Gulati Sonia, Ekland Eric H, Ruggles Kelly V, Chan Robin B, Jayabalasingham Bamini, Zhou Bowen, Mantel Pierre-Yves, Lee Marcus C S, Spottiswoode Natasha, Coburn-Flynn Olivia, Hjelmqvist Daisy, Worgall Tilla S, Marti Matthias, Di Paolo Gilbert, Fidock David A
Department of Microbiology and Immunology, Columbia University College of Physicians and Surgeons, New York, NY 10032, USA.
Department of Population Health, New York University School of Medicine, New York, NY 10032, USA.
Cell Host Microbe. 2015 Sep 9;18(3):371-81. doi: 10.1016/j.chom.2015.08.003.
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.
在其生命周期中,恶性疟原虫通过从头合成和获取宿主细胞脂质实现快速增殖。鉴于这一关键作用,疟原虫脂质合成酶正成为潜在的药物靶点。为了探索它们在治疗干预方面更广泛的潜力,我们分析了恶性疟原虫有性和无性血液阶段(ABS)发育过程中的整体脂质情况。利用液相色谱 - 质谱联用技术,我们分析了ABS阶段寄生虫、感染红细胞(RBC)衍生的微泡、配子体和未感染RBC中构成24类的304种脂质。有10类脂质此前在恶性疟原虫中未被鉴定,并且70% - 75%的脂质类别在ABS和配子体发育过程中丰度发生了变化。利用靶向脂质代谢的化合物,我们证实了包括三酰甘油在内的主要脂质类别的重要性。这些研究突出了宿主与寄生虫脂质代谢之间的相互作用,并为药物研发工作提供了对恶性疟原虫脂质及候选途径的全面分析。