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Fungal and bacterial microbiome dysbiosis and imbalance of trans-kingdom network in asthma

BACKGROUND: Fungal and bacterial microbiota play an important role in development of asthma. We aim to characterize airway microbiome (mycobiome, bacteriome) and functional genes in asthmatics and controls. METHODS: Sputum microbiome of controls, untreated asthma patients and inhaled corticosteroid...

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Autores principales: Huang, Chunrong, Yu, Youchao, Du, Wei, Liu, Yahui, Dai, Ranran, Tang, Wei, Wang, Ping, Zhang, Chenhong, Shi, Guochao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7583303/
https://www.ncbi.nlm.nih.gov/pubmed/33110490
http://dx.doi.org/10.1186/s13601-020-00345-8
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author Huang, Chunrong
Yu, Youchao
Du, Wei
Liu, Yahui
Dai, Ranran
Tang, Wei
Wang, Ping
Zhang, Chenhong
Shi, Guochao
author_facet Huang, Chunrong
Yu, Youchao
Du, Wei
Liu, Yahui
Dai, Ranran
Tang, Wei
Wang, Ping
Zhang, Chenhong
Shi, Guochao
author_sort Huang, Chunrong
collection PubMed
description BACKGROUND: Fungal and bacterial microbiota play an important role in development of asthma. We aim to characterize airway microbiome (mycobiome, bacteriome) and functional genes in asthmatics and controls. METHODS: Sputum microbiome of controls, untreated asthma patients and inhaled corticosteroid (ICS) receiving patients was detected using high throughput sequencing. Metagenomic sequencing was used to examine the functional genes of microbiome. RESULTS: 1. Mycobiome: α diversity was lower in untreated asthma group than that in controls. Mycobiome compositions differed among the three groups. Compared with controls, untreated asthma group has higher abundance of Wallemia, Mortierella and Fusarium. Compared with untreated asthma patients, ICS receiving patients has higher abundance of Fusarium and Mortierella, lower frequency of Wallemia, Alternaria and Aspergillus. 2. Bacteriome: α diversity was lower in untreated asthma group than that in controls. There are some overlaps of bacteriome compositions between controls and untreated asthma patients which were distinct from ICS receiving patients. Untreated asthma group has higher Streptococcus than controls. 3. Potential fungal and bacterial biomarkers of asthma: Trametes, Aspergillus, Streptococcus, Gemella, Neisseria, etc. 4. Correlation network: There are dense and homogenous correlations in controls but a dramatically unbalanced network in untreated asthma and ICS receiving patients, which suggested the existence of disease-specific inter-kingdom and intra-kingdom alterations. 5. Metagenomic analysis: functional pathways were associated with the status of asthma, microbiome and functional genes showed different correlations in different environment. CONCLUSION: We showed mycobiome and bacteriome dysbiosis in asthma featured by alterations in biodiversity, community composition, inter-kingdom and intra-kingdom network. We also observed several functional genes associated with asthma.
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spelling pubmed-75833032020-10-26 Fungal and bacterial microbiome dysbiosis and imbalance of trans-kingdom network in asthma Huang, Chunrong Yu, Youchao Du, Wei Liu, Yahui Dai, Ranran Tang, Wei Wang, Ping Zhang, Chenhong Shi, Guochao Clin Transl Allergy Research BACKGROUND: Fungal and bacterial microbiota play an important role in development of asthma. We aim to characterize airway microbiome (mycobiome, bacteriome) and functional genes in asthmatics and controls. METHODS: Sputum microbiome of controls, untreated asthma patients and inhaled corticosteroid (ICS) receiving patients was detected using high throughput sequencing. Metagenomic sequencing was used to examine the functional genes of microbiome. RESULTS: 1. Mycobiome: α diversity was lower in untreated asthma group than that in controls. Mycobiome compositions differed among the three groups. Compared with controls, untreated asthma group has higher abundance of Wallemia, Mortierella and Fusarium. Compared with untreated asthma patients, ICS receiving patients has higher abundance of Fusarium and Mortierella, lower frequency of Wallemia, Alternaria and Aspergillus. 2. Bacteriome: α diversity was lower in untreated asthma group than that in controls. There are some overlaps of bacteriome compositions between controls and untreated asthma patients which were distinct from ICS receiving patients. Untreated asthma group has higher Streptococcus than controls. 3. Potential fungal and bacterial biomarkers of asthma: Trametes, Aspergillus, Streptococcus, Gemella, Neisseria, etc. 4. Correlation network: There are dense and homogenous correlations in controls but a dramatically unbalanced network in untreated asthma and ICS receiving patients, which suggested the existence of disease-specific inter-kingdom and intra-kingdom alterations. 5. Metagenomic analysis: functional pathways were associated with the status of asthma, microbiome and functional genes showed different correlations in different environment. CONCLUSION: We showed mycobiome and bacteriome dysbiosis in asthma featured by alterations in biodiversity, community composition, inter-kingdom and intra-kingdom network. We also observed several functional genes associated with asthma. BioMed Central 2020-10-22 /pmc/articles/PMC7583303/ /pubmed/33110490 http://dx.doi.org/10.1186/s13601-020-00345-8 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research
Huang, Chunrong
Yu, Youchao
Du, Wei
Liu, Yahui
Dai, Ranran
Tang, Wei
Wang, Ping
Zhang, Chenhong
Shi, Guochao
Fungal and bacterial microbiome dysbiosis and imbalance of trans-kingdom network in asthma
title Fungal and bacterial microbiome dysbiosis and imbalance of trans-kingdom network in asthma
title_full Fungal and bacterial microbiome dysbiosis and imbalance of trans-kingdom network in asthma
title_fullStr Fungal and bacterial microbiome dysbiosis and imbalance of trans-kingdom network in asthma
title_full_unstemmed Fungal and bacterial microbiome dysbiosis and imbalance of trans-kingdom network in asthma
title_short Fungal and bacterial microbiome dysbiosis and imbalance of trans-kingdom network in asthma
title_sort fungal and bacterial microbiome dysbiosis and imbalance of trans-kingdom network in asthma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7583303/
https://www.ncbi.nlm.nih.gov/pubmed/33110490
http://dx.doi.org/10.1186/s13601-020-00345-8
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