Evidence map›Paper›PMID 39816006›Full record

ArticleMycoses2025

Airway Mycobiota-Microbiota During Pulmonary Exacerbation of Cystic Fibrosis Patients: A Culture and Targeted Sequencing Study.

Cécile Angebault, Louise-Eva Vandenborght, Laurence Bassinet, Nathalie Wizla, Agnès Ferroni, Rodrigue Dessein, Natacha Remus, Caroline Thumerelle, Nathalie Fauchet, Ralph Epaud and 2 more

Abstract readMulticenter Study
In one paragraph

Article in Mycoses, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
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

12 authors.

Cécile AngebaultUnité de Parasitologie-Mycologie, Département de Prévention, Diagnostic et Traitement Des Infections, CHU Henri Mondor, Assistance Publique Des Hôpitaux de Paris (APHP), Creteil, France.ORCID https://orcid.org/0000-0001-7641-3002
Louise-Eva VandenborghtGenoScreen, Lille, France.
Laurence BassinetService de Pneumologie, Centre Hospitalier Intercommunal de Creteil, Creteil, France.
Nathalie WizlaService de Gastro-Entérologie, Hépatologie Pédiatrique, CHU Lille, Lille, France.
Agnès FerroniService de Microbiologie Clinique, CHU Necker-Enfants Malades, Assistance Publique Des Hôpitaux de Paris (APHP), Paris, France.
Rodrigue DesseinService de Bactériologie, CHU Lille, Lille, France.
Natacha RemusService de Pédiatrie Générale, Centre Hospitalier Intercommunal de Creteil, Creteil, France.
Caroline ThumerelleService de Pédiatrie, CHU Lille, Lille, France.
Nathalie FauchetService de Microbiologie, Centre Hospitalier Intercommunal de Creteil, Creteil, France.
Ralph EpaudService de Pédiatrie Générale, Centre Hospitalier Intercommunal de Creteil, Creteil, France.ORCID https://orcid.org/0000-0003-3830-1039
Laurence DelhaesService de Parasitologie-Mycologie, CHU Bordeaux, Groupe Hospitalier Pellegrin, Bordeaux, France.
Françoise BotterelUnité de Parasitologie-Mycologie, Département de Prévention, Diagnostic et Traitement Des Infections, CHU Henri Mondor, Assistance Publique Des Hôpitaux de Paris (APHP), Creteil, France.

Funding

Association Vaincre la Mucoviscidose 2013/2013-047/03
6 · The paper itself

Abstract

backgroundThe airways of patients with cystic fibrosis (pwCF) harbour complex fungal and bacterial microbiota involved in pulmonary exacerbations (PEx) and requiring antimicrobial treatment. Descriptive studies analysing bacterial and fungal microbiota concomitantly are scarce, especially using both culture and high-throughput-sequencing (HTS).

objectivesWe analysed bacterial-fungal microbiota and inter-kingdom correlations in two French CF centres according to clinical parameters and antimicrobial choices.

methodsForty-eight pwCF with PEx from Creteil (n = 24) and Lille (n = 24) CF centres were included over 2 years. Sputa were collected for culture and targeted-HTS (ITS2 and V3-V4 targets). Sequencing and culture data, along with clinical, radiological and treatment data, were analysed. Two-level stratified analysis was performed to study potential confounding factors (age, CF mutation, FEV1 and antibiotics) on the centre factor. Inter-kingdom correlations were analysed.

resultsSignificant differences in the bacterial microbiota profile were found between centres (p-value = 0.03). For mycobiota, the taxonomic distribution and diversity were comparable. HTS provided concordant but more detailed information than culture and increased detection of main CF fungi (> 25% more positive samples for Aspergillus or Scedosporium). FEV1 and systemic antibiotic before PEx influenced bacterial microbiota, but no clinical association was found with the mycobiota. No inter-kingdom correlation between Pseudomonas and fungi was found.

conclusionsDescribing concomitant bacterial and fungal communities of pwCF at the beginning of PEx using culture and HTS shows greater diversity in HTS and better detection in case of low microbial load. Interesting inter-kingdom correlations were observed, requiring further research on larger cohorts to understand the potential microbial interactions.

Indexed as

BacteriaCystic FibrosisFungiMicrobiotaMycobiomeAdolescentAdultAnti-Bacterial AgentsChildFemaleFranceHigh-Throughput Nucleotide SequencingHumansMaleMiddle AgedSputumAnti-Bacterial AgentsAspergillusCandidacolonizationcystic fibrosisinternal transcribed spacerpneumoniaScedosporium apiospermum

Identifiers

PMID39816006
PMCPMC11736540

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.