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Malaria Immunology - download pdf or read online

By A. Perlmann, M. Troye-Bloomberg

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Inset: A pellicular complex consists of a parasitophorous vacuole membrane (PVM), a gametocyte plasmalemma (GPM), and an inner layer composed of two closely apposed membranes (IL). 1 ␮m. b Vacuolated gametocyte from the 3’CO clone. Vacuolation originates at the plasmalemma of the gametocyte (G). 5 ␮m. Reprinted with permission from Lobo et al. (1999) [97]; courtesy of Molecular Cell. micro- (male) or macro- (female) gametocyte in the red blood cells. Infected erythrocytes in the fine capillaries of bone marrow and spleen only develop the gametocytes.

As the young oocyst grows, vacuoles appear beneath the oocyst capsule (fig. 8a). The vacuoles enlarge and form large clefts that subdivide the oocyst cytoplasm into sporoblasts. From these sporoblasts, sporozoites bud into the inter-space of the oocyst (fig. 8b). The circumsporozoite (CS) protein is selectively expressed during the sporoblast formation process. CS-knockout mutants differentiate normally to the early oocyst stage but fail to form viable sporozoites [107], suggesting that the CS protein may be essential for the budding process of sporozoites in the oocyst.

All merozoites from a committed schizont will give rise to gametocytes [3]. The molecular basis for commitment is unknown. Gametocyte morphology is distinct from that of asexual blood stages and mirrored by an equally distinct transcriptional activity that prepares the long-lived, circulating mature male and female gametocyte sexual precursors for the sudden re-initiation of development in the mosquito midgut. The extent of transcriptional reprogramming is emphasised by recent microarray experiments with P.

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Malaria Immunology by A. Perlmann, M. Troye-Bloomberg


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