Titre
Azithromycin alters spatial and temporal dynamics of airway microbiota in idiopathic pulmonary fibrosis.
Type
article
Institution
UNIL/CHUV/Unisanté + institutions partenaires
Périodique
Auteur(s)
Gijs, P.J.
Auteure/Auteur
Daccord, C.
Auteure/Auteur
Bernasconi, E.
Auteure/Auteur
Brutsche, M.
Auteure/Auteur
Clarenbach, C.F.
Auteure/Auteur
Hostettler, K.
Auteure/Auteur
Guler, S.A.
Auteure/Auteur
Mercier, L.
Auteure/Auteur
Ubags, N.
Auteure/Auteur
Funke-Chambour, M.
Auteure/Auteur
von Garnier, C.
Auteure/Auteur
Liens vers les personnes
Liens vers les unités
ISSN
2312-0541
Statut éditorial
Publié
Date de publication
2023-05
Volume
9
Numéro
3
Première page
00720
Dernière page/numéro d’article
2022
Peer-reviewed
Oui
Langue
anglais
Notes
Publication types: Journal Article
Publication Status: epublish
Publication Status: epublish
Résumé
High bacterial burden in the lung microbiota predicts progression of idiopathic pulmonary fibrosis (IPF). Azithromycin (AZT) is a macrolide antibiotic known to alter the lung microbiota in several chronic pulmonary diseases, and observational studies have shown a positive effect of AZT on mortality and hospitalisation rate in IPF. However, the effect of AZT on the lung microbiota in IPF remains unknown.
We sought to determine the impact of a 3-month course of AZT on the lung microbiota in IPF. We assessed sputum and oropharyngeal swab specimens from 24 adults with IPF included in a randomised controlled crossover trial of oral AZT 500 mg 3 times per week. 16S rRNA gene amplicon sequencing and quantitative PCR (qPCR) were performed to assess bacterial communities. Antibiotic resistance genes (ARGs) were assessed using real-time qPCR.
AZT significantly decreased community diversity with a stronger and more persistent effect in the lower airways (sputum). AZT treatment altered the temporal kinetics of the upper (oropharyngeal swab) and lower airway microbiota, increasing community similarity between the two sites for 1 month after macrolide cessation. Patients with an increase in ARG carriage had lower bacterial density and enrichment of the genus Streptococcus. In contrast, patients with more stable ARG carriage had higher bacterial density and enrichment in Prevotella.
AZT caused sustained changes in the diversity and composition of the upper and lower airway microbiota in IPF, with effects on the temporal and spatial dynamics between the two sites.
We sought to determine the impact of a 3-month course of AZT on the lung microbiota in IPF. We assessed sputum and oropharyngeal swab specimens from 24 adults with IPF included in a randomised controlled crossover trial of oral AZT 500 mg 3 times per week. 16S rRNA gene amplicon sequencing and quantitative PCR (qPCR) were performed to assess bacterial communities. Antibiotic resistance genes (ARGs) were assessed using real-time qPCR.
AZT significantly decreased community diversity with a stronger and more persistent effect in the lower airways (sputum). AZT treatment altered the temporal kinetics of the upper (oropharyngeal swab) and lower airway microbiota, increasing community similarity between the two sites for 1 month after macrolide cessation. Patients with an increase in ARG carriage had lower bacterial density and enrichment of the genus Streptococcus. In contrast, patients with more stable ARG carriage had higher bacterial density and enrichment in Prevotella.
AZT caused sustained changes in the diversity and composition of the upper and lower airway microbiota in IPF, with effects on the temporal and spatial dynamics between the two sites.
PID Serval
serval:BIB_A193A919A5E2
PMID
Open Access
Oui
Date de création
2023-06-05T13:51:32.976Z
Date de création dans IRIS
2025-05-20T23:08:11Z
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Article.pdf
Version du manuscrit
preprint
Licence
https://creativecommons.org/licenses/by/4.0
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1.41 MB
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Adobe PDF
PID Serval
serval:BIB_A193A919A5E2.P001
URN
urn:nbn:ch:serval-BIB_A193A919A5E20
Somme de contrôle
(MD5):deabb4586295724f8f4979964496cbc4
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Imprimatur.pdf
Version du manuscrit
preprint
Taille
69.05 KB
Format
Adobe PDF
PID Serval
serval:BIB_A193A919A5E2.S001
Somme de contrôle
(MD5):14ce6d619f9e468c8ce0627156482a30