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Characteristics and intrasubject variation in the respiratory microbiome in interstitial lung disease

Recent studies have reported that the lower airway microbiome may play an essential role in the development and progression of interstitial lung disease (ILD). The aim of the current study was to evaluate the characteristics of the respiratory microbiome and intrasubject variation in patients with I...

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Autores principales: Cho, Jun Yeun, Kim, Mi Yeon, Kim, Ji Hyoun, Kim, Eung-Gook, Kim, Sun-Hyung, Yang, Bumhee, Kang, Hyeran, Lee, Ki Man, Choe, Kang Hyeon, Shin, Yoon Mi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10082288/
https://www.ncbi.nlm.nih.gov/pubmed/37026952
http://dx.doi.org/10.1097/MD.0000000000033402
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author Cho, Jun Yeun
Kim, Mi Yeon
Kim, Ji Hyoun
Kim, Eung-Gook
Kim, Sun-Hyung
Yang, Bumhee
Kang, Hyeran
Lee, Ki Man
Choe, Kang Hyeon
Shin, Yoon Mi
author_facet Cho, Jun Yeun
Kim, Mi Yeon
Kim, Ji Hyoun
Kim, Eung-Gook
Kim, Sun-Hyung
Yang, Bumhee
Kang, Hyeran
Lee, Ki Man
Choe, Kang Hyeon
Shin, Yoon Mi
author_sort Cho, Jun Yeun
collection PubMed
description Recent studies have reported that the lower airway microbiome may play an essential role in the development and progression of interstitial lung disease (ILD). The aim of the current study was to evaluate the characteristics of the respiratory microbiome and intrasubject variation in patients with ILD. Patients with ILD were recruited prospectively for 12 months. The sample size was small (n = 11) owing to delayed recruitment during the COVID-19 pandemic. All subjects were hospitalized and were evaluated by a questionnaire survey, blood sampling, pulmonary function test, and bronchoscopy. Bronchoalveolar lavage fluid (BALF) was obtained at 2 sites, the most and least disease-affected lesions. Sputum collection was also performed. Furthermore, 16S ribosomal RNA gene sequencing was performed using the Illumina platform and indexes of α- and β-diversity were evaluated. Species diversity and richness tended to be lower in the most-affected lesion than in the least-affected lesion. However, taxonomic abundance patterns were similar in these 2 groups. The phylum Fusobacteria was more prevalent in fibrotic ILD than in nonfibrotic ILD. Inter-sample differences in relative abundances were more prominent in BALF versus sputum specimens. Rothia and Veillonella were more prevalent in the sputum than in BALF. We did not detect site-specific dysbiosis in the ILD lung. BALF was an effective respiratory specimen type for evaluating the lung microbiome in patients with ILD. Further studies are needed to evaluate the causal links between the lung microbiome and the pathogenesis of ILD.
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spelling pubmed-100822882023-04-09 Characteristics and intrasubject variation in the respiratory microbiome in interstitial lung disease Cho, Jun Yeun Kim, Mi Yeon Kim, Ji Hyoun Kim, Eung-Gook Kim, Sun-Hyung Yang, Bumhee Kang, Hyeran Lee, Ki Man Choe, Kang Hyeon Shin, Yoon Mi Medicine (Baltimore) 6700 Recent studies have reported that the lower airway microbiome may play an essential role in the development and progression of interstitial lung disease (ILD). The aim of the current study was to evaluate the characteristics of the respiratory microbiome and intrasubject variation in patients with ILD. Patients with ILD were recruited prospectively for 12 months. The sample size was small (n = 11) owing to delayed recruitment during the COVID-19 pandemic. All subjects were hospitalized and were evaluated by a questionnaire survey, blood sampling, pulmonary function test, and bronchoscopy. Bronchoalveolar lavage fluid (BALF) was obtained at 2 sites, the most and least disease-affected lesions. Sputum collection was also performed. Furthermore, 16S ribosomal RNA gene sequencing was performed using the Illumina platform and indexes of α- and β-diversity were evaluated. Species diversity and richness tended to be lower in the most-affected lesion than in the least-affected lesion. However, taxonomic abundance patterns were similar in these 2 groups. The phylum Fusobacteria was more prevalent in fibrotic ILD than in nonfibrotic ILD. Inter-sample differences in relative abundances were more prominent in BALF versus sputum specimens. Rothia and Veillonella were more prevalent in the sputum than in BALF. We did not detect site-specific dysbiosis in the ILD lung. BALF was an effective respiratory specimen type for evaluating the lung microbiome in patients with ILD. Further studies are needed to evaluate the causal links between the lung microbiome and the pathogenesis of ILD. Lippincott Williams & Wilkins 2022-04-07 /pmc/articles/PMC10082288/ /pubmed/37026952 http://dx.doi.org/10.1097/MD.0000000000033402 Text en Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle 6700
Cho, Jun Yeun
Kim, Mi Yeon
Kim, Ji Hyoun
Kim, Eung-Gook
Kim, Sun-Hyung
Yang, Bumhee
Kang, Hyeran
Lee, Ki Man
Choe, Kang Hyeon
Shin, Yoon Mi
Characteristics and intrasubject variation in the respiratory microbiome in interstitial lung disease
title Characteristics and intrasubject variation in the respiratory microbiome in interstitial lung disease
title_full Characteristics and intrasubject variation in the respiratory microbiome in interstitial lung disease
title_fullStr Characteristics and intrasubject variation in the respiratory microbiome in interstitial lung disease
title_full_unstemmed Characteristics and intrasubject variation in the respiratory microbiome in interstitial lung disease
title_short Characteristics and intrasubject variation in the respiratory microbiome in interstitial lung disease
title_sort characteristics and intrasubject variation in the respiratory microbiome in interstitial lung disease
topic 6700
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10082288/
https://www.ncbi.nlm.nih.gov/pubmed/37026952
http://dx.doi.org/10.1097/MD.0000000000033402
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