Evidence map›Paper›PMID 35250930›Full record

ArticleFrontiers in microbiology2022

Murine Model for Measuring Effects of Humanized-Dosing of Antibiotics on the Gut Microbiome.

Shana R Leopold, Kamilia Abdelraouf, David P Nicolau, Hanako Agresta, Jethro Johnson, Kathleen Teter, Wm Michael Dunne, David Broadwell, Alex van Belkum, Lisa M Schechter and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in microbiology, 2022. 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 43% 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, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Antibiotic perturbations to the gut microbiome.Nature reviews. Microbiology · 2023
    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

12 authors at 5 institutions in 2 countries.

Shana R LeopoldThe Jackson Laboratory for Genomic Medicine, Farmington, CT, United States.
Kamilia AbdelraoufCenter for Anti-Infective Research and Development, Hartford Hospital, Hartford, CT, United States.
David P NicolauCenter for Anti-Infective Research and Development, Hartford Hospital, Hartford, CT, United States.
Hanako AgrestaThe Jackson Laboratory for Genomic Medicine, Farmington, CT, United States.
Jethro JohnsonThe Jackson Laboratory for Genomic Medicine, Farmington, CT, United States.
Kathleen TeterThe Jackson Laboratory for Genomic Medicine, Farmington, CT, United States.
Wm Michael DunneBioMérieux Inc., Durham, NC, United States.
David BroadwellBioMérieux Inc., Durham, NC, United States.
Alex van BelkumBioMérieux SA, Clinical Unit, Grenoble, France.
Lisa M SchechterBioMérieux SA, Clinical Unit, Hazelwood, MO, United States.
Erica J SodergrenThe Jackson Laboratory for Genomic Medicine, Farmington, CT, United States.
George M WeinstockThe Jackson Laboratory for Genomic Medicine, Farmington, CT, United States.
Jackson Laboratory · USbioMérieux (United States) · USbioMérieux (France) · FRHartford Financial Services (United States)Hartford Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is a current need for enhancing our insight in the effects of antimicrobial treatment on the composition of human microbiota. Also, the spontaneous restoration of the microbiota after antimicrobial treatment requires better understanding. This is best addressed in well-defined animal models. We here present a model in which immune-competent or neutropenic mice were administered piperacillin-tazobactam (TZP) according to human treatment schedules. Before, during and after the TZP treatment, fecal specimens were longitudinally collected at established intervals over several weeks. Gut microbial taxonomic distribution and abundance were assessed through culture and molecular means during all periods. Non-targeted metabolomics analyses of stool samples using Quadrupole Time of Flight mass spectrometry (QTOF MS) were also applied to determine if a metabolic fingerprint correlated with antibiotic use, immune status, and microbial abundance. TZP treatment led to a 5-10-fold decrease in bacterial fecal viability counts which were not fully restored during post-antibiotic follow up. Two distinct, relatively uniform and reproducible restoration scenarios of microbiota changes were seen in post TZP-treatment mice. Post-antibiotic flora could consist of predominantly Firmicutes or, alternatively, a more diverse mix of taxa. In general, the pre-treatment microbial communities were not fully restored within the screening periods applied. A new species, closely related to

Indexed as

gastro-intestinal tracthumanized antibiotic treatmentmetabolomemicrobiome dynamicsnon-infected mouse modelpiperacillin-tazobactam

Identifiers

PMID35250930
PMCPMC8892246
OpenAlexW4213275903

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.