School of Interdisciplinary Informatics, University of Nebraska at Omaha, Omaha, 68182, NE, USA.
College of Information Science and Technology, University of Nebraska at Omaha, Omaha, 68182, NE, USA.
BMC Genomics. 2019 Dec 20;20(Suppl 11):945. doi: 10.1186/s12864-019-6288-7.
Microbiomes play vital roles in shaping environments and stabilize them based on their compositions and inter-species relationships among its species. Variations in microbial properties have been reported to have significant impact on their host environment. For example, variants in gut microbiomes have been reported to be associated with several chronic conditions, such as inflammatory disease and irritable bowel syndrome. However, how microbial bacteria contribute to pathogenesis still remains unclear and major research questions in this domain remain unanswered.
We propose a split graph model to represent the composition and interactions of a given microbiome. We used metagenomes from Korean populations in this study. The dataset consists of three different types of samples, viz. mucosal tissue and stool from Crohn's disease patients and stool from healthy individuals. We use the split graph model to analyze the impact of microbial compositions on various host phenotypes. Utilizing the graph model, we have developed a pipeline that integrates genomic information and pathway analysis to characterize both critical informative components of inter-bacterial correlations and associations between bacterial taxa and various metabolic pathways.
The obtained results highlight the importance of the microbial communities and their inter-relationships and show how these microbial structures are correlated with Crohn's disease. We show that there are significant positive associations between detected taxonomic biomarkers as well as multiple functional modules in the split graph of mucosal tissue samples from CD patients. Bacteria Moraxellaceae and Pseudomonadaceae were detected as taxonomic biomarkers in CD groups. Higher abundance of these bacteria have been reported in previous study and several metabolic pathways associated with these bacteria were characterized in CD samples.
The proposed pipeline provides a new way to approach the analysis of complex microbiomes. The results obtained from this study show great potential in unraveling mechansims in complex biological systems to understand how various components in such complex environments are associated with critical biological functions.
微生物组在基于其组成和物种间的相互关系塑造环境并使其稳定方面发挥着至关重要的作用。微生物特性的变化已被报道对其宿主环境有重大影响。例如,肠道微生物组的变异已被报道与几种慢性疾病有关,如炎症性疾病和肠易激综合征。然而,微生物细菌如何导致发病机制仍不清楚,该领域的主要研究问题仍未得到解答。
我们提出了一个分裂图模型来表示给定微生物组的组成和相互作用。我们在这项研究中使用了来自韩国人群的宏基因组。该数据集包含三种不同类型的样本,即克罗恩病患者的粘膜组织和粪便以及健康个体的粪便。我们使用分裂图模型来分析微生物组成对各种宿主表型的影响。利用图模型,我们开发了一个集成基因组信息和途径分析的管道,以描述细菌间相互关系的关键信息成分以及细菌分类群与各种代谢途径之间的关联。
获得的结果强调了微生物群落及其相互关系的重要性,并展示了这些微生物结构如何与克罗恩病相关。我们表明,在 CD 患者的粘膜组织样本的分裂图中,检测到的分类生物标志物以及多个功能模块之间存在显著的正相关。在 CD 组中检测到细菌莫拉氏菌科和假单胞菌科作为分类生物标志物。以前的研究报道了这些细菌的丰度较高,并且在 CD 样本中对与这些细菌相关的几种代谢途径进行了表征。
所提出的管道为分析复杂微生物组提供了一种新方法。这项研究的结果显示出在揭示复杂生物系统中的机制方面具有很大的潜力,以了解复杂环境中的各种成分如何与关键的生物学功能相关联。