Department of Pathology, Microbiology and Immunology, University of California Davis, School of Veterinary Medicine, Davis, California, United States of America.
PLoS One. 2012;7(2):e29998. doi: 10.1371/journal.pone.0029998. Epub 2012 Feb 13.
Sexual reproduction of Toxoplasma gondii occurs exclusively within enterocytes of the definitive felid host. The resulting immature oocysts are excreted into the environment during defecation, where in the days following, they undergo a complex developmental process. Within each oocyst, this culminates in the generation of two sporocysts, each containing 4 sporozoites. A single felid host is capable of shedding millions of oocysts, which can survive for years in the environment, are resistant to most methods of microbial inactivation during water-treatment and are capable of producing infection in warm-blooded hosts at doses as low as 1-10 ingested oocysts. Despite its extremely interesting developmental biology and crucial role in initiating an infection, almost nothing is known about the oocyst stage beyond morphological descriptions. Here, we present a complete transcriptomic analysis of the oocyst from beginning to end of its development. In addition, and to identify genes whose expression is unique to this developmental form, we compared the transcriptomes of developing oocysts with those of in vitro-derived tachyzoites and in vivo-derived bradyzoites. Our results reveal many genes whose expression is specifically up- or down-regulated in different developmental stages, including many genes that are likely critical to oocyst development, wall formation, resistance to environmental destruction and sporozoite infectivity. Of special note is the up-regulation of genes that appear "off" in tachyzoites and bradyzoites but that encode homologues of proteins known to serve key functions in those asexual stages, including a novel pairing of sporozoite-specific paralogues of AMA1 and RON2, two proteins that have recently been shown to form a crucial bridge during tachyzoite invasion of host cells. This work provides the first in-depth insight into the development and functioning of one of the most important but least studied stages in the Toxoplasma life cycle.
刚地弓形虫的有性生殖仅发生在终末宿主的肠上皮细胞内。由此产生的未成熟卵囊在粪便中排出到环境中,在接下来的几天里,它们经历了一个复杂的发育过程。在每个卵囊内,最终产生两个孢子囊,每个孢子囊含有 4 个孢子。一只猫科宿主能够排出数百万个卵囊,这些卵囊可以在环境中存活多年,对水处理过程中大多数微生物灭活方法具有抗性,并且能够在低至 1-10 个摄入卵囊的剂量下感染温血宿主。尽管其发育生物学极其有趣,并且在引发感染方面起着至关重要的作用,但除了形态描述之外,对卵囊阶段几乎一无所知。在这里,我们对卵囊从发育开始到结束的整个过程进行了全面的转录组分析。此外,为了鉴定仅在这种发育形式中表达的基因,我们比较了发育中的卵囊与体外衍生的速殖子和体内衍生的缓殖子的转录组。我们的研究结果揭示了许多基因的表达在不同的发育阶段特异性地上调或下调,包括许多可能对卵囊发育、壁形成、抵抗环境破坏和孢子活力至关重要的基因。特别值得注意的是,一些基因的表达上调,而这些基因在速殖子和缓殖子中是“关闭”的,但它们编码的蛋白同源物在这些无性阶段中具有关键功能,包括与 AMA1 和 RON2 的孢子特异性同源物的新配对,这两种蛋白最近被证明在速殖子入侵宿主细胞期间形成了一个关键的桥梁。这项工作首次深入了解了刚地弓形虫生命周期中最重要但研究最少的阶段之一的发育和功能。