Shoaie Saeed, Nielsen Jens
Department of Chemical and Biological Engineering, Chalmers University of Technology Gothenburg, Sweden.
Front Genet. 2014 Apr 22;5:86. doi: 10.3389/fgene.2014.00086. eCollection 2014.
Increased understanding of the interactions between the gut microbiota, diet and environmental effects may allow us to design efficient treatment strategies for addressing global health problems. Existence of symbiotic microorganisms in the human gut provides different functions for the host such as conversion of nutrients, training of the immune system, and resistance to pathogens. The gut microbiome also plays an influential role in maintaining human health, and it is a potential target for prevention and treatment of common disorders including obesity, type 2 diabetes, and atherosclerosis. Due to the extreme complexity of such disorders, it is necessary to develop mathematical models for deciphering the role of its individual elements as well as the entire system and such models may assist in better understanding of the interactions between the bacteria in the human gut and the host by use of genome-scale metabolic models (GEMs). Recently, GEMs have been employed to explore the interactions between predominant bacteria in the gut ecosystems. Additionally, these models enabled analysis of the contribution of each species to the overall metabolism of the microbiota through the integration of omics data. The outcome of these studies can be used for proposing optimal conditions for desired microbiome phenotypes. Here, we review the recent progress and challenges for elucidating the interactions between the human gut microbiota and host through metabolic modeling. We discuss how these models may provide scaffolds for analyzing high-throughput data, developing probiotics and prebiotics, evaluating the effects of probiotics and prebiotics and eventually designing clinical interventions.
对肠道微生物群、饮食和环境影响之间相互作用的深入了解,可能使我们能够设计出有效的治疗策略,以解决全球健康问题。人类肠道中存在的共生微生物为宿主提供了不同的功能,如营养物质的转化、免疫系统的训练以及对病原体的抵抗。肠道微生物群在维持人类健康方面也发挥着重要作用,它是预防和治疗包括肥胖、2型糖尿病和动脉粥样硬化在内的常见疾病的潜在靶点。由于这些疾病极其复杂,有必要开发数学模型来解读其各个要素以及整个系统的作用,此类模型可能有助于通过使用基因组规模代谢模型(GEMs)更好地理解人类肠道细菌与宿主之间的相互作用。最近,GEMs已被用于探索肠道生态系统中主要细菌之间的相互作用。此外,这些模型通过整合组学数据,能够分析每个物种对微生物群整体代谢的贡献。这些研究结果可用于提出理想微生物组表型的最佳条件。在此,我们综述了通过代谢建模阐明人类肠道微生物群与宿主之间相互作用的最新进展和挑战。我们讨论了这些模型如何为分析高通量数据、开发益生菌和益生元、评估益生菌和益生元的效果以及最终设计临床干预措施提供框架。