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DOI 10.3389/fcimb.2026.1905007

Медицинская библиотека · Frontiers in cellular and infection microbiology · 2026

Employing Metagenomics Capture targeted next-generation sequencing for the etiological diagnosis of bloodstream infections.

Lao Chuyu, Li Zihuan, Lin Guanwen, Li Congrong, Wang Yuqi

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Аннотация

BACKGROUND

Bloodstream infections (BSIs) represent a significant public health concern. Metagenomic Capture targeted next-generation sequencing technology, as a newly emerging method for pathogen detection, has been applied in the etiological diagnosis of various infectious diseases and demonstrates good diagnostic efficacy. However, there is relatively limited research on the diagnostic value of this technology for the etiological diagnosis of BSIs.

METHODS

A comprehensive retrospective analysis was performed on patients suspected of having BSIs who were admitted to the Affiliated Guangdong Second Provincial General Hospital of Jinan University in 2024. These patients underwent both blood culture analysis and Metagenomic Capture targeted next-generation sequencing technology for diagnostic testing, and a detailed comparison of the results was conducted.

RESULTS

It was found that the Metagenomic Capture-targeted next-generation sequencing method has a shorter time to result [1.33 (1.18 - 1.69) vs 2.73 (1.89 - 3.84) days, p < 0.001], more pathogenic microbial species detected, higher positive detection rate and higher sensitivity than blood culture.

CONCLUSIONS

Metagenomic Capture targeted next-generation sequencing technology is a promising tool for pathogen identification in BSIs, offering substantial methodological advantages in terms of turnaround time, detection breadth, and sensitivity. These diagnostic performance characteristics support its potential utility in clinical microbiology practice.

Для цитирования: Lao Chuyu, Li Zihuan, Lin Guanwen, Li Congrong, Wang Yuqi. Employing Metagenomics Capture targeted next-generation sequencing for the etiological diagnosis of bloodstream infections.. Frontiers in cellular and infection microbiology. 2026. DOI: 10.3389/fcimb.2026.1905007.

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