Gut microbiome stability and dynamics in healthy donors and patients with non-gastrointestinal cancers

Author:

Byrd Allyson L.1ORCID,Liu Menghan12ORCID,Fujimura Kei E.1ORCID,Lyalina Svetlana3ORCID,Nagarkar Deepti R.1ORCID,Charbit Bruno4ORCID,Bergstedt Jacob5ORCID,Patin Etienne5ORCID,Harrison Oliver J.6ORCID,Quintana-Murci Lluís57ORCID,Mellman Ira1ORCID,Duffy Darragh48ORCID,Albert Matthew L.9ORCID,

Affiliation:

1. Department of Cancer Immunology, Genentech Inc., San Francisco, CA

2. Sackler Institute of Graduate Biomedical Sciences, New York University School of Medicine, New York, NY

3. Personalized Health Care, Genentech Inc., San Francisco, CA

4. Cytometry and Biomarkers UTechS, CRT, Institut Pasteur, Paris, France

5. Human Evolutionary Genetics Unit, Institut Pasteur, UMR 2000, Centre National de la Recherche Scientifique, Paris, France

6. Center for Fundamental Immunology, Benaroya Research Institute, Seattle, WA

7. Collège de France, Paris, France

8. Translational Immunology Lab, Institut Pasteur, Paris, France

9. Insitro, South San Francisco, CA

Abstract

As microbial therapeutics are increasingly being tested in diverse patient populations, it is essential to understand the host and environmental factors influencing the microbiome. Through analysis of 1,359 gut microbiome samples from 946 healthy donors of the Milieu Intérieur cohort, we detail how microbiome composition is associated with host factors, lifestyle parameters, and disease states. Using a genome-based taxonomy, we found biological sex was the strongest driver of community composition. Additionally, bacterial populations shift across decades of life (age 20–69), with Bacteroidota species consistently increased with age while Actinobacteriota species, including Bifidobacterium, decreased. Longitudinal sampling revealed that short-term stability exceeds interindividual differences. By accounting for these factors, we defined global shifts in the microbiomes of patients with non-gastrointestinal tumors compared with healthy donors. Together, these results demonstrated that the microbiome displays predictable variations as a function of sex, age, and disease state. These variations must be considered when designing microbiome-targeted therapies or interpreting differences thought to be linked to pathophysiology or therapeutic response.

Funder

French government

Agence Nationale de la Recherche

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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