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严重恶性疟原虫感染中毒力基因表达的表观遗传失调。

Epigenetic dysregulation of virulence gene expression in severe Plasmodium falciparum malaria.

机构信息

School of Life Sciences, Keele University, Staffs ST5 5BG, United Kingdom.

出版信息

J Infect Dis. 2012 May 15;205(10):1593-600. doi: 10.1093/infdis/jis239. Epub 2012 Mar 23.

Abstract

Chronic infections with the human malaria parasite Plasmodium falciparum depend on antigenic variation. P. falciparum erythrocyte membrane protein 1 (PfEMP1), the major erythrocyte surface antigen mediating parasite sequestration in the microvasculature, is encoded in parasites by a highly diverse family of var genes. Antigenic switching is mediated by clonal variation in var expression, and recent in vitro studies have demonstrated a role for epigenetic processes in var regulation. Expression of particular PfEMP1 variants may result in parasite enrichment in different tissues, a factor in the development of severe disease. Here, we study in vivo human infections and provide evidence that infection-induced stress responses in the host can modify PfEMP1 expression via the perturbation of epigenetic mechanisms. Our work suggests that severe disease may not be the direct result of an adaptive virulence strategy to maximize parasite survival but that it may indicate a loss of control of the carefully regulated process of antigenic switching that maintains chronic infections.

摘要

慢性感染人类疟原虫依赖于抗原变异。疟原虫红细胞膜蛋白 1(PfEMP1)是主要的红细胞表面抗原,介导寄生虫在微血管中的隔离,由高度多样化的 var 基因家族在寄生虫中编码。抗原转换由 var 表达的克隆变异介导,最近的体外研究表明表观遗传过程在 var 调节中起作用。特定 PfEMP1 变体的表达可能导致寄生虫在不同组织中的富集,这是严重疾病发展的一个因素。在这里,我们研究体内人类感染,并提供证据表明宿主的感染诱导应激反应可以通过干扰表观遗传机制来改变 PfEMP1 的表达。我们的工作表明,严重疾病可能不是寄生虫为了最大限度地生存而采取的适应性毒力策略的直接结果,而是可能表明对维持慢性感染的精心调控的抗原转换过程失去了控制。

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