Limited effects of azithromycin on the oropharyngeal microbiome in children with CF and early pseudomonas infection

Abstract Background Tobramycin inhalation solution (TIS) and chronic azithromycin (AZ) have known clinical benefits for children with CF, likely due to antimicrobial and anti-inflammatory activity. The effects of chronic AZ in combination with TIS on the airway microbiome have not been extensively i...

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Main Authors: Brandie D. Wagner, Edith T. Zemanick, Scott D. Sagel, Charles E. Robertson, Mark J. Stevens, Nicole Mayer-Hamblett, George Retsch-Bogart, Bonnie W. Ramsey, J. Kirk Harris
Format: Article
Language:English
Published: BMC 2023-10-01
Series:BMC Microbiology
Subjects:
Online Access:https://doi.org/10.1186/s12866-023-03073-8
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author Brandie D. Wagner
Edith T. Zemanick
Scott D. Sagel
Charles E. Robertson
Mark J. Stevens
Nicole Mayer-Hamblett
George Retsch-Bogart
Bonnie W. Ramsey
J. Kirk Harris
author_facet Brandie D. Wagner
Edith T. Zemanick
Scott D. Sagel
Charles E. Robertson
Mark J. Stevens
Nicole Mayer-Hamblett
George Retsch-Bogart
Bonnie W. Ramsey
J. Kirk Harris
author_sort Brandie D. Wagner
collection DOAJ
description Abstract Background Tobramycin inhalation solution (TIS) and chronic azithromycin (AZ) have known clinical benefits for children with CF, likely due to antimicrobial and anti-inflammatory activity. The effects of chronic AZ in combination with TIS on the airway microbiome have not been extensively investigated. Oropharyngeal swab samples were collected in the OPTIMIZE multicenter, randomized, placebo-controlled trial examining the addition of AZ to TIS in 198 children with CF and early P. aeruginosa infection. Bacterial small subunit rRNA gene community profiles were determined. The effects of TIS and AZ were assessed on oropharyngeal microbial diversity and composition to uncover whether effects on the bacterial community may be a mechanism of action related to the observed changes in clinical outcomes. Results Substantial changes in bacterial communities (total bacterial load, diversity and relative abundance of specific taxa) were observed by week 3 of TIS treatment for both the AZ and placebo groups. On average, these shifts were due to changes in non-traditional CF taxa that were not sustained at the later study visits (weeks 13 and 26). Bacterial community measures did not differ between the AZ and placebo groups. Conclusions This study provides further evidence that the mechanism for AZ’s effect on clinical outcomes is not due solely to action on airway microbial composition.
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spelling doaj.art-d5da65057c594b7ab884fe12599e5df72023-10-29T12:16:24ZengBMCBMC Microbiology1471-21802023-10-0123111110.1186/s12866-023-03073-8Limited effects of azithromycin on the oropharyngeal microbiome in children with CF and early pseudomonas infectionBrandie D. Wagner0Edith T. Zemanick1Scott D. Sagel2Charles E. Robertson3Mark J. Stevens4Nicole Mayer-Hamblett5George Retsch-Bogart6Bonnie W. Ramsey7J. Kirk Harris8Department of Biostatistics and Informatics, Colorado School of Public Health, University of ColoradoChildren’s Hospital ColoradoChildren’s Hospital ColoradoDepartment of Infectious Diseases, University of ColoradoChildren’s Hospital ColoradoDepartment of Pediatrics, University of WashingtonDepartment of Pediatrics, University of North CarolinaDepartment of Pediatrics, University of WashingtonChildren’s Hospital ColoradoAbstract Background Tobramycin inhalation solution (TIS) and chronic azithromycin (AZ) have known clinical benefits for children with CF, likely due to antimicrobial and anti-inflammatory activity. The effects of chronic AZ in combination with TIS on the airway microbiome have not been extensively investigated. Oropharyngeal swab samples were collected in the OPTIMIZE multicenter, randomized, placebo-controlled trial examining the addition of AZ to TIS in 198 children with CF and early P. aeruginosa infection. Bacterial small subunit rRNA gene community profiles were determined. The effects of TIS and AZ were assessed on oropharyngeal microbial diversity and composition to uncover whether effects on the bacterial community may be a mechanism of action related to the observed changes in clinical outcomes. Results Substantial changes in bacterial communities (total bacterial load, diversity and relative abundance of specific taxa) were observed by week 3 of TIS treatment for both the AZ and placebo groups. On average, these shifts were due to changes in non-traditional CF taxa that were not sustained at the later study visits (weeks 13 and 26). Bacterial community measures did not differ between the AZ and placebo groups. Conclusions This study provides further evidence that the mechanism for AZ’s effect on clinical outcomes is not due solely to action on airway microbial composition.https://doi.org/10.1186/s12866-023-03073-8MicrobiomeOropharyngeal swabMacrolidesPulmonary exacerbationTobramycinBeta diversity
spellingShingle Brandie D. Wagner
Edith T. Zemanick
Scott D. Sagel
Charles E. Robertson
Mark J. Stevens
Nicole Mayer-Hamblett
George Retsch-Bogart
Bonnie W. Ramsey
J. Kirk Harris
Limited effects of azithromycin on the oropharyngeal microbiome in children with CF and early pseudomonas infection
BMC Microbiology
Microbiome
Oropharyngeal swab
Macrolides
Pulmonary exacerbation
Tobramycin
Beta diversity
title Limited effects of azithromycin on the oropharyngeal microbiome in children with CF and early pseudomonas infection
title_full Limited effects of azithromycin on the oropharyngeal microbiome in children with CF and early pseudomonas infection
title_fullStr Limited effects of azithromycin on the oropharyngeal microbiome in children with CF and early pseudomonas infection
title_full_unstemmed Limited effects of azithromycin on the oropharyngeal microbiome in children with CF and early pseudomonas infection
title_short Limited effects of azithromycin on the oropharyngeal microbiome in children with CF and early pseudomonas infection
title_sort limited effects of azithromycin on the oropharyngeal microbiome in children with cf and early pseudomonas infection
topic Microbiome
Oropharyngeal swab
Macrolides
Pulmonary exacerbation
Tobramycin
Beta diversity
url https://doi.org/10.1186/s12866-023-03073-8
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