Centre for Immunity, Infection and Evolution, Institute of Immunology and Infection Research, School of Biological Sciences, University of Edinburgh, Kings Buildings, West Mains Road, Edinburgh, EH9 3JT, UK.
J Mol Med (Berl). 2010 Sep;88(9):865-71. doi: 10.1007/s00109-010-0637-y. Epub 2010 Jun 5.
The sleeping sickness parasite, Trypanosoma brucei, must differentiate in response to the changing environments that it encounters during its complex life cycle. One developmental form, the bloodstream stumpy stage, plays an important role in infection dynamics and transmission of the parasite. Recent advances have shed light on the molecular mechanisms by which these stumpy forms differentiate as they are transmitted from the mammalian host to the insect vector of sleeping sickness, tsetse flies. These molecular advances now provide improved experimental tools for the study of stumpy formation and function within the mammalian bloodstream. They also offer new routes to therapy via high-throughput screens for agents that accelerate parasite development. Here, we shall discuss the recent advances that have been made and the prospects for future research now available.
昏睡病寄生虫,布氏锥虫,必须根据其在复杂生命周期中遇到的环境变化进行分化。一种发育形式,血液短循环阶段,在寄生虫的感染动力学和传播中起着重要作用。最近的进展揭示了这些短循环形式在从哺乳动物宿主传播到昏睡病的昆虫载体——采采蝇时分化的分子机制。这些分子进展现在为在哺乳动物血液中研究短循环形成和功能提供了改进的实验工具。它们还通过高通量筛选加速寄生虫发育的药物,为治疗提供了新途径。在这里,我们将讨论已经取得的最新进展以及未来研究的前景。