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Plasmodium falciparum STEVOR Proteins Are Highly Expressed in Patient Isolates and Located in the Surface Membranes of Infected Red Blood Cells and the Apical Tips of Merozoites

机译:恶性疟原虫STEVOR蛋白在患者分离株中高表达,并位于感染红细胞的表面膜和裂殖子的顶端

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The human parasite Plasmodium falciparum has the potential to express a vast repertoire of variant proteins on the surface of the infected red blood cell (iRBC). Variation in the expression pattern of these proteins is linked to antigenic variation and thereby evasion of host antibody-mediated immunity. The genes in the stevor multigene family code for small variant antigens that are expressed in blood-stage parasites where they can be detected in membranous structures called Maurer's clefts (MC). Some studies have indicated that STEVOR protein may also be trafficked to the iRBC membrane. To address the location of STEVOR protein in more detail, we have analyzed expression in several cultured parasite lines and in parasites obtained directly from patients. We detected STEVOR expression in a higher proportion of parasites recently isolated from patients than in cultured parasite lines and show that STEVOR is trafficked in schizont-stage parasites from the MC to the RBC cytosol and the iRBC membrane. Furthermore, STEVOR protein is also detected at the apical end of merozoites. Importantly, we show that culture-adapted parasites do not require STEVOR for survival. These findings provide new insights into the role of the stevor multigene family during both the schizont and merozoite stages of the parasite and highlight the importance of studying freshly isolated parasites, rather than parasite lines maintained in culture, when investigating potential mediators of host-parasite interactions.
机译:人类寄生虫恶性疟原虫具有在受感染的红细胞(iRBC)表面表达大量变异蛋白的潜力。这些蛋白质表达模式的变化与抗原变化有关,从而逃避了宿主抗体介导的免疫力。 stevor 多基因家族中的基因编码在血液阶段寄生虫中表达的小变异抗原,在那里可以在称为Maurer裂隙(MC)的膜状结构中检测到它们。一些研究表明,STEVOR蛋白也可能被转运到iRBC膜上。为了更详细地解决STEVOR蛋白的位置,我们分析了几种培养的寄生虫品系和直接从患者获得的寄生虫中的表达。我们检测到最近从患者体内分离出的寄生虫中STEVOR表达的比例高于培养的寄生虫系,表明STEVOR在从精神分裂症阶段的寄生虫中贩运到MC到RBC胞质溶胶和iRBC膜。此外,在裂殖子的顶端也检测到STEVOR蛋白。重要的是,我们表明适应文化的寄生虫不需要生存就需要STEVOR。这些发现为寄生虫的裂殖体和裂殖子阶段的 多基因家族的作用提供了新的见解,并强调了在调查时研究新鲜分离的寄生虫而非培养中保持的寄生虫系的重要性。宿主-寄生虫相互作用的潜在介体。

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