceum zygotes to ookinetes. J Biol Chem 277:14085-91
Wang, P; Conrad, J T; Shahabuddin, M (2001) Localization of midgut-specific protein antigens from Aedes aegypti (Diptera: Culicidae) using monoclonal antibodies. J Med Entomol 38:223-30
Shahabuddin, M; Costero, A (2001) Spatial distribution of factors that determine sporogonic development of malaria parasites in mosquitoes. Insect Biochem Mol Biol 31:231-40
Park, S S; Shahabuddin, M (2000) Structural organization of posterior midgut muscles in mosquitoes, Aedes aegypti and Anopheles gambiae. J Struct Biol 129:30-7
Killeen, G F; Foy, B D; Shahabuddin, M et al. (2000) Tagging bloodmeals with phagemids allows feeding of multiple-sample arrays to single cages of mosquitoes (Diptera: Culicidae) and the recovery of single recombinant antibody fragment genes from individual insects. J Med Entomol 37:528-33
Schneider, D; Shahabuddin, M (2000) Malaria parasite development in a Drosophila model. Science 288:2376-9
Zieler, H; Garon, C F; Fischer, E R et al. (2000) A tubular network associated with the brush-border surface of the Aedes aegypti midgut: implications for pathogen transmission by mosquitoes. J Exp Biol 203:1599-611
Zieler, H; Nawrocki, J P; Shahabuddin, M (1999) Plasmodium gallinaceum ookinetes adhere specifically to the midgut epithelium of Aedes aegypti by interaction with a carbohydrate ligand. J Exp Biol 202:485-95
Shahabuddin, M; Vinetz, J M (1999) Chitinases of human parasites and their implications as antiparasitic targets. EXS 87:223-34

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