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药物和环境污染物对肠道细菌产生胺类物质的影响。

Impact of drugs and environmental contaminants on amine production by gut bacteria.

作者信息

Kamrad Stephan, Davis Tara F, Patil Kiran R

机构信息

The Medical Research Council Toxicology Unit and Department of Biochemistry, University of Cambridge, Cambridge, UK.

出版信息

Mol Syst Biol. 2025 Jun 30. doi: 10.1038/s44320-025-00130-4.

Abstract

Xenobiotics like drugs are recognised as key influencers of gut bacterial growth. Yet, their impact on the production of metabolites involved in microbiota-host interactions is largely unknown. Here, we report the impact of commonly ingested xenobiotics-therapeutic drugs, pesticides, industrial chemicals, and sweeteners-on gut bacterial amine metabolism. We tested >13,000 interactions between >1700 compounds and 4 amine-producing bacteria, uncovering 747 xenobiotic-species-metabolite interactions involving 275 compounds. These compounds span all tested classes, with the majority being antimicrobial drugs. In 66% of the cases, amine production was correlated with growth, while the rest showed xenobiotic-induced decoupling between growth and metabolite production. The latter includes transient bursts in polyamine production by Escherichia coli in response to β-lactam antibiotics, and overproduction of aromatic amines by Ruminococcus gnavus treated with 15 diverse chemicals. Xenobiotics thus can disrupt metabolic homeostasis in both growth-dependent and -independent manner. We also find that metabolic responses have non-monotonic dose-dependency, resulting in lower doses sometimes having stronger effects. Our results bring forward the potential of common xenobiotics to disrupt the amine metabolism of gut bacteria.

摘要

像药物这样的外源性物质被认为是肠道细菌生长的关键影响因素。然而,它们对参与微生物群与宿主相互作用的代谢物产生的影响在很大程度上尚不清楚。在此,我们报告了常见摄入的外源性物质——治疗药物、农药、工业化学品和甜味剂——对肠道细菌胺代谢的影响。我们测试了1700多种化合物与4种产胺细菌之间的13000多种相互作用,发现了涉及275种化合物的747种外源性物质-物种-代谢物相互作用。这些化合物涵盖了所有测试类别,其中大多数是抗菌药物。在66%的情况下,胺的产生与生长相关,而其余情况则显示外源性物质导致生长与代谢物产生之间的解耦。后者包括大肠杆菌对β-内酰胺抗生素的反应中多胺产生的短暂爆发,以及用15种不同化学物质处理的纤细瘤胃球菌芳香胺的过量产生。因此,外源性物质可以以生长依赖和非依赖的方式破坏代谢稳态。我们还发现代谢反应具有非单调剂量依赖性,有时较低剂量会产生更强的影响。我们的结果揭示了常见外源性物质破坏肠道细菌胺代谢的可能性。

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