The Parkinson’s disease drug entacapone disrupts gut microbiome homeostasis via iron sequestration

Many human-targeted drugs alter the gut microbiome, leading to implications for host health. However, the mechanisms underlying these effects are not well known. Here we combined quantitative microbiome profiling, long-read metagenomics, stable isotope probing and single-cell chemical imaging to investigate the impact of two widely prescribed drugs on the gut microbiome. Physiologically relevant concentrations of entacapone, a treatment for Parkinson's disease, or loxapine succinate, used to treat schizophrenia, were incubated ex vivo with human faecal samples. Both drugs significantly impact microbial activity, more so than microbial abundance. Mechanistically, entacapone can complex and deplete available iron resulting in gut microbiome composition and function changes. Microbial growth can be rescued by replenishing levels of microbiota-accessible iron. Further, entacapone-induced iron starvation selected for iron-scavenging gut microbiome members encoding antimicrobial resistance and virulence genes. These findings reveal the impact of two under-investigated drugs on whole microbiomes and identify metal sequestration as a mechanism of drug-induced microbiome disturbance.

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Publication Details

Journal
Nature Microbiology
Published
2024-11-21
DOI
https://doi.org/10.1038/s41564-024-01853-0
Citations
15
Primary Topic
Parkinson's Disease Mechanisms and Treatments
Type
article
Field-Weighted Citation Impact
5.54

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article

The Parkinson’s disease drug entacapone disrupts gut microbiome homeostasis via iron sequestration

Dávid Szamosvári, David Berry, Bela Hausmann, Michael Wagner et al.
15 citations
Nature Microbiology
Parkinson's Disease Mechanisms and Treatments
5.54
article

The Parkinson’s disease drug entacapone disrupts gut microbiome homeostasis via iron sequestration

Dávid Szamosvári, David Berry, Bela Hausmann, Michael Wagner, Jannie Munk Kristensen, Stefanie Imminger, David Seki, Xiaowei Ge, Fátima C. Pereira, Thomas Böttcher, Yifan Zhu, Kenneth Wasmund, Rasmus Hansen Kirkegaard, Arno Schintlmeister, Ji‐Xin Cheng, Klara Maritsch, Marie Decorte, Juwairiyah B. Shazzad
article en
15 citations

Abstract

Many human-targeted drugs alter the gut microbiome, leading to implications for host health. However, the mechanisms underlying these effects are not well known. Here we combined quantitative microbiome profiling, long-read metagenomics, stable isotope probing and single-cell chemical imaging to investigate the impact of two widely prescribed drugs on the gut microbiome. Physiologically relevant concentrations of entacapone, a treatment for Parkinson's disease, or loxapine succinate, used to treat schizophrenia, were incubated ex vivo with human faecal samples. Both drugs significantly impact microbial activity, more so than microbial abundance. Mechanistically, entacapone can complex and deplete available iron resulting in gut microbiome composition and function changes. Microbial growth can be rescued by replenishing levels of microbiota-accessible iron. Further, entacapone-induced iron starvation selected for iron-scavenging gut microbiome members encoding antimicrobial resistance and virulence genes. These findings reveal the impact of two under-investigated drugs on whole microbiomes and identify metal sequestration as a mechanism of drug-induced microbiome disturbance.

Nature MicrobiologyVol. 9(12)
Boston University (US), University of Vienna (AT), University of Southampton (GB), University of Portsmouth (GB), Medical University of Vienna (AT), Aalborg University (DK)
University of Southampton, Austrian Science Fund, Universität Wien, Medizinische Universität Wien, National Institutes of Health, Biotechnology and Biological Sciences Research Council
Good health and well-being
Openalex Percentile: Top 3%
Parkinson's Disease Mechanisms and Treatments
5.54
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