Evidence map›Paper›PMID 34874778›Full record

ArticlemSystems2021

Changes in Gut Bacterial Translation Occur before Symptom Onset and Dysbiosis in Dextran Sodium Sulfate-Induced Murine Colitis.

M Taguer, E Darbinian, K Wark, A Ter-Cheam, D A Stephens, C F Maurice

Open access · goldAbstract read
In one paragraph

Article in mSystems, 2021. 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
0.4field-weighted citation impact, top 40% of its field
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, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
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

6 authors at 1 institution in 1 country.

M TaguerDepartment of Microbiology & Immunology, Faculty of Medicine and Health Sciences, McGill Universitygrid.14709.3b, Montreal, Quebec, Canada.
E DarbinianDepartment of Microbiology & Immunology, Faculty of Medicine and Health Sciences, McGill Universitygrid.14709.3b, Montreal, Quebec, Canada.
K WarkDepartment of Microbiology & Immunology, Faculty of Medicine and Health Sciences, McGill Universitygrid.14709.3b, Montreal, Quebec, Canada.
A Ter-CheamDepartment of Mathematics and Statistics, Faculty of Science, McGill Universitygrid.14709.3b, Montreal, Quebec, Canada.
D A StephensDepartment of Mathematics and Statistics, Faculty of Science, McGill Universitygrid.14709.3b, Montreal, Quebec, Canada.
C F MauriceDepartment of Microbiology & Immunology, Faculty of Medicine and Health Sciences, McGill Universitygrid.14709.3b, Montreal, Quebec, Canada.ORCID 0000-0001-7187-3472
McGill University · CA

Funding

Canada Research Chairs (Chaires de recherche du Canada) 950-230748 X-242502Canadian Institute for Advanced Research (ICRA) Azrieli Global ScholarGouvernement du Canada | Canadian Institutes of Health Research (CIHR) PJT-149098Gouvernement du Canada | Natural Sciences and Engineering Research Council of Canada (NSERC) DiscoveryGouvernement du Canada | Natural Sciences and Engineering Research Council of Canada (NSERC) PGSD3-504903-2017
6 · The paper itself

Abstract

Longitudinal studies on the gut microbiome that follow the effect of a perturbation are critical in understanding the microbiome's response and succession to disease. Here, we use a dextran sodium sulfate (DSS) mouse model of colitis as a tractable perturbation to study how gut bacteria change their physiology over the course of a perturbation. Using single-cell methods such as flow cytometry, bioorthogonal noncanonical amino acid tagging (BONCAT), and population-based cell sorting combined with 16S rRNA sequencing, we determine the diversity of physiologically distinct fractions of the gut microbiota and how they respond to a controlled perturbation. The physiological markers of bacterial activity studied here include relative nucleic acid content, membrane damage, and protein production. There is a distinct and reproducible succession in bacterial physiology, with an increase in bacteria with membrane damage and diversity changes in the translationally active fraction, both, critically, occurring before symptom onset. Large increases in the relative abundance of

Indexed as

bacterial physiologyBONCATcolitisflow cytometryhigh nucleic acidlongitudinallow nucleic acid

Identifiers

PMID34874778
PMCPMC8651081
OpenAlexW4200366135

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.