| Literature DB >> 26355219 |
Sonia Gulati1, Eric H Ekland1, Kelly V Ruggles2, Robin B Chan3, Bamini Jayabalasingham1, Bowen Zhou3, Pierre-Yves Mantel4, Marcus C S Lee1, Natasha Spottiswoode1, Olivia Coburn-Flynn1, Daisy Hjelmqvist4, Tilla S Worgall3, Matthias Marti4, Gilbert Di Paolo3, David A Fidock5.
Abstract
During its life cycle, Plasmodium falciparum undergoes rapid proliferation fueled by de novo synthesis and acquisition of host cell lipids. Consistent with this essential role, Plasmodium lipid synthesis enzymes are emerging as potential drug targets. To explore their broader potential for therapeutic interventions, we assayed the global lipid landscape during P. falciparum sexual and asexual blood stage (ABS) development. Using liquid chromatography-mass spectrometry, we analyzed 304 lipids constituting 24 classes in ABS parasites, infected red blood cell (RBC)-derived microvesicles, gametocytes, and uninfected RBCs. Ten lipid classes were previously uncharacterized in P. falciparum, and 70%-75% of the lipid classes exhibited changes in abundance during ABS and gametocyte development. Utilizing compounds that target lipid metabolism, we affirmed the essentiality of major classes, including triacylglycerols. These studies highlight the interplay between host and parasite lipid metabolism and provide a comprehensive analysis of P. falciparum lipids with candidate pathways for drug discovery efforts.Entities:
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Year: 2015 PMID: 26355219 PMCID: PMC4567697 DOI: 10.1016/j.chom.2015.08.003
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023