Department of Veterinary and Biomedical Sciences, College of Veterinary Medicine, University of Minnesota, St. Paul, Minnesota, United States of America.
PLoS One. 2012;7(3):e31715. doi: 10.1371/journal.pone.0031715. Epub 2012 Mar 15.
Cryptosporidiosis is caused by an obligate intracellular parasite that has eluded global transcriptional or proteomic analysis of the intracellular developmental stages. The transcript abundance for 3,302 genes (87%) of the Cryptosporidium parvum protein coding genome was elucidated over a 72 hr infection within HCT8 cells using Real Time-PCR. The parasite had detectable transcription of all genes in vitro within at least one time point tested, and adjacent genes were not co-regulated. Five genes were not detected within the first 24 hr of infection, one containing two AP2 domains. The fewest genes detected were at 2 hr post infection, while 30% (985) of the genes have their highest expression at 48 and/or 72 hr. Nine expression clusters were formed over the entire 72 hr time course and indicate patterns of transcriptional increases at each of the 7 time points collected except 36 hr, including genes paralleling parasite 18S rRNA transcript levels. Clustering within only the first 24 hr of infection indicates spikes in expression at each of the 4 time points, a group paralleling 18S rRNA transcript levels, and a cluster with peaks at both 6 and 24 hr. All genes were classified into 18 functional categories, which were unequally distributed across clusters. Expression of metabolic, ribosomal and proteasome proteins did not parallel 18S rRNA levels indicating distinct biochemical profiles during developmental stage progression. Proteins involved in translation are over-represented at 6 hr, while structural proteins are over-represented at 12 hr. Standardization methods identified 107 genes with <80% at a single of its total expression at a single time point over 72 hr. This comprehensive transcriptome of the intracellular stages of C. parvum provides insight for understanding its complex development following parasitization of intestinal epithelial cells.
隐孢子虫病是由一种专性细胞内寄生虫引起的,这种寄生虫逃避了全球对细胞内发育阶段的转录组或蛋白质组分析。使用实时 PCR,在 HCT8 细胞中感染 72 小时内,阐明了微小隐孢子虫蛋白编码基因组的 3302 个基因(87%)的转录丰度。在至少一个测试时间点,寄生虫在体外检测到所有基因的可检测转录,并且相邻基因没有共调控。在感染的前 24 小时内未检测到 5 个基因,其中一个包含两个 AP2 结构域。在感染后 2 小时检测到的基因最少,而 30%(985 个)的基因在 48 和/或 72 小时表达最高。在整个 72 小时的时间过程中形成了 9 个表达簇,表明在每个收集的 7 个时间点上都有转录增加的模式,包括与寄生虫 18S rRNA 转录水平平行的基因。仅在感染的前 24 小时内聚类表明,在每个 4 个时间点上的表达均出现高峰,一组与 18S rRNA 转录水平平行,并且在 6 和 24 小时时都有一个峰。所有基因均被分类为 18 个功能类别,这些类别在聚类中分布不均。代谢,核糖体和蛋白酶体蛋白的表达与 18S rRNA 水平不平行,表明在发育阶段进展过程中具有独特的生化特征。参与翻译的蛋白质在 6 小时时表达过高,而结构蛋白在 12 小时时表达过高。标准化方法在 72 小时内,在单个时间点的总表达的 80%以下鉴定了 107 个基因。该微小隐孢子虫细胞内阶段的综合转录组为理解其寄生肠上皮细胞后的复杂发育提供了见解。