Host Cell Phosphatidylcholine Is a Key Mediator of Malaria Parasite Survival during Liver Stage Infection
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Author(s) • • • • • • • • •
Itoe, Maurice A.
Cabal, Ghislain G.
Real, Eliana
Zuzarte-Luis, Vanessa
Bhatia, Sangeeta N.
Frischknecht, Friedrich
Thiele, Christoph
Shevchenko, Andrej
Mota, Maria M.
Sampaio, Julio L.
Date Issued
December 2014
Journal
Cell Host & Microbe
Publisher
Elsevier
Citation
Itoe, Maurice A., Julio L. Sampaio, Ghislain G. Cabal, Eliana Real, Vanessa Zuzarte-Luis, Sandra March, Sangeeta N. Bhatia, et al. “Host Cell Phosphatidylcholine Is a Key Mediator of Malaria Parasite Survival During Liver Stage Infection.” Cell Host & Microbe 16, no. 6 (December 2014): 778–786.
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Final published version
Abstract
During invasion, Plasmodium, the causative agent of malaria, wraps itself in a parasitophorous vacuole membrane (PVM), which constitutes a critical interface between the parasite and its host cell. Within hepatocytes, each Plasmodium sporozoite generates thousands of new parasites, creating high demand for lipids to support this replication and enlarge the PVM. Here, a global analysis of the total lipid repertoire of Plasmodium-infected hepatocytes reveals an enrichment of neutral lipids and the major membrane phospholipid, phosphatidylcholine (PC). While infection is unaffected in mice deficient in key enzymes involved in neutral lipid synthesis and lipolysis, ablation of rate-limiting enzymes in hepatic PC biosynthetic pathways significantly decreases parasite numbers. Host PC is taken up by both P. berghei and P. falciparum and is necessary for correct localization of parasite proteins to the PVM, which is essential for parasite survival. Thus, Plasmodium relies on the abundance of these lipids within hepatocytes to support infection.
MIT Department
Massachusetts Institute of Technology. Institute for Medical Engineering & Science
Harvard University--MIT Division of Health Sciences and Technology
Koch Institute for Integrative Cancer Research at MIT
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DOI of Published Version
https://doi.org/10.1016/j.chom.2014.11.006