Literature DB >> 2189114

Commitment of the malaria parasite Plasmodium falciparum to sexual and asexual development.

M C Bruce1, P Alano, S Duthie, R Carter.   

Abstract

Blood-stage malaria parasites in the vertebrate host can develop either into the asexual, multiplying forms, called schizonts, or into gametocytes, the sexual stages of the parasite. In the present work we studied the differentiation into asexual parasites or gametocytes of the progeny of single, isolated schizonts of the clone 3D7A of Plasmodium falciparum, using monoclonal antibodies specific for the sexual or asexual stages of the parasite. We observed that schizonts obtained from a continuous culture undergoing serial cycles of growth and dilution with fresh red blood cells produced either only gametocytes or only asexual parasites, showing a high degree of commitment to one or the other developmental pathway. The relative proportion of schizonts which produced gametocytes was very low at low parasite densities in culture, while at high parasite densities a much greater proportion of schizonts produced gametocytes. Nevertheless, at both low and high parasite densities individual schizonts were almost always fully committed to producing only gametocytes or only asexual parasites.

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Year:  1990        PMID: 2189114     DOI: 10.1017/s0031182000061199

Source DB:  PubMed          Journal:  Parasitology        ISSN: 0031-1820            Impact factor:   3.234


  87 in total

1.  Mixed-genotype infections of malaria parasites: within-host dynamics and transmission success of competing clones.

Authors:  L H Taylor; D Walliker; A F Read
Journal:  Proc Biol Sci       Date:  1997-06-22       Impact factor: 5.349

Review 2.  Sexual development in Plasmodium parasites: knowing when it's time to commit.

Authors:  Gabrielle A Josling; Manuel Llinás
Journal:  Nat Rev Microbiol       Date:  2015-09       Impact factor: 60.633

3.  Identification of a continuous and cross-reacting epitope for Plasmodium falciparum transmission-blocking immunity.

Authors:  B Wizel; N Kumar
Journal:  Proc Natl Acad Sci U S A       Date:  1991-11-01       Impact factor: 11.205

4.  Markedly enhanced immunogenicity of a Pfs25 DNA-based malaria transmission-blocking vaccine by in vivo electroporation.

Authors:  Ralph LeBlanc; Yessika Vasquez; Drew Hannaman; Nirbhay Kumar
Journal:  Vaccine       Date:  2007-11-20       Impact factor: 3.641

5.  Response to chloroquine treatment in children with or without gametocytes during uncomplicated Plasmodium falciparum malaria.

Authors:  A A Adedeji; B A Fateye; A O J Amoo; A Sowunmi
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2006-02       Impact factor: 3.267

6.  Predicting optimal transmission investment in malaria parasites.

Authors:  Megan A Greischar; Nicole Mideo; Andrew F Read; Ottar N Bjørnstad
Journal:  Evolution       Date:  2016-06-24       Impact factor: 3.694

7.  Isolation and functional characterization of two distinct sexual-stage-specific promoters of the human malaria parasite Plasmodium falciparum.

Authors:  K J Dechering; A M Kaan; W Mbacham; D F Wirth; W Eling; R N Konings; H G Stunnenberg
Journal:  Mol Cell Biol       Date:  1999-02       Impact factor: 4.272

8.  Commitment Isn't for Everyone.

Authors:  Gabrielle A Josling; Manuel Llinás
Journal:  Trends Parasitol       Date:  2019-04-30

9.  A semi-automated method for counting fluorescent malaria oocysts increases the throughput of transmission blocking studies.

Authors:  Michael J Delves; Robert E Sinden
Journal:  Malar J       Date:  2010-01-29       Impact factor: 2.979

Review 10.  Malaria gametocytogenesis.

Authors:  David A Baker
Journal:  Mol Biochem Parasitol       Date:  2010-04-08       Impact factor: 1.759

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