ZIPCO, a putative metal ion transporter, is crucial for Plasmodium liver-stage development

EMBO Mol Med. 2014 Nov;6(11):1387-97. doi: 10.15252/emmm.201403868.

Abstract

The malaria parasite, Plasmodium, requires iron for growth, but how it imports iron remains unknown. We characterize here a protein that belongs to the ZIP (Zrt-, Irt-like Protein) family of metal ion transport proteins and have named ZIP domain-containing protein (ZIPCO). Inactivation of the ZIPCO-encoding gene in Plasmodium berghei, while not affecting the parasite's ability to multiply in mouse blood and to infect mosquitoes, greatly impairs its capacity to develop inside hepatocytes. Iron/zinc supplementation and depletion experiments suggest that ZIPCO is required for parasite utilization of iron and possibly zinc, consistent with its predicted function as a metal transporter. This is the first report of a ZIP protein having a crucial role in Plasmodium liver-stage development, as well as the first metal ion transporter identified in Plasmodium pre-erythrocytic stages. Because of the drastic dependence on iron of Plasmodium growth, ZIPCO and related proteins might constitute attractive drug targets to fight against malaria.

Keywords: Plasmodium; ZIP; iron; liver stage; transporter.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Anopheles
  • Female
  • Gene Knockout Techniques
  • Hep G2 Cells
  • Hepatocytes / parasitology
  • Humans
  • Ions / metabolism
  • Iron / metabolism*
  • Liver / parasitology*
  • Malaria / parasitology*
  • Membrane Transport Proteins / genetics
  • Membrane Transport Proteins / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Molecular Sequence Data
  • Phylogeny
  • Plasmodium berghei / genetics
  • Plasmodium berghei / growth & development*
  • Plasmodium berghei / metabolism*
  • Sequence Homology, Amino Acid
  • Zinc / metabolism

Substances

  • Ions
  • Membrane Transport Proteins
  • Iron
  • Zinc