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小变异体STEVOR抗原独特地位于恶性疟原虫感染的红细胞的毛氏裂体内。

Small variant STEVOR antigen is uniquely located within Maurer's clefts in Plasmodium falciparum-infected red blood cells.

作者信息

Kaviratne M, Khan S M, Jarra W, Preiser P R

机构信息

Division of Parasitology, National Institute for Medical Research, London, United Kingdom.

出版信息

Eukaryot Cell. 2002 Dec;1(6):926-35. doi: 10.1128/EC.1.6.926-935.2002.

Abstract

Malaria parasite antigens encoded by multigene families are important factors in virulence and in disease pathology. In Plasmodium falciparum, the virulence factor PfEMP-1 is encoded by the var multigene family and is exposed at the infected erythrocyte surface. PfEMP-1 is clonally variant, allowing the parasite to evade host immunity. The recently identified P. falciparum stevor multigene family and its products also have the potential to be involved in similar important aspects of host-parasite interactions. Here, we show tightly regulated stage-specific transcription of stevor occurring over just a few hours of the asexual parasite life cycle. Only a subset of stevor genes are transcribed in parasite populations maintained in cultures and in single micromanipulated parasites. Antibodies against STEVOR recognize proteins of the expected size (approximately 37 kDa) and localize STEVOR in Maurer's clefts, unique membranous structures located in the cytoplasm of infected erythrocytes. The fact that the timing of stevor expression and the location of STEVOR are clearly distinct from those of other parasite variant antigens suggests that this gene family may have a novel role in P. falciparum biology.

摘要

由多基因家族编码的疟原虫抗原是毒力和疾病病理过程中的重要因素。在恶性疟原虫中,毒力因子PfEMP-1由var多基因家族编码,并暴露于被感染红细胞表面。PfEMP-1具有克隆变异特性,使疟原虫能够逃避宿主免疫。最近发现的恶性疟原虫stevor多基因家族及其产物也有可能参与宿主-寄生虫相互作用的类似重要方面。在此,我们展示了stevor在无性疟原虫生命周期仅几个小时内受到严格调控的阶段特异性转录。在培养物中维持的寄生虫群体以及单个经显微操作的寄生虫中,只有一部分stevor基因被转录。针对STEVOR的抗体识别预期大小(约37 kDa)的蛋白质,并将STEVOR定位在毛氏小体中,毛氏小体是位于被感染红细胞细胞质中的独特膜结构。stevor表达的时间和STEVOR的定位与其他寄生虫变异抗原明显不同,这一事实表明该基因家族可能在恶性疟原虫生物学中具有新的作用。

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