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Metagenomic Next-Generation Sequencing for Diagnosing Infections in Lung Transplant Recipients: A Retrospective Study

Background: Accurate identification of pathogens is essential for the diagnosis and control of infections. We aimed to compare the diagnostic performance of metagenomic next-generation sequencing (mNGS) and conventional detection methods (CDM) in lung transplant recipients (LTRs). Methods: We retros...

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Autores principales: Ju, Chun-Rong, Lian, Qiao-Yan, Guan, Wei-Jie, Chen, Ao, Zhang, Jian-Heng, Xu, Xin, Chen, Rong-Chang, Li, Shi-Yue, He, Jian-Xing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8866178/
https://www.ncbi.nlm.nih.gov/pubmed/35221789
http://dx.doi.org/10.3389/ti.2022.10265
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author Ju, Chun-Rong
Lian, Qiao-Yan
Guan, Wei-Jie
Chen, Ao
Zhang, Jian-Heng
Xu, Xin
Chen, Rong-Chang
Li, Shi-Yue
He, Jian-Xing
author_facet Ju, Chun-Rong
Lian, Qiao-Yan
Guan, Wei-Jie
Chen, Ao
Zhang, Jian-Heng
Xu, Xin
Chen, Rong-Chang
Li, Shi-Yue
He, Jian-Xing
author_sort Ju, Chun-Rong
collection PubMed
description Background: Accurate identification of pathogens is essential for the diagnosis and control of infections. We aimed to compare the diagnostic performance of metagenomic next-generation sequencing (mNGS) and conventional detection methods (CDM) in lung transplant recipients (LTRs). Methods: We retrospectively analyzed 107 LTRs with suspected infection of pulmonary, blood, central nervous system or chest wall between March 2018 and November 2020. Bronchoalveolar lavage fluid and other body fluids were subject to pathogen detection by both mNGS and CDM. Results: Of the 163 specimens, 84 (51.5%) tested positive for both mNGS and culture, 19 (11.7%) of which were completely consistent, 44 (27.0%) were partially congruent, and 21 (12.9%) were discordant (kappa = .215; p = .001). Compared with CDM, mNGS detected a higher diversity of pathogens. Moreover, the turn-around time was significantly shorter for mNGS compared with culture (2.7 ± .4 vs. 5.5 ± 1.6 days, p < .001). As an auxiliary method, treatment strategies were adjusted according to mNGS findings in 31 cases (29.0%), including eight patients with non-infectious diseases, who were finally cured. Conclusion: mNGS can identify pathogens with a shorter turn-around time and therefore provide a more accurate and timely diagnostic information to ascertaining pulmonary infections. mNGS might have a role in differentiating infectious from non-infectious lung diseases in LTRs.
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spelling pubmed-88661782022-02-25 Metagenomic Next-Generation Sequencing for Diagnosing Infections in Lung Transplant Recipients: A Retrospective Study Ju, Chun-Rong Lian, Qiao-Yan Guan, Wei-Jie Chen, Ao Zhang, Jian-Heng Xu, Xin Chen, Rong-Chang Li, Shi-Yue He, Jian-Xing Transpl Int Health Archive Background: Accurate identification of pathogens is essential for the diagnosis and control of infections. We aimed to compare the diagnostic performance of metagenomic next-generation sequencing (mNGS) and conventional detection methods (CDM) in lung transplant recipients (LTRs). Methods: We retrospectively analyzed 107 LTRs with suspected infection of pulmonary, blood, central nervous system or chest wall between March 2018 and November 2020. Bronchoalveolar lavage fluid and other body fluids were subject to pathogen detection by both mNGS and CDM. Results: Of the 163 specimens, 84 (51.5%) tested positive for both mNGS and culture, 19 (11.7%) of which were completely consistent, 44 (27.0%) were partially congruent, and 21 (12.9%) were discordant (kappa = .215; p = .001). Compared with CDM, mNGS detected a higher diversity of pathogens. Moreover, the turn-around time was significantly shorter for mNGS compared with culture (2.7 ± .4 vs. 5.5 ± 1.6 days, p < .001). As an auxiliary method, treatment strategies were adjusted according to mNGS findings in 31 cases (29.0%), including eight patients with non-infectious diseases, who were finally cured. Conclusion: mNGS can identify pathogens with a shorter turn-around time and therefore provide a more accurate and timely diagnostic information to ascertaining pulmonary infections. mNGS might have a role in differentiating infectious from non-infectious lung diseases in LTRs. Frontiers Media S.A. 2022-02-10 /pmc/articles/PMC8866178/ /pubmed/35221789 http://dx.doi.org/10.3389/ti.2022.10265 Text en Copyright © 2022 Ju, Lian, Guan, Chen, Zhang, Xu, Chen, Li and He. https://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 Health Archive
Ju, Chun-Rong
Lian, Qiao-Yan
Guan, Wei-Jie
Chen, Ao
Zhang, Jian-Heng
Xu, Xin
Chen, Rong-Chang
Li, Shi-Yue
He, Jian-Xing
Metagenomic Next-Generation Sequencing for Diagnosing Infections in Lung Transplant Recipients: A Retrospective Study
title Metagenomic Next-Generation Sequencing for Diagnosing Infections in Lung Transplant Recipients: A Retrospective Study
title_full Metagenomic Next-Generation Sequencing for Diagnosing Infections in Lung Transplant Recipients: A Retrospective Study
title_fullStr Metagenomic Next-Generation Sequencing for Diagnosing Infections in Lung Transplant Recipients: A Retrospective Study
title_full_unstemmed Metagenomic Next-Generation Sequencing for Diagnosing Infections in Lung Transplant Recipients: A Retrospective Study
title_short Metagenomic Next-Generation Sequencing for Diagnosing Infections in Lung Transplant Recipients: A Retrospective Study
title_sort metagenomic next-generation sequencing for diagnosing infections in lung transplant recipients: a retrospective study
topic Health Archive
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8866178/
https://www.ncbi.nlm.nih.gov/pubmed/35221789
http://dx.doi.org/10.3389/ti.2022.10265
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