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刚地弓形虫:体外缓殖子-速殖子相互转化的动力学

Toxoplasma gondii: kinetics of bradyzoite-tachyzoite interconversion in vitro.

作者信息

Soete M, Fortier B, Camus D, Dubremetz J F

机构信息

INSERM Unité 42, Villeneuve d' Ascq, France.

出版信息

Exp Parasitol. 1993 May;76(3):259-64. doi: 10.1006/expr.1993.1031.

Abstract

Stage-specific monoclonal antibodies have been used to investigate the bradyzoite-tachyzoite interconversion of Toxoplasma gondii in vitro. The differentiation of bradyzoites isolated from brain cysts (strains 76K and BQNC2) and grown in culture proceeded through intermediate stages which expressed both the specific markers of bradyzoites (P36, P34, P21, and P18) and a specific marker of tachyzoites (SAG1-P30). Differentiation started before parasite division, but large vacuoles containing intermediate stages were also found, suggesting that these were able to multiply. Intermediate stages were also observed during the differentiation of peritoneal tachyzoites (strain Prugniaud) into bradyzoites in vitro. Triggering of bradyzoite protein synthesis is not a single event since one of the four bradyzoite-specific proteins (P21) always appeared later than the others during bradyzoite differentiation. During interconversion, heterogeneous vacuoles containing parasites expressing different levels of bradyzoite or tachyzoite proteins were observed. This observation together with the fact that differentiation is not synchronous within a culture or within a host cell suggest a complex triggering process.

摘要

阶段特异性单克隆抗体已被用于体外研究刚地弓形虫缓殖子与速殖子的相互转化。从脑囊肿分离并在培养中生长的缓殖子(76K和BQNC2株)的分化过程经历中间阶段,这些中间阶段同时表达缓殖子的特异性标志物(P36、P34、P21和P18)和速殖子的特异性标志物(SAG1-P30)。分化在寄生虫分裂之前就开始了,但也发现了含有中间阶段的大液泡,这表明这些中间阶段能够增殖。在体外将腹腔速殖子(Prugniaud株)分化为缓殖子的过程中也观察到了中间阶段。缓殖子蛋白合成的触发不是一个单一事件,因为在缓殖子分化过程中,四种缓殖子特异性蛋白之一(P21)总是比其他蛋白出现得晚。在相互转化过程中,观察到含有表达不同水平缓殖子或速殖子蛋白的寄生虫的异质液泡。这一观察结果以及分化在培养物或宿主细胞内不同步的事实表明存在一个复杂的触发过程。

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