Disruption of a Plasmodium falciparum gene linked to male sexual development causes early arrest in gametocytogenesis

Proc Natl Acad Sci U S A. 2005 Nov 15;102(46):16813-8. doi: 10.1073/pnas.0501858102. Epub 2005 Nov 7.

Abstract

A male gametocyte defect in the Plasmodium falciparum Dd2 parasite was previously discovered through the observation that all progeny clones in a Dd2 x HB3 genetic cross were the result of fertilization events between Dd2 female and HB3 male gametes. A determinant linked to the defect in Dd2 was subsequently mapped to an 800-kb segment on chromosome 12. Here, we report further mapping of the determinant to an 82-kb region and the identification of a candidate gene, P. falciparum male development gene 1 (pfmdv-1), that is expressed at a lower level in Dd2 compared with the wild-type normal male gametocyte-producing ancestor W2. Pfmdv-1 protein is sexual-stage specific and is located on the gametocyte plasma membrane, parasitophorous vacuole membrane, and the membranes of cleft-like structures within the erythrocyte. Disruption of pfmdv-1 results in a dramatic reduction in mature gametocytes, especially functional male gametocytes, with the majority of sexually committed parasites developmentally arrested at stage I. The pfmdv-1-knockout parasites show disturbed membrane structures, particularly multimembrane vesicles/tubes that likely derive from deformed cleft-like structures. Mosquito infectivity of the knockout parasites was also greatly reduced but not completely lost. The results suggest that pfmdv-1 plays a key role in gametocyte membrane formation and integrity.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Animals
  • Cytoplasm / metabolism
  • Down-Regulation
  • Erythrocytes / parasitology
  • Genes, Protozoan
  • Germ Cells / cytology*
  • Plasmodium falciparum / genetics*
  • Plasmodium falciparum / growth & development*
  • Reverse Transcriptase Polymerase Chain Reaction