Azithromycin alters spatial and temporal dynamics of airway microbiota in idiopathic pulmonary fibrosis

Background 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...

Full description

Bibliographic Details
Main Authors: Pieter-Jan Gijs, Cécile Daccord, Eric Bernasconi, Martin Brutsche, Christian F. Clarenbach, Katrin Hostettler, Sabina A. Guler, Louis Mercier, Niki Ubags, Manuela Funke-Chambour, Christophe von Garnier
Format: Article
Language:English
Published: European Respiratory Society 2023-05-01
Series:ERJ Open Research
Online Access:http://openres.ersjournals.com/content/9/3/00720-2022.full
_version_ 1797689386513465344
author Pieter-Jan Gijs
Cécile Daccord
Eric Bernasconi
Martin Brutsche
Christian F. Clarenbach
Katrin Hostettler
Sabina A. Guler
Louis Mercier
Niki Ubags
Manuela Funke-Chambour
Christophe von Garnier
author_facet Pieter-Jan Gijs
Cécile Daccord
Eric Bernasconi
Martin Brutsche
Christian F. Clarenbach
Katrin Hostettler
Sabina A. Guler
Louis Mercier
Niki Ubags
Manuela Funke-Chambour
Christophe von Garnier
author_sort Pieter-Jan Gijs
collection DOAJ
description Background 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. Methods 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. Results 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. Conclusions 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.
first_indexed 2024-03-12T01:44:59Z
format Article
id doaj.art-fa18904419d44ceb858658e86c5de4eb
institution Directory Open Access Journal
issn 2312-0541
language English
last_indexed 2024-03-12T01:44:59Z
publishDate 2023-05-01
publisher European Respiratory Society
record_format Article
series ERJ Open Research
spelling doaj.art-fa18904419d44ceb858658e86c5de4eb2023-09-09T13:53:54ZengEuropean Respiratory SocietyERJ Open Research2312-05412023-05-019310.1183/23120541.00720-202200720-2022Azithromycin alters spatial and temporal dynamics of airway microbiota in idiopathic pulmonary fibrosisPieter-Jan Gijs0Cécile Daccord1Eric Bernasconi2Martin Brutsche3Christian F. Clarenbach4Katrin Hostettler5Sabina A. Guler6Louis Mercier7Niki Ubags8Manuela Funke-Chambour9Christophe von Garnier10 Division of Pulmonology, Department of Medicine, CHUV, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland Division of Pulmonology, Department of Medicine, CHUV, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland Division of Pulmonology, Department of Medicine, CHUV, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland Lungenzentrum, Kantonsspital St Gallen, St Gallen, Switzerland Division of Pulmonary Medicine, University Hospital of Zurich, Zurich, Switzerland Clinics of Respiratory Medicine, University Hospital Basel, Basel, Switzerland Department of Pulmonary Medicine, Inselspital, Bern University Hospital, Bern, Switzerland Division of Pulmonology, Department of Medicine, CHUV, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland Division of Pulmonology, Department of Medicine, CHUV, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland Department of Pulmonary Medicine, Inselspital, Bern University Hospital, Bern, Switzerland Division of Pulmonology, Department of Medicine, CHUV, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland Background 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. Methods 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. Results 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. Conclusions 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.http://openres.ersjournals.com/content/9/3/00720-2022.full
spellingShingle Pieter-Jan Gijs
Cécile Daccord
Eric Bernasconi
Martin Brutsche
Christian F. Clarenbach
Katrin Hostettler
Sabina A. Guler
Louis Mercier
Niki Ubags
Manuela Funke-Chambour
Christophe von Garnier
Azithromycin alters spatial and temporal dynamics of airway microbiota in idiopathic pulmonary fibrosis
ERJ Open Research
title Azithromycin alters spatial and temporal dynamics of airway microbiota in idiopathic pulmonary fibrosis
title_full Azithromycin alters spatial and temporal dynamics of airway microbiota in idiopathic pulmonary fibrosis
title_fullStr Azithromycin alters spatial and temporal dynamics of airway microbiota in idiopathic pulmonary fibrosis
title_full_unstemmed Azithromycin alters spatial and temporal dynamics of airway microbiota in idiopathic pulmonary fibrosis
title_short Azithromycin alters spatial and temporal dynamics of airway microbiota in idiopathic pulmonary fibrosis
title_sort azithromycin alters spatial and temporal dynamics of airway microbiota in idiopathic pulmonary fibrosis
url http://openres.ersjournals.com/content/9/3/00720-2022.full
work_keys_str_mv AT pieterjangijs azithromycinaltersspatialandtemporaldynamicsofairwaymicrobiotainidiopathicpulmonaryfibrosis
AT ceciledaccord azithromycinaltersspatialandtemporaldynamicsofairwaymicrobiotainidiopathicpulmonaryfibrosis
AT ericbernasconi azithromycinaltersspatialandtemporaldynamicsofairwaymicrobiotainidiopathicpulmonaryfibrosis
AT martinbrutsche azithromycinaltersspatialandtemporaldynamicsofairwaymicrobiotainidiopathicpulmonaryfibrosis
AT christianfclarenbach azithromycinaltersspatialandtemporaldynamicsofairwaymicrobiotainidiopathicpulmonaryfibrosis
AT katrinhostettler azithromycinaltersspatialandtemporaldynamicsofairwaymicrobiotainidiopathicpulmonaryfibrosis
AT sabinaaguler azithromycinaltersspatialandtemporaldynamicsofairwaymicrobiotainidiopathicpulmonaryfibrosis
AT louismercier azithromycinaltersspatialandtemporaldynamicsofairwaymicrobiotainidiopathicpulmonaryfibrosis
AT nikiubags azithromycinaltersspatialandtemporaldynamicsofairwaymicrobiotainidiopathicpulmonaryfibrosis
AT manuelafunkechambour azithromycinaltersspatialandtemporaldynamicsofairwaymicrobiotainidiopathicpulmonaryfibrosis
AT christophevongarnier azithromycinaltersspatialandtemporaldynamicsofairwaymicrobiotainidiopathicpulmonaryfibrosis