Ferreira da Silva Marialice da Fonseca, Barbosa Helene S, Gross Uwe, Lüder Carsten G K
Institute for Medical Microbiology, Georg-August-University, Kreuzbergring 57, D-37075 Göttingen, Germany.
Mol Biosyst. 2008 Aug;4(8):824-34. doi: 10.1039/b800520f. Epub 2008 Jun 2.
Toxoplasma gondii is an obligatory intracellular parasitic protozoan that infects a variety of avian and mammalian hosts including up to one third of the human population worldwide. Developmental differentiation between distinct stages, i.e. sporozoites, tachyzoites and bradyzoites is fundamental for the parasite life cycle and for transmission between hosts. It is also interconnected with the pathogenesis of overt toxoplasmosis and makes T. gondii an important opportunistic pathogen of humans. In order to delineate the underlying mechanisms, several cell culture differentiation systems have been developed which mimic the transition from fast-replicating tachyzoites to slowly proliferating bradyzoites in vitro. Since exogenous stress factors, i.e. alkaline pH, IFN-gamma and other proinflammatory cytokines, chemicals or drugs, heat shock, and deprivation of nutrients have been shown to increase the efficacy of bradyzoite development in vitro, Toxoplasma stage differentiation is largely viewed as a stress-related response to hostile environmental conditions. However, tachyzoite to bradyzoite differentiation also occurs spontaneously in vitro and this raises questions about the importance of stress conditions for triggering stage conversion. High frequencies of spontaneous bradyzoite development in primary and permanent skeletal muscle cells, i.e. cells that preferentially harbour bradyzoite-containing tissue cysts in vivo suggest that the host cell type may be critical. Furthermore, the host cell transcriptome, including the expression of distinct host cell genes, has recently been shown to trigger bradyzoite development and cyst formation. Together, these results strongly indicate that the complex cellular environment, besides exogenous stress factors, may govern the developmental differentiation of T. gondii.
刚地弓形虫是一种专性细胞内寄生原生动物,可感染多种鸟类和哺乳动物宿主,全球多达三分之一的人口受其感染。不同阶段(即子孢子、速殖子和缓殖子)之间的发育分化对于寄生虫的生命周期以及宿主间的传播至关重要。它还与显性弓形虫病的发病机制相互关联,使刚地弓形虫成为人类重要的机会性病原体。为了阐明其潜在机制,已开发了几种细胞培养分化系统,这些系统可在体外模拟从快速复制的速殖子到缓慢增殖的缓殖子的转变。由于外源性应激因素,如碱性pH值、干扰素-γ和其他促炎细胞因子、化学物质或药物、热休克以及营养物质剥夺已被证明可提高体外缓殖子发育的效率,因此弓形虫阶段分化在很大程度上被视为对恶劣环境条件的应激相关反应。然而,速殖子向缓殖子的分化在体外也会自发发生,这就引发了关于应激条件在触发阶段转换中的重要性的问题。在原代和永久性骨骼肌细胞(即体内优先含有含缓殖子组织囊肿的细胞)中,自发缓殖子发育的频率很高,这表明宿主细胞类型可能至关重要。此外,最近已证明宿主细胞转录组,包括不同宿主细胞基因的表达,可触发缓殖子发育和囊肿形成。总之,这些结果强烈表明,除了外源性应激因素外,复杂的细胞环境可能控制着刚地弓形虫的发育分化。