Evidence map›Paper›PMID 40128848›Full record

ArticleMicrobiome2025

Temporal dynamics and metagenomics of phosphorothioate epigenomes in the human gut microbiome.

Shane R Byrne, Michael S DeMott, Yifeng Yuan, Farzan Ghanegolmohammadi, Stefanie Kaiser, James G Fox, Eric J Alm, Peter C Dedon

Abstract read
In one paragraph

Article in Microbiome, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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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

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Shane R Byrne *Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.
Michael S DeMott *Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.
Yifeng YuanDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.
Farzan GhanegolmohammadiDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.
Stefanie KaiserPharmaceutical Chemistry, Goethe University, Frankfurt, Germany.
James G FoxDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.
Eric J AlmDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.
Peter C DedonDepartment of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA. pcdedon@mit.edu.

Funding

TOXICOLOGY CORE UNITP30ES002109 · NIEHS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI NILES, JACQUIN C · 1985 to 2020
$25.6M
TRAINING GRANTS IN ENVIROMENTAL TOXICOLOGYT32ES007020 · NIEHS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI ESSIGMANN, JOHN M · 1985 to 2024
$13.1M
Interactions Between the Microbiota and Helicobacter pylori in Gastric CarcinogenesisR01CA281732 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI JAMES G FOX, RICHARD M. PEEK · 2023 to 2026
$2.7M
NCI NIH HHS R01 CA281732NIEHS Core Center Grant P30-ES002109NIEHS NIH HHS P30 ES002109NIEHS NIH HHS T32 ES007020NIEHS Training Grant in Environmental Toxicology T32-ES007020NIH Transformative Award R01-OD028099-01
6 · The paper itself

Abstract

backgroundEpigenetic regulation of gene expression and host defense is well established in microbial communities, with dozens of DNA modifications comprising the epigenomes of prokaryotes and bacteriophage. Phosphorothioation (PT) of DNA, in which a chemically reactive sulfur atom replaces a non-bridging oxygen in the sugar-phosphate backbone, is catalyzed by dnd and ssp gene families widespread in bacteria and archaea. However, little is known about the role of PTs or other microbial epigenetic modifications in the human microbiome. Here we optimized and applied fecal DNA extraction, mass spectrometric, and metagenomics technologies to characterize the landscape and temporal dynamics of gut microbes possessing PT modifications.

resultsExploiting the nuclease-resistance of PTs, mass spectrometric analysis of limit digests of PT-containing DNA reveals PT dinucleotides as part of genomic consensus sequences, with 16 possible dinucleotide combinations. Analysis of mouse fecal DNA revealed a highly uniform spectrum of 11 PT dinucleotides in all littermates, with PTs estimated to occur in 5-10% of gut microbes. Though at similar levels, PT dinucleotides in fecal DNA from 11 healthy humans possessed signature combinations and levels of individual PTs. Comparison with a widely distributed microbial epigenetic mark, m

Indexed as

BacteriaEpigenesis, GeneticEpigenomeGastrointestinal MicrobiomeMetagenomicsPhosphatesAnimalsFecesFemaleHumansMaleMass SpectrometryMetagenomeMicePhosphatesthiophosphoric acidEpigeneticsHuman gut microbiomeMass spectrometryMetagenomic analysisMouse gut microbiomePhosphorothioatePT-seq

Identifiers

PMID40128848
PMCPMC11931770

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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.