Institut Pasteur, Université Paris Cité, Inserm U1201, CNRS EMR9195, Unité de Biologie des Interactions Hôte-Parasite, 25 Rue du Dr Roux, F-75015 Paris, France.
Institut Pasteur, Université Paris Cité, Inserm U1201, CNRS EMR9195, Unité de Biologie des Interactions Hôte-Parasite, 25 Rue du Dr Roux, F-75015 Paris, France.
Curr Opin Microbiol. 2022 Dec;70:102207. doi: 10.1016/j.mib.2022.102207. Epub 2022 Sep 29.
A commonly observed survival strategy in protozoan parasites is the sequential expression of clonally variant-surface antigens to avoid elimination by the host's immune response. In malaria-causing P. falciparum, the immunovariant erythrocyte-membrane protein-1 (PfEMP1) adhesin family, encoded by var genes, is responsible for both antigenic variation and cytoadherence of infected erythrocytes to the microvasculature. Until recently, the biological function of these variant genes was believed to be restricted to intraerythrocytic developmental stages. With the advent of new technologies, var gene expression has been confirmed in transmission and pre-erythrocytic stages. Here, we discuss how repurposing of var gene expression beyond chronic blood-stage infection may be critical for successful transmission.
在原生动物寄生虫中,一种常见的生存策略是顺序表达克隆变异的表面抗原,以避免被宿主的免疫反应所清除。在引起疟疾的恶性疟原虫中,免疫变异红细胞膜蛋白 1(PfEMP1)黏附素家族由 var 基因编码,负责感染红细胞的抗原变异和与微血管的细胞黏附。直到最近,人们还认为这些变异基因的生物学功能仅限于红细胞内的发育阶段。随着新技术的出现,var 基因的表达已在传播和红细胞前期阶段得到证实。在这里,我们讨论了超越慢性血期感染重新利用 var 基因表达如何对成功传播至关重要。