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Fine Particulate Matter Exposure Alters Pulmonary Microbiota Composition and Aggravates Pneumococcus-Induced Lung Pathogenesis

Exposure to fine particulate matter (PM) with aerodynamic diameter ≤2.5 μm (PM(2.)(5)) is closely correlated with respiratory diseases. Microbiota plays a key role in maintaining body homeostasis including regulation of host immune status and metabolism. As reported recently, PM(2.)(5) exposure caus...

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Autores principales: Chen, Yu-Wen, Li, Shiao-Wen, Lin, Chia-Der, Huang, Mei-Zi, Lin, Hwai-Jeng, Chin, Chia-Yin, Lai, Yi-Ru, Chiu, Cheng-Hsun, Yang, Chia-Yu, Lai, Chih-Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7649221/
https://www.ncbi.nlm.nih.gov/pubmed/33195201
http://dx.doi.org/10.3389/fcell.2020.570484
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author Chen, Yu-Wen
Li, Shiao-Wen
Lin, Chia-Der
Huang, Mei-Zi
Lin, Hwai-Jeng
Chin, Chia-Yin
Lai, Yi-Ru
Chiu, Cheng-Hsun
Yang, Chia-Yu
Lai, Chih-Ho
author_facet Chen, Yu-Wen
Li, Shiao-Wen
Lin, Chia-Der
Huang, Mei-Zi
Lin, Hwai-Jeng
Chin, Chia-Yin
Lai, Yi-Ru
Chiu, Cheng-Hsun
Yang, Chia-Yu
Lai, Chih-Ho
author_sort Chen, Yu-Wen
collection PubMed
description Exposure to fine particulate matter (PM) with aerodynamic diameter ≤2.5 μm (PM(2.)(5)) is closely correlated with respiratory diseases. Microbiota plays a key role in maintaining body homeostasis including regulation of host immune status and metabolism. As reported recently, PM(2.)(5) exposure causes microbiota dysbiosis and thus promotes disease progression. However, whether PM(2.)(5) alters pulmonary microbiota distribution and aggravates bacteria-induced pathogenesis remains unknown. In this study, we used mouse experimental models of PM(2.)(5) exposure combined with Streptococcus pneumonia infection. We characterized the airway microbiota of bronchoalveolar lavage fluid (BALF) by sequencing the 16S rRNA V3–V4 amplicon on the Illumina MiSeq platform, followed by a combination of bioinformatics and statistical analyses. Shannon-diversity index, observed ASVs, and Fisher’s diversity index indicated that microbiota richness was significantly decreased in the mice treated with either PM(2.)(5) or pneumococcus when compared with the control group. The genera Streptococcus, Prevotella, Leptotrichia, and Granulicatella were remarkably increased in mice exposed to PM(2.)(5) combined with pneumococcal infection as compared to mice with pneumococcal infection alone. Histopathological examination exhibited that a more pronounced inflammation was present in lungs of mice treated with PM(2.)(5) and pneumococcus than that in mouse groups exposed to either PM(2.)(5) or pneumococcal infection alone. Our results demonstrate that PM(2.)(5) alters the microbiota composition, thereby enhancing susceptibility to pneumococcal infection and exacerbating lung pathogenesis.
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spelling pubmed-76492212020-11-13 Fine Particulate Matter Exposure Alters Pulmonary Microbiota Composition and Aggravates Pneumococcus-Induced Lung Pathogenesis Chen, Yu-Wen Li, Shiao-Wen Lin, Chia-Der Huang, Mei-Zi Lin, Hwai-Jeng Chin, Chia-Yin Lai, Yi-Ru Chiu, Cheng-Hsun Yang, Chia-Yu Lai, Chih-Ho Front Cell Dev Biol Cell and Developmental Biology Exposure to fine particulate matter (PM) with aerodynamic diameter ≤2.5 μm (PM(2.)(5)) is closely correlated with respiratory diseases. Microbiota plays a key role in maintaining body homeostasis including regulation of host immune status and metabolism. As reported recently, PM(2.)(5) exposure causes microbiota dysbiosis and thus promotes disease progression. However, whether PM(2.)(5) alters pulmonary microbiota distribution and aggravates bacteria-induced pathogenesis remains unknown. In this study, we used mouse experimental models of PM(2.)(5) exposure combined with Streptococcus pneumonia infection. We characterized the airway microbiota of bronchoalveolar lavage fluid (BALF) by sequencing the 16S rRNA V3–V4 amplicon on the Illumina MiSeq platform, followed by a combination of bioinformatics and statistical analyses. Shannon-diversity index, observed ASVs, and Fisher’s diversity index indicated that microbiota richness was significantly decreased in the mice treated with either PM(2.)(5) or pneumococcus when compared with the control group. The genera Streptococcus, Prevotella, Leptotrichia, and Granulicatella were remarkably increased in mice exposed to PM(2.)(5) combined with pneumococcal infection as compared to mice with pneumococcal infection alone. Histopathological examination exhibited that a more pronounced inflammation was present in lungs of mice treated with PM(2.)(5) and pneumococcus than that in mouse groups exposed to either PM(2.)(5) or pneumococcal infection alone. Our results demonstrate that PM(2.)(5) alters the microbiota composition, thereby enhancing susceptibility to pneumococcal infection and exacerbating lung pathogenesis. Frontiers Media S.A. 2020-10-26 /pmc/articles/PMC7649221/ /pubmed/33195201 http://dx.doi.org/10.3389/fcell.2020.570484 Text en Copyright © 2020 Chen, Li, Lin, Huang, Lin, Chin, Lai, Chiu, Yang and Lai. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Chen, Yu-Wen
Li, Shiao-Wen
Lin, Chia-Der
Huang, Mei-Zi
Lin, Hwai-Jeng
Chin, Chia-Yin
Lai, Yi-Ru
Chiu, Cheng-Hsun
Yang, Chia-Yu
Lai, Chih-Ho
Fine Particulate Matter Exposure Alters Pulmonary Microbiota Composition and Aggravates Pneumococcus-Induced Lung Pathogenesis
title Fine Particulate Matter Exposure Alters Pulmonary Microbiota Composition and Aggravates Pneumococcus-Induced Lung Pathogenesis
title_full Fine Particulate Matter Exposure Alters Pulmonary Microbiota Composition and Aggravates Pneumococcus-Induced Lung Pathogenesis
title_fullStr Fine Particulate Matter Exposure Alters Pulmonary Microbiota Composition and Aggravates Pneumococcus-Induced Lung Pathogenesis
title_full_unstemmed Fine Particulate Matter Exposure Alters Pulmonary Microbiota Composition and Aggravates Pneumococcus-Induced Lung Pathogenesis
title_short Fine Particulate Matter Exposure Alters Pulmonary Microbiota Composition and Aggravates Pneumococcus-Induced Lung Pathogenesis
title_sort fine particulate matter exposure alters pulmonary microbiota composition and aggravates pneumococcus-induced lung pathogenesis
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7649221/
https://www.ncbi.nlm.nih.gov/pubmed/33195201
http://dx.doi.org/10.3389/fcell.2020.570484
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