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VAR2CSA is the principal ligand for chondroitin sulfate A in two allogeneic isolates of Plasmodium falciparum.
- Source :
-
Molecular and biochemical parasitology [Mol Biochem Parasitol] 2006 Aug; Vol. 148 (2), pp. 117-24. Date of Electronic Publication: 2006 Apr 07. - Publication Year :
- 2006
-
Abstract
- Malaria during pregnancy causes serious disease that is associated with sequestration in the placenta of Plasmodium falciparum infected erythrocytes that adhere to several host receptors, including chondroitin sulfate A (CSA). The principal CSA binding ligand associated with placental sequestration is the P. falciparum erythrocyte membrane protein 1 (PfEMP1), encoded by the var2csa gene. We disrupted the var2csa gene in two allogeneic parasites and ablated CSA binding. However, in one parasite line we were able to re-select for adhesion to bovine trachea CSA associated with transcription of two var genes, var-CS2 and varP. Parasites transcribing parts of var-CS2 and varP were present in the placentae of some infected women but the mutant parasites that transcribed var-CS2 and varP were recognized by sera from men and pregnant women independent of parity. This work raises the possibility that the PfEMP1 molecules encoded by var-CS2 and varP may be minor contributors to placental malaria but also confirms the importance of the immunodominant, conserved var2csa PfEMP1s in pregnancy associated malaria and strengthens the case for var2csa as a pregnancy-specific malaria vaccine.
- Subjects :
- Animals
Antigens, Protozoan genetics
Cattle
Cell Adhesion
Erythrocytes parasitology
Female
Humans
Ligands
Malaria Vaccines
Male
Placenta chemistry
Placenta parasitology
Plasmodium falciparum genetics
Pregnancy
Transfection
Antigens, Protozoan metabolism
Chondroitin Sulfates metabolism
Malaria, Falciparum parasitology
Plasmodium falciparum isolation & purification
Pregnancy Complications, Parasitic parasitology
Subjects
Details
- Language :
- English
- ISSN :
- 0166-6851
- Volume :
- 148
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Molecular and biochemical parasitology
- Publication Type :
- Academic Journal
- Accession number :
- 16631964
- Full Text :
- https://doi.org/10.1016/j.molbiopara.2006.03.006