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Evaluation of respiratory samples in etiology diagnosis and microbiome characterization by metagenomic sequencing

BACKGROUND: The application of clinical mNGS for diagnosing respiratory infections improves etiology diagnosis, however at the same time, it brings new challenges as an unbiased sequencing method informing all identified microbiomes in the specimen. METHODS: Strategy evaluation and metagenomic analy...

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Autores principales: Miao, Qing, Liang, Tianzhu, Pei, Na, Liu, Chunjiao, Pan, Jue, Li, Na, Wang, Qingqing, Chen, Yanqiong, Chen, Yu, Ma, Yuyan, Jin, Wenting, Zhang, Yao, Su, Yi, Yao, Yumeng, Huang, Yingnan, Zhou, Chunmei, Bao, Rong, Xu, Xiaoling, Chen, Weijun, Hu, Bijie, Li, Junhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9748891/
https://www.ncbi.nlm.nih.gov/pubmed/36517824
http://dx.doi.org/10.1186/s12931-022-02230-3
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author Miao, Qing
Liang, Tianzhu
Pei, Na
Liu, Chunjiao
Pan, Jue
Li, Na
Wang, Qingqing
Chen, Yanqiong
Chen, Yu
Ma, Yuyan
Jin, Wenting
Zhang, Yao
Su, Yi
Yao, Yumeng
Huang, Yingnan
Zhou, Chunmei
Bao, Rong
Xu, Xiaoling
Chen, Weijun
Hu, Bijie
Li, Junhua
author_facet Miao, Qing
Liang, Tianzhu
Pei, Na
Liu, Chunjiao
Pan, Jue
Li, Na
Wang, Qingqing
Chen, Yanqiong
Chen, Yu
Ma, Yuyan
Jin, Wenting
Zhang, Yao
Su, Yi
Yao, Yumeng
Huang, Yingnan
Zhou, Chunmei
Bao, Rong
Xu, Xiaoling
Chen, Weijun
Hu, Bijie
Li, Junhua
author_sort Miao, Qing
collection PubMed
description BACKGROUND: The application of clinical mNGS for diagnosing respiratory infections improves etiology diagnosis, however at the same time, it brings new challenges as an unbiased sequencing method informing all identified microbiomes in the specimen. METHODS: Strategy evaluation and metagenomic analysis were performed for the mNGS data generated between March 2017 and October 2019. Diagnostic strengths of four specimen types were assessed to pinpoint the more appropriate type for mNGS diagnosis of respiratory infections. Microbiome complexity was revealed between patient cohorts and infection types. A bioinformatic pipeline resembling diagnosis results was built based upon multiple bioinformatic parameters. RESULTS: The positive predictive values (PPVs) for mNGS diagnosing of non-mycobacterium, Nontuberculous Mycobacteria (NTM), and Aspergillus were obviously higher in bronchoalveolar lavage fluid (BALF) demonstrating the potency of BALF in mNGS diagnosis. Lung tissues and sputum were acceptable for diagnosis of the Mycobacterium tuberculosis (MTB) infections. Interestingly, significant taxonomy differences were identified in sufficient BALF specimens, and unique bacteriome and virome compositions were found in the BALF specimens of tumor patients. Our pipeline showed comparative diagnostic strength with the clinical microbiological diagnosis. CONCLUSIONS: To achieve reliable mNGS diagnosis result, BALF specimens for suspicious common infections, and lung tissues and sputum for doubtful MTB infections are recommended to avoid the false results given by the complexed respiratory microbiomes. Our developed bioinformatic pipeline successful helps mNGS data interpretation and reduces manual corrections for etiology diagnosis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12931-022-02230-3.
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spelling pubmed-97488912022-12-14 Evaluation of respiratory samples in etiology diagnosis and microbiome characterization by metagenomic sequencing Miao, Qing Liang, Tianzhu Pei, Na Liu, Chunjiao Pan, Jue Li, Na Wang, Qingqing Chen, Yanqiong Chen, Yu Ma, Yuyan Jin, Wenting Zhang, Yao Su, Yi Yao, Yumeng Huang, Yingnan Zhou, Chunmei Bao, Rong Xu, Xiaoling Chen, Weijun Hu, Bijie Li, Junhua Respir Res Research BACKGROUND: The application of clinical mNGS for diagnosing respiratory infections improves etiology diagnosis, however at the same time, it brings new challenges as an unbiased sequencing method informing all identified microbiomes in the specimen. METHODS: Strategy evaluation and metagenomic analysis were performed for the mNGS data generated between March 2017 and October 2019. Diagnostic strengths of four specimen types were assessed to pinpoint the more appropriate type for mNGS diagnosis of respiratory infections. Microbiome complexity was revealed between patient cohorts and infection types. A bioinformatic pipeline resembling diagnosis results was built based upon multiple bioinformatic parameters. RESULTS: The positive predictive values (PPVs) for mNGS diagnosing of non-mycobacterium, Nontuberculous Mycobacteria (NTM), and Aspergillus were obviously higher in bronchoalveolar lavage fluid (BALF) demonstrating the potency of BALF in mNGS diagnosis. Lung tissues and sputum were acceptable for diagnosis of the Mycobacterium tuberculosis (MTB) infections. Interestingly, significant taxonomy differences were identified in sufficient BALF specimens, and unique bacteriome and virome compositions were found in the BALF specimens of tumor patients. Our pipeline showed comparative diagnostic strength with the clinical microbiological diagnosis. CONCLUSIONS: To achieve reliable mNGS diagnosis result, BALF specimens for suspicious common infections, and lung tissues and sputum for doubtful MTB infections are recommended to avoid the false results given by the complexed respiratory microbiomes. Our developed bioinformatic pipeline successful helps mNGS data interpretation and reduces manual corrections for etiology diagnosis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12931-022-02230-3. BioMed Central 2022-12-14 2022 /pmc/articles/PMC9748891/ /pubmed/36517824 http://dx.doi.org/10.1186/s12931-022-02230-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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
Miao, Qing
Liang, Tianzhu
Pei, Na
Liu, Chunjiao
Pan, Jue
Li, Na
Wang, Qingqing
Chen, Yanqiong
Chen, Yu
Ma, Yuyan
Jin, Wenting
Zhang, Yao
Su, Yi
Yao, Yumeng
Huang, Yingnan
Zhou, Chunmei
Bao, Rong
Xu, Xiaoling
Chen, Weijun
Hu, Bijie
Li, Junhua
Evaluation of respiratory samples in etiology diagnosis and microbiome characterization by metagenomic sequencing
title Evaluation of respiratory samples in etiology diagnosis and microbiome characterization by metagenomic sequencing
title_full Evaluation of respiratory samples in etiology diagnosis and microbiome characterization by metagenomic sequencing
title_fullStr Evaluation of respiratory samples in etiology diagnosis and microbiome characterization by metagenomic sequencing
title_full_unstemmed Evaluation of respiratory samples in etiology diagnosis and microbiome characterization by metagenomic sequencing
title_short Evaluation of respiratory samples in etiology diagnosis and microbiome characterization by metagenomic sequencing
title_sort evaluation of respiratory samples in etiology diagnosis and microbiome characterization by metagenomic sequencing
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9748891/
https://www.ncbi.nlm.nih.gov/pubmed/36517824
http://dx.doi.org/10.1186/s12931-022-02230-3
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