Multiple var gene transcripts are expressed in Plasmodium falciparum infected erythrocytes selected for adhesion

被引:54
作者
Noviyanti, R
Brown, GV [1 ]
Wickham, ME
Duffy, MF
Cowman, AF
Reeder, JC
机构
[1] Univ Melbourne, Royal Melbourne Hosp, Dept Med, Melbourne, Vic 3050, Australia
[2] Papua New Guinea Inst Med Res, Goroka, Papua N Guinea
[3] Eijkman Inst Mol Biol, Jakarta, Indonesia
[4] Walter & Eliza Hall Inst Med Res, Div Infect & Immun, Melbourne, Vic 3050, Australia
基金
英国医学研究理事会;
关键词
Plasmodium falciparum; malaria; var genes; PfEMP1; cytoadherence;
D O I
10.1016/S0166-6851(01)00266-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Adherence of Plasmodium falciparum-infected erythrocytes to the post-capillary endothelium is an important characteristic of malaria infection. The adhesion is mediated predominantly by P. falciparum Erythrocyte Membrane Protein-1 (PfEMP1), a clonally variant protein expressed on the surface of infected red blood cells that appears to be a target of protective immunity. A multi-membered var gene family encodes PfEMP1 and switching expression of different var genes conveys different antigenic and adhesive properties to infected red blood cells. Knowledge about transcriptional control of phenotypic expression, or the mechanisms that allow multiple binding specificities, is very limited. Here, we describe a series of phenotypic selection experiments, which resulted in the expression of different PfEMP1 acid the detection of multiple full-length var gene transcripts in the mature trophozoite stage. However, a dominant form of PFEMP1 appeared to be expressed, which suggested that most var transcripts do not lead to a surface expressed PfEMP1 molecule. Parasites bound to specific receptors still expressed multiple full-length var. genes and mature trophozoites selected for increased adhesion to a specific receptor retained the ability to bind to multiple receptors. Our findings suggest that a defined adhesive phenotype can be associated with expression of multiple oar genes. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:227 / 237
页数:11
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