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在糖尿病前期患者和未经治疗的 2 型糖尿病患者中存在明显不同的肠道宏基因组和宏蛋白质组特征。

Distinct gut metagenomics and metaproteomics signatures in prediabetics and treatment-naïve type 2 diabetics.

机构信息

BGI-Shenzhen, Shenzhen 518083, China; China National GeneBank, Shenzhen 518120, China; Laboratory of Genomics and Molecular Biomedicine, Department of Biology, University of Copenhagen, 2100 Copenhagen, Denmark.

Suzhou Centre for Disease Control and Prevention, Suzhou 215007, China.

出版信息

EBioMedicine. 2019 Sep;47:373-383. doi: 10.1016/j.ebiom.2019.08.048. Epub 2019 Sep 3.

Abstract

BACKGROUND

The gut microbiota plays important roles in modulating host metabolism. Previous studies have demonstrated differences in the gut microbiome of T2D and prediabetic individuals compared to healthy individuals, with distinct disease-related microbial profiles being reported in groups of different age and ethnicity. However, confounding factors such as anti-diabetic medication hamper identification of the gut microbial changes in disease development.

METHOD

We used a combination of in-depth metagenomics and metaproteomics analyses of faecal samples from treatment-naïve type 2 diabetic (TN-T2D, n = 77), pre-diabetic (Pre-DM, n = 80), and normal glucose tolerant (NGT, n = 97) individuals to investigate compositional and functional changes of the gut microbiota and the faecal content of microbial and host proteins in Pre-DM and treatment-naïve T2D individuals to elucidate possible host-microbial interplays characterizing different disease stages.

FINDINGS

We observed distinct differences characterizing the gut microbiota of these three groups and validated several key features in an independent TN-T2D cohort. We also demonstrated that the content of several human antimicrobial peptides and pancreatic enzymes differed in faecal samples between three groups.

INTERPRETATION

Our findings suggest a complex, disease stage-dependent interplay between the gut microbiota and the host and point to the value of metaproteomics to gain further insight into interplays between the gut microbiota and the host. FUND: The study was supported by the National Natural Science Foundation of China (No. 31601073), the National Key Research and Development Program of China (No. 2017YFC0909703) and the Shenzhen Municipal Government of China (No. JCYJ20170817145809215). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

摘要

背景

肠道微生物群在调节宿主代谢方面发挥着重要作用。先前的研究表明,2 型糖尿病(T2D)和糖尿病前期个体的肠道微生物组与健康个体存在差异,并且在不同年龄和种族的群体中报告了不同的与疾病相关的微生物特征。然而,抗糖尿病药物等混杂因素阻碍了对疾病发展过程中肠道微生物变化的识别。

方法

我们使用深度宏基因组学和粪便样本代谢组学分析相结合的方法,对未经治疗的 2 型糖尿病(TN-T2D,n=77)、糖尿病前期(Pre-DM,n=80)和正常糖耐量(NGT,n=97)个体的粪便样本进行分析,以研究肠道微生物群的组成和功能变化,以及 Pre-DM 和未经治疗的 T2D 个体中微生物和宿主蛋白的粪便含量,以阐明可能表征不同疾病阶段的宿主-微生物相互作用。

结果

我们观察到这三个组的肠道微生物群具有明显的差异,并在独立的 TN-T2D 队列中验证了几个关键特征。我们还表明,在三个组的粪便样本中,几种人类抗菌肽和胰腺酶的含量存在差异。

结论

我们的研究结果表明,肠道微生物群与宿主之间存在复杂的、依赖疾病阶段的相互作用,并指出代谢组学在进一步深入了解肠道微生物群与宿主之间的相互作用方面具有价值。

资助

本研究得到了中国国家自然科学基金(No. 31601073)、中国国家重点研发计划(No. 2017YFC0909703)和中国深圳市政府(No. JCYJ20170817145809215)的支持。资助者在研究设计、数据收集和分析、决策发表或手稿准备方面没有作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa65/6796533/32bbad1527cf/gr1.jpg

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