Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
PLoS Negl Trop Dis. 2010 Jan 26;4(1):e586. doi: 10.1371/journal.pntd.0000586.
In order to proceed through their life cycle, Leishmania parasites switch between sandflies and mammals. The flagellated promastigote cells transmitted by the insect vector are phagocytized by macrophages within the mammalian host and convert into the amastigote stage, which possesses a rudimentary flagellum only. During an earlier proteomic study of the stage differentiation of the parasite we identified a component of the outer dynein arm docking complex, a structure of the flagellar axoneme. The 70 kDa subunit of the outer dynein arm docking complex consists of three subunits altogether and is essential for the assembly of the outer dynein arm onto the doublet microtubule of the flagella. According to the nomenclature of the well-studied Chlamydomonas reinhardtii complex we named the Leishmania protein LdDC2.
METHODOLOGY/PRINCIPAL FINDINGS: This study features a characterization of the protein over the life cycle of the parasite. It is synthesized exclusively in the promastigote stage and localizes to the flagellum. Gene replacement mutants of lddc2 show reduced growth rates and diminished flagellar length. Additionally, the normally spindle-shaped promastigote parasites reveal a more spherical cell shape giving them an amastigote-like appearance. The mutants lose their motility and wiggle in place. Ultrastructural analyses reveal that the outer dynein arm is missing. Furthermore, expression of the amastigote-specific A2 gene family was detected in the deletion mutants in the absence of a stage conversion stimulus. In vitro infectivity is slightly increased in the mutant cell line compared to wild-type Leishmania donovani parasites.
CONCLUSIONS/SIGNIFICANCE: Our results indicate that the correct assembly of the flagellum has a great influence on the investigated characteristics of Leishmania parasites. The lack of a single flagellar protein causes an aberrant morphology, impaired growth and altered infectiousness of the parasite.
为了完成生命周期,利什曼原虫在白蛉和哺乳动物之间切换。昆虫媒介传播的鞭毛前体滋养体被哺乳动物宿主体内的巨噬细胞吞噬,并转化为无鞭毛的阿米巴阶段,仅具有原始鞭毛。在寄生虫阶段分化的早期蛋白质组学研究中,我们鉴定了一种动体外侧臂对接复合物的成分,该复合物是鞭毛轴丝的结构。动体外侧臂对接复合物的 70kDa 亚基由三个亚基组成,对于将外侧动体臂组装到鞭毛的双联体微管上至关重要。根据研究充分的衣藻 Reinhardtii 复合物的命名法,我们将利什曼蛋白 LdDC2 命名为。
方法/主要发现:本研究的特点是在寄生虫的整个生命周期中对该蛋白进行了表征。它仅在前体滋养体阶段合成,并定位于鞭毛。lddc2 的基因替换突变体显示出生长速度降低和鞭毛长度减小。此外,正常的纺锤形前体滋养体寄生虫呈现出更球形的细胞形状,使它们具有类似无鞭毛体的外观。突变体失去了它们的运动能力,只能原地摆动。超微结构分析显示,外侧动体臂缺失。此外,在没有阶段转换刺激的情况下,缺失突变体中检测到了动基体特异性 A2 基因家族的表达。与野生型利什曼原虫相比,突变细胞系的体外感染性略有增加。
结论/意义:我们的结果表明,正确组装鞭毛对利什曼原虫的研究特征有很大影响。单个鞭毛蛋白的缺失会导致寄生虫的形态异常、生长受损和感染力改变。