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The feeding mechanism of avian malarial parasites

TLDR
Electron microscope studies of the erythrocytic forms, including gametocytes and asexual schizonts, of the protozoa Plasmodium fallax, P. lophurae, and P. cathemerium have revealed a "cytostome," a specialized organelle of the pellicular membrane which is active in the ingestion of host cell cytoplasm.
Abstract
Electron microscope studies of the erythrocytic forms, including gametocytes and asexual schizonts, of the protozoa Plasmodium fallax, P. lophurae, and P. cathemerium, have revealed a "cytostome," a specialized organelle of the pellicular membrane which is active in the ingestion of host cell cytoplasm. In material fixed in glutaraldehyde and postfixed in OsO(4), the cytostome appears in face view as a pore limited by two dense circular membranes and having an inside diameter of approximately 190 mmicro. In cross-section, the cytostome is a cavity bounded on each side by two dense segments corresponding to the two dense circles observed in face view; its base consists of a single unit membrane. In the process of feeding, the cytostome cavity enlarges by expansion of its membrane, permitting a large quantity of red cell cytoplasm to come into contact with the cytostome wall. Subsequent digestion of erythrocyte cytoplasm occurs exclusively in food vacuoles which emanate from the cytostome invagination. As digestion progresses, the food vacuoles initially stain more densely and there is a marked build-up of hemozoin granules. In the final stage of digestion, a single membrane surrounds a cluster of residual pigment particles and very little of the original host cell cytoplasm remains. The cytostome in exoerythrocytic stages of P. fallax has been observed only in merozoites and does not seem to play the same role in the feeding mechanism.

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Journal ArticleDOI

Hemoglobin metabolism in the malaria parasite Plasmodium falciparum.

TL;DR: Understanding the disposition of hemoglobin has allowed identification of essential processes and metabolic weakpoints that can be exploited to combat this scourge of mankind.
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A Brief Illustrated Guide to the Ultrastructure of Plasmodium falciparum Asexual Blood Stages

TL;DR: An illustrated overview of the three-dimensional (3-D) organization of the merozoite, ring, trophozoite and schizont stages of the parasite, based on available data that include 3-D reconstruc-tion from serial electron microscope sections is given.
Journal ArticleDOI

Order and specificity of the Plasmodium falciparum hemoglobin degradation pathway.

TL;DR: Three vacuolar proteases are isolated that account for most of the globin-degrading activity of the digestive vacuole and suggest an ordered pathway of hemoglobin catabolism that presents an excellent target for chemotherapy.
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Fate of haem iron in the malaria parasite Plasmodium falciparum.

TL;DR: Fe-Mössbauer spectroscopy shows that haemozoin is the only detectable iron species in trophozoites, and electron spectroscopic imaging confirms this conclusion.
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4-Aminoquinolines—Past, present, and future; A chemical perspective

TL;DR: This review describes structure-activity relationships for the 4-aminoquinolines, along with views on the mechanism of action and parasite resistance, and potential approaches to the design of new synthetic derivatives.
References
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THE USE OF LEAD CITRATE AT HIGH pH AS AN ELECTRON-OPAQUE STAIN IN ELECTRON MICROSCOPY

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Cytochemistry and electron microscopy. The preservation of cellular ultrastructure and enzymatic activity by aldehyde fixation.

TL;DR: A postfixation in osmium tetroxide, even after long periods of storage, developed an image that—notable in the case of glutaraldehyde—was largely indistinguishable from that of tissues fixed under optimal conditions with osmia tetroxides alone.
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Phagotrophy and two new structures in the malaria parasite Plasmodium berghei.

TL;DR: Continuity between these bodies and the host cytoplasm was found in a number of electron micrographs, showing that the bodies are formed by invagination of the double plasma membrane of the parasite.
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