Structural and Computational Biology Unit, European Molecular Biology Laboratory, Heidelberg, Germany.
The Medical Research Council Toxicology Unit, University of Cambridge, Cambridge, UK.
Mol Syst Biol. 2021 Mar;17(3):e10116. doi: 10.15252/msb.202010116.
Broad-spectrum antibiotics target multiple gram-positive and gram-negative bacteria, and can collaterally damage the gut microbiota. Yet, our knowledge of the extent of damage, the antibiotic activity spectra, and the resistance mechanisms of gut microbes is sparse. This limits our ability to mitigate microbiome-facilitated spread of antibiotic resistance. In addition to antibiotics, non-antibiotic drugs affect the human microbiome, as shown by metagenomics as well as in vitro studies. Microbiome-drug interactions are bidirectional, as microbes can also modulate drugs. Chemical modifications of antibiotics mostly function as antimicrobial resistance mechanisms, while metabolism of non-antibiotics can also change the drugs' pharmacodynamic, pharmacokinetic, and toxic properties. Recent studies have started to unravel the extensive capacity of gut microbes to metabolize drugs, the mechanisms, and the relevance of such events for drug treatment. These findings raise the question whether and to which degree these reciprocal drug-microbiome interactions will differ across individuals, and how to take them into account in drug discovery and precision medicine. This review describes recent developments in the field and discusses future study areas that will benefit from systems biology approaches to better understand the mechanistic role of the human gut microbiota in drug actions.
广谱抗生素针对多种革兰氏阳性菌和革兰氏阴性菌,并可能间接地破坏肠道微生物组。然而,我们对肠道微生物损伤的程度、抗生素的活性谱以及抗生素耐药性的机制知之甚少。这限制了我们减轻微生物组促进抗生素耐药性传播的能力。除了抗生素外,非抗生素药物也会影响人类微生物组,这一点已通过宏基因组学和体外研究得到证实。微生物组-药物相互作用是双向的,因为微生物也可以调节药物。抗生素的化学修饰主要作为抗菌耐药性机制起作用,而非抗生素的代谢也可以改变药物的药效学、药代动力学和毒性特性。最近的研究开始揭示肠道微生物广泛代谢药物的能力、相关机制,以及这些事件对药物治疗的相关性。这些发现提出了一个问题,即这些相互的药物-微生物组相互作用是否会在个体之间存在差异,以及在药物发现和精准医学中如何考虑这些差异。这篇综述描述了该领域的最新进展,并讨论了未来将受益于系统生物学方法的研究领域,以更好地理解人类肠道微生物组在药物作用中的机制作用。