Differential var gene transcription in Plasmodium falciparum isolates from patients with cerebral malaria compared to hyperparasitaemia

• DOI: 10.1016/j.molbiopara.2006.08.005
• Publication Date: 2006-09-06T14:32:41Z
• Authors: Helen M. Kyriacou; Graham N. Stone; Richard J. Challis; Ahmed Raza; Kirsten E. Lyke; Mahamadou A. Thera; Abdoulaye K. Koné; Ogobara K. Doumbo; Christopher V. Plowe; J. Alexandra Rowe
• Keywords: Transcription, Genetic; Genes, Protozoan; Molecular Sequence Data; Plasmodium falciparum; Malaria, Cerebral; Protozoan Proteins; Parasitemia; Article; 03 medical and health sciences; Animals; Humans; Amino Acid Sequence; Malaria, Falciparum; Molecular Biology; Phylogeny; Expressed Sequence Tags; 0303 health sciences; Virulence; Infant; Protein Structure, Tertiary; 3. Good health; Gene Expression Regulation; Child, Preschool; Parasitology; Sequence Alignment

The Plasmodium falciparum variant erythrocyte surface antigens known as PfEMP1, encoded by the var gene family, are thought to play a crucial role in malaria pathogenesis because they mediate adhesion to host cells and immuno-modulation. Var genes have been divided into three major groups (A, B and C) and two intermediate groups (B/A and B/C) on the basis of their genomic location and upstream sequence. We analysed expressed sequence tags of the var gene DBLalpha domain to investigate var gene transcription in relation to disease severity in Malian children. We found that P. falciparum isolates from children with cerebral malaria (unrousable coma) predominantly transcribe var genes with DBLalpha1-like domains that are characteristic of Group A or B/A var genes. In contrast, isolates from children with equally high parasite burdens but no symptoms or signs of severe malaria (hyperparasitaemia patients) predominantly transcribe var genes with DBLalpha0-like domains that are characteristic of the B and C-related var gene groups. These results suggest that var genes with DBLalpha1-like domains (Group A or B/A) may be implicated in the pathogenesis of cerebral malaria, while var genes with DBLalpha0-like domains promote less virulent malaria infections.