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iTRAQ-based comparative proteomic analysis of cells infected with Eimeria tenella sporozoites

机译:基于iTRAQ的艾美球虫孢子体感染细胞的比较蛋白质组学分析

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摘要

Eimeria tenella is an obligate intracellular parasite that actively invades cecal epithelial cells of chickens. When E. tenella infects a host cell, the host produces a corresponding change to deal with damage caused by this infection. To date, our knowledge on the mechanism of how the host cell responds to E. tenella infection is highly limited at both the molecular and cellular levels. In this study, isobaric tags for relative and absolute quantitation (iTRAQ) coupled with LC-MS/MS was used to screen the differentially expressed proteins (DEPs) in BHK-21 cells infected with E. tenella sporozoites for 24 h post infection. In total, 6139 non-redundant distinct proteins were identified and 195 of these were found to have a fold change ratio ≥1.3 or ≤0.7 and p < 0.05, including 151 up-regulated proteins and 44 down-regulated proteins. The reliability of the proteomic data was further validated with qPCR and western blot. Gene Ontology enrichment indicated that the up-regulated DEPs were mainly involved in binding and catalytic activity, whereas the down-regulated DEPs were catalytic activity and molecular function regulators. Furthermore, KEGG pathway analysis showed that the DEPs participated in the PI3K-Akt, chemokine, Ras, Wnt, and p53 signaling pathways and so on, and the up-regulated and down-regulated DEPs mainly related to the ribosome and mRNA surveillance pathway, respectively. The data in this study provide an important basis to further analyze E. tenella host cell interactions.
机译:艾美球虫是一种专性的细胞内寄生虫,可主动侵入鸡的盲肠上皮细胞。当E. tenella感染宿主细胞时,宿主会产生相应的变化以应对这种感染引起的损害。迄今为止,我们对宿主细胞对大肠杆菌的反应机理的知识在分子和细胞水平上都非常有限。在这项研究中,等压和绝对定量(iTRAQ)标记与LC-MS / MS结合使用,用于在感染后24 h的Tenella子孢子虫感染的BHK-21细胞中筛选差异表达的蛋白(DEP)。总共鉴定出6139个非冗余的不同蛋白质,其中195个的倍数变化率≥1.3或≤0.7和p <0.05,其中包括151个上调蛋白和44个下调蛋白。蛋白质组学数据的可靠性通过qPCR和Western blot进一步验证。基因本体论的丰富表明,上调的DEPs主要参与结合和催化活性,而下调的DEPs是催化活性和分子功能调节剂。此外,KEGG通路分析显示DEP参与了PI3K-Akt,趋化因子,Ras,Wnt和p53信号通路等,而DEP的上调和下调主要与核糖体和mRNA监测通路有关,分别。这项研究中的数据为进一步分析大肠杆菌的宿主细胞相互作用提供了重要的基础。

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