Role of plasma and blood-cell co-metagenomic sequencing in precise diagnosis and severity evaluation of sepsis, a prospective cohort study in sepsis patients

被引:0
|
作者
Zhu, Ying [1 ,2 ]
Miao, Hui [3 ]
Zhang, Jingjia [1 ]
Jiang, Zhi [3 ]
Chu, Xiaobing [1 ,2 ]
Xu, Yingchun [1 ]
Tian, Wenjia [3 ]
Gao, Haotian [1 ]
Zhu, Yun [3 ]
Li, Lifeng [3 ]
Yang, Qiwen [1 ,4 ]
机构
[1] Chinese Acad Med Sci, Peking Union Med Coll Hosp, Dept Clin Lab, State Key Lab Complex Severe & Rare Dis, Beijing, Peoples R China
[2] Chinese Acad Med Sci, Peking Union Med Coll, Grad Sch, Beijing, Peoples R China
[3] Genskey Med Technol Co Ltd, Beijing, Peoples R China
[4] Peking Union Med Coll, Key Lab Pathogen Infect Prevent & Control, Minist Educ, Beijing, Peoples R China
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
Plasma; Blood-cell; Metagenomic next-generation sequencing; Sepsis; Intensive care unit;
D O I
10.1016/j.jinf.2025.106434
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Purposes: Sepsis caused great clinical burden all over the world. This study clarified the value of plasma metagenomic next-generation sequencing (p-mNGS) and blood cell mNGS (bc-mNGS) in sepsis diagnosis and evaluation. Methods: One hundred and fourty-seven blood samples were collected from sepsis patients who met sepsis 3.0 criteria. Blood culture (BC), qPCR, p-mNGS, bc-mNGS and necessary routine assays were conducted. Taking BC and qPCR as reference, diagnosis performance of p-mNGS and bc-mNGS was analyzed. Blood transcriptome was conducted to evaluate the immunological response of patients in groups with different p/bc-mNGS results. Impact of antibiotic use on different methods was also analyzed. Results: The p-mNGS demonstrated a sensitivity of 100% for bacteria/fungi and 97% for viruses, which was higher than bc-mNGS (88% for bacteria and fungi, 71% for viruses). However, bc-mNGS showed higher concordance with BC results, which indicated that co-mNGS (p-mNGS plus bc-mNGS) protocol increased sensitivity and was helpful to justify viable blood pathogens in sepsis patients. This study showed that pmNGS(+) & bc-mNGS(+) samples represented more activated immunity response (low expression of interferon-induced genes and high expression of JAK-STAT pathway genes), poorer clinical laboratory indicators (higher Sequential Organ Failure Assessment, higher procalcitonin and higher C-reactive protein) and lower survival rate. This study also proved that the use of broad-spectrum antibiotics affected much less on p/bc-mNGS diagnostic ability than on BC. Conclusions: This research highlighted the potential value of plasma and blood-cell co-metagenomic sequencing in precise diagnosis and severity evaluation of sepsis patients, which will benefit the management of sepsis patients. (c) 2025 The Author(s). Published by Elsevier Ltd on behalf of The British Infection Association. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
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页数:9
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