Noviyanti R, Brown G V, Wickham M E, Duffy M F, Cowman A F, Reeder J C
Infection and Immunity Division, The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria 3050, Australia.
Mol Biochem Parasitol. 2001 May;114(2):227-37. doi: 10.1016/s0166-6851(01)00266-3.
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 and 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 var genes.
恶性疟原虫感染的红细胞与毛细血管后内皮细胞的黏附是疟疾感染的一个重要特征。这种黏附主要由恶性疟原虫红细胞膜蛋白1(PfEMP1)介导,PfEMP1是一种在受感染红细胞表面表达的克隆变异蛋白,似乎是保护性免疫的靶点。一个多成员的var基因家族编码PfEMP1,不同var基因的切换表达赋予受感染红细胞不同的抗原性和黏附特性。关于表型表达的转录控制,即允许多种结合特异性的机制的知识非常有限。在这里,我们描述了一系列表型选择实验,这些实验导致了不同PfEMP1的表达,并在成熟滋养体阶段检测到多个全长var基因转录本。然而,一种占主导地位的PfEMP1形式似乎被表达出来,这表明大多数var转录本不会导致表面表达的PfEMP1分子。与特定受体结合的寄生虫仍然表达多个全长var基因,并且为增加对特定受体的黏附而选择的成熟滋养体保留了与多种受体结合的能力。我们的研究结果表明,一种确定的黏附表型可能与多个var基因的表达相关。