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The effects of inhaled aztreonam on the cystic fibrosis lung microbiome

BACKGROUND: Aztreonam lysine for inhalation (AZLI) is an inhaled antibiotic used to treat chronic Pseudomonas aeruginosa infection in CF. AZLI improves lung function and quality of life, and reduces exacerbations-improvements attributed to its antipseudomonal activity. Given the extremely high aztre...

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Autores principales: Heirali, Alya A., Workentine, Matthew L., Acosta, Nicole, Poonja, Ali, Storey, Douglas G., Somayaji, Ranjani, Rabin, Harvey R., Whelan, Fiona J., Surette, Michael G., Parkins, Michael D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5420135/
https://www.ncbi.nlm.nih.gov/pubmed/28476135
http://dx.doi.org/10.1186/s40168-017-0265-7
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author Heirali, Alya A.
Workentine, Matthew L.
Acosta, Nicole
Poonja, Ali
Storey, Douglas G.
Somayaji, Ranjani
Rabin, Harvey R.
Whelan, Fiona J.
Surette, Michael G.
Parkins, Michael D.
author_facet Heirali, Alya A.
Workentine, Matthew L.
Acosta, Nicole
Poonja, Ali
Storey, Douglas G.
Somayaji, Ranjani
Rabin, Harvey R.
Whelan, Fiona J.
Surette, Michael G.
Parkins, Michael D.
author_sort Heirali, Alya A.
collection PubMed
description BACKGROUND: Aztreonam lysine for inhalation (AZLI) is an inhaled antibiotic used to treat chronic Pseudomonas aeruginosa infection in CF. AZLI improves lung function and quality of life, and reduces exacerbations-improvements attributed to its antipseudomonal activity. Given the extremely high aztreonam concentrations achieved in the lower airways by nebulization, we speculate this may extend its spectrum of activity to other organisms. As such, we sought to determine if AZLI affects the CF lung microbiome and whether community constituents can be used to predict treatment responsiveness. METHODS: Patients were included if they had chronic P. aeruginosa infection and repeated sputum samples collected before and after AZLI. Sputum DNA was extracted, and the V3-hypervariable region of the 16S ribosomal RNA (rRNA) gene amplified and sequenced. RESULTS: Twenty-four patients naïve to AZLI contributed 162 samples. The cohort had a median age of 37.1 years, and a  median FEV(1) of 44% predicted. Fourteen patients were a priori defined as responders for achieving ≥3% FEV(1) improvement following initiation. No significant changes in alpha diversity were noted following AZLI. Furthermore, beta diversity demonstrated clustering with respect to patients, but had no association with AZLI use. However, we did observe a decline in the relative abundance of several individual operational taxonomic units (OTUs) following AZLI initiation suggesting that specific sub-populations of organisms may be impacted. Patients with higher abundance of Staphylococcus and anaerobic organisms including Prevotella and Fusobacterium were less likely to respond to therapy. CONCLUSIONS: Results from our study suggest potential alternate/additional mechanisms by which AZLI functions. Moreover, our study suggests that the CF microbiota may be used as a biomarker to predict patient responsiveness to therapy suggesting the microbiome may be harnessed for the personalization of therapies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40168-017-0265-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-54201352017-05-08 The effects of inhaled aztreonam on the cystic fibrosis lung microbiome Heirali, Alya A. Workentine, Matthew L. Acosta, Nicole Poonja, Ali Storey, Douglas G. Somayaji, Ranjani Rabin, Harvey R. Whelan, Fiona J. Surette, Michael G. Parkins, Michael D. Microbiome Research BACKGROUND: Aztreonam lysine for inhalation (AZLI) is an inhaled antibiotic used to treat chronic Pseudomonas aeruginosa infection in CF. AZLI improves lung function and quality of life, and reduces exacerbations-improvements attributed to its antipseudomonal activity. Given the extremely high aztreonam concentrations achieved in the lower airways by nebulization, we speculate this may extend its spectrum of activity to other organisms. As such, we sought to determine if AZLI affects the CF lung microbiome and whether community constituents can be used to predict treatment responsiveness. METHODS: Patients were included if they had chronic P. aeruginosa infection and repeated sputum samples collected before and after AZLI. Sputum DNA was extracted, and the V3-hypervariable region of the 16S ribosomal RNA (rRNA) gene amplified and sequenced. RESULTS: Twenty-four patients naïve to AZLI contributed 162 samples. The cohort had a median age of 37.1 years, and a  median FEV(1) of 44% predicted. Fourteen patients were a priori defined as responders for achieving ≥3% FEV(1) improvement following initiation. No significant changes in alpha diversity were noted following AZLI. Furthermore, beta diversity demonstrated clustering with respect to patients, but had no association with AZLI use. However, we did observe a decline in the relative abundance of several individual operational taxonomic units (OTUs) following AZLI initiation suggesting that specific sub-populations of organisms may be impacted. Patients with higher abundance of Staphylococcus and anaerobic organisms including Prevotella and Fusobacterium were less likely to respond to therapy. CONCLUSIONS: Results from our study suggest potential alternate/additional mechanisms by which AZLI functions. Moreover, our study suggests that the CF microbiota may be used as a biomarker to predict patient responsiveness to therapy suggesting the microbiome may be harnessed for the personalization of therapies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40168-017-0265-7) contains supplementary material, which is available to authorized users. BioMed Central 2017-05-05 /pmc/articles/PMC5420135/ /pubmed/28476135 http://dx.doi.org/10.1186/s40168-017-0265-7 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Research
Heirali, Alya A.
Workentine, Matthew L.
Acosta, Nicole
Poonja, Ali
Storey, Douglas G.
Somayaji, Ranjani
Rabin, Harvey R.
Whelan, Fiona J.
Surette, Michael G.
Parkins, Michael D.
The effects of inhaled aztreonam on the cystic fibrosis lung microbiome
title The effects of inhaled aztreonam on the cystic fibrosis lung microbiome
title_full The effects of inhaled aztreonam on the cystic fibrosis lung microbiome
title_fullStr The effects of inhaled aztreonam on the cystic fibrosis lung microbiome
title_full_unstemmed The effects of inhaled aztreonam on the cystic fibrosis lung microbiome
title_short The effects of inhaled aztreonam on the cystic fibrosis lung microbiome
title_sort effects of inhaled aztreonam on the cystic fibrosis lung microbiome
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5420135/
https://www.ncbi.nlm.nih.gov/pubmed/28476135
http://dx.doi.org/10.1186/s40168-017-0265-7
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