| Literature DB >> 25011110 |
Makhtar Niang1, Amy Kristine Bei2, Kripa Gopal Madnani1, Shaaretha Pelly1, Selasi Dankwa2, Usheer Kanjee2, Karthigayan Gunalan1, Anburaj Amaladoss3, Kim Pin Yeo1, Ndeye Sakha Bob1, Benoit Malleret4, Manoj Theodore Duraisingh2, Peter Rainer Preiser5.
Abstract
Variant surface antigens play an important role in Plasmodium falciparum malaria pathogenesis and in immune evasion by the parasite. Although most work to date has focused on P. falciparum Erythrocyte Membrane Protein 1 (PfEMP1), two other multigene families encoding STEVOR and RIFIN are expressed in invasive merozoites and on the infected erythrocyte surface. However, their role during parasite infection remains to be clarified. Here we report that STEVOR functions as an erythrocyte-binding protein that recognizes Glycophorin C (GPC) on the red blood cell (RBC) surface and that its binding correlates with the level of GPC on the RBC surface. STEVOR expression on the RBC leads to PfEMP1-independent binding of infected RBCs to uninfected RBCs (rosette formation), while antibodies targeting STEVOR in the merozoite can effectively inhibit invasion. Our results suggest a PfEMP1-independent role for STEVOR in enabling infected erythrocytes at the schizont stage to form rosettes and in promoting merozoite invasion.Entities:
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Year: 2014 PMID: 25011110 PMCID: PMC4382205 DOI: 10.1016/j.chom.2014.06.004
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023