Cargando…

Bacterial biogeography of adult airways in atopic asthma

BACKGROUND: Perturbations to the composition and function of bronchial bacterial communities appear to contribute to the pathophysiology of asthma. Unraveling the nature and mechanisms of these complex associations will require large longitudinal studies, for which bronchoscopy is poorly suited. Stu...

Descripción completa

Detalles Bibliográficos
Autores principales: Durack, Juliana, Huang, Yvonne J., Nariya, Snehal, Christian, Laura S., Mark Ansel, K., Beigelman, Avraham, Castro, Mario, Dyer, Anne-Marie, Israel, Elliot, Kraft, Monica, Martin, Richard J., Mauger, David T., Rosenberg, Sharon R., King, Tonya S., White, Steven R., Denlinger, Loren C., Holguin, Fernando, Lazarus, Stephen C., Lugogo, Njira, Peters, Stephen P., Smith, Lewis J., Wechsler, Michael E., Lynch, Susan V., Boushey, Homer A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5994066/
https://www.ncbi.nlm.nih.gov/pubmed/29885665
http://dx.doi.org/10.1186/s40168-018-0487-3
_version_ 1783330348946423808
author Durack, Juliana
Huang, Yvonne J.
Nariya, Snehal
Christian, Laura S.
Mark Ansel, K.
Beigelman, Avraham
Castro, Mario
Dyer, Anne-Marie
Israel, Elliot
Kraft, Monica
Martin, Richard J.
Mauger, David T.
Rosenberg, Sharon R.
King, Tonya S.
White, Steven R.
Denlinger, Loren C.
Holguin, Fernando
Lazarus, Stephen C.
Lugogo, Njira
Peters, Stephen P.
Smith, Lewis J.
Wechsler, Michael E.
Lynch, Susan V.
Boushey, Homer A.
author_facet Durack, Juliana
Huang, Yvonne J.
Nariya, Snehal
Christian, Laura S.
Mark Ansel, K.
Beigelman, Avraham
Castro, Mario
Dyer, Anne-Marie
Israel, Elliot
Kraft, Monica
Martin, Richard J.
Mauger, David T.
Rosenberg, Sharon R.
King, Tonya S.
White, Steven R.
Denlinger, Loren C.
Holguin, Fernando
Lazarus, Stephen C.
Lugogo, Njira
Peters, Stephen P.
Smith, Lewis J.
Wechsler, Michael E.
Lynch, Susan V.
Boushey, Homer A.
author_sort Durack, Juliana
collection PubMed
description BACKGROUND: Perturbations to the composition and function of bronchial bacterial communities appear to contribute to the pathophysiology of asthma. Unraveling the nature and mechanisms of these complex associations will require large longitudinal studies, for which bronchoscopy is poorly suited. Studies of samples obtained by sputum induction and nasopharyngeal brushing or lavage have also reported asthma-associated microbiota characteristics. It remains unknown, however, whether the microbiota detected in these less-invasive sample types reflect the composition of bronchial microbiota in asthma. RESULTS: Bacterial microbiota in paired protected bronchial brushings (BB; n = 45), induced sputum (IS; n = 45), oral wash (OW; n = 45), and nasal brushings (NB; n = 27) from adults with mild atopic asthma (AA), atopy without asthma (ANA), and healthy controls (HC) were profiled using 16S rRNA gene sequencing. Though microbiota composition varied with sample type (p < 0.001), compositional similarity was greatest for BB-IS, particularly in AAs and ANAs. The abundance of genera detected in BB correlated with those detected in IS and OW (r median [IQR] 0.869 [0.748–0.942] and 0.822 [0.687–0.909] respectively), but not with those in NB (r = 0.004 [− 0.003–0.011]). The number of taxa shared between IS-BB and NB-BB was greater in AAs than in HCs (p < 0.05) and included taxa previously associated with asthma. Of the genera abundant in NB, only Moraxella correlated positively with abundance in BB; specific members of this genus were shared between the two compartments only in AAs. Relative abundance of Moraxella in NB of AAs correlated negatively with that of Corynebacterium but positively with markers of eosinophilic inflammation in the blood and BAL fluid. The genus, Corynebacterium, trended to dominate all NB samples of HCs but only half of AAs (p = 0.07), in whom abundance of this genus was negatively associated with markers of eosinophilic inflammation. CONCLUSIONS: Induced sputum is superior to nasal brush or oral wash for assessing bronchial microbiota composition in asthmatic adults. Although compositionally similar to the bronchial microbiota, the microbiota in induced sputum are distinct, reflecting enrichment of oral bacteria. Specific bacterial genera are shared between the nasal and the bronchial mucosa which are associated with markers of systemic and bronchial inflammation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40168-018-0487-3) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5994066
