Related Experiment Video
Updated: Jun 20, 2026

10:09
Selection of Plasmodium falciparum Parasites for Cytoadhesion to Human Brain Endothelial Cells
Published on: January 3, 2012
Competitive endothelial adhesion between Plasmodium falciparum isolates under physiological flow conditions
Happy Phiri1, Jacqui Montgomery, Malcolm Molyneux
1Malawi-Liverpool-Wellcome Trust Clinical Research Programme, College of Medicine, Chichiri, Blantyre 3, Malawi. hphiri@mlw.medcol.mw
Malaria Journal
|September 24, 2009
Summary
Different Plasmodium falciparum variants compete for binding to endothelium. This competition, based on adhesive efficiency, influences cytoadherence and disease severity in falciparum malaria.
Area of Science:
- Malariology
- Cellular Biology
- Pathogenesis
Background:
- Severe falciparum malaria pathogenesis involves sequestration of parasitized red blood cells (pRBCs) in microvasculature.
- Plasmodium falciparum infections often comprise parasite subpopulations with diverse adhesive properties.
- Competition for endothelial adhesion among these subpopulations is a key unanswered question.
Purpose of the Study:
- To investigate competition for endothelial binding between P. falciparum pRBCs with variant adhesive phenotypes.
- To assess cytoadherence competition under laboratory conditions, particularly under flow.
Main Methods:
- Four P. falciparum isolates with known adherence phenotypes were paired and mixed.
- In vitro static and flow-based competitive adhesion assays were used to test binding to cultured human endothelium.
- Adherence levels were quantified and analyzed using statistical tests.
Main Results:
- P. falciparum parasite lines exhibited significant variations in their efficiency of endothelial adhesion.
- Differential adhesion efficiencies were observed between paired parasite lines.
Conclusions:
- Plasmodium falciparum variants actively compete for endothelial adhesion.
- Variants can be ranked by their binding efficiency, indicating differential cytoadherence capabilities.
- Mixed infections with variants may lead to non-uniform cytoadherence and varied disease severity.

