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Pathogen Diagnosis Value of Nanopore Sequencing in Severe Hospital-Acquired Pneumonia Patients

BACKGROUND: Next-generation sequencing of the metagenome (mNGS) is increasingly used in pathogen diagnosis for infectious diseases due to its short detection time. The time for Oxford Nanopore Technologies (ONT) sequencing-based etiology detection is further shortened compared with that of mNGS, but...

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Autores principales: Zhao, Xin, Ge, Yue, Zhang, Yuan, Zhang, WenJie, Hu, HongBin, Li, LuLan, Sha, Tong, Zeng, ZhenHua, Wu, Feng, Chen, ZhongQing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10228525/
https://www.ncbi.nlm.nih.gov/pubmed/37260782
http://dx.doi.org/10.2147/IDR.S410593
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author Zhao, Xin
Ge, Yue
Zhang, Yuan
Zhang, WenJie
Hu, HongBin
Li, LuLan
Sha, Tong
Zeng, ZhenHua
Wu, Feng
Chen, ZhongQing
author_facet Zhao, Xin
Ge, Yue
Zhang, Yuan
Zhang, WenJie
Hu, HongBin
Li, LuLan
Sha, Tong
Zeng, ZhenHua
Wu, Feng
Chen, ZhongQing
author_sort Zhao, Xin
collection PubMed
description BACKGROUND: Next-generation sequencing of the metagenome (mNGS) is increasingly used in pathogen diagnosis for infectious diseases due to its short detection time. The time for Oxford Nanopore Technologies (ONT) sequencing-based etiology detection is further shortened compared with that of mNGS, but only a few studies have verified the time advantage and accuracy of ONT sequencing for etiology diagnosis. In 2022, a study confirmed that there was no significant difference in sensitivity and specificity between ONT and mNGS in suspected community-acquired pneumonia patients, which there was no clinical study verified in patients with SHAP. METHODS: From October 24 to November 20, 2022, 10 patients with severe hospital-acquired pneumonia (SHAP) in the Nanfang Hospital intensive care unit (ICU) were prospectively enrolled. Bronchoalveolar lavage fluid (BALF) was collected for ONT sequencing, mNGS, and traditional culture. The differences in pathogen detection time and diagnostic agreement among ONT sequencing, mNGS, traditional culture method, and clinical composite diagnosis were compared. RESULTS: Compared with mNGS and the traditional culture method, ONT sequencing had a significant advantage in pathogen detection time (9.6±0.7 h versus 24.7±2.7 h versus 132±58 h, P <0.05). The agreement rate between ONT sequencing and the clinical composite diagnosis was 73.3% (kappa value=0.737, P <0.05). CONCLUSION: ONT sequencing has a potential advantage for rapidly identifying pathogens.
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spelling pubmed-102285252023-05-31 Pathogen Diagnosis Value of Nanopore Sequencing in Severe Hospital-Acquired Pneumonia Patients Zhao, Xin Ge, Yue Zhang, Yuan Zhang, WenJie Hu, HongBin Li, LuLan Sha, Tong Zeng, ZhenHua Wu, Feng Chen, ZhongQing Infect Drug Resist Original Research BACKGROUND: Next-generation sequencing of the metagenome (mNGS) is increasingly used in pathogen diagnosis for infectious diseases due to its short detection time. The time for Oxford Nanopore Technologies (ONT) sequencing-based etiology detection is further shortened compared with that of mNGS, but only a few studies have verified the time advantage and accuracy of ONT sequencing for etiology diagnosis. In 2022, a study confirmed that there was no significant difference in sensitivity and specificity between ONT and mNGS in suspected community-acquired pneumonia patients, which there was no clinical study verified in patients with SHAP. METHODS: From October 24 to November 20, 2022, 10 patients with severe hospital-acquired pneumonia (SHAP) in the Nanfang Hospital intensive care unit (ICU) were prospectively enrolled. Bronchoalveolar lavage fluid (BALF) was collected for ONT sequencing, mNGS, and traditional culture. The differences in pathogen detection time and diagnostic agreement among ONT sequencing, mNGS, traditional culture method, and clinical composite diagnosis were compared. RESULTS: Compared with mNGS and the traditional culture method, ONT sequencing had a significant advantage in pathogen detection time (9.6±0.7 h versus 24.7±2.7 h versus 132±58 h, P <0.05). The agreement rate between ONT sequencing and the clinical composite diagnosis was 73.3% (kappa value=0.737, P <0.05). CONCLUSION: ONT sequencing has a potential advantage for rapidly identifying pathogens. Dove 2023-05-26 /pmc/articles/PMC10228525/ /pubmed/37260782 http://dx.doi.org/10.2147/IDR.S410593 Text en © 2023 Zhao et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Zhao, Xin
Ge, Yue
Zhang, Yuan
Zhang, WenJie
Hu, HongBin
Li, LuLan
Sha, Tong
Zeng, ZhenHua
Wu, Feng
Chen, ZhongQing
Pathogen Diagnosis Value of Nanopore Sequencing in Severe Hospital-Acquired Pneumonia Patients
title Pathogen Diagnosis Value of Nanopore Sequencing in Severe Hospital-Acquired Pneumonia Patients
title_full Pathogen Diagnosis Value of Nanopore Sequencing in Severe Hospital-Acquired Pneumonia Patients
title_fullStr Pathogen Diagnosis Value of Nanopore Sequencing in Severe Hospital-Acquired Pneumonia Patients
title_full_unstemmed Pathogen Diagnosis Value of Nanopore Sequencing in Severe Hospital-Acquired Pneumonia Patients
title_short Pathogen Diagnosis Value of Nanopore Sequencing in Severe Hospital-Acquired Pneumonia Patients
title_sort pathogen diagnosis value of nanopore sequencing in severe hospital-acquired pneumonia patients
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10228525/
https://www.ncbi.nlm.nih.gov/pubmed/37260782
http://dx.doi.org/10.2147/IDR.S410593
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