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Characterizing temporal and inter-individual functional differences in infant gut microbiome by a metaproteomics approach

机译:通过标准瘤方法表征婴幼儿肠道微生物组的时间和间间功能差异

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In this study, we employed a metaproteomic pipeline to characterize the temporal microbial functions and interactions with human host in four premature infant gut, aiming to examine the inter-individual functional commonalities and differences among multiple infants. KEGG mapping of all identified proteins revealed both host- and microbiome- associated metabolic pathways/activities. In addition to these core metabolisms, several pathways/proteins were found unique to a particular infant, indicating types of unique microbial functions. Trefoil factor 3 and tight junction proteins were detected with low abundance or not detected, suggesting that the epithelial barrier was immature or still under development in these premature infants. In addition, proteins participating in the host immunity were constantly abundant over time as essential components in the balance and control of gut microbiome and the maturation of human immune system.
机译:在这项研究中,我们使用了一个月形管道,以表征了四个过早婴儿肠道中的时间微生物功能和与人宿主的相互作用,旨在检查多个婴儿的个体间官能共性和差异。所有已识别的蛋白质的Kegg映射揭示了宿主和微生物组合相关的代谢途径/活动。除了这些核心代谢外,还发现了几种途径/蛋白质特定婴儿,表明独特微生物功能的类型。用低丰度或未检测到的三叶屈光度沉积物3和紧密结蛋白,表明上皮屏障在这些早产儿中不成熟或仍处于开发。此外,参与宿主免疫力的蛋白质随着肠道微生物组平衡和控制的基本组分以及人类免疫系统的成熟而不断充分。

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