Evidence map›Paper›PMID 39242817›Full record

ArticleNature microbiology2024

Primary succession of Bifidobacteria drives pathogen resistance in neonatal microbiota assembly.

Yan Shao, Cristina Garcia-Mauriño, Simon Clare, Nicholas J R Dawson, Andre Mu, Anne Adoum, Katherine Harcourt, Junyan Liu, Hilary P Browne, Mark D Stares and 4 more

Abstract read
In one paragraph

Article in Nature microbiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

39 citing papers in PubMed.

  1. Trial
  2. Review
  3. Observational
  4. Review
  5. Review
  6. Exploring the Adhesion Potential ofFoods (Basel, Switzerland) · 2026
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Early supplementation with live combinedFrontiers in cellular and infection microbiology · 2026
    Observational
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Yan ShaoHost-Microbiota Interactions Laboratory, Wellcome Sanger Institute, Hinxton, UK. ys4@sanger.ac.uk.ORCID http://orcid.org/0000-0002-8662-0504
Cristina Garcia-MauriñoInstitute for Global Health, University College London, London, UK.
Simon ClareHost-Microbiota Interactions Laboratory, Wellcome Sanger Institute, Hinxton, UK.
Nicholas J R DawsonHost-Microbiota Interactions Laboratory, Wellcome Sanger Institute, Hinxton, UK.
Andre MuHost-Microbiota Interactions Laboratory, Wellcome Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0002-0853-9743
Anne AdoumHost-Microbiota Interactions Laboratory, Wellcome Sanger Institute, Hinxton, UK.
Katherine HarcourtHost-Microbiota Interactions Laboratory, Wellcome Sanger Institute, Hinxton, UK.
Junyan LiuHost-Microbiota Interactions Laboratory, Wellcome Sanger Institute, Hinxton, UK.
Hilary P BrowneHost-Microbiota Interactions Laboratory, Wellcome Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0002-1305-2470
Mark D StaresHost-Microbiota Interactions Laboratory, Wellcome Sanger Institute, Hinxton, UK.
Alison RodgerInstitute for Global Health, University College London, London, UK.
Peter BrocklehurstBirmingham Clinical Trials Unit, University of Birmingham, Birmingham, UK.
Nigel FieldInstitute for Global Health, University College London, London, UK.
Trevor D LawleyHost-Microbiota Interactions Laboratory, Wellcome Sanger Institute, Hinxton, UK. tl2@sanger.ac.uk.ORCID http://orcid.org/0000-0002-4805-621X

Funding

Wellcome TrustWellcome Trust (Wellcome) WT101169MA, 206194 and 108413/A/15/D
6 · The paper itself

Abstract

Human microbiota assembly commences at birth, seeded by both maternal and environmental microorganisms. Ecological theory postulates that primary colonizers dictate microbial community assembly outcomes, yet such microbial priority effects in the human gut remain underexplored. Here using longitudinal faecal metagenomics, we characterized neonatal microbiota assembly for a cohort of 1,288 neonates from the UK. We show that the pioneering neonatal gut microbiota can be stratified into one of three distinct community states, each dominated by a single microbial species and influenced by clinical and host factors, such as maternal age, ethnicity and parity. A community state dominated by Enterococcus faecalis displayed stochastic microbiota assembly with persistent high pathogen loads into infancy. In contrast, community states dominated by Bifidobacterium, specifically B. longum and particularly B. breve, exhibited a stable assembly trajectory and long-term pathogen colonization resistance, probably due to strain-specific functional adaptions to a breast milk-rich neonatal diet. Consistent with our human cohort observation, B. breve demonstrated priority effects and conferred pathogen colonization resistance in a germ-free mouse model. Our findings solidify the crucial role of Bifidobacteria as primary colonizers in shaping the microbiota assembly and functions in early life.

Indexed as

BifidobacteriumFecesGastrointestinal MicrobiomeAnimalsEnterococcus faecalisFemaleHumansInfant, NewbornMaleMetagenomicsMiceMilk, HumanUnited Kingdom

Identifiers

PMID39242817
PMCPMC11445081

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.