» Articles » PMID: 19915077

The Malaria Parasite Cyclic GMP-dependent Protein Kinase Plays a Central Role in Blood-stage Schizogony

Overview
Journal Eukaryot Cell
Specialty Molecular Biology
Date 2009 Nov 17
PMID 19915077
Citations 113
Authors
Affiliations
Soon will be listed here.
Abstract

A role for the Plasmodium falciparum cyclic GMP (cGMP)-dependent protein kinase (PfPKG) in gametogenesis in the malaria parasite was elucidated previously. In the present study we examined the role of PfPKG in the asexual blood-stage of the parasite life cycle, the stage that causes malaria pathology. A specific PKG inhibitor (compound 1, a trisubstituted pyrrole) prevented the progression of P. falciparum schizonts through to ring stages in erythrocyte invasion assays. Addition of compound 1 to ring-stage parasites allowed normal development up to 30 h postinvasion, and segmented schizonts were able to form. However, synchronized schizonts treated with compound 1 for > or =6 h became large and dysmorphic and were unable to rupture or liberate merozoites. To conclusively demonstrate that the effect of compound 1 on schizogony was due to its selective action on PfPKG, we utilized genetically manipulated P. falciparum parasites expressing a compound 1-insensitive PfPKG. The mutant parasites were able to complete schizogony in the presence of compound 1 but not in the presence of the broad-spectrum protein kinase inhibitor staurosporine. This shows that PfPKG is the primary target of compound 1 during schizogony and provides direct evidence of a role for PfPKG in this process. Discovery of essential roles for the P. falciparum PKG in both asexual and sexual development demonstrates that cGMP signaling is a key regulator of both of these crucial life cycle phases and defines this molecule as an exciting potential drug target for both therapeutic and transmission blocking action against malaria.

Citing Articles

Plasmodium blood stage development requires the chromatin remodeller Snf2L.

Watzlowik M, Silberhorn E, Das S, Singhal R, Venugopal K, Holzinger S Nature. 2025; .

PMID: 39972139 DOI: 10.1038/s41586-025-08595-x.


The malaria parasite PP1 phosphatase controls the initiation of the egress pathway of asexual blood-stages by regulating the rounding-up of the vacuole.

Seveno M, Loubens M, Berry L, Graindorge A, Lebrun M, Lavazec C PLoS Pathog. 2025; 21(1):e1012455.

PMID: 39808636 PMC: 11731718. DOI: 10.1371/journal.ppat.1012455.


Inhibitors of malaria parasite cyclic nucleotide phosphodiesterases block asexual blood-stage development and mosquito transmission.

Gomez-Gonzalez P, Gupta A, Drought L, Patel A, Okombo J, van der Watt M Sci Adv. 2024; 10(49):eadq1383.

PMID: 39642214 PMC: 11623267. DOI: 10.1126/sciadv.adq1383.


Activation loop phosphorylation and cGMP saturation of PKG regulate egress of malaria parasites.

Koussis K, Haase S, Withers-Martinez C, Flynn H, Kunzelmann S, Christodoulou E PLoS Pathog. 2024; 20(6):e1012360.

PMID: 38935780 PMC: 11236177. DOI: 10.1371/journal.ppat.1012360.


Post-Translational Modifications of Proteins of Malaria Parasites during the Life Cycle.

Schwarzer E, Skorokhod O Int J Mol Sci. 2024; 25(11).

PMID: 38892332 PMC: 11173270. DOI: 10.3390/ijms25116145.


References
1.
Carruthers V, Giddings O, Sibley L . Secretion of micronemal proteins is associated with toxoplasma invasion of host cells. Cell Microbiol. 2001; 1(3):225-35. DOI: 10.1046/j.1462-5822.1999.00023.x. View

2.
Francis S, Smith J, Colbran J, Grimes K, Walsh K, Kumar S . Arginine 75 in the pseudosubstrate sequence of type Ibeta cGMP-dependent protein kinase is critical for autoinhibition, although autophosphorylated serine 63 is outside this sequence. J Biol Chem. 1996; 271(34):20748-55. View

3.
Schlossmann J, Hofmann F . cGMP-dependent protein kinases in drug discovery. Drug Discov Today. 2005; 10(9):627-34. DOI: 10.1016/S1359-6446(05)03406-9. View

4.
Roger N, Dubremetz J, Delplace P, FORTIER B, Tronchin G, Vernes A . Characterization of a 225 kilodalton rhoptry protein of Plasmodium falciparum. Mol Biochem Parasitol. 1988; 27(2-3):135-41. DOI: 10.1016/0166-6851(88)90033-3. View

5.
Brossier F, Jewett T, Lovett J, Sibley L . C-terminal processing of the toxoplasma protein MIC2 is essential for invasion into host cells. J Biol Chem. 2002; 278(8):6229-34. DOI: 10.1074/jbc.M209837200. View