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Comprehensive transcriptome analysis of peripheral blood unravels key lncRNAs implicated in ABPA and asthma

Allergic bronchopulmonary aspergillosis (ABPA) is a complex hypersensitivity lung disease caused by a fungus known as Aspergillus fumigatus. It complicates and aggravates asthma. Despite their potential associations, the underlying mechanisms of asthma developing into ABPA remain obscure. Here we pe...

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Autores principales: Huang, Chen, Leng, Dongliang, Zheng, Peiyan, Deng, Min, Li, Lu, Wu, Ge, Sun, Baoqing, Zhang, Xiaohua Douglas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8236232/
https://www.ncbi.nlm.nih.gov/pubmed/34221710
http://dx.doi.org/10.7717/peerj.11453
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author Huang, Chen
Leng, Dongliang
Zheng, Peiyan
Deng, Min
Li, Lu
Wu, Ge
Sun, Baoqing
Zhang, Xiaohua Douglas
author_facet Huang, Chen
Leng, Dongliang
Zheng, Peiyan
Deng, Min
Li, Lu
Wu, Ge
Sun, Baoqing
Zhang, Xiaohua Douglas
author_sort Huang, Chen
collection PubMed
description Allergic bronchopulmonary aspergillosis (ABPA) is a complex hypersensitivity lung disease caused by a fungus known as Aspergillus fumigatus. It complicates and aggravates asthma. Despite their potential associations, the underlying mechanisms of asthma developing into ABPA remain obscure. Here we performed an integrative transcriptome analysis based on three types of human peripheral blood, which derived from ABPA patients, asthmatic patients and health controls, aiming to identify crucial lncRNAs implicated in ABPA and asthma. Initially, a high-confidence dataset of lncRNAs was identified using a stringent filtering pipeline. A comparative mutational analysis revealed no significant difference among these samples. Differential expression analysis disclosed several immune-related mRNAs and lncRNAs differentially expressed in ABPA and asthma. For each disease, three sub-networks were established using differential network analysis. Many key lncRNAs implicated in ABPA and asthma were identified, respectively, i.e., AL139423.1-201, AC106028.4-201, HNRNPUL1-210, PUF60-218 and SREBF1-208. Our analysis indicated that these lncRNAs exhibits in the loss-of-function networks, and the expression of which were repressed in the occurrences of both diseases, implying their important roles in the immune-related processes in response to the occurrence of both diseases. Above all, our analysis proposed a new point of view to explore the relationship between ABPA and asthma, which might provide new clues to unveil the pathogenic mechanisms for both diseases.
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spelling pubmed-82362322021-07-02 Comprehensive transcriptome analysis of peripheral blood unravels key lncRNAs implicated in ABPA and asthma Huang, Chen Leng, Dongliang Zheng, Peiyan Deng, Min Li, Lu Wu, Ge Sun, Baoqing Zhang, Xiaohua Douglas PeerJ Bioinformatics Allergic bronchopulmonary aspergillosis (ABPA) is a complex hypersensitivity lung disease caused by a fungus known as Aspergillus fumigatus. It complicates and aggravates asthma. Despite their potential associations, the underlying mechanisms of asthma developing into ABPA remain obscure. Here we performed an integrative transcriptome analysis based on three types of human peripheral blood, which derived from ABPA patients, asthmatic patients and health controls, aiming to identify crucial lncRNAs implicated in ABPA and asthma. Initially, a high-confidence dataset of lncRNAs was identified using a stringent filtering pipeline. A comparative mutational analysis revealed no significant difference among these samples. Differential expression analysis disclosed several immune-related mRNAs and lncRNAs differentially expressed in ABPA and asthma. For each disease, three sub-networks were established using differential network analysis. Many key lncRNAs implicated in ABPA and asthma were identified, respectively, i.e., AL139423.1-201, AC106028.4-201, HNRNPUL1-210, PUF60-218 and SREBF1-208. Our analysis indicated that these lncRNAs exhibits in the loss-of-function networks, and the expression of which were repressed in the occurrences of both diseases, implying their important roles in the immune-related processes in response to the occurrence of both diseases. Above all, our analysis proposed a new point of view to explore the relationship between ABPA and asthma, which might provide new clues to unveil the pathogenic mechanisms for both diseases. PeerJ Inc. 2021-06-24 /pmc/articles/PMC8236232/ /pubmed/34221710 http://dx.doi.org/10.7717/peerj.11453 Text en © 2021 Huang et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Bioinformatics
Huang, Chen
Leng, Dongliang
Zheng, Peiyan
Deng, Min
Li, Lu
Wu, Ge
Sun, Baoqing
Zhang, Xiaohua Douglas
Comprehensive transcriptome analysis of peripheral blood unravels key lncRNAs implicated in ABPA and asthma
title Comprehensive transcriptome analysis of peripheral blood unravels key lncRNAs implicated in ABPA and asthma
title_full Comprehensive transcriptome analysis of peripheral blood unravels key lncRNAs implicated in ABPA and asthma
title_fullStr Comprehensive transcriptome analysis of peripheral blood unravels key lncRNAs implicated in ABPA and asthma
title_full_unstemmed Comprehensive transcriptome analysis of peripheral blood unravels key lncRNAs implicated in ABPA and asthma
title_short Comprehensive transcriptome analysis of peripheral blood unravels key lncRNAs implicated in ABPA and asthma
title_sort comprehensive transcriptome analysis of peripheral blood unravels key lncrnas implicated in abpa and asthma
topic Bioinformatics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8236232/
https://www.ncbi.nlm.nih.gov/pubmed/34221710
http://dx.doi.org/10.7717/peerj.11453
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