Literature DB >> 338177

Variations in structure and function during the life cycle of malarial parasites.

M Aikawa.   

Abstract

The fine structure of malarial parasites is reviewed and the function of the intracellular organelles is discussed. When the erythrocytic, exoerythrocytic, and mosquito stages of plasmodia are compared, substantial differences are seen. The major differences involve the amount of surface coat of the motile forms, the structure and function of the mitochondria, and the ingestion and digestion of nutrients. Significant structural differences are also observed between comparable stages of mammalian and avian parasites. These differences indicate that malarial parasites adapt themselves to the different environments in which the parasite resides.When host cell changes induced by malarial parasite infection are reviewed, alterations characteristic of the infecting plasmodia are observed in erythrocytes. Erythrocyte changes include caveola-vesicle complexes, excrescences, and clefts. The caveola-vesicle complexes possess malarial antigens and exhibit pinocytotic activities. The excrescences form focal junctions with adjacent cells and may be responsible for infected erythrocyte sequestration in organs. The significance of these host cell changes specific to certain species of malarial parasite is still unknown.

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Year:  1977        PMID: 338177      PMCID: PMC2366740     

Source DB:  PubMed          Journal:  Bull World Health Organ        ISSN: 0042-9686            Impact factor:   9.408


  21 in total

1.  Erythrocyte membrane alterations induced by Plasmodium simium infection in Saimiri sciureus: relation to Schüffner's dots.

Authors:  C R Sterling; T M Seed; M Aikawa; J Rabbege
Journal:  J Parasitol       Date:  1975-04       Impact factor: 1.276

2.  Electron microscope study of the blood stages of Plasmodium tropiduri, a lizard malaria parasite.

Authors:  J V Scorza
Journal:  Parasitology       Date:  1971-08       Impact factor: 3.234

3.  Localization of acid phosphatase activity in Plasmodium berghei and P. gallinaceum: an electron microscopic observation.

Authors:  M Aikawa; P E Thompson
Journal:  J Parasitol       Date:  1971-06       Impact factor: 1.276

Review 4.  Parasitological review. Plasmodium: the fine structure of malarial parasites.

Authors:  M Aikawa
Journal:  Exp Parasitol       Date:  1971-10       Impact factor: 2.011

5.  The fine structure of trophozoites and gametocytes in Plasmodium coatneyi.

Authors:  M A Rudzinska; W Trager
Journal:  J Protozool       Date:  1968-02

6.  Sporoblast and sporozoite formation in Plasmodium gallinaceum infection of Aedes aegypti.

Authors:  J A Terzakis; H Sprinz; R A Ward
Journal:  Mil Med       Date:  1966-09       Impact factor: 1.437

7.  Fine structure of the exoerythrocytic stage of Plasmodium cynomolgi.

Authors:  T Sodeman; B Schnitzer; T Durkee; P Jcontacos
Journal:  Science       Date:  1970-10-16       Impact factor: 47.728

8.  Plasmodium falciparum malaria. Ultrastructure of parasitized erythrocytes in cardiac vessels.

Authors:  S A Luse; L H Miller
Journal:  Am J Trop Med Hyg       Date:  1971-09       Impact factor: 2.345

9.  Antibody-induced ultrastructural changes of malarial sporozoites.

Authors:  A H Cochrane; M Aikawa; M Jeng; R S Nussenzweig
Journal:  J Immunol       Date:  1976-03       Impact factor: 5.422

10.  Phagotrophy and two new structures in the malaria parasite Plasmodium berghei.

Authors:  M A RUDZINSKA; W TRAGER
Journal:  J Biophys Biochem Cytol       Date:  1959-08
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  13 in total

1.  Antimalarial activities of dermaseptin S4 derivatives.

Authors:  M Krugliak; R Feder; V Y Zolotarev; L Gaidukov; A Dagan; H Ginsburg; A Mor
Journal:  Antimicrob Agents Chemother       Date:  2000-09       Impact factor: 5.191

2.  A novel alternate secretory pathway for the export of Plasmodium proteins into the host erythrocyte.

Authors:  M F Wiser; H N Lanners; R A Bafford; J M Favaloro
Journal:  Proc Natl Acad Sci U S A       Date:  1997-08-19       Impact factor: 11.205

Review 3.  Biochemistry of Plasmodium (malarial parasites).

Authors:  I W Sherman
Journal:  Microbiol Rev       Date:  1979-12

4.  Membrane specific mapping and colocalization of malarial and host skeletal proteins in the Plasmodium falciparum infected erythrocyte by dual-color near-field scanning optical microscopy.

Authors:  T Enderle; T Ha; D F Ogletree; D S Chemla; C Magowan; S Weiss
Journal:  Proc Natl Acad Sci U S A       Date:  1997-01-21       Impact factor: 11.205

5.  Intracellular structures of normal and aberrant Plasmodium falciparum malaria parasites imaged by soft x-ray microscopy.

Authors:  C Magowan; J T Brown; J Liang; J Heck; R L Coppel; N Mohandas; W Meyer-Ilse
Journal:  Proc Natl Acad Sci U S A       Date:  1997-06-10       Impact factor: 11.205

6.  Transformation of sporozoites of Plasmodium berghei into exoerythrocytic forms in the liver of its mammalian host.

Authors:  J F Meis; J P Verhave; P H Jap; J H Meuwissen
Journal:  Cell Tissue Res       Date:  1985       Impact factor: 5.249

Review 7.  The biology of tissue forms and other asexual stages in mammalian plasmodia.

Authors:  J P Verhave; J F Meis
Journal:  Experientia       Date:  1984-12-15

8.  Comparative morphology of human and animal malaria parasites. I. Host-parasite interface.

Authors:  U Mackenstedt; C R Brockelman; H Mehlhorn; W Raether
Journal:  Parasitol Res       Date:  1989       Impact factor: 2.289

9.  Interaction between Plasmodium falciparum apical membrane antigen 1 and the rhoptry neck protein complex defines a key step in the erythrocyte invasion process of malaria parasites.

Authors:  Dave Richard; Christopher A MacRaild; David T Riglar; Jo-Anne Chan; Michael Foley; Jake Baum; Stuart A Ralph; Raymond S Norton; Alan F Cowman
Journal:  J Biol Chem       Date:  2010-03-12       Impact factor: 5.157

10.  Ultrastructure of erythrocytes from Aotus trivirgatus and Saimiri sciureus monkeys infected by Plasmodium vivax.

Authors:  H N Lanners
Journal:  Parasitol Res       Date:  1991       Impact factor: 2.289

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