Evidence map›Paper›PMID 32635564›Full record

ArticleMicroorganisms2020

Untargeted Metagenomic Investigation of the Airway Microbiome of Cystic Fibrosis Patients with Moderate-Severe Lung Disease.

Giovanni Bacci, Giovanni Taccetti, Daniela Dolce, Federica Armanini, Nicola Segata, Francesca Di Cesare, Vincenzina Lucidi, Ersilia Fiscarelli, Patrizia Morelli, Rosaria Casciaro and 3 more

Open access · goldAbstract read
In one paragraph

Article in Microorganisms, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.5field-weighted citation impact, top 8% 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

20 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
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  8. 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
  9. Review
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  11. Article
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  15. Microorganisms · 2021
    Article
  16. Review
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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 at 6 institutions in 1 country.

Giovanni BacciDepartment of Biology, University of Florence, Sesto Fiorentino, 50019 Florence, Italy.ORCID 0000-0003-4406-7816
Giovanni TaccettiCystic Fibrosis Center, Anna Meyer Children's University Hospital, Department of Pediatrics Medicine, 50139 Florence, Italy.
Daniela DolceCystic Fibrosis Center, Anna Meyer Children's University Hospital, Department of Pediatrics Medicine, 50139 Florence, Italy.
Federica ArmaniniCentre for Integrative Biology, University of Trento, 38122 Trento, Italy.
Nicola SegataCentre for Integrative Biology, University of Trento, 38122 Trento, Italy.ORCID 0000-0002-1583-5794
Francesca Di CesareDepartment of Biology, University of Florence, Sesto Fiorentino, 50019 Florence, Italy.
Vincenzina LucidiChildren's Hospital and Research Institute Bambino Gesù, 00165 Rome, Italy.
Ersilia FiscarelliChildren's Hospital and Research Institute Bambino Gesù, 00165 Rome, Italy.
Patrizia MorelliCystic Fibrosis Center, IRCCS G. Gaslini Institute, Department of Pediatrics, 16147 Genoa, Italy.
Rosaria CasciaroCystic Fibrosis Center, IRCCS G. Gaslini Institute, Department of Pediatrics, 16147 Genoa, Italy.
Anna NegroniDepartment for Sustainability, Italian National Agency for New Technologies, Energy and Sustainable Economic Development, ENEA Casaccia Research Center, 00123 Rome, Italy.ORCID 0000-0002-2273-8837
Alessio MengoniDepartment of Biology, University of Florence, Sesto Fiorentino, 50019 Florence, Italy.ORCID 0000-0002-1265-8251
Annamaria BevivinoDepartment for Sustainability, Italian National Agency for New Technologies, Energy and Sustainable Economic Development, ENEA Casaccia Research Center, 00123 Rome, Italy.ORCID 0000-0003-4277-7048
University of Florence · ITBambino Gesù Children's Hospital · ITIstituto Giannina Gaslini · ITMeyer Children's Hospital · ITNational Agency for New Technologies, Energy and Sustainable Economic Development · ITUniversity of Trento · IT

Funding

Fondazione per la Ricerca sulla Fibrosi Cistica FFC#19/2017
6 · The paper itself

Abstract

Although the cystic fibrosis (CF) lung microbiota has been characterized in several studies, little is still known about the temporal changes occurring at the whole microbiome level using untargeted metagenomic analysis. The aim of this study was to investigate the taxonomic and functional temporal dynamics of the lower airway microbiome in a cohort of CF patients. Multiple sputum samples were collected over 15 months from 22 patients with advanced lung disease regularly attending three Italian CF Centers, given a total of 79 samples. DNA extracted from samples was subjected to shotgun metagenomic sequencing allowing both strain-level taxonomic profiling and assessment of the functional metagenomic repertoire. High inter-patient taxonomic heterogeneity was found with short-term compositional changes across clinical status. Each patient exhibited distinct sputum microbial communities at the taxonomic level, and strain-specific colonization of both traditional and atypical CF pathogens. A large core set of genes, including antibiotic resistance genes, were shared across patients despite observed differences in clinical status, and consistently detected in the lung microbiome of all subjects independently from known antibiotic exposure. In conclusion, an overall stability in the microbiome-associated genes was found despite taxonomic fluctuations of the communities.

Indexed as

airway microbiomeantibiotic resistance genescystic fibrosismetagenome composition

Identifiers

PMID32635564
PMCPMC7409339
OpenAlexW3040580712

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.