Evidence map›Paper›PMID 25878338›Full record

ArticleJournal of clinical microbiology2015

Rapid Detection of Emerging Pathogens and Loss of Microbial Diversity Associated with Severe Lung Disease in Cystic Fibrosis.

William G Flight, Ann Smith, Christopher Paisey, Julian R Marchesi, Matthew J Bull, Phillip J Norville, Ken J Mutton, A Kevin Webb, Rowland J Bright-Thomas, Andrew M Jones and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of clinical microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 1 pooled it
8.1field-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

55 citing papers in PubMed, 1 synthesis or guideline pooled it, 105 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Journal of bacteriology · 2026
    Article
  5. Article
  6. Review
  7. The cystic fibrosis pathogenJournal of medical microbiology · 2025
    Article
  8. Article
  9. Journal of bacteriology · 2025
    Article
  10. Article
  11. Article
  12. Review
  13. Changing profile of bacterial infection and microbiome in cystic fibrosis: when to use antibiotics in the era of CFTR-modulator therapy.European respiratory review : an official journal of the European Respiratory Society · 2024
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. A clinicians' review of the respiratory microbiome.Breathe (Sheffield, England) · 2022
    Review
  19. Commensal Bacteria in the Cystic Fibrosis Airway Microbiome ReduceFrontiers in cellular and infection microbiology · 2022
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

William G FlightUniversity Hospital of South Manchester NHS Foundation Trust, Manchester, United Kingdom Institute of Inflammation & Repair, University of Manchester, Manchester, United Kingdom Oxford University Hospitals NHS Trust, Oxford, United Kingdom.
Ann SmithOrganisms and Environment Division, School of Biosciences, Cardiff University, Cardiff, United Kingdom.
Christopher PaiseyOrganisms and Environment Division, School of Biosciences, Cardiff University, Cardiff, United Kingdom.
Julian R MarchesiOrganisms and Environment Division, School of Biosciences, Cardiff University, Cardiff, United Kingdom Department of Hepatology & Gastroenterology, St. Mary's Hospital, Imperial College London, London, United Kingdom.
Matthew J BullOrganisms and Environment Division, School of Biosciences, Cardiff University, Cardiff, United Kingdom.
Phillip J NorvilleOrganisms and Environment Division, School of Biosciences, Cardiff University, Cardiff, United Kingdom.
Ken J MuttonInstitute of Inflammation & Repair, University of Manchester, Manchester, United Kingdom Central Manchester University Hospitals NHS Foundation Trust and Public Health England Laboratory, Manchester, United Kingdom.
A Kevin WebbUniversity Hospital of South Manchester NHS Foundation Trust, Manchester, United Kingdom Institute of Inflammation & Repair, University of Manchester, Manchester, United Kingdom.
Rowland J Bright-ThomasUniversity Hospital of South Manchester NHS Foundation Trust, Manchester, United Kingdom Institute of Inflammation & Repair, University of Manchester, Manchester, United Kingdom.
Andrew M JonesUniversity Hospital of South Manchester NHS Foundation Trust, Manchester, United Kingdom Institute of Inflammation & Repair, University of Manchester, Manchester, United Kingdom.
Eshwar MahenthiralingamOrganisms and Environment Division, School of Biosciences, Cardiff University, Cardiff, United Kingdom MahenthiralingamE@cardiff.ac.uk.ORCID http://orcid.org/0000-0001-9014-3790
Cardiff University · GBUniversity of Manchester · GBSt Mary's Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Respiratory infection in cystic fibrosis (CF) is polymicrobial, but standard sputum microbiology does not account for the lung microbiome or detect changes in microbial diversity associated with disease. As a clinically applicable CF microbiome surveillance scheme, total sputum nucleic acids isolated by a standard high-throughput robotic method for accredited viral diagnosis were profiled for bacterial diversity using ribosomal intergenic spacer analysis (RISA) PCR. Conventional culture and RISA were performed on 200 paired sputum samples from 93 CF adults; pyrosequencing of the 16S rRNA gene was applied to 59 patients to systematically determine bacterial diversity. Compared to the microbiology data, RISA profiles clustered into two groups: the emerging nonfermenting Gram-negative organisms (eNFGN) and Pseudomonas groups. Patients who were culture positive for Burkholderia, Achromobacter, Stenotrophomonas, and Ralstonia clustered within the eNFGN group. Pseudomonas group RISA profiles were associated with Pseudomonas aeruginosa culture-positive patients. Sequence analysis confirmed the abundance of eNFGN genera and Pseudomonas within these respective groups. Low bacterial diversity was associated with severe lung disease (P < 0.001) and the presence of Burkholderia (P < 0.001). An absence of Streptococcus (P < 0.05) occurred in individuals with lung function in the lowest quartile. In summary, nucleic acids isolated from CF sputum can serve as a single template for both molecular virology and bacteriology, with a RISA PCR rapidly detecting the presence of dominant eNFGN pathogens or P. aeruginosa missed by culture (11% of cases). We provide guidance for how this straightforward CF microbiota profiling scheme may be adopted by clinical laboratories.

Indexed as

BiodiversityAdultAutomation, LaboratoryBacteriaCystic FibrosisFemaleHumansMaleMolecular Diagnostic TechniquesPneumonia, BacterialPneumonia, ViralSpecimen HandlingSputumVirusesYoung Adult

Identifiers

PMID25878338
PMCPMC4473198
OpenAlexW2096288151

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.