Sato Yuko, Hliscs Marion, Dunst Josefine, Goosmann Christian, Brinkmann Volker, Montagna Georgina N, Matuschewski Kai
Parasitology Unit, Max Planck Institute for Infection Biology, 10117 Berlin, Germany Infectious Diseases Interdisciplinary Research Group, Singapore-Massachusetts Institute of Technology Alliance for Research and Technology, 138602 Singapore
Parasitology Unit, Max Planck Institute for Infection Biology, 10117 Berlin, Germany School of BioSciences, University of Melbourne, Parkville, 3010 Victoria, Australia.
Mol Biol Cell. 2016 Jul 15;27(14):2234-44. doi: 10.1091/mbc.E15-10-0734. Epub 2016 May 25.
Plasmodium relies on actin-based motility to migrate from the site of infection and invade target cells. Using a substrate-dependent gliding locomotion, sporozoites are able to move at fast speed (1-3 μm/s). This motility relies on a minimal set of actin regulatory proteins and occurs in the absence of detectable filamentous actin (F-actin). Here we report an overexpression strategy to investigate whether perturbations of F-actin steady-state levels affect gliding locomotion and host invasion. We selected two vital Plasmodium berghei G-actin-binding proteins, C-CAP and profilin, in combination with three stage-specific promoters and mapped the phenotypes afforded by overexpression in all three extracellular motile stages. We show that in merozoites and ookinetes, additional expression does not impair life cycle progression. In marked contrast, overexpression of C-CAP and profilin in sporozoites impairs circular gliding motility and salivary gland invasion. The propensity for productive motility correlates with actin accumulation at the parasite tip, as revealed by combinations of an actin-stabilizing drug and transgenic parasites. Strong expression of profilin, but not C-CAP, resulted in complete life cycle arrest. Comparative overexpression is an alternative experimental genetic strategy to study essential genes and reveals effects of regulatory imbalances that are not uncovered from deletion-mutant phenotyping.
疟原虫依靠基于肌动蛋白的运动性从感染部位迁移并侵入靶细胞。子孢子利用依赖于底物的滑行运动,能够快速移动(1-3μm/s)。这种运动性依赖于一组最少的肌动蛋白调节蛋白,并且在没有可检测到的丝状肌动蛋白(F-肌动蛋白)的情况下发生。在这里,我们报告一种过表达策略,以研究F-肌动蛋白稳态水平的扰动是否会影响滑行运动和宿主入侵。我们选择了两种重要的伯氏疟原虫G-肌动蛋白结合蛋白C-CAP和肌动蛋白结合蛋白,并结合三个阶段特异性启动子,绘制了在所有三个细胞外运动阶段过表达所产生的表型。我们表明,在裂殖子和动合子中,额外的表达不会损害生命周期的进展。与之形成鲜明对比的是,在子孢子中过表达C-CAP和肌动蛋白结合蛋白会损害圆周滑行运动和唾液腺入侵。如肌动蛋白稳定药物和转基因寄生虫的组合所示,有效运动的倾向与寄生虫顶端的肌动蛋白积累相关。肌动蛋白结合蛋白的强烈表达而非C-CAP导致整个生命周期停滞。比较过表达是研究必需基因的另一种实验性遗传策略,揭示了缺失突变体表型分析未发现的调节失衡的影响。