Soldati Dominique, Foth Bernardo J, Cowman Alan F
Department of Microbiology and Molecular Medicine, C.M.U. Faculty of Medicine, University of Geneva, 1 rue Michel-Servet, 1211 Geneva 4, Switzerland. dominique
Trends Parasitol. 2004 Dec;20(12):567-74. doi: 10.1016/j.pt.2004.09.009.
Apicomplexan parasites have evolved an efficient mechanism to gain entry into non-phagocytic cells, hence challenging their hosts by the establishment of infection in immuno-privileged tissues. Gliding motility is a prerequisite for the invasive stage of most apicomplexans, allowing them to migrate across tissues, and actively invade and egress host cells. In the late 1960s, detailed morphological studies revealed that motile apicomplexans share an elaborate architecture comprising a subpellicular cytoskeleton and apical organelles. Since 1993, the development of technologies for transient and stable transfection have provided powerful tools with which to identify gene products associated with these structures and organelles, as well as to understand their functions. In combination with access to several parasite genomes, it is now possible to compare and contrast the strategies and molecular machines that have been selectively designed by distinct life stages within a species, or by different apicomplexan species, to optimize infection.
顶复门寄生虫已经进化出一种有效的机制来进入非吞噬细胞,从而通过在免疫特权组织中建立感染来挑战它们的宿主。滑行运动是大多数顶复门寄生虫侵入阶段的先决条件,使它们能够在组织中迁移,并主动侵入和离开宿主细胞。在20世纪60年代末,详细的形态学研究表明,运动的顶复门寄生虫具有一种精细的结构,包括皮层下细胞骨架和顶端细胞器。自1993年以来,瞬时和稳定转染技术的发展提供了强大的工具,可用于识别与这些结构和细胞器相关的基因产物,并了解它们的功能。结合对几种寄生虫基因组的研究,现在可以比较和对比一个物种内不同生命阶段或不同顶复门物种为优化感染而选择性设计的策略和分子机制。