Paternal effect of the nuclear formin-like protein MISFIT on Plasmodium development in the mosquito vector

Malaria parasites must undergo sexual and sporogonic development in mosquitoes before they can infect their vertebrate hosts. We report the discovery and characterization of MISFIT, the first protein with paternal effect on the development of the rodent malaria parasite Plasmodium berghei in Anophel...

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Published inPLoS pathogens Vol. 5; no. 8; pp. e1000539 - 1000539
Main Authors Bushell, Ellen S C, Ecker, Andrea, Schlegelmilch, Timm, Goulding, David, Dougan, Gordon, Sinden, Robert E, Christophides, George K, Kafatos, Fotis C, Vlachou, Dina
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 01.08.2009
Public Library of Science (PLoS)
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Summary:Malaria parasites must undergo sexual and sporogonic development in mosquitoes before they can infect their vertebrate hosts. We report the discovery and characterization of MISFIT, the first protein with paternal effect on the development of the rodent malaria parasite Plasmodium berghei in Anopheles mosquitoes. MISFIT is expressed in male gametocytes and localizes to the nuclei of male gametocytes, zygotes and ookinetes. Gene disruption results in mutant ookinetes with reduced genome content, microneme defects and altered transcriptional profiles of putative cell cycle regulators, which yet successfully invade the mosquito midgut. However, developmental arrest ensues during the ookinete transformation to oocysts leading to malaria transmission blockade. Genetic crosses between misfit mutant parasites and parasites that are either male or female gamete deficient reveal a strict requirement for a male misfit allele. MISFIT belongs to the family of formin-like proteins, which are known regulators of the dynamic remodeling of actin and microtubule networks. Our data identify the ookinete-to-oocyst transition as a critical cell cycle checkpoint in Plasmodium development and lead us to hypothesize that MISFIT may be a regulator of cell cycle progression. This study offers a new perspective for understanding the male contribution to malaria parasite development in the mosquito vector.
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Carried out the majority of the experiments and contributed to data analysis and drafting the manuscript: ESCB. Contributed to genetic crosses and generation of transgenic parasites: AE. Performed confocal microscopy and assisted microarray analysis: TS. Conducted TEM: DG. Supervised TEM and provided materials: GD. Provided scientific advice and feedback on the manuscript: RES. Contributed to experimental design and data interpretation: GKC. Provided scientific advice and feedback on the manuscript, and contributed reagents and materials: FCK. Designed experiments, analyzed the data, oversaw the project, and wrote the manuscript: DV.
ISSN:1553-7374
1553-7366
1553-7374
DOI:10.1371/journal.ppat.1000539