Evidence map›Paper›PMID 37347185›Full record

ArticleMicrobiology spectrum2023

The Impact of Long-Term Macrolide Exposure on the Gut Microbiome and Its Implications for Metabolic Control.

Jocelyn M Choo, Alyce M Martin, Steven L Taylor, Emily Sun, Fredrick M Mobegi, Tokuwa Kanno, Alyson Richard, Lucy D Burr, Stevie Lingman, Megan Martin and 3 more

Open access · goldAbstract read
In one paragraph

Article in Microbiology spectrum, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 14% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
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  4. Review
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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

13 authors at 4 institutions in 2 countries.

Jocelyn M ChooMicrobiome and Host Health Program, South Australian Health and Medical Research Institute, Adelaide, South Australia, Australia.ORCID 0000-0001-9500-8360
Alyce M MartinFlinders Health and Medical Research Institute, College of Medicine and Public Health, Flinders University, Adelaide, South Australia, Australia.
Steven L TaylorMicrobiome and Host Health Program, South Australian Health and Medical Research Institute, Adelaide, South Australia, Australia.
Emily SunFlinders Health and Medical Research Institute, College of Medicine and Public Health, Flinders University, Adelaide, South Australia, Australia.
Fredrick M MobegiMicrobiome and Host Health Program, South Australian Health and Medical Research Institute, Adelaide, South Australia, Australia.
Tokuwa KannoInstitute of Pharmaceutical Science, School of Cancer & Pharmaceutical Sciences, King's College London, London, United Kingdom.
Alyson RichardMicrobiome and Host Health Program, South Australian Health and Medical Research Institute, Adelaide, South Australia, Australia.
Lucy D BurrDepartment of Respiratory and Sleep Medicine, Mater Adult Hospital, Brisbane, Queensland, Australia.
Stevie LingmanDepartment of Respiratory and Sleep Medicine, Mater Adult Hospital, Brisbane, Queensland, Australia.
Megan MartinDepartment of Respiratory and Sleep Medicine, Mater Adult Hospital, Brisbane, Queensland, Australia.
Damien J KeatingFlinders Health and Medical Research Institute, College of Medicine and Public Health, Flinders University, Adelaide, South Australia, Australia.
A James MasonInstitute of Pharmaceutical Science, School of Cancer & Pharmaceutical Sciences, King's College London, London, United Kingdom.ORCID 0000-0003-0411-602X
Geraint B RogersMicrobiome and Host Health Program, South Australian Health and Medical Research Institute, Adelaide, South Australia, Australia.
Flinders University · AUKing's College London · GBMater Adult Hospital · AUMater Research · AU

Funding

British Heart Foundation
6 · The paper itself

Abstract

Long-term low-dose macrolide therapy is now widely used in the treatment of chronic respiratory diseases for its immune-modulating effects, although the antimicrobial properties of macrolides can also have collateral impacts on the gut microbiome. We investigated whether such treatment altered intestinal commensal microbiology and whether any such changes affected systemic immune and metabolic regulation. In healthy adults exposed to 4 weeks of low-dose erythromycin or azithromycin, as used clinically, we observed consistent shifts in gut microbiome composition, with a reduction in microbial capacity related to carbohydrate metabolism and short-chain fatty acid biosynthesis. These changes were accompanied by alterations in systemic biomarkers relating to immune (interleukin 5 [IL-5], IL-10, monocyte chemoattractant protein 1 [MCP-1]) and metabolic (serotonin [5-HT], C-peptide) homeostasis. Transplantation of erythromycin-exposed murine microbiota into germ-free mice demonstrated that changes in metabolic homeostasis and gastrointestinal motility, but not systemic immune regulation, resulted from changes in intestinal microbiology caused by macrolide treatment. Our findings highlight the potential for long-term low-dose macrolide therapy to influence host physiology via alteration of the gut microbiome.

Indexed as

Gastrointestinal MicrobiomeRespiratory Tract DiseasesAnimalsAnti-Bacterial AgentsErythromycinMacrolidesMiceAnti-Bacterial AgentsErythromycinMacrolidesazithromycinerythromycingnotobiotic modelgut microbiomeimmunoregulationmetabolic healthmurine antibiotic model

Identifiers

PMID37347185
PMCPMC10433835
OpenAlexW4381598845

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.