Multiple essential functions of Plasmodium falciparum actin-1 during malaria blood-stage development

Authors:
Sujaan Das, Leandro Lemgruber, Chwen L. Tay, Jake Baum, Markus Meissner
In:
Source: BMC Biol.
Publication Date: (2017)
Issue: 15: 70
Research Area:
Parasitology
Cells used in publication:
Plasmodium falciparum
Species: unicellular
Tissue Origin:
Platform:
4D-Nucleofector® X-Unit
Experiment

The Amaxa™ P3 primary cell 4D-Nucleofector™ X Kit L (Lonza, Cologne, Germany) was used for transfections. The input DNA was added to 100 µL P3 primary cell solution, mixed with 10–20 µL of packed synchronous mature schizonts and added to the cuvette, which was electroporated in a 4D-Nucleofector machine (Lonza) using the program FP158.

Abstract

The phylum Apicomplexa includes intracellular parasites causing immense global disease burden, the deadliest of them being the human malaria parasite Plasmodium falciparum, which invades and replicates within erythrocytes. The cytoskeletal protein actin is well conserved within apicomplexans but divergent from mammalian actins, and was primarily reported to function during host cell invasion. However, novel invasion mechanisms have been described for several apicomplexans, and specific functions of the acto-myosin system are being reinvestigated. Of the two actin genes in P. falciparum, actin-1 (pfact1) is ubiquitously expressed in all life-cycle stages and is thought to be required for erythrocyte invasion, although its functions during parasite development are unknown, and definitive in vivo characterisation during invasion is lacking.