Evidence map›Paper›PMID 25898134›Full record

ArticlePloS one2015

Changes in cystic fibrosis airway microbial community associated with a severe decline in lung function.

Patrizia Paganin, Ersilia Vita Fiscarelli, Vanessa Tuccio, Manuela Chiancianesi, Giovanni Bacci, Patrizia Morelli, Daniela Dolce, Claudia Dalmastri, Alessandra De Alessandri, Vincenzina Lucidi and 3 more

Abstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing 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

38 citing papers in PubMed.

  1. Trial
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  12. Observational
  13. Review
  14. Bacterial Interactions withMicroorganisms · 2021
    Review
  15. Article
  16. Review
  17. Static Growth Promotes PrrF and 2-Alkyl-4(1Journal of bacteriology · 2020
    Article
  18. Article
  19. Article
  20. Article
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

13 authors.

Patrizia PaganinTechnical Unit for Sustainable Development and Innovation of Agro-Industrial System, ENEA (Italian National Agency for New Technologies, Energy and Sustainable Economic Development), Casaccia Research Center, Rome, Italy.
Ersilia Vita FiscarelliCystic Fibrosis Microbiology and Cystic Fibrosis Center, Children's Hospital and Research Institute Bambino Gesù, Rome, Italy.
Vanessa TuccioCystic Fibrosis Microbiology and Cystic Fibrosis Center, Children's Hospital and Research Institute Bambino Gesù, Rome, Italy.
Manuela ChiancianesiDepartment of Evolutionary Biology, University of Florence, Florence, Italy.
Giovanni BacciDepartment of Evolutionary Biology, University of Florence, Florence, Italy.
Patrizia MorelliDepartment of Pediatrics, Cystic Fibrosis Center, G. Gaslini Institute, Genoa, Italy.
Daniela DolceDepartment of Pediatrics, Cystic Fibrosis Center, Meyer Hospital, Florence, Italy.
Claudia DalmastriTechnical Unit for Sustainable Development and Innovation of Agro-Industrial System, ENEA (Italian National Agency for New Technologies, Energy and Sustainable Economic Development), Casaccia Research Center, Rome, Italy.
Alessandra De AlessandriDepartment of Pediatrics, Cystic Fibrosis Center, G. Gaslini Institute, Genoa, Italy.
Vincenzina LucidiCystic Fibrosis Microbiology and Cystic Fibrosis Center, Children's Hospital and Research Institute Bambino Gesù, Rome, Italy.
Giovanni TaccettiDepartment of Pediatrics, Cystic Fibrosis Center, Meyer Hospital, Florence, Italy.
Alessio MengoniDepartment of Evolutionary Biology, University of Florence, Florence, Italy.
Annamaria BevivinoTechnical Unit for Sustainable Development and Innovation of Agro-Industrial System, ENEA (Italian National Agency for New Technologies, Energy and Sustainable Economic Development), Casaccia Research Center, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cystic fibrosis (CF) is a genetic disease resulting in chronic polymicrobial infections of the airways and progressive decline in lung function. To gain insight into the underlying causes of severe lung diseases, we aimed at comparing the airway microbiota detected in sputum of CF patients with stable lung function (S) versus those with a substantial decline in lung function (SD). Microbiota composition was investigated by using culture-based and culture-independent methods, and by performing multivariate and statistical analyses. Culture-based methods identified some microbial species associated with a worse lung function, i.e. Pseudomonas aeruginosa, Rothia mucilaginosa, Streptococcus pneumoniae and Candida albicans, but only the presence of S. pneumoniae and R. mucilaginosa was found to be associated with increased severe decline in forced expiratory volume in 1 second (FEV1). Terminal-Restriction Fragment Length Polymorphism (T-RFLP) analysis revealed a higher bacterial diversity than that detected by culture-based methods. Molecular signatures with a statistically significant odds ratio for SD status were detected, and classified as Pseudomonas, Burkholderia and Shewanella, while for other Terminal Restriction Fragments (T-RFs) no species assignation was achieved. The analysis of T-RFLP data using ecological biodiversity indices showed reduced Evenness in SD patients compared to S ones, suggesting an impaired ecology of the bacterial community in SD patients. Statistically significant differences of the ecological biodiversity indices among the three sub-groups of FEV1 (normal/mild vs moderate vs severe) were also found, suggesting that the patients with moderate lung disease experienced changes in the airway assembly of taxa. Overall, changes in CF airway microbial community associated with a severe lung function decline were detected, allowing us to define some discriminatory species as well as some discriminatory T-RFs that represent good candidates for the development of predictive biomarkers of substantial decline in lung function.

Indexed as

AdolescentAdultBurkholderiaCandida albicansCystic FibrosisDisease ProgressionFemaleForced Expiratory VolumeHumansLungMaleMicrobiotaMolecular TypingPolymorphism, Restriction Fragment LengthPseudomonas aeruginosaShewanella

Identifiers

PMID25898134
PMCPMC4405530

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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.