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Azithromycin and the microbiota of cystic fibrosis sputum
BACKGROUND: Azithromycin is commonly prescribed drug for individuals with cystic fibrosis (CF), with demonstrated benefits in reducing lung function decline, exacerbation occurrence and improving nutrition. As azithromycin has antimicrobial activity against components of the uncultured microbiome an...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8008652/ https://www.ncbi.nlm.nih.gov/pubmed/33784986 http://dx.doi.org/10.1186/s12866-021-02159-5 |
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author | Acosta, Nicole Thornton, Christina S. Surette, Michael G. Somayaji, Ranjani Rossi, Laura Rabin, Harvey R. Parkins, Michael D. |
author_facet | Acosta, Nicole Thornton, Christina S. Surette, Michael G. Somayaji, Ranjani Rossi, Laura Rabin, Harvey R. Parkins, Michael D. |
author_sort | Acosta, Nicole |
collection | PubMed |
description | BACKGROUND: Azithromycin is commonly prescribed drug for individuals with cystic fibrosis (CF), with demonstrated benefits in reducing lung function decline, exacerbation occurrence and improving nutrition. As azithromycin has antimicrobial activity against components of the uncultured microbiome and increasingly the CF microbiome is implicated in disease pathogenesis – we postulated azithromycin may act through its manipulation. Herein we sought to determine if the CF microbiome changed following azithromycin use and if clinical benefit observed during azithromycin use associated with baseline community structure. RESULTS: Drawing from a prospectively collected biobank we identified patients with sputum samples prior to, during and after initiating azithromycin and determined the composition of the CF microbial community by sequencing the V3-V4 region of the 16S rRNA gene. We categorized patients as responders if their rate of lung function decline improved after azithromycin initiation. Thirty-eight adults comprised our cohort, nine who had not utilized azithromycin in at least 3 years, and 29 who were completely naïve. We did not observe a major impact in the microbial community structure of CF sputum in the 2 years following azithromycin usage in either alpha or beta-diversity metrics. Seventeen patients (45%) were classified as Responders – demonstrating reduced lung function decline after azithromycin. Responders who were naïve to azithromycin had a modest clustering effect distinguishing them from those who were non-Responders, and had communities enriched with several organisms including Stenotrophomonas, but not Pseudomonas. CONCLUSIONS: Azithromycin treatment did not associate with subsequent large changes in the CF microbiome structure. However, we found that baseline community structure associated with subsequent azithromycin response in CF adults. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-021-02159-5. |
format | Online Article Text |
id | pubmed-8008652 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-80086522021-03-31 Azithromycin and the microbiota of cystic fibrosis sputum Acosta, Nicole Thornton, Christina S. Surette, Michael G. Somayaji, Ranjani Rossi, Laura Rabin, Harvey R. Parkins, Michael D. BMC Microbiol Research Article BACKGROUND: Azithromycin is commonly prescribed drug for individuals with cystic fibrosis (CF), with demonstrated benefits in reducing lung function decline, exacerbation occurrence and improving nutrition. As azithromycin has antimicrobial activity against components of the uncultured microbiome and increasingly the CF microbiome is implicated in disease pathogenesis – we postulated azithromycin may act through its manipulation. Herein we sought to determine if the CF microbiome changed following azithromycin use and if clinical benefit observed during azithromycin use associated with baseline community structure. RESULTS: Drawing from a prospectively collected biobank we identified patients with sputum samples prior to, during and after initiating azithromycin and determined the composition of the CF microbial community by sequencing the V3-V4 region of the 16S rRNA gene. We categorized patients as responders if their rate of lung function decline improved after azithromycin initiation. Thirty-eight adults comprised our cohort, nine who had not utilized azithromycin in at least 3 years, and 29 who were completely naïve. We did not observe a major impact in the microbial community structure of CF sputum in the 2 years following azithromycin usage in either alpha or beta-diversity metrics. Seventeen patients (45%) were classified as Responders – demonstrating reduced lung function decline after azithromycin. Responders who were naïve to azithromycin had a modest clustering effect distinguishing them from those who were non-Responders, and had communities enriched with several organisms including Stenotrophomonas, but not Pseudomonas. CONCLUSIONS: Azithromycin treatment did not associate with subsequent large changes in the CF microbiome structure. However, we found that baseline community structure associated with subsequent azithromycin response in CF adults. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-021-02159-5. BioMed Central 2021-03-30 /pmc/articles/PMC8008652/ /pubmed/33784986 http://dx.doi.org/10.1186/s12866-021-02159-5 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Acosta, Nicole Thornton, Christina S. Surette, Michael G. Somayaji, Ranjani Rossi, Laura Rabin, Harvey R. Parkins, Michael D. Azithromycin and the microbiota of cystic fibrosis sputum |
title | Azithromycin and the microbiota of cystic fibrosis sputum |
title_full | Azithromycin and the microbiota of cystic fibrosis sputum |
title_fullStr | Azithromycin and the microbiota of cystic fibrosis sputum |
title_full_unstemmed | Azithromycin and the microbiota of cystic fibrosis sputum |
title_short | Azithromycin and the microbiota of cystic fibrosis sputum |
title_sort | azithromycin and the microbiota of cystic fibrosis sputum |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8008652/ https://www.ncbi.nlm.nih.gov/pubmed/33784986 http://dx.doi.org/10.1186/s12866-021-02159-5 |
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