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Proteomic differences between developmental stages of Toxoplasma gondii revealed by iTRAQ-based quantitative proteomics

机译:基于iTRAQ的定量蛋白质组学揭示了弓形虫发育阶段之间的蛋白质组学差异

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摘要

Toxoplasma gondii has a complex two-host life-cycle between intermediate host and definitive host. Understanding proteomic variations across the life-cycle stages of T. gondii may improve the understanding of molecular adaption mechanism of T. gondii across life-cycle stages, and should have implications for the development of new treatment and prevention interventions against T. gondii infection. Here, we utilized LC–MS/MS coupled with iTRAQ labeling technology to identify differentially expressed proteins (DEPs) specific to tachyzoite (T), bradyzoites-containing cyst (C) and sporulated oocyst (O) stages of the cyst-forming T. gondii Prugniuad (Pru) strain. A total of 6285 proteins were identified in the three developmental stages of T. gondii. Our analysis also revealed 875, 656, and 538 DEPs in O vs. T, T vs. C, and C vs. O, respectively. The up- and down-regulated proteins were analyzed by Gene Ontology enrichment, KEGG pathway and STRING analyses. Some virulence-related factors and ribosomal proteins exhibited distinct expression patterns across the life-cycle stages. The virulence factors expressed in sporulated oocysts and the number of up-regulated virulence factors in the cyst stage were about twice as many as in tachyzoites. Of the 79 ribosomal proteins identified in T. gondii, the number of up-regulated ribosomal proteins was 33 and 46 in sporulated oocysts and cysts, respectively, compared with tachyzoites. These results support the hypothesis that oocyst and cystic stages are able to adapt to adverse environmental conditions and selection pressures induced by the host’s immune response, respectively. These findings have important implications for understanding of the developmental biology of T. gondii, which may facilitate the discovery of novel therapeutic targets to better control toxoplasmosis.
机译:弓形虫在中间宿主和确定宿主之间具有复杂的两宿主生命周期。了解弓形虫整个生命周期阶段的蛋白质组学变异可能会增进对弓形虫整个生命周期阶段的分子适应机制的理解,并且应该对开发针对弓形虫感染的新治疗和预防措施有影响。在这里,我们利用LC-MS / MS与iTRAQ标记技术相结合,鉴定了特定于速殖子(T),含缓殖子的囊肿(C)和形成囊肿的T的孢子卵囊(O)阶段的差异表达蛋白(DEP)。刚地Prugniuad(Pru)菌株。在弓形虫的三个发育阶段共鉴定出6285种蛋白质。我们的分析还显示,O对T,T对C和C对O分别为875、656和538个DEP。通过基因本体富集,KEGG途径和STRING分析来分析上调和下调的蛋白质。在整个生命周期阶段,一些毒性相关因子和核糖体蛋白表现出不同的表达模式。在孢子卵囊中表达的毒力因子和在囊肿阶段上调的毒力因子的数量大约是速殖子的两倍。与速殖子相比,在刚地弓形虫中鉴定的79种核糖体蛋白中,孢子化卵囊和囊肿中核糖体蛋白上调的数目分别为33和46。这些结果支持以下假设:卵囊和囊性阶段能够分别适应不利的环境条件和宿主免疫反应诱导的选择压力。这些发现对理解弓形虫的发育生物学具有重要意义,这可能有助于发现新的治疗靶标以更好地控制弓形虫病。

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