Evidence map›Paper›PMID 26266556›Full record

ArticleAmerican journal of respiratory and critical care medicine2015

The Role of Short-Chain Fatty Acids, Produced by Anaerobic Bacteria, in the Cystic Fibrosis Airway.

Bojana Mirković, Michelle A Murray, Gillian M Lavelle, Kevin Molloy, Ahmed Abdul Azim, Cedric Gunaratnam, Fiona Healy, Dubhfeasa Slattery, Paul McNally, Joe Hatch and 6 more

Open access · greenAbstract read
In one paragraph

Article in American journal of respiratory and critical care medicine, 2015. 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
8.8field-weighted citation impact, top 2% 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, 136 citations in OpenAlex.

  1. Journal of bacteriology · 2026
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  5. Functional CFTR may be required for Prevotella melaninogenica regulation of epithelial cell defense against Staphylococcus aureus.Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2026
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23 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 7 institutions in 3 countries.

Bojana Mirković1 Respiratory Research Division, Department of Medicine, Royal College of Surgeons in Ireland, Education and Research Centre, Beaumont Hospital, Dublin, Ireland.
Michelle A Murray1 Respiratory Research Division, Department of Medicine, Royal College of Surgeons in Ireland, Education and Research Centre, Beaumont Hospital, Dublin, Ireland.
Gillian M Lavelle1 Respiratory Research Division, Department of Medicine, Royal College of Surgeons in Ireland, Education and Research Centre, Beaumont Hospital, Dublin, Ireland.
Kevin Molloy1 Respiratory Research Division, Department of Medicine, Royal College of Surgeons in Ireland, Education and Research Centre, Beaumont Hospital, Dublin, Ireland.
Ahmed Abdul Azim1 Respiratory Research Division, Department of Medicine, Royal College of Surgeons in Ireland, Education and Research Centre, Beaumont Hospital, Dublin, Ireland.
Cedric Gunaratnam1 Respiratory Research Division, Department of Medicine, Royal College of Surgeons in Ireland, Education and Research Centre, Beaumont Hospital, Dublin, Ireland.
Fiona Healy2 Temple Street Children's University Hospital, Dublin, Ireland.
Dubhfeasa Slattery2 Temple Street Children's University Hospital, Dublin, Ireland.
Paul McNally3 Our Lady's Children's Hospital, Crumlin, Dublin, Ireland.
Joe Hatch4 Cystic Fibrosis/Pulmonary Research and Treatment Center.
Matthew Wolfgang4 Cystic Fibrosis/Pulmonary Research and Treatment Center.
Michael M Tunney6 CF & Airways Microbiology Group and.
Marianne S Muhlebach8 Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
Rosaleen Devery9 School of Biotechnology, Dublin City University, Dublin, Ireland.
Catherine M Greene1 Respiratory Research Division, Department of Medicine, Royal College of Surgeons in Ireland, Education and Research Centre, Beaumont Hospital, Dublin, Ireland.
Noel G McElvaney1 Respiratory Research Division, Department of Medicine, Royal College of Surgeons in Ireland, Education and Research Centre, Beaumont Hospital, Dublin, Ireland.
Royal College of Surgeons in Ireland · IETemple Street Children's University Hospital · IEChildren's Health Ireland at Crumlin · IECystic Fibrosis Foundation · USDublin City University · IEQueen's University Belfast · GBUniversity of North Carolina at Chapel Hill · US

Funding

The Role of Anaerobic Bacterial Infection in Cystic FibrosisR01HL092964 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BOUCHER, RICHARD CHARLES · 2010 to 2013
$2.9M
NHLBI NIH HHS 5R01 HL092964-04NHLBI NIH HHS R01 HL092964
6 · The paper itself

Abstract

rationaleAnaerobic bacteria are present in large numbers in the airways of people with cystic fibrosis (PWCF). In the gut, anaerobes produce short-chain fatty acids (SCFAs) that modulate immune and inflammatory processes.

objectivesTo investigate the capacity of anaerobes to contribute to cystic fibrosis (CF) airway pathogenesis via SCFAs.

methodsSamples of 109 PWCF were processed using anaerobic microbiological culture with bacteria present identified by 16S RNA sequencing. SCFA levels in anaerobic supernatants and bronchoalveolar lavage (BAL) were determined by gas chromatography. The mRNA and/or protein expression of two SCFA receptors, GPR41 and GPR43, in CF and non-CF bronchial brushings and 16HBE14o(-) and CFBE41o(-) cells were evaluated using reverse transcription polymerase chain reaction, Western blot analysis, laser scanning cytometry, and confocal microscopy. SCFA-induced IL-8 secretion was monitored by ELISA. MEASUREMENTS AND MAIN

resultsFifty-seven (52.3%) of 109 PWCF were anaerobe positive. Prevalence increased with age, from 33.3% to 57.7% in PWCF younger (n = 24) and older (n = 85) than 6 years of age. All evaluated anaerobes produced millimolar concentrations of SCFAs, including acetic, propionic, and butyric acids. SCFA levels were higher in BAL samples of adults than in those of children. GPR41 levels were elevated in CFBE41o(-) versus 16HBE14o(-) cells; CF versus non-CF bronchial brushings; and 16HBE14o(-) cells after treatment with cystic fibrosis transmembrane conductance regulator inhibitor CFTR(inh)-172, CF BAL, or inducers of endoplasmic reticulum stress. SCFAs induced a dose-dependent and pertussis toxin-sensitive IL-8 response in bronchial epithelial cells, with a higher production of IL-8 in CFBE41o(-) than in 16HBE14o(-) cells.

conclusionsThis study illustrates that SCFAs contribute to excessive production of IL-8 in CF airways colonized with anaerobes via up-regulated GPR41.

Indexed as

Bacteria, AnaerobicAdolescentAdultAge FactorsBlotting, WesternBronchoalveolar Lavage FluidChildChild, PreschoolChromatography, GasCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorEnzyme-Linked Immunosorbent AssayEpithelial CellsFatty AcidsFemaleHumansCystic Fibrosis Transmembrane Conductance RegulatorFatty Acidsanaerobic bacteriacystic fibrosisinflammationshort-chain fatty acids

Identifiers

PMID26266556
PMCPMC4731701
OpenAlexW2189008731

What OpenQuestion holds

Textmetadata
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.