Industrialization drives convergent microbial and physiological shifts in the human metaorganism

Authors:

Mathilde Poyet, Malte Rühlemann, Ana Schaan, Yue Ma, Lucas Moitinho-Silva, Eike Wacker, Hannah Jebens, Lucas Patel, Le Thanh Tu Nguyen, Alexis Zimmer, Damian Plichta, Daniel McDonald, Christine Stevens, Adwoa Agyei, Mary Afihene, Shadrack Asibey, Yaw Awuku, Aida Badiane, Lee Ching, Chris Corzett, Awa Deme, Manuel Dominguez-Rodrigo, Amoako Duah, Alain Fezeu, Alain Froment, Sean Gibbons, Catherine Girard, Jeff Hooker, Fatimah Ibrahim, Deborah Iqaluk, Vanessa Juimo, Pinja Kettunen, Sophie Lafosse, Ernest Lango-Yaya, Jenni Lehtimäki, Yvonne Lim, Audax Mabulla, Varocha Mahachai, Rihlat Mohamed, Katya Moniz, Ivan Mwikarago, Yvonne Nartey, Daouda Ndiaye, Mary Noel, Charles Onyekwere, Tan Pin, Amelie Plymoth, Lewis Roberts, Lasse Ruokolainen, John Rusine, Laure Segurel, Jesse Shapiro, Shani Sigwazi, Ainara Sistiaga, Kenneth Valles, Tommi Vatanen, Ratha-korn Vilaichone, Philip Rosenstiel, John Baines, Andre Franke, David Ellinghaus, Rob Knight, Mark Daly, Ramnik Xavier, Eric Alm, Mathieu Groussin

Year of publication:

2025

Volume:

Issue:

ISSN:

Journal (long):

Unknown Journal

Journal (short):

UKN

Impact factor:

PubMed: -
Abstract:

Summary

Understanding how host lifestyle and industrialization shape the human gut microbiome and intestinal physiology requires multimodal analyses across diverse global host contexts. Here, we generate multivariate data from the Global Microbiome Conservancy cohort, including gut microbiome, IgA-sequencing, host genotyping, diet, lifestyle and fecal biomarker profiles, to investigate host–microbiome interactions across gradients of industrialization and geography. We show that industrialization is associated with homogenized microbial compositions, reduced microbial diversity, and lower community stability, independent of host confounders. We further show that industrialization is linked to elevated markers of gut stress, increased IgA secretion, and altered patterns of IgA-bacteria interactions. Finally, we show that microbiome-based disease predictors trained on industrialized populations lose accuracy in less industrialized cohorts, highlighting limited cross-population transferability. Together, our results suggest profound restructuring of host-microbiome interactions due to industrialized lifestyles, and emphasize the need for inclusive, globally representative data to improve translational microbiome applications across diverse human populations.

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