Evidence map›Paper›PMID 25514533›Full record

ArticleThe ISME journal2015

A Winogradsky-based culture system shows an association between microbial fermentation and cystic fibrosis exacerbation.

Robert A Quinn, Katrine Whiteson, Yan-Wei Lim, Peter Salamon, Barbara Bailey, Simone Mienardi, Savannah E Sanchez, Don Blake, Doug Conrad, Forest Rohwer

Erratum issuedAbstract read
In one paragraph

Article in The ISME journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
–field-weighted citation impact
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

44 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Simulated Media for Mimicking the Human Environment In Vitro.APMIS : acta pathologica, microbiologica, et immunologica Scandinavica · 2025
    Review
  6. Review
  7. Fungal lung disease.The European respiratory journal · 2024
    Review
  8. Article
  9. Review
  10. Longitudinal changes in the cystic fibrosis airway microbiota with time and treatment.Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2024
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. What Makes Pseudomonas aeruginosa a Pathogen?Advances in experimental medicine and biology · 2022
    Article
  18. Multi-Omics Study of Keystone Species in a Cystic Fibrosis Microbiome.International journal of molecular sciences · 2021
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Robert A QuinnDepartment of Biology, San Diego State University, San Diego, CA, USA.
Katrine WhitesonDepartment of Biology, San Diego State University, San Diego, CA, USA.
Yan-Wei LimDepartment of Biology, San Diego State University, San Diego, CA, USA.
Peter SalamonDepartment of Mathematics and Statistics, San Diego State University, San Diego, CA, USA.
Barbara BaileyDepartment of Mathematics and Statistics, San Diego State University, San Diego, CA, USA.
Simone MienardiDepartment of Chemistry, University of California, Irvine, CA, USA.
Savannah E SanchezDepartment of Biology, San Diego State University, San Diego, CA, USA.
Don BlakeDepartment of Chemistry, University of California, Irvine, CA, USA.
Doug ConradDepartment of Medicine, University of California, San Diego, CA, USA.
Forest RohwerDepartment of Biology, San Diego State University, San Diego, CA, USA.

Funding

San Diego Clinical and Translational Research InstituteUL1TR000100 · NCATS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI FIRESTEIN, GARY S · 2012 to 2015
$19.7M
SAN DIEGO CLINICAL AND TRANSLATIONAL RESEARCH INSTITUTEUL1RR031980 · NCRR · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI FIRESTEIN, GARY S · 2010 to 2011
$14.0M
Ecology of Cystic Fibrosis: Administrative SupplementR01GM095384 · NIGMS · SAN DIEGO STATE UNIVERSITY · PI ROHWER, FOREST L · 2011 to 2014
$1.9M
NCATS NIH HHS UL1 TR000100NCATS NIH HHS UL1TR000100NCRR NIH HHS UL1 RR031980NCRR NIH HHS UL1RR031980NIGMS NIH HHS R01 GM095384NIGMS NIH HHS R01 GM095384-01
6 · The paper itself

Abstract

There is a poor understanding of how the physiology of polymicrobial communities in cystic fibrosis (CF) lungs contributes to pulmonary exacerbations and lung function decline. In this study, a microbial culture system based on the principles of the Winogradsky column (WinCF system) was developed to study the physiology of CF microbes. The system used glass capillary tubes filled with artificial sputum medium to mimic a clogged airway bronchiole. Chemical indicators were added to observe microbial physiology within the tubes. Characterization of sputum samples from seven patients showed variation in pH, respiration, biofilm formation and gas production, indicating that the physiology of CF microbial communities varied among patients. Incubation of homogenized tissues from an explant CF lung mirrored responses of a Pseudomonas aeruginosa pure culture, supporting evidence that end-stage lungs are dominated by this pathogen. Longitudinal sputum samples taken through two exacerbation events in a single patient showed that a two-unit drop in pH and a 30% increase in gas production occurred in the tubes prior to exacerbation, which was reversed with antibiotic treatment. Microbial community profiles obtained through amplification and sequencing of the 16S rRNA gene showed that fermentative anaerobes became more abundant during exacerbation and were then reduced during treatment where P. aeruginosa became the dominant bacterium. Results from the WinCF experiments support the model where two functionally different CF microbial communities exist, the persistent Climax Community and the acute Attack Community. Fermentative anaerobes are hypothesized to be the core members of the Attack Community and production of acidic and gaseous products from fermentation may drive developing exacerbations. Treatment targeting the Attack Community may better resolve exacerbations and resulting lung damage.

Indexed as

FermentationBacteriaBacteria, AnaerobicBacteriological TechniquesCystic FibrosisHumansLungPseudomonas aeruginosaSputum

Identifiers

PMID25514533
PMCPMC4817692

What OpenQuestion holds

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Registered trials

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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.