Evidence map›Paper›PMID 24401860›Full record

ArticleThe ISME journal2014

Breath gas metabolites and bacterial metagenomes from cystic fibrosis airways indicate active pH neutral 2,3-butanedione fermentation.

Katrine L Whiteson, Simone Meinardi, Yan Wei Lim, Robert Schmieder, Heather Maughan, Robert Quinn, Donald R Blake, Douglas Conrad, Forest Rohwer

Open access · hybridAbstract read
In one paragraph

Article in The ISME journal, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing 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

77 citing papers in PubMed, 134 citations in OpenAlex.

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17 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

9 authors at 4 institutions in 1 country.

Katrine L WhitesonDepartment of Biology, San Diego State University, San Diego, CA, USA.
Simone MeinardiDepartment of Chemistry, University of California, Irvine, CA, USA.
Yan Wei LimDepartment of Biology, San Diego State University, San Diego, CA, USA.
Robert SchmiederDepartment of Biology, San Diego State University, San Diego, CA, USA.
Heather MaughanRonin Institute, Montclair, NJ, USA.
Robert QuinnDepartment of Biology, San Diego State University, San Diego, CA, USA.
Donald R BlakeDepartment of Chemistry, University of California, Irvine, CA, USA.
Douglas ConradDepartment of Medicine, University of California, San Diego, La Jolla, CA, USA.
Forest RohwerDepartment of Biology, San Diego State University, San Diego, CA, USA.
San Diego State University · USUniversity of California, Irvine · USRonin Institute · USUniversity of California, San Diego · US

Funding

Ecology of Cystic Fibrosis: Administrative SupplementR01GM095384 · NIGMS · SAN DIEGO STATE UNIVERSITY · PI ROHWER, FOREST L · 2011 to 2014
$1.9M
NIGMS NIH HHS R01 GM095384NIGMS NIH HHS R01 GM095384-01NIGMS NIH HHS R01GM095384-01S1
6 · The paper itself

Abstract

The airways of cystic fibrosis (CF) patients are chronically colonized by patient-specific polymicrobial communities. The conditions and nutrients available in CF lungs affect the physiology and composition of the colonizing microbes. Recent work in bioreactors has shown that the fermentation product 2,3-butanediol mediates cross-feeding between some fermenting bacteria and Pseudomonas aeruginosa, and that this mechanism increases bacterial current production. To examine bacterial fermentation in the respiratory tract, breath gas metabolites were measured and several metagenomes were sequenced from CF and non-CF volunteers. 2,3-butanedione was produced in nearly all respiratory tracts. Elevated levels in one patient decreased during antibiotic treatment, and breath concentrations varied between CF patients at the same time point. Some patients had high enough levels of 2,3-butanedione to irreversibly damage lung tissue. Antibiotic therapy likely dictates the activities of 2,3-butanedione-producing microbes, which suggests a need for further study with larger sample size. Sputum microbiomes were dominated by P. aeruginosa, Streptococcus spp. and Rothia mucilaginosa, and revealed the potential for 2,3-butanedione biosynthesis. Genes encoding 2,3-butanedione biosynthesis were disproportionately abundant in Streptococcus spp, whereas genes for consumption of butanedione pathway products were encoded by P. aeruginosa and R. mucilaginosa. We propose a model where low oxygen conditions in CF lung lead to fermentation and a decrease in pH, triggering 2,3-butanedione fermentation to avoid lethal acidification. We hypothesize that this may also increase phenazine production by P. aeruginosa, increasing reactive oxygen species and providing additional electron acceptors to CF microbes.

Indexed as

Genome, BacterialMetagenomeAnti-Bacterial AgentsBreath TestsButylene GlycolsCoinfectionCystic FibrosisDiacetylFermentationHumansHydrogen-Ion ConcentrationMaleSputum2,3-butylene glycolAnti-Bacterial AgentsButylene GlycolsDiacetyl

Identifiers

PMID24401860
PMCPMC4030226
OpenAlexW2072676969

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.