A vacuolar iron-transporter homologue acts as a detoxifier in Plasmodium

Iron is an essential micronutrient but is also highly toxic. In yeast and plant cells, a key detoxifying mechanism involves iron sequestration into intracellular storage compartments, mediated by members of the vacuolar iron-transporter (VIT) family of proteins. Here we study the VIT homologue from the malaria parasites Plasmodium falciparum (PfVIT) and Plasmodium berghei (PbVIT). PfVIT-mediated iron transport in a yeast heterologous expression system is saturable (K_m~14.7 μM), and selective for Fe²⁺ over other divalent cations. PbVIT-deficient P. berghei lines (Pbvit^-) show a reduction in parasite load in both liver and blood stages of infection in mice. Moreover, Pbvit^- parasites have higher levels of labile iron in blood stages and are more sensitive to increased iron levels in liver stages, when compared with wild-type parasites. Our data are consistent with Plasmodium VITs playing a major role in iron detoxification and, thus, normal development of malaria parasites in their mammalian host.