Evidence map›Paper›PMID 26691591›Full record

ArticlePloS one2015

Antibiotic Treatment Affects Intestinal Permeability and Gut Microbial Composition in Wistar Rats Dependent on Antibiotic Class.

Monica Vera-Lise Tulstrup, Ellen Gerd Christensen, Vera Carvalho, Caroline Linninge, Siv Ahrné, Ole Højberg, Tine Rask Licht, Martin Iain Bahl

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 123 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
123citing papers in PubMed, 1 pooled it
5.7field-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

123 citing papers in PubMed, 1 synthesis or guideline pooled it, 218 citations in OpenAlex.

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63 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

8 authors at 3 institutions in 2 countries.

Monica Vera-Lise TulstrupDivision of Diet, Disease prevention and Toxicology, National Food Institute, Technical University of Denmark, Søborg, Denmark.
Ellen Gerd ChristensenDivision of Diet, Disease prevention and Toxicology, National Food Institute, Technical University of Denmark, Søborg, Denmark.
Vera CarvalhoDivision of Diet, Disease prevention and Toxicology, National Food Institute, Technical University of Denmark, Søborg, Denmark.
Caroline LinningeDepartment of Food Technology, Engineering and Nutrition, Lund University, Lund, Sweden.
Siv AhrnéDepartment of Food Technology, Engineering and Nutrition, Lund University, Lund, Sweden.
Ole HøjbergDepartment of Animal Science, Aarhus University, Tjele, Denmark.
Tine Rask LichtDivision of Diet, Disease prevention and Toxicology, National Food Institute, Technical University of Denmark, Søborg, Denmark.
Martin Iain BahlDivision of Diet, Disease prevention and Toxicology, National Food Institute, Technical University of Denmark, Søborg, Denmark.
Technical University of Denmark · DKLund University · SEAarhus University · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antibiotics are frequently administered orally to treat bacterial infections not necessarily related to the gastrointestinal system. This has adverse effects on the commensal gut microbial community, as it disrupts the intricate balance between specific bacterial groups within this ecosystem, potentially leading to dysbiosis. We hypothesized that modulation of community composition and function induced by antibiotics affects intestinal integrity depending on the antibiotic administered. To address this a total of 60 Wistar rats (housed in pairs with 6 cages per group) were dosed by oral gavage with either amoxicillin (AMX), cefotaxime (CTX), vancomycin (VAN), metronidazole (MTZ), or water (CON) daily for 10-11 days. Bacterial composition, alpha diversity and caecum short chain fatty acid levels were significantly affected by AMX, CTX and VAN, and varied among antibiotic treatments. A general decrease in diversity and an increase in the relative abundance of Proteobacteria was observed for all three antibiotics. Additionally, the relative abundance of Bifidobacteriaceae was increased in the CTX group and both Lactobacillaceae and Verrucomicrobiaceae were increased in the VAN group compared to the CON group. No changes in microbiota composition or function were observed following MTZ treatment. Intestinal permeability to 4 kDa FITC-dextran decreased after CTX and VAN treatment and increased following MTZ treatment. Plasma haptoglobin levels were increased by both AMX and CTX but no changes in expression of host tight junction genes were found in any treatment group. A strong correlation between the level of caecal succinate, the relative abundance of Clostridiaceae 1 family in the caecum, and the level of acute phase protein haptoglobin in blood plasma was observed. In conclusion, antibiotic-induced changes in microbiota may be linked to alterations in intestinal permeability, although the specific interactions remain to be elucidated as changes in permeability did not always result from major changes in microbiota and vice versa.

Indexed as

AnimalsAnti-Bacterial AgentsBacteriaFemaleGastrointestinal MicrobiomeHaptoglobinsIntestinal MucosaIntestinesPermeabilityRatsRats, WistarAnti-Bacterial AgentsHaptoglobins

Identifiers

PMID26691591
PMCPMC4686753
OpenAlexW755088251

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.