Literature DB >> 22926648

Hemozoin accumulation in Garnham bodies of Plasmodium falciparum gametocytes.

Augustine U Orjih1.   

Abstract

Garnham bodies are curious objects exclusive in erythrocytes containing sexual forms (gametocytes) of Plasmodium falciparum. Although the name is familiar, only a few photographs of Garnham bodies (G-bodies) have been published. Considering that other objects in malaria-infected erythrocytes, such as Schuffner's dots of Plasmodium vivax and Maurer's clefts of P. falciparum, have been found to have some functions, it has become necessary to pay closer attention to G-bodies. The present study presents previously unknown features of G-bodies and suggests a protective role for them. Wild isolates of P. falciparum were encouraged to grow in vitro under conditions that promote gametocytogenesis. Thin and thick smears of the cells were stained with Giemsa stain and examined under a light microscope. Production of G-bodies was detected in two isolates both in immature and mature gametocytes. Sometimes, the objects are found both at the top and below the parasite, contrary to previous suggestion of it being only on one side. They are highly diverse in morphology, including those that are shaped like m or S. Hemozoin accumulation was detected in some of the bodies, indicating direct opening into the cystoplasm of the parasite. It is possible that hemozoin was first produced in the parasite's food vacuole before being transported to G-bodies. Alternatively, hemoglobin transport vesicles could first accumulate in G-bodies where metabolically released ferriprotoporphyrin IX (FP) could be polymerized; but this would need acidic environment comparable to that in food vacuole. Electron microscopy has revealed that G-bodies consist of membranous whorls and it has been demonstrated experimentally that both infected and uninfected membranes promote β-hematin formation. Whatever the mechanism, storing hemozoin in G-bodies outside the cytoplasm of the parasite could provide intraerythrocytic sexual forms of P. falciparum additional protection against FP toxicity.

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Year:  2012        PMID: 22926648     DOI: 10.1007/s00436-012-3090-8

Source DB:  PubMed          Journal:  Parasitol Res        ISSN: 0932-0113            Impact factor:   2.289


  20 in total

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2.  Observations on gametogenesis in Plasmodium falciparum from continuous culture.

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Journal:  J Protozool       Date:  1979-02

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4.  Involvement of lipids in ferriprotoporphyrin IX polymerization in malaria.

Authors:  C D Fitch; G Z Cai; Y F Chen; J D Shoemaker
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5.  Gametocytogenesis of Plasmodium falciparum in vitro: an electron microscopic study.

Authors:  R E Sinden
Journal:  Parasitology       Date:  1982-02       Impact factor: 3.234

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Authors:  Augustine U Orjih; Thazhumpal C Mathew; Preethi T Cherian
Journal:  Exp Biol Med (Maywood)       Date:  2012-08-13

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Review 8.  The role of the Maurer's clefts in protein transport in Plasmodium falciparum.

Authors:  Tobili Y Sam-Yellowe
Journal:  Trends Parasitol       Date:  2009-05-11

9.  Evidence for environmental modulation of gametocytogenesis in Plasmodium falciparum in continuous culture.

Authors:  R Carter; L H Miller
Journal:  Bull World Health Organ       Date:  1979       Impact factor: 9.408

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Authors:  Dewal Jani; Rana Nagarkatti; Wandy Beatty; Ross Angel; Carla Slebodnick; John Andersen; Sanjai Kumar; Dharmendar Rathore
Journal:  PLoS Pathog       Date:  2008-04-25       Impact factor: 6.823

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4.  Budding pouches and associated bubbles: 3D visualization of exo-membrane structures in plasmodium falciparum gametocytes.

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