Plasmodium male development gene-1 (mdv-1) is important for female sexual development and identifies a polarised plasma membrane during zygote development

Int J Parasitol. 2009 Jun;39(7):755-61. doi: 10.1016/j.ijpara.2008.11.008. Epub 2008 Dec 24.

Abstract

Successful development of Plasmodium sexual stages is essential for parasite survival, but the genes involved are poorly understood. We 'knocked out' the male development gene-1 (mdv-1) locus in Plasmodium berghei and found it to be important in female gametocyte activation. Indirect immunofluorescence assays show MDV-1 has a punctate cytoplasmic distribution in gametocytes. After activation of both females and males, MDV-1 is more peripherally located but in males exclusively it becomes concentrated in a few large foci. In vitro ookinete conversion assays that test the ability of activated female gametocytes to develop into retort stage ookinetes, suggests a complicit role for MDV-1, with the knock-out parasite producing 86% reduction in ookinetes. The retort stage ookinete develops from the zygote by increasing growth of an apical protrusion and MDV-1 locates at the 'leading' extracellular apical pole of this protrusion. In the fully developed ookinete MDV-1 is localised to the posterior pole. In vivo, the knock-out parasites demonstrate a phenotype in which there is a 90% reduction of parasite transmission to oocysts in mosquitoes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Animals, Genetically Modified
  • Anopheles / parasitology
  • Blotting, Western
  • Cell Cycle Proteins / metabolism
  • Cell Membrane / metabolism*
  • Cell Membrane / parasitology
  • Female
  • Fluorescent Antibody Technique, Indirect
  • Gametogenesis / physiology*
  • Gene Deletion
  • Genes, Developmental / physiology
  • Male
  • Mice
  • Molecular Sequence Data
  • Oocysts / growth & development
  • Oocysts / physiology
  • Phenotype
  • Plasmodium berghei / genetics
  • Plasmodium berghei / growth & development*
  • Plasmodium berghei / parasitology
  • Proteome / physiology
  • Protozoan Proteins / genetics
  • Protozoan Proteins / metabolism*
  • Rabbits
  • Sex Ratio
  • Sexual Development*
  • Zygote / growth & development*
  • Zygote / metabolism

Substances

  • Cell Cycle Proteins
  • Proteome
  • Protozoan Proteins