Evidence map›Paper›PMID 27709125›Full record

ArticlemSystems

Genetic and transcriptional analysis of human host response to healthy gut microbiota.

Allison L Richards, Michael B Burns, Adnan Alazizi, Luis B Barreiro, Roger Pique-Regi, Ran Blekhman, Francesca Luca

Abstract read
In one paragraph

Article in mSystems. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Piceatannol Attenuates Benzo[Journal of agricultural and food chemistry · 2025
    Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Microbial control of host gene regulation and the evolution of host-microbiome interactions in primates.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
    Review
  15. Article
  16. A Novel View of HumanBiomolecules · 2019
    Review
  17. Review
  18. An insight into gut microbiota and its functionalities.Cellular and molecular life sciences : CMLS · 2019
    Review
  19. Review
  20. Review
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

7 authors.

Allison L RichardsCenter for Molecular Medicine and Genetics, Wayne State University, Detroit, MI.
Michael B BurnsDepartments of Genetics, Cell Biology, and Development, The University of Minnesota, Minneapolis, MN; Department of Ecology, Evolution, and Behavior, The University of Minnesota, Minneapolis, MN.
Adnan AlaziziCenter for Molecular Medicine and Genetics, Wayne State University, Detroit, MI.
Luis B BarreiroDepartment of Pediatrics, Sainte-Justine Hospital Research Centre, University of Montreal, Montreal, QC, Canada.
Roger Pique-RegiCenter for Molecular Medicine and Genetics, Wayne State University, Detroit, MI; Department of Obstetrics and Gynecology, Wayne State University, Detroit, MI.
Ran BlekhmanDepartments of Genetics, Cell Biology, and Development, The University of Minnesota, Minneapolis, MN; Department of Ecology, Evolution, and Behavior, The University of Minnesota, Minneapolis, MN.
Francesca LucaCenter for Molecular Medicine and Genetics, Wayne State University, Detroit, MI; Department of Obstetrics and Gynecology, Wayne State University, Detroit, MI.

Funding

University of Minnesota Clinical and Translational Science Institute (UMN CTSI)UL1TR000114 · NCATS · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R · 2012 to 2015
$35.0M
Functional Characterization of the Genetic and Environmental Determinants of Complex TraitsR01GM109215 · NIGMS · WAYNE STATE UNIVERSITY · PI Francesca Luca, Roger Pique-Regi · 2014 to 2026
$3.2M
NCATS NIH HHS UL1 TR000114NIGMS NIH HHS R01 GM109215United States NIGMS
6 · The paper itself

Abstract

Many studies have demonstrated the importance of the gut microbiota in healthy and disease states. However, establishing the causality of host-microbiota interactions in humans is still challenging. Here, we describe a novel experimental system to define the transcriptional response induced by the microbiota in human cells and to shed light on the molecular mechanisms underlying host-gut microbiota interactions. In primary human colonic epithelial cells, we identified over 6,000 genes that change expression at various time points following co-culturing with the gut microbiota of a healthy individual. Among the differentially expressed genes we found a 1.8-fold enrichment of genes associated with diseases that have been previously linked to the microbiome, such as obesity and colorectal cancer. In addition, our experimental system allowed us to identify 87 host SNPs that show allele-specific expression in 69 genes. Furthermore, for 12 SNPs in 12 different genes, allele-specific expression is conditional on the exposure to the microbiota. Of these 12 genes, eight have been associated with diseases linked to the gut microbiota, specifically colorectal cancer, obesity and type 2 diabetes. Our study demonstrates a scalable approach to study host-gut microbiota interactions and can be used to identify putative mechanisms for the interplay between host genetics and microbiota in health and disease.

Identifiers

PMID27709125
PMCPMC5047527

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LicenceCC BY
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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.