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The Murine Lung Microbiome Changes During Lung Inflammation and Intranasal Vancomycin Treatment

Most microbiome research related to airway diseases has focused on the gut microbiome. This is despite advances in culture independent microbial identification techniques revealing that even healthy lungs possess a unique dynamic microbiome. This conceptual change raises the question; if lung diseas...

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Autores principales: Barfod, Kenneth Klingenberg, Vrankx, Katleen, Mirsepasi-Lauridsen, Hengameh Chloé, Hansen, Jitka Stilund, Hougaard, Karin Sørig, Larsen, Søren Thor, Ouwenhand, Arthur C., Krogfelt, Karen Angeliki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Open 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4676059/
https://www.ncbi.nlm.nih.gov/pubmed/26668669
http://dx.doi.org/10.2174/1874285801509010167
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author Barfod, Kenneth Klingenberg
Vrankx, Katleen
Mirsepasi-Lauridsen, Hengameh Chloé
Hansen, Jitka Stilund
Hougaard, Karin Sørig
Larsen, Søren Thor
Ouwenhand, Arthur C.
Krogfelt, Karen Angeliki
author_facet Barfod, Kenneth Klingenberg
Vrankx, Katleen
Mirsepasi-Lauridsen, Hengameh Chloé
Hansen, Jitka Stilund
Hougaard, Karin Sørig
Larsen, Søren Thor
Ouwenhand, Arthur C.
Krogfelt, Karen Angeliki
author_sort Barfod, Kenneth Klingenberg
collection PubMed
description Most microbiome research related to airway diseases has focused on the gut microbiome. This is despite advances in culture independent microbial identification techniques revealing that even healthy lungs possess a unique dynamic microbiome. This conceptual change raises the question; if lung diseases could be causally linked to local dysbiosis of the local lung microbiota. Here, we manipulate the murine lung and gut microbiome, in order to show that the lung microbiota can be changed experimentally. We have used four different approaches: lung inflammation by exposure to carbon nano-tube particles, oral probiotics and oral or intranasal exposure to the antibiotic vancomycin. Bacterial DNA was extracted from broncho-alveolar and nasal lavage fluids, caecum samples and compared by DGGE. Our results show that: the lung microbiota is sex dependent and not just a reflection of the gut microbiota, and that induced inflammation can change lung microbiota. This change is not transferred to offspring. Oral probiotics in adult mice do not change lung microbiome detectible by DGGE. Nasal vancomycin can change the lung microbiome preferentially, while oral exposure does not. These observations should be considered in future studies of the causal relationship between lung microbiota and lung diseases.
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spelling pubmed-46760592015-12-14 The Murine Lung Microbiome Changes During Lung Inflammation and Intranasal Vancomycin Treatment Barfod, Kenneth Klingenberg Vrankx, Katleen Mirsepasi-Lauridsen, Hengameh Chloé Hansen, Jitka Stilund Hougaard, Karin Sørig Larsen, Søren Thor Ouwenhand, Arthur C. Krogfelt, Karen Angeliki Open Microbiol J Article Most microbiome research related to airway diseases has focused on the gut microbiome. This is despite advances in culture independent microbial identification techniques revealing that even healthy lungs possess a unique dynamic microbiome. This conceptual change raises the question; if lung diseases could be causally linked to local dysbiosis of the local lung microbiota. Here, we manipulate the murine lung and gut microbiome, in order to show that the lung microbiota can be changed experimentally. We have used four different approaches: lung inflammation by exposure to carbon nano-tube particles, oral probiotics and oral or intranasal exposure to the antibiotic vancomycin. Bacterial DNA was extracted from broncho-alveolar and nasal lavage fluids, caecum samples and compared by DGGE. Our results show that: the lung microbiota is sex dependent and not just a reflection of the gut microbiota, and that induced inflammation can change lung microbiota. This change is not transferred to offspring. Oral probiotics in adult mice do not change lung microbiome detectible by DGGE. Nasal vancomycin can change the lung microbiome preferentially, while oral exposure does not. These observations should be considered in future studies of the causal relationship between lung microbiota and lung diseases. Bentham Open 2015-11-03 /pmc/articles/PMC4676059/ /pubmed/26668669 http://dx.doi.org/10.2174/1874285801509010167 Text en © Barfodet al.; Licensee Bentham Open. https://creativecommons.org/licenses/by/4.0/legalcode This is an open access article licensed under the terms of the (https://creativecommons.org/licenses/by/4.0/legalcode), which permits unrestricted, noncommercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Barfod, Kenneth Klingenberg
Vrankx, Katleen
Mirsepasi-Lauridsen, Hengameh Chloé
Hansen, Jitka Stilund
Hougaard, Karin Sørig
Larsen, Søren Thor
Ouwenhand, Arthur C.
Krogfelt, Karen Angeliki
The Murine Lung Microbiome Changes During Lung Inflammation and Intranasal Vancomycin Treatment
title The Murine Lung Microbiome Changes During Lung Inflammation and Intranasal Vancomycin Treatment
title_full The Murine Lung Microbiome Changes During Lung Inflammation and Intranasal Vancomycin Treatment
title_fullStr The Murine Lung Microbiome Changes During Lung Inflammation and Intranasal Vancomycin Treatment
title_full_unstemmed The Murine Lung Microbiome Changes During Lung Inflammation and Intranasal Vancomycin Treatment
title_short The Murine Lung Microbiome Changes During Lung Inflammation and Intranasal Vancomycin Treatment
title_sort murine lung microbiome changes during lung inflammation and intranasal vancomycin treatment
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4676059/
https://www.ncbi.nlm.nih.gov/pubmed/26668669
http://dx.doi.org/10.2174/1874285801509010167
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