Transition of Plasmodium sporozoites into liver stage-like forms is regulated by the RNA binding protein Pumilio

PLoS Pathog. 2011 May;7(5):e1002046. doi: 10.1371/journal.ppat.1002046. Epub 2011 May 19.

Abstract

Many eukaryotic developmental and cell fate decisions that are effected post-transcriptionally involve RNA binding proteins as regulators of translation of key mRNAs. In malaria parasites (Plasmodium spp.), the development of round, non-motile and replicating exo-erythrocytic liver stage forms from slender, motile and cell-cycle arrested sporozoites is believed to depend on environmental changes experienced during the transmission of the parasite from the mosquito vector to the vertebrate host. Here we identify a Plasmodium member of the RNA binding protein family PUF as a key regulator of this transformation. In the absence of Pumilio-2 (Puf2) sporozoites initiate EEF development inside mosquito salivary glands independently of the normal transmission-associated environmental cues. Puf2- sporozoites exhibit genome-wide transcriptional changes that result in loss of gliding motility, cell traversal ability and reduction in infectivity, and, moreover, trigger metamorphosis typical of early Plasmodium intra-hepatic development. These data demonstrate that Puf2 is a key player in regulating sporozoite developmental control, and imply that transformation of salivary gland-resident sporozoites into liver stage-like parasites is regulated by a post-transcriptional mechanism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anopheles / parasitology
  • Gene Expression Profiling
  • Liver / parasitology
  • Malaria / parasitology*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Microarray Analysis
  • Plasmodium berghei / genetics
  • Plasmodium berghei / growth & development*
  • Plasmodium berghei / metabolism
  • Plasmodium berghei / pathogenicity
  • Protein Processing, Post-Translational
  • Protozoan Proteins / genetics
  • Protozoan Proteins / metabolism*
  • RNA-Binding Proteins / genetics
  • RNA-Binding Proteins / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Salivary Glands / parasitology
  • Sporozoites / growth & development*
  • Sporozoites / metabolism
  • Sporozoites / ultrastructure

Substances

  • Protozoan Proteins
  • RNA-Binding Proteins