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-59940662018-06-21 Bacterial biogeography of adult airways in atopic asthma Durack, Juliana Huang, Yvonne J. Nariya, Snehal Christian, Laura S. Mark Ansel, K. Beigelman, Avraham Castro, Mario Dyer, Anne-Marie Israel, Elliot Kraft, Monica Martin, Richard J. Mauger, David T. Rosenberg, Sharon R. King, Tonya S. White, Steven R. Denlinger, Loren C. Holguin, Fernando Lazarus, Stephen C. Lugogo, Njira Peters, Stephen P. Smith, Lewis J. Wechsler, Michael E. Lynch, Susan V. Boushey, Homer A. Microbiome Research BACKGROUND: Perturbations to the composition and function of bronchial bacterial communities appear to contribute to the pathophysiology of asthma. Unraveling the nature and mechanisms of these complex associations will require large longitudinal studies, for which bronchoscopy is poorly suited. Studies of samples obtained by sputum induction and nasopharyngeal brushing or lavage have also reported asthma-associated microbiota characteristics. It remains unknown, however, whether the microbiota detected in these less-invasive sample types reflect the composition of bronchial microbiota in asthma. RESULTS: Bacterial microbiota in paired protected bronchial brushings (BB; n = 45), induced sputum (IS; n = 45), oral wash (OW; n = 45), and nasal brushings (NB; n = 27) from adults with mild atopic asthma (AA), atopy without asthma (ANA), and healthy controls (HC) were profiled using 16S rRNA gene sequencing. Though microbiota composition varied with sample type (p < 0.001), compositional similarity was greatest for BB-IS, particularly in AAs and ANAs. The abundance of genera detected in BB correlated with those detected in IS and OW (r median [IQR] 0.869 [0.748–0.942] and 0.822 [0.687–0.909] respectively), but not with those in NB (r = 0.004 [− 0.003–0.011]). The number of taxa shared between IS-BB and NB-BB was greater in AAs than in HCs (p < 0.05) and included taxa previously associated with asthma. Of the genera abundant in NB, only Moraxella correlated positively with abundance in BB; specific members of this genus were shared between the two compartments only in AAs. Relative abundance of Moraxella in NB of AAs correlated negatively with that of Corynebacterium but positively with markers of eosinophilic inflammation in the blood and BAL fluid. The genus, Corynebacterium, trended to dominate all NB samples of HCs but only half of AAs (p = 0.07), in whom abundance of this genus was negatively associated with markers of eosinophilic inflammation. CONCLUSIONS: Induced sputum is superior to nasal brush or oral wash for assessing bronchial microbiota composition in asthmatic adults. Although compositionally similar to the bronchial microbiota, the microbiota in induced sputum are distinct, reflecting enrichment of oral bacteria. Specific bacterial genera are shared between the nasal and the bronchial mucosa which are associated with markers of systemic and bronchial inflammation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40168-018-0487-3) contains supplementary material, which is available to authorized users. BioMed Central 2018-06-09 /pmc/articles/PMC5994066/ /pubmed/29885665 http://dx.doi.org/10.1186/s40168-018-0487-3 Text en © The Author(s). 2018 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
Durack, Juliana
Huang, Yvonne J.
Nariya, Snehal
Christian, Laura S.
Mark Ansel, K.
Beigelman, Avraham
Castro, Mario
Dyer, Anne-Marie
Israel, Elliot
Kraft, Monica
Martin, Richard J.
Mauger, David T.
Rosenberg, Sharon R.
King, Tonya S.
White, Steven R.
Denlinger, Loren C.
Holguin, Fernando
Lazarus, Stephen C.
Lugogo, Njira
Peters, Stephen P.
Smith, Lewis J.
Wechsler, Michael E.
Lynch, Susan V.
Boushey, Homer A.
Bacterial biogeography of adult airways in atopic asthma
title Bacterial biogeography of adult airways in atopic asthma
title_full Bacterial biogeography of adult airways in atopic asthma
title_fullStr Bacterial biogeography of adult airways in atopic asthma
title_full_unstemmed Bacterial biogeography of adult airways in atopic asthma
title_short Bacterial biogeography of adult airways in atopic asthma
title_sort bacterial biogeography of adult airways in atopic asthma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5994066/
https://www.ncbi.nlm.nih.gov/pubmed/29885665
http://dx.doi.org/10.1186/s40168-018-0487-3
work_keys_str_mv AT durackjuliana bacterialbiogeographyofadultairwaysinatopicasthma
AT huangyvonnej bacterialbiogeographyofadultairwaysinatopicasthma
AT nariyasnehal bacterialbiogeographyofadultairwaysinatopicasthma
AT christianlauras bacterialbiogeographyofadultairwaysinatopicasthma
AT markanselk bacterialbiogeographyofadultairwaysinatopicasthma
AT beigelmanavraham bacterialbiogeographyofadultairwaysinatopicasthma
AT castromario bacterialbiogeographyofadultairwaysinatopicasthma
AT dyerannemarie bacterialbiogeographyofadultairwaysinatopicasthma
AT israelelliot bacterialbiogeographyofadultairwaysinatopicasthma
AT kraftmonica bacterialbiogeographyofadultairwaysinatopicasthma
AT martinrichardj bacterialbiogeographyofadultairwaysinatopicasthma
AT maugerdavidt bacterialbiogeographyofadultairwaysinatopicasthma
AT rosenbergsharonr bacterialbiogeographyofadultairwaysinatopicasthma
AT kingtonyas bacterialbiogeographyofadultairwaysinatopicasthma
AT whitestevenr bacterialbiogeographyofadultairwaysinatopicasthma
AT denlingerlorenc bacterialbiogeographyofadultairwaysinatopicasthma
AT holguinfernando bacterialbiogeographyofadultairwaysinatopicasthma
AT lazarusstephenc bacterialbiogeographyofadultairwaysinatopicasthma
AT lugogonjira bacterialbiogeographyofadultairwaysinatopicasthma
AT petersstephenp bacterialbiogeographyofadultairwaysinatopicasthma
AT smithlewisj bacterialbiogeographyofadultairwaysinatopicasthma
AT wechslermichaele bacterialbiogeographyofadultairwaysinatopicasthma
AT lynchsusanv bacterialbiogeographyofadultairwaysinatopicasthma
AT bousheyhomera bacterialbiogeographyofadultairwaysinatopicasthma
AT bacterialbiogeographyofadultairwaysinatopicasthma