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Evaluation of Cell-Free DNA-Based Next-Generation Sequencing for Identifying Pathogens in Bacteremia Patients

Rapid detection of bloodstream pathogens would greatly facilitate clinicians to make precise antimicrobial treatment in patients with bacteremia. In this study, 114 plasma samples were collected from patients with identified or suspected bacteremia, and pathogens were detected by the conventional bl...

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Autores principales: Zhang, Chaoqin, Cheng, Hang, Zhao, Yuxi, Chen, Jinlian, Li, Meng, Yu, Zhijian, Sun, Xiang, Li, Peiyu, Shang, Yongpeng, Ma, Jinmin, Zheng, Jinxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sciendo 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9944966/
https://www.ncbi.nlm.nih.gov/pubmed/36369999
http://dx.doi.org/10.33073/pjm-2022-043
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author Zhang, Chaoqin
Cheng, Hang
Zhao, Yuxi
Chen, Jinlian
Li, Meng
Yu, Zhijian
Sun, Xiang
Li, Peiyu
Shang, Yongpeng
Ma, Jinmin
Zheng, Jinxin
author_facet Zhang, Chaoqin
Cheng, Hang
Zhao, Yuxi
Chen, Jinlian
Li, Meng
Yu, Zhijian
Sun, Xiang
Li, Peiyu
Shang, Yongpeng
Ma, Jinmin
Zheng, Jinxin
author_sort Zhang, Chaoqin
collection PubMed
description Rapid detection of bloodstream pathogens would greatly facilitate clinicians to make precise antimicrobial treatment in patients with bacteremia. In this study, 114 plasma samples were collected from patients with identified or suspected bacteremia, and pathogens were detected by the conventional blood culture (BC) and cell-free DNA metagenomics next-generation sequencing (cfDNA mNGS). The present study indicated that 76% (38/50) of positive conventional blood culture (BC(+) group) patients were positively detected by cfDNA mNGS, and only 4% were mismatched between cfDNA mNGS and conventional bacteria culture. Pathogens in 32.8% of suspected bacteremia patients with negative conventional blood culture (BC(–) group) were determined accurately by cfDNA mNGS combined with analyzing the patients’ clinical manifestations. Escherichia coli and Klebsiella pneumoniae were the most detected pathogens in identified bacteremia patients by cfDNA mNGS. 76.2% (16/21) of E. coli and 92.3% (12/13) of K. pneumoniae in bacteremia patients were identified by conventional blood cultures that were also detected by cfDNA mNGS. This study demonstrated that genomic coverage of E. coli and K. pneumoniae were more often detected in BC(+) group patients and genomic coverage of Acinetobacter johnsonii and Paucibacter sp. KCTC 42545 was more often detected in BC(–) group patients. In conclusion, cfDNA mNGS could rapidly and precisely provide an alternative detection method for the diagnosis of bacteremia.
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spelling pubmed-99449662023-02-23 Evaluation of Cell-Free DNA-Based Next-Generation Sequencing for Identifying Pathogens in Bacteremia Patients Zhang, Chaoqin Cheng, Hang Zhao, Yuxi Chen, Jinlian Li, Meng Yu, Zhijian Sun, Xiang Li, Peiyu Shang, Yongpeng Ma, Jinmin Zheng, Jinxin Pol J Microbiol Original Paper Rapid detection of bloodstream pathogens would greatly facilitate clinicians to make precise antimicrobial treatment in patients with bacteremia. In this study, 114 plasma samples were collected from patients with identified or suspected bacteremia, and pathogens were detected by the conventional blood culture (BC) and cell-free DNA metagenomics next-generation sequencing (cfDNA mNGS). The present study indicated that 76% (38/50) of positive conventional blood culture (BC(+) group) patients were positively detected by cfDNA mNGS, and only 4% were mismatched between cfDNA mNGS and conventional bacteria culture. Pathogens in 32.8% of suspected bacteremia patients with negative conventional blood culture (BC(–) group) were determined accurately by cfDNA mNGS combined with analyzing the patients’ clinical manifestations. Escherichia coli and Klebsiella pneumoniae were the most detected pathogens in identified bacteremia patients by cfDNA mNGS. 76.2% (16/21) of E. coli and 92.3% (12/13) of K. pneumoniae in bacteremia patients were identified by conventional blood cultures that were also detected by cfDNA mNGS. This study demonstrated that genomic coverage of E. coli and K. pneumoniae were more often detected in BC(+) group patients and genomic coverage of Acinetobacter johnsonii and Paucibacter sp. KCTC 42545 was more often detected in BC(–) group patients. In conclusion, cfDNA mNGS could rapidly and precisely provide an alternative detection method for the diagnosis of bacteremia. Sciendo 2022-11-12 /pmc/articles/PMC9944966/ /pubmed/36369999 http://dx.doi.org/10.33073/pjm-2022-043 Text en © 2022 Chaoqin Zhang et al., published by Sciendo https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
spellingShingle Original Paper
Zhang, Chaoqin
Cheng, Hang
Zhao, Yuxi
Chen, Jinlian
Li, Meng
Yu, Zhijian
Sun, Xiang
Li, Peiyu
Shang, Yongpeng
Ma, Jinmin
Zheng, Jinxin
Evaluation of Cell-Free DNA-Based Next-Generation Sequencing for Identifying Pathogens in Bacteremia Patients
title Evaluation of Cell-Free DNA-Based Next-Generation Sequencing for Identifying Pathogens in Bacteremia Patients
title_full Evaluation of Cell-Free DNA-Based Next-Generation Sequencing for Identifying Pathogens in Bacteremia Patients
title_fullStr Evaluation of Cell-Free DNA-Based Next-Generation Sequencing for Identifying Pathogens in Bacteremia Patients
title_full_unstemmed Evaluation of Cell-Free DNA-Based Next-Generation Sequencing for Identifying Pathogens in Bacteremia Patients
title_short Evaluation of Cell-Free DNA-Based Next-Generation Sequencing for Identifying Pathogens in Bacteremia Patients
title_sort evaluation of cell-free dna-based next-generation sequencing for identifying pathogens in bacteremia patients
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9944966/
https://www.ncbi.nlm.nih.gov/pubmed/36369999
http://dx.doi.org/10.33073/pjm-2022-043
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