Behnke Michael S, Zhang Tiange P, Dubey Jitender P, Sibley L David
Department of Molecular Microbiology, Washington University School of Medicine, 660 S, Euclid Ave,, St Louis, MO 63110, USA.
BMC Genomics. 2014 May 8;15(1):350. doi: 10.1186/1471-2164-15-350.
Considerable work has been carried out to understand the biology of tachyzoites and bradyzoites of Toxoplasma gondii in large part due to in vitro culture methods for these stages. However, culturing methods for stages that normally develop in the gut of the definitive felid host, including the merozoite and sexual stages, have not been developed hindering the ability to study a large portion of the parasite's life cycle. Here, we begin to unravel the molecular aspects of enteric stages by providing new data on merozoite stage gene expression.
To profile gene expression differences in enteric stages we harvested merozoites from the intestine of infected cats and hybridized mRNA to the Affymetrix Toxoplasma GeneChip. We analyzed the merozoite data in context of the life cycle by comparing it to previously published data for the oocyst, tachyzoite, and bradyzoite stages. Principal component analysis highlighted the unique profile of merozoites, placing them approximately half-way on a continuum between the tachyzoite/bradyzoite and oocyst samples. Prior studies have shown that antibodies to surface antigen one (SAG1) and many dense granule proteins do not label merozoites: our microarray data confirms that these genes were not expressed at this stage. Also, the expression for many rhoptry and microneme proteins was drastically reduced while the expression for many surface antigens was increased at the merozoite stage. Gene Ontology and KEGG analysis revealed that genes involved in transcription/translation and many metabolic pathways were upregulated at the merozoite stage, highlighting unique growth requirements of this stage. To functionally test these predictions, we demonstrated that an upstream promoter region of a merozoite specific gene was sufficient to control expression in merozoites in vivo.
Merozoites are the first developmental stage in the coccidian cycle that takes place within the gut of the definitive host. The data presented here describe the global gene expression profile of the merozoite stage and the creation of transgenic parasite strains that show stage-specific expression of reporter genes in the cat intestine. These data and reagents will be useful in unlocking how the parasite senses and responds to the felid gut environment to initiate enteric development.
为了解刚地弓形虫速殖子和缓殖子的生物学特性,已经开展了大量工作,这在很大程度上归功于这些阶段的体外培养方法。然而,针对通常在终末宿主猫科动物肠道中发育的阶段(包括裂殖子和有性阶段)的培养方法尚未开发出来,这阻碍了对寄生虫大部分生命周期进行研究的能力。在此,我们通过提供关于裂殖子阶段基因表达的新数据,开始揭示肠道阶段的分子层面。
为了剖析肠道阶段的基因表达差异,我们从受感染猫的肠道中收获裂殖子,并将mRNA与Affymetrix弓形虫基因芯片进行杂交。我们通过将裂殖子数据与先前发表的卵囊、速殖子和缓殖子阶段的数据进行比较,在生命周期的背景下分析裂殖子数据。主成分分析突出了裂殖子的独特图谱,使其在速殖子/缓殖子和卵囊样本之间的连续体上大致处于中间位置。先前的研究表明,针对表面抗原1(SAG1)和许多致密颗粒蛋白的抗体不会标记裂殖子:我们的微阵列数据证实这些基因在这个阶段不表达。此外,许多棒状体和微线体蛋白的表达大幅降低,而许多表面抗原的表达在裂殖子阶段增加。基因本体论和KEGG分析表明,参与转录/翻译和许多代谢途径的基因在裂殖子阶段上调,突出了该阶段独特的生长需求。为了在功能上验证这些预测,我们证明裂殖子特异性基因的上游启动子区域足以在体内控制裂殖子中的表达。
裂殖子是球虫生命周期中在终末宿主肠道内发生的第一个发育阶段。此处呈现的数据描述了裂殖子阶段的全局基因表达图谱以及创建在猫肠道中显示报告基因阶段特异性表达的转基因寄生虫株。这些数据和试剂将有助于揭示寄生虫如何感知和响应猫科动物肠道环境以启动肠道发育。