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Infection and Immunity, November 2004, p. 6597-6602, Vol. 72, No. 11
0019-9567/04/$08.00+0 DOI: 10.1128/IAI.72.11.6597-6602.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.
Department of Infectious & Tropical Diseases, London School of Hygiene & Tropical Medicine,1 Division of Parasitology, National Institute for Medical Research, London, United Kingdom,2 School of Biological Sciences, Nanyang Technological University, Singapore, Singapore,3 Departement d'Immunologie, Institut Cochin, INSERM U567, CNRS UMR 8104, Paris, France4
Received 22 January 2004/ Returned for modification 21 March 2004/ Accepted 25 July 2004
The genome of Plasmodium falciparum harbors three extensive multigene families, var, rif, and stevor (for subtelomeric variable open reading frame), located mainly in the subtelomeric regions of the parasite's 14 chromosomes. STEVOR variants are known to be expressed in asexual parasites, but no function has as yet been ascribed to this protein family. We have examined the expression of STEVOR proteins in intraerythrocytic sexual stages, gametocytes, and extracellular sporozoites isolated from infected Anopheles mosquitoes. In gametocytes, stevor transcripts appear transiently early in development but STEVOR proteins persist for several days and are transported out of the parasite, travel through the host cell cytoplasm, and localize to the erythrocyte plasma membrane. In contrast to asexual parasites, gametocytes move STEVOR to the periphery via a trafficking pathway independent of Maurer's clefts. In sporozoites, STEVOR appear dispersed throughout the cytoplasm in vesicle-like structures. The pattern of STEVOR localization we have observed in gametocytes and sporozoites differs significantly from that in asexual parasite stages. STEVOR variants are therefore likely to perform different functions in each stage of the parasites life cycle in which they occur.
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