NG2: Metabolism of Microbial Pathogens, Robert Koch-Institute, 13353, Berlin, Germany.
Institute of Virology, Medical Center University of Freiburg, 79104, Freiburg, Germany.
Nat Commun. 2022 Mar 4;13(1):1168. doi: 10.1038/s41467-022-28730-w.
The apicomplexan parasite Toxoplasma gondii forms bradyzoite-containing tissue cysts that cause chronic and drug-tolerant infections. However, current in vitro models do not allow long-term culture of these cysts to maturity. Here, we developed a human myotube-based in vitro culture model of functionally mature tissue cysts that are orally infectious to mice and tolerate exposure to a range of antibiotics and temperature stresses. Metabolomic characterization of purified cysts reveals global changes that comprise increased levels of amino acids and decreased abundance of nucleobase- and tricarboxylic acid cycle-associated metabolites. In contrast to fast replicating tachyzoite forms of T. gondii these tissue cysts tolerate exposure to the aconitase inhibitor sodium fluoroacetate. Direct access to persistent stages of T. gondii under defined cell culture conditions will be essential for the dissection of functionally important host-parasite interactions and drug evasion mechanisms. It will also facilitate the identification of new strategies for therapeutic intervention.
刚地弓形虫是一种顶端复合体寄生虫,会形成含有缓殖子的包囊,导致慢性和耐药性感染。然而,目前的体外模型无法使这些包囊长期培养至成熟。在这里,我们开发了一种基于人肌管的体外培养模型,可培养成熟的、具有口服感染能力的组织包囊,且可耐受多种抗生素和温度应激。对纯化包囊进行代谢组学分析表明,其包含广泛的变化,包括氨基酸水平升高和核碱基及三羧酸循环相关代谢物丰度降低。与快速复制的速殖子形式的刚地弓形虫不同,这些组织包囊能够耐受乌头酸酶抑制剂氟乙酸钠的作用。在明确的细胞培养条件下直接接触持久存在的刚地弓形虫阶段对于解析功能重要的宿主-寄生虫相互作用和药物逃逸机制至关重要。它还将促进新的治疗干预策略的确定。