Bohne W, Gross U, Ferguson D J, Heesemann J
Institute of Hygiene and Microbiology, University of Würzburg, Germany.
Mol Microbiol. 1995 Jun;16(6):1221-30. doi: 10.1111/j.1365-2958.1995.tb02344.x.
Stage conversion between the tachyzoite and bradyzoite forms of the protozoan parasite Toxoplasma gondii is an important aspect in the pathogenesis of toxoplasmosis. In an initial investigation of molecular regulation of stage conversion in T. gondii, we describe the cloning and characterization of a bradyzoite-specifically expressed gene (hsp30/bag1). Bradyzoite formation was induced in cell culture by alkaline pH, and this was followed by purification of this parasitic stage using magnetic cell sorting. A bradyzoite cDNA library was constructed by random amplification using the polymerase chain reaction. Screening with a bradyzoite-specific monoclonal antibody identified a reactive clone. The amino acid sequence derived from the 687 bp open reading frame showed similarity to the conserved C-terminal region of small heat-shock proteins from plants. Stage-specific expression of the naturally occurring 30 kDa antigen in bradyzoites was confirmed by polyclonal antisera generated against the recombinant antigen. Immunoelectron microscopy indicated a cytosolic location of this antigen in bradyzoites. The expression of HSP30/BAG1 seems to be regulated at the mRNA level, since reverse polymerase chain reaction using bradyzoite-specific primers amplified transcripts in bradyzoites only, not in tachyzoites.
原生动物寄生虫刚地弓形虫速殖子与缓殖子形式之间的阶段转换是弓形虫病发病机制中的一个重要方面。在对刚地弓形虫阶段转换的分子调控进行的初步研究中,我们描述了一个缓殖子特异性表达基因(hsp30/bag1)的克隆与特性分析。通过碱性pH在细胞培养中诱导缓殖子形成,随后使用磁性细胞分选法纯化该寄生虫阶段。利用聚合酶链反应通过随机扩增构建了一个缓殖子cDNA文库。用缓殖子特异性单克隆抗体进行筛选鉴定出一个反应性克隆。从687 bp开放阅读框推导的氨基酸序列显示与植物小热休克蛋白保守的C末端区域相似。针对重组抗原产生的多克隆抗血清证实了天然存在的30 kDa抗原在缓殖子中的阶段特异性表达。免疫电子显微镜显示该抗原在缓殖子的胞质中定位。HSP30/BAG1的表达似乎在mRNA水平受到调控,因为使用缓殖子特异性引物的逆转录聚合酶链反应仅在缓殖子中扩增出转录本,而在速殖子中未扩增出。