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低丰度微生物物种产生的脱氧胆酸与葡萄糖代谢受损有关。

Production of deoxycholic acid by low-abundant microbial species is associated with impaired glucose metabolism.

机构信息

Wallenberg Laboratory and Department of Molecular and Clinical Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.

Department of Bioengineering, Stanford University, Stanford, CA, USA.

出版信息

Nat Commun. 2024 May 20;15(1):4276. doi: 10.1038/s41467-024-48543-3.

Abstract

Alterations in gut microbiota composition are suggested to contribute to cardiometabolic diseases, in part by producing bioactive molecules. Some of the metabolites are produced by very low abundant bacterial taxa, which largely have been neglected due to limits of detection. However, the concentration of microbially produced metabolites from these taxa can still reach high levels and have substantial impact on host physiology. To explore this concept, we focused on the generation of secondary bile acids by 7α-dehydroxylating bacteria and demonstrated that addition of a very low abundant bacteria to a community can change the metabolic output dramatically. We show that Clostridium scindens converts cholic acid into the secondary bile acid deoxycholic acid (DCA) very efficiently even though the abundance of C. scindens is low, but still detectable by digital droplet PCR. We also show that colonization of germ-free female mice with a community containing C. scindens induces DCA production and affects host metabolism. Finally, we show that DCA correlates with impaired glucose metabolism and a worsened lipid profile in individuals with type 2 diabetes, which implies that this metabolic pathway may contribute to the development of cardiometabolic disease.

摘要

肠道微生物组成的改变被认为是导致代谢性心血管疾病的原因之一,部分原因是它们产生了生物活性分子。一些代谢物是由丰度非常低的细菌产生的,由于检测限的限制,这些细菌在很大程度上被忽视了。然而,这些细菌产生的微生物代谢物的浓度仍然可以达到很高的水平,并对宿主的生理机能产生实质性的影响。为了探索这一概念,我们专注于 7α-脱羟化细菌产生次级胆汁酸的过程,并证明向群落中添加一种丰度非常低的细菌可以显著改变其代谢产物。我们发现,尽管梭菌属的丰度很低,但仍然可以通过数字液滴 PCR 检测到,它可以非常有效地将胆酸转化为次级胆汁酸脱氧胆酸(DCA)。我们还表明,用含有梭菌属的群落定植无菌雌性小鼠会诱导 DCA 的产生,并影响宿主的新陈代谢。最后,我们发现 DCA 与 2 型糖尿病患者的葡萄糖代谢受损和脂质谱恶化相关,这意味着这种代谢途径可能有助于代谢性心血管疾病的发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d26/11106306/5c57fcc8a1ca/41467_2024_48543_Fig1_HTML.jpg

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