Evidence map›Paper›PMID 23019655›Full record

ArticleScience translational medicine2012

Quantitative analysis of the human airway microbial ecology reveals a pervasive signature for cystic fibrosis.

Paul C Blainey, Carlos E Milla, David N Cornfield, Stephen R Quake

Abstract read
In one paragraph

Article in Science translational medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed, 2 pooled it
12.7field-weighted citation impact, top 1% 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

67 citing papers in PubMed, 2 syntheses or guidelines pooled it, 116 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Cross-talk between immune system and microbiota in COVID-19.Expert review of gastroenterology & hepatology · 2021
    Review
  10. Review
  11. Article
  12. The Role of Respiratory Microbiota in Lung Cancer.International journal of biological sciences · 2021
    Review
  13. Analysis of airway microbiota in adults from a Brazilian cystic fibrosis center.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2020
    Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. 16S rRNA gene sequencing reveals site-specific signatures of the upper and lower airways of cystic fibrosis patients.Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2018
    Article
  20. Article

7 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

4 authors at 1 institution in 1 country.

Paul C BlaineyDepartment of Bioengineering, Stanford University, Stanford, CA 94305, USA.
Carlos E Milla
David N Cornfield
Stephen R Quake
Stanford University · US

Funding

NIH Director's Pioneer Award (RMI)DP1OD000251 · OD · STANFORD UNIVERSITY · PI QUAKE, STEPHEN R · 2004 to 2008
$3.9M
Molecular regulation of pulmonary vascular KCa ChannelsR01HL070628 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI CORNFIELD, DAVID N. · 2003 to 2015
$2.8M
Optimization of a microfluidic device for single bacterial cell genomicsR01HG004863 · NHGRI · STANFORD UNIVERSITY · PI RELMAN, DAVID A. · 2008 to 2010
$1.8M
NHGRI NIH HHS 5R01HG004863-02NHGRI NIH HHS R01 HG004863NHLBI NIH HHS R01 HL070628NIH HHS DP1 OD000251
6 · The paper itself

Abstract

Cystic fibrosis (CF) is an autosomal recessive disease caused by mutations in the gene encoding the CF transmembrane conductance regulator. Disruption of electrolyte homeostasis at mucosal surfaces leads to severe lung, pancreatic, intestinal, hepatic, and reproductive abnormalities. Loss of lung function as a result of chronic lung disease is the primary cause of death from CF. Using high-throughput sequencing to survey microbes in the sputum of 16 CF patients and 9 control individuals, we identified diverse microbial communities in the healthy samples, contravening conventional wisdom that healthy airways are not significantly colonized. Comparing these communities with those from the CF patients revealed significant differences in microbial ecology, including differential representation of uncultivated phylotypes. Despite patient-specific differences, our analysis revealed a focal microbial profile characteristic of CF. The profile differentiated case and control groups even when classically recognized CF pathogens were excluded. As a control, lung explant tissues were also processed from a group of patients with pulmonary disease. The findings in lung tissue corroborated the presence of taxa identified in the sputum samples. Comparing the sequencing results with clinical data indicated that diminished microbial diversity is associated with severity of pulmonary inflammation within our adult CF cohort.

Indexed as

AdultBacteriaBase SequenceCase-Control StudiesCystic FibrosisFemaleForced Expiratory VolumeHumansLungMalePhylogenyPrincipal Component AnalysisRNA, Ribosomal, 16SVital CapacityRNA, Ribosomal, 16S

Identifiers

PMID23019655
PMCPMC3898170
OpenAlexW2143194130

What OpenQuestion holds

Textmetadata
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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.