scholarly journals A patatin-like phospholipase is crucial for gametocyte induction in the malaria parasite Plasmodium falciparum

2019 ◽  
Author(s):  
Ansgar Flammersfeld ◽  
Atscharah Panyot ◽  
Yoshiki Yamaryo ◽  
Philipp Auraß ◽  
Jude M. Pryborski ◽  
...  

AbstractPatatin-like phospholipases (PNPLAs) are highly conserved enzymes of prokaryotic and eukaryotic organisms with major roles in lipid homeostasis. The genome of the malaria parasite Plasmodium falciparum encodes four putative PNPLAs with predicted functions during phospholipid degradation. We here investigated the role of one of the plasmodial PNPLAs, a putative PLA2 termed PNPLA1, during blood stage replication and gametocyte development. PNPLA1 is present in the asexual and sexual blood stages and here localizes to the cytoplasm. PNPLA1-deficiency due to gene disruption or conditional gene-knockdown had no effect on erythrocytic replication, gametocyte maturation and gametogenesis. However, blood stage parasites lacking PNPLA1 were severely impaired in gametocyte induction, while PNPLA1 overexpression promotes gametocyte formation. The loss of PNPLA1 further leads to transcriptional down-regulation of genes related to gametocytogenesis, including the gene encoding the sexual commitment regulator AP2-G. Additionally, lipidomics of PNPLA1-deficient asexual blood stage parasites revealed overall increased levels of major phospholipids, including phosphatidylcholine (PC), which is a substrate of PLA2. Because PC synthesis is pivotal for erythrocytic replication, while the reduced availability of PC precursors drives the parasite into gametocytogenesis, we hypothesize that the high PC levels due to PNPLA1-deficiency prevent the blood stage parasites from entering the sexual pathway.

Science ◽  
2020 ◽  
Vol 368 (6492) ◽  
pp. 754-759 ◽  
Author(s):  
Lauren M. Smith ◽  
Francis C. Motta ◽  
Garima Chopra ◽  
J. Kathleen Moch ◽  
Robert R. Nerem ◽  
...  

The blood stage of the infection of the malaria parasite Plasmodium falciparum exhibits a 48-hour developmental cycle that culminates in the synchronous release of parasites from red blood cells, which triggers 48-hour fever cycles in the host. This cycle could be driven extrinsically by host circadian processes or by a parasite-intrinsic oscillator. To distinguish between these hypotheses, we examine the P. falciparum cycle in an in vitro culture system and show that the parasite has molecular signatures associated with circadian and cell cycle oscillators. Each of the four strains examined has a different period, which indicates strain-intrinsic period control. Finally, we demonstrate that parasites have low cell-to-cell variance in cycle period, on par with a circadian oscillator. We conclude that an intrinsic oscillator maintains Plasmodium’s rhythmic life cycle.


2019 ◽  
Vol 116 (3) ◽  
pp. 456a
Author(s):  
Matthias Garten ◽  
Josh R. Beck ◽  
Robyn Roth ◽  
Christopher K.E. Bleck ◽  
John E. Heuser ◽  
...  

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