Evidence map›Paper›PMID 28449706›Full record

ArticleMicrobiome2017

Chemical and pathogen-induced inflammation disrupt the murine intestinal microbiome.

Mikayla A Borton, Anice Sabag-Daigle, Jikang Wu, Lindsey M Solden, Bridget S O'Banion, Rebecca A Daly, Richard A Wolfe, Juan F Gonzalez, Vicki H Wysocki, Brian M M Ahmer and 1 more

Open access · goldAbstract read
In one paragraph

Article in Microbiome, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

83 citing papers in PubMed, 162 citations in OpenAlex.

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23 more citing papers are in PubMed but not listed here.

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

11 authors at 2 institutions in 1 country.

Mikayla A BortonDepartment of Microbiology, The Ohio State University, 484 W. 12th Avenue, 440 Biological Sciences Building, Columbus, OH, 43210, USA.
Anice Sabag-DaigleDepartment of Microbial Infection and Immunity, The Ohio State University, Columbus, OH, 43210, USA.
Jikang WuDepartment of Chemistry and Biochemistry, The Ohio State University, Columbus, OH, 43210, USA.
Lindsey M SoldenDepartment of Microbiology, The Ohio State University, 484 W. 12th Avenue, 440 Biological Sciences Building, Columbus, OH, 43210, USA.
Bridget S O'BanionDepartment of Microbiology, The Ohio State University, 484 W. 12th Avenue, 440 Biological Sciences Building, Columbus, OH, 43210, USA.
Rebecca A DalyDepartment of Microbiology, The Ohio State University, 484 W. 12th Avenue, 440 Biological Sciences Building, Columbus, OH, 43210, USA.
Richard A WolfeDepartment of Microbiology, The Ohio State University, 484 W. 12th Avenue, 440 Biological Sciences Building, Columbus, OH, 43210, USA.
Juan F GonzalezDepartment of Microbial Infection and Immunity, The Ohio State University, Columbus, OH, 43210, USA.
Vicki H WysockiDepartment of Chemistry and Biochemistry, The Ohio State University, Columbus, OH, 43210, USA.
Brian M M AhmerDepartment of Microbiology, The Ohio State University, 484 W. 12th Avenue, 440 Biological Sciences Building, Columbus, OH, 43210, USA.
Kelly C WrightonDepartment of Microbiology, The Ohio State University, 484 W. 12th Avenue, 440 Biological Sciences Building, Columbus, OH, 43210, USA. wrighton.1@osu.edu.
The Ohio State University · USInterface (United States) · US

Funding

Microbial ecology of the inflamed intestineR01AI143288 · NIAID · OHIO STATE UNIVERSITY · PI AHMER, BRIAN M, WRIGHTON, KELLY C · 2018 to 2022
$3.5M
Salmonella, colonization resistance, and fructose-asparagineR01AI116119 · NIAID · OHIO STATE UNIVERSITY · PI AHMER, BRIAN M, BEHRMAN, EDWARD J. · 2015 to 2019
$2.5M
NIAID NIH HHS R01 AI116119NIAID NIH HHS R01 AI143288
6 · The paper itself

Abstract

backgroundSalmonella is one of the most significant food-borne pathogens to affect humans and agriculture. While it is well documented that Salmonella infection triggers host inflammation, the impacts on the gut environment are largely unknown. A CBA/J mouse model was used to evaluate intestinal responses to Salmonella-induced inflammation. In parallel, we evaluated chemically induced inflammation by dextran sodium sulfate (DSS) and a non-inflammation control. We profiled gut microbial diversity by sequencing 16S ribosomal ribonucleic acid (rRNA) genes from fecal and cecal samples. These data were correlated to the inflammation marker lipocalin-2 and short-chain fatty acid concentrations.

resultsWe demonstrated that inflammation, chemically or biologically induced, restructures the chemical and microbial environment of the gut over a 16-day period. We observed that the ten mice within the Salmonella treatment group had a variable Salmonella relative abundance, with three high responding mice dominated by >46% Salmonella at later time points and the remaining seven mice denoted as low responders. These low- and high-responding Salmonella groups, along with the chemical DSS treatment, established an inflammation gradient with chemical and low levels of Salmonella having at least 3 log-fold lower lipocalin-2 concentration than the high-responding Salmonella mice. Total short-chain fatty acid and individual butyrate concentrations each negatively correlated with inflammation levels. Microbial communities were also structured along this inflammation gradient. Low levels of inflammation, regardless of chemical or biological induction, enriched for Akkermansia spp. in the Verrucomicrobiaceae and members of the Bacteroidetes family S24-7. Relative to the control or low inflammation groups, high levels of Salmonella drastically decreased the overall microbial diversity, specifically driven by the reduction of Alistipes and Lachnospiraceae in the Bacteroidetes and Firmicutes phyla, respectively. Conversely, members of the Enterobacteriaceae and Lactobacillus were positively correlated to high levels of Salmonella-induced inflammation.

conclusionsOur results show that enteropathogenic infection and intestinal inflammation are interrelated factors modulating gut homeostasis. These findings may prove informative with regard to prophylactic or therapeutic strategies to prevent disruption of microbial communities, or promote their restoration.

Indexed as

Gastrointestinal MicrobiomeAnimalsBacteriaCecumDextran SulfateDNA, BacterialDNA, RibosomalFecesLipocalin-2MiceRNA, Ribosomal, 16SSalmonella Infections, AnimalSequence Analysis, DNADextran SulfateDNA, BacterialDNA, RibosomalLcn2 protein, mouseLipocalin-2RNA, Ribosomal, 16SBeta diversityCBA/JInflammationLEfSeLipocalin-2SalmonellaShort-chain fatty acids

Identifiers

PMID28449706
PMCPMC5408407
OpenAlexW2607531920

What OpenQuestion holds

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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.