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Exploring the microbiota of upper respiratory tract during the development of pneumonia in a mouse model
The alteration of the microbial community in the upper respiratory tract (URT) can contribute to the colonization and invasion of respiratory pathogens. However, there are no studies regarding whether the characteristics of the URT microbiota can be affected by infections in lower respiratory tract...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764665/ https://www.ncbi.nlm.nih.gov/pubmed/31560693 http://dx.doi.org/10.1371/journal.pone.0222589 |
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author | Morinaga, Yoshitomo Take, Yuki Sasaki, Daisuke Ota, Kenji Kaku, Norihito Uno, Naoki Sakamoto, Kei Kosai, Kosuke Miyazaki, Taiga Hasegawa, Hiroo Izumikawa, Koichi Mukae, Hiroshi Yanagihara, Katsunori |
author_facet | Morinaga, Yoshitomo Take, Yuki Sasaki, Daisuke Ota, Kenji Kaku, Norihito Uno, Naoki Sakamoto, Kei Kosai, Kosuke Miyazaki, Taiga Hasegawa, Hiroo Izumikawa, Koichi Mukae, Hiroshi Yanagihara, Katsunori |
author_sort | Morinaga, Yoshitomo |
collection | PubMed |
description | The alteration of the microbial community in the upper respiratory tract (URT) can contribute to the colonization and invasion of respiratory pathogens. However, there are no studies regarding whether the characteristics of the URT microbiota can be affected by infections in lower respiratory tract (LRT). To elucidate the microbial profiles of the URT during pneumonia, the oral, nasal, and lung microbiota was evaluated at the early phase in a murine pneumonia model by direct intratracheal inoculation of Klebsiella pneumoniae. The meta 16S rRNA sequencing of bronchoalveolar lavage fluid after K. pneumoniae inoculation presented alterations in the beta diversity of the microbes, but not in the alpha diversity. At this point, a significant increase in microbial alpha diversity was observed in the oral cavity, but not in the nasal cavity. The significant increase was observed in the family Carnobacteriaceae and family Enterococcaceae. These results suggest that characterizing the microbial community of the respiratory tract may not just involve a simple downstream relationship from the URT to the LRT. The health status of the LRT may influence the oral microbiota. Thus, evaluation of the oral microbiota may contribute towards monitoring lung health; the oral microbiota may act as a diagnostic marker of pneumonia. |
format | Online Article Text |
id | pubmed-6764665 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-67646652019-10-12 Exploring the microbiota of upper respiratory tract during the development of pneumonia in a mouse model Morinaga, Yoshitomo Take, Yuki Sasaki, Daisuke Ota, Kenji Kaku, Norihito Uno, Naoki Sakamoto, Kei Kosai, Kosuke Miyazaki, Taiga Hasegawa, Hiroo Izumikawa, Koichi Mukae, Hiroshi Yanagihara, Katsunori PLoS One Research Article The alteration of the microbial community in the upper respiratory tract (URT) can contribute to the colonization and invasion of respiratory pathogens. However, there are no studies regarding whether the characteristics of the URT microbiota can be affected by infections in lower respiratory tract (LRT). To elucidate the microbial profiles of the URT during pneumonia, the oral, nasal, and lung microbiota was evaluated at the early phase in a murine pneumonia model by direct intratracheal inoculation of Klebsiella pneumoniae. The meta 16S rRNA sequencing of bronchoalveolar lavage fluid after K. pneumoniae inoculation presented alterations in the beta diversity of the microbes, but not in the alpha diversity. At this point, a significant increase in microbial alpha diversity was observed in the oral cavity, but not in the nasal cavity. The significant increase was observed in the family Carnobacteriaceae and family Enterococcaceae. These results suggest that characterizing the microbial community of the respiratory tract may not just involve a simple downstream relationship from the URT to the LRT. The health status of the LRT may influence the oral microbiota. Thus, evaluation of the oral microbiota may contribute towards monitoring lung health; the oral microbiota may act as a diagnostic marker of pneumonia. Public Library of Science 2019-09-27 /pmc/articles/PMC6764665/ /pubmed/31560693 http://dx.doi.org/10.1371/journal.pone.0222589 Text en © 2019 Morinaga et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Morinaga, Yoshitomo Take, Yuki Sasaki, Daisuke Ota, Kenji Kaku, Norihito Uno, Naoki Sakamoto, Kei Kosai, Kosuke Miyazaki, Taiga Hasegawa, Hiroo Izumikawa, Koichi Mukae, Hiroshi Yanagihara, Katsunori Exploring the microbiota of upper respiratory tract during the development of pneumonia in a mouse model |
title | Exploring the microbiota of upper respiratory tract during the development of pneumonia in a mouse model |
title_full | Exploring the microbiota of upper respiratory tract during the development of pneumonia in a mouse model |
title_fullStr | Exploring the microbiota of upper respiratory tract during the development of pneumonia in a mouse model |
title_full_unstemmed | Exploring the microbiota of upper respiratory tract during the development of pneumonia in a mouse model |
title_short | Exploring the microbiota of upper respiratory tract during the development of pneumonia in a mouse model |
title_sort | exploring the microbiota of upper respiratory tract during the development of pneumonia in a mouse model |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764665/ https://www.ncbi.nlm.nih.gov/pubmed/31560693 http://dx.doi.org/10.1371/journal.pone.0222589 |
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