Cited by 59Gut microbiota and healthClostridium difficile and Clostridium perfringens researchMicrobial Community Ecology and Physiology

Endospores and other lysis-resistant bacteria comprise a widely shared core community within the human microbiota

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Kearney, Sean M, Gibbons, Sean M, Poyet, Mathilde, Gurry, Thomas, Bullock, Kevin, Allegretti, Jessica R, Clish, Clary B, Alm, Eric J·2018·The ISME Journal

Published version of a preprint

Abstract

Endospore-formers in the human microbiota are well adapted for host-to-host transmission, and an emerging consensus points to their role in determining health and disease states in the gut. The human gut, more than any other environment, encourages the maintenance of endospore formation, with recent culture-based work suggesting that over 50% of genera in the microbiome carry genes attributed to this trait. However, there has been limited work on the ecological role of endospores and other stress-resistant cellular states in the human gut. In fact, there is no data to indicate whether organisms with the genetic potential to form endospores actually form endospores in situ and how sporulation varies across individuals and over time. Here we applied a culture-independent protocol to enrich for endospores and other stress-resistant cells in human feces to identify variation in these states across people and within an individual over time. We see that cells with resistant states are more likely than those without to be shared among multiple individuals, which suggests that these resistant states are particularly adapted for cross-host dissemination. Furthermore, we use untargeted fecal metabolomics in 24 individuals and within a person over time to show that these organisms respond to shared environmental signals, and in particular, dietary fatty acids, that likely mediate colonization of recently disturbed human guts.

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References 65 · Cited by 59

Research works printed but not linked: 2

  1. Smith PM, Howitt MR, Panikov N, Michaud M, Gallini CA, Bohlooly-Y M, et al. The microbial metabolites, short-chain fatty acids, regulate colonic treg cell homeostasis. Science. 2013;341: 569-73.
  2. Van den Abbeele P, Belzer C, Goossens M, Kleerebezem M, De Vos WM, Thas O, et al. Butyrate-producing Clostridium cluster XIVa species specifically colonize mucins in an in vitro gut model. ISME J. 2013;7:949-61.

Authors
Kearney, S. M., Gibbons, S. M., Poyet, M., Gurry, T., Bullock, K., Allegretti, J. R., Clish, C. B., & Alm, E. J.
Affiliations
  • Broad Institute (US)
  • Brigham and Women's Hospital (US)
Corresponding author
Alm, Eric J
Venue
The ISME Journal
Published
2018-06-13
Volume
12
Issue
10
Pages
2403-2416
ISSN
  • 1751-7362 (ISSN-L)
  • 1751-7370
OpenAlex
W2949372008
Cited by
59
References
65
Citations by year
2026: 3 · 2025: 9 · 2024: 4 · 2023: 5 · 2022: 10 · 2021: 8 · 2020: 11 · 2019: 5 · 2018: 4
FWCI
2.48
Type
journal article
Language
en
Open access
Locations
  • The ISME Journal (publishedVersion)
  • bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
Broad Institute BN10 Trainee Grant NSF Graduate Research Fellowship
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
  • Health Sciences › Medicine › Infectious Diseases › Clostridium difficile and Clostridium perfringens research
  • Physical Sciences › Environmental Science › Ecology › Microbial Community Ecology and Physiology
Keywords
endospores, endospore-forming bacteria, human gut microbiome, cross-host transmission, core microbiome, fecal metabolomics, dietary fatty acids, intestinal colonization, sporulation, interindividual variability
MeSH terms
Gastrointestinal Microbiome, Bacteria, Feces, Humans, Spores, Bacterial, Biodiversity

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