Integrated Multi‐Cohort Analysis of the Parkinson's Disease Gut Metagenome

Author:

Boktor Joseph C.12ORCID,Sharon Gil1ORCID,Verhagen Metman Leo A.3ORCID,Hall Deborah A.3,Engen Phillip A.4ORCID,Zreloff Zoe5,Hakim Daniel J.6,Bostick John W.12ORCID,Ousey James1ORCID,Lange Danielle5,Humphrey Gregory6,Ackermann Gail7ORCID,Carlin Martha5ORCID,Knight Rob678ORCID,Keshavarzian Ali49ORCID,Mazmanian Sarkis K.12ORCID

Affiliation:

1. Division of Biology and Biological Engineering California Institute of Technology Pasadena California USA

2. Aligning Science Across Parkinson's (ASAP) Collaborative Research Network Chevy Chase Maryland USA

3. Department of Neurology Sciences Rush University Medical Center Chicago Illinois USA

4. Rush Center for Integrated Microbiome and Chronobiology Research Rush University Medical Center Chicago Illinois USA

5. The BioCollective, LLC Denver Colorado USA

6. Center for Microbiome Innovation, Jacobs School of Engineering University of California San Diego La Jolla California USA

7. Department of Pediatrics, School of Medicine University of California San Diego California USA

8. Department of Bioengineering University of California, San Diego La Jolla California USA

9. Departments of Internal Medicine, Anatomy & Cell Biology Rush University Medical Center Chicago Illinois USA

Abstract

AbstractBackgroundThe gut microbiome is altered in several neurologic disorders, including Parkinson's disease (PD).ObjectivesThe aim is to profile the fecal gut metagenome in PD for alterations in microbial composition, taxon abundance, metabolic pathways, and microbial gene products, and their relationship with disease progression.MethodsShotgun metagenomic sequencing was conducted on 244 stool donors from two independent cohorts in the United States, including individuals with PD (n = 48, n = 47, respectively), environmental household controls (HC, n = 29, n = 30), and community population controls (PC, n = 41, n = 49). Microbial features consistently altered in PD compared to HC and PC subjects were identified. Data were cross‐referenced to public metagenomic data sets from two previous studies in Germany and China to determine generalizable microbiome features.ResultsWe find several significantly altered taxa between PD and controls within the two cohorts sequenced in this study. Analysis across global cohorts returns consistent changes only in Intestinimonas butyriciproducens. Pathway enrichment analysis reveals disruptions in microbial carbohydrate and lipid metabolism and increased amino acid and nucleotide metabolism in PD. Global gene‐level signatures indicate an increased response to oxidative stress, decreased cellular growth and microbial motility, and disrupted intercommunity signaling.ConclusionsA metagenomic meta‐analysis of PD shows consistent and novel alterations in functional metabolic potential and microbial gene abundance across four independent studies from three continents. These data reveal that stereotypic changes in the functional potential of the gut microbiome are a consistent feature of PD, highlighting potential diagnostic and therapeutic avenues for future research. © 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Funder

Michael J. Fox Foundation

U.S. Department of Defense

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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