Evidence map›Paper›PMID 39826551›Full record

ArticleCell systems2025

Subspecies phylogeny in the human gut revealed by co-evolutionary constraints across the bacterial kingdom.

Benjamin A Doran, Robert Y Chen, Hannah Giba, Vivek Behera, Bidisha Barat, Anitha Sundararajan, Huaiying Lin, Ashley Sidebottom, Eric G Pamer, Arjun S Raman

Abstract read
In one paragraph

Article in Cell systems, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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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

10 authors.

Benjamin A DoranDuchossois Family Institute, University of Chicago, Chicago, IL 60637, USA; Pritzker School of Molecular Engineering, University of Chicago, Chicago, IL 60637, USA.
Robert Y ChenDepartment of Psychiatry, University of Washington, Seattle, WA 98195, USA.
Hannah GibaDuchossois Family Institute, University of Chicago, Chicago, IL 60637, USA; Department of Pathology, University of Chicago, Chicago, IL 60637, USA.
Vivek BeheraDepartment of Medicine, University of Chicago, Chicago, IL 60637, USA.
Bidisha BaratDuchossois Family Institute, University of Chicago, Chicago, IL 60637, USA.
Anitha SundararajanDuchossois Family Institute, University of Chicago, Chicago, IL 60637, USA.
Huaiying LinDuchossois Family Institute, University of Chicago, Chicago, IL 60637, USA.
Ashley SidebottomDuchossois Family Institute, University of Chicago, Chicago, IL 60637, USA.
Eric G PamerDuchossois Family Institute, University of Chicago, Chicago, IL 60637, USA; Department of Medicine, University of Chicago, Chicago, IL 60637, USA.
Arjun S RamanDuchossois Family Institute, University of Chicago, Chicago, IL 60637, USA; Department of Pathology, University of Chicago, Chicago, IL 60637, USA; Center for the Physics of Evolving Systems, University of Chicago, Chicago, IL 60637, USA. Electronic address: araman@bsd.uchicago.edu.

Funding

Using co-evolution to understand the emergence of bacterial phenotype from proteome variationR35GM146702 · NIGMS · UNIVERSITY OF CHICAGO · PI Arjun Raman · 2022 to 2026
$2.0M
NIGMS NIH HHS R35 GM146702
6 · The paper itself

Abstract

The human gut microbiome contains many bacterial strains of the same species ("strain-level variants") that shape microbiome function. The tremendous scale and molecular resolution at which microbial communities are being interrogated motivates addressing how to describe strain-level variants. We introduce the "Spectral Tree"-an inferred tree of relatedness built from patterns of co-evolutionary constraint between greater than 7,000 diverse bacteria. Using the Spectral Tree to describe over 600 diverse gut commensal strains that we isolated, whole-genome sequenced, and metabolically profiled revealed (1) widespread phylogenetic structure among strain-level variants, (2) the origins of subspecies phylogeny as a shared history of phage infections across humans, and (3) the key role of inter-human strain variation in predicting strain-level metabolic qualities. Overall, our work demonstrates the existence and metabolic importance of structured phylogeny below the level of species for commensal gut bacteria, motivating a redefinition of individual strains according to their evolutionary context. A record of this paper's transparent peer review process is included in the supplemental information.

Indexed as

BacteriaGastrointestinal MicrobiomePhylogenyEvolution, MolecularGenome, BacterialHumanscomputational systems biologyevolutionary modelsmicrobiomestatistical inference

Identifiers

PMID39826551
PMCPMC12626139

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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.