首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Novel Systems Modeling Methodology in Comparative Microbial Metabolomics: Identifying Key Enzymes and Metabolites Implicated in Autism Spectrum Disorders
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Novel Systems Modeling Methodology in Comparative Microbial Metabolomics: Identifying Key Enzymes and Metabolites Implicated in Autism Spectrum Disorders

机译:比较微生物代谢组学中的新型系统建模方法:识别自闭症谱系障碍中涉及的关键酶和代谢物

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摘要

Autism spectrum disorders are a group of mental illnesses highly correlated with gastrointestinal dysfunction. Recent studies have shown that there may be one or more microbial “fingerprints” in terms of the composition characterizing individuals with autism, which could be used for diagnostic purposes. This paper proposes a computational approach whereby metagenomes characteristic of “healthy” and autistic individuals are artificially constructed via genomic information, analyzed for the enzymes coded within, and then these enzymes are compared in detail. This is a text mining application. A custom-designed online application was built and used for the comparative metabolomics study and made publically available. Several of the enzyme-catalyzing reactions involved with the amino acid glutamate were curiously missing from the “autism” microbiome and were coded within almost every organism included in the “control” microbiome. Interestingly, there exists a leading hypothesis regarding autism and glutamate involving a neurological excitation/inhibition imbalance; but the association with this study is unclear. The results included data on the transsulfuration and transmethylation pathways, involved with oxidative stress, also of importance to autism. The results from this study are in alignment with leading hypotheses in the field, which is impressive, considering the purely in silico nature of this study. The present study provides new insight into the complex metabolic interactions underlying autism, and this novel methodology has potential to be useful for developing new hypotheses. However, limitations include sparse genome data availability and conflicting literature experimental data. We believe our software tool and methodology has potential for having great utility as data become more available, comprehensive and reliable.
机译:自闭症谱系障碍是一组与胃肠功能障碍高度相关的精神疾病。最近的研究表明,就自闭症患者的特征而言,可能存在一种或多种微生物“指纹”,可用于诊断目的。本文提出了一种计算方法,通过基因组信息人工构建“健康”和自闭症个体的特征基因组,分析其中编码的酶,然后对这些酶进行详细比较。这是一个文本挖掘应用程序。建立了定制设计的在线应用程序,并将其用于比较代谢组学研究,并向公众公开。奇怪的是,“自闭症”微生物组中缺少几种与氨基酸谷氨酸有关的酶催化反应,并被编码为“对照”微生物组中几乎每个生物体内的编码。有趣的是,关于自闭症和谷氨酸存在神经兴奋/抑制失衡的主要假设。但是与这项研究的关联尚不清楚。结果包括与氧化应激有关的转硫和转甲基化途径的数据,这对自闭症也很重要。考虑到这项研究的纯计算机性质,这项研究的结果与该领域的主要假设相吻合。本研究提供了对自闭症潜在的复杂的代谢相互作用的新见解,这种新颖的方法学有可能用于发展新的假设。但是,局限性包括基因组数据稀疏和文献实验数据矛盾。我们相信,随着数据变得更加可用,全面和可靠,我们的软件工具和方法论具有巨大的实用性。

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