加强血流感染诊断:精确识别病原体的新型过滤和定向下一代测序方法。

IF 4 2区 生物学 Q2 MICROBIOLOGY
Frontiers in Microbiology Pub Date : 2025-03-20 eCollection Date: 2025-01-01 DOI:10.3389/fmicb.2025.1538265
Ting-Syuan Lin, ZiHao Zhu, XiaoHong Lin, Hsi-Yuan Huang, Li-Ping Li, Jing Li, Jie Ni, PeiZhi Li, LanChun Chen, WeiXin Tang, HuiXin Liu, XiaoLong Se, MingFei Xie, Canling Long, Chih-Min Chiu, Szu-Han Fang, JiaMing Zhao, Yang-Chi-Dung Lin, XueTao Yu, Hsien-Da Huang
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引用次数: 0

摘要

血流感染(bsi)是一项重大的诊断挑战,主要是由于血培养等传统方法的局限性。这些方法通常产生较低的阳性率,处理时间长,延误治疗,并且仅限于检测范围狭窄的病原体。这种延误和不准确可能严重阻碍及时的临床干预,潜在地损害患者的预后。新一代测序(NGS)是快速、精确鉴定病原体的有力工具。虽然宏基因组NGS (mNGS)提供了广泛的病原体覆盖范围,但它往往昂贵且复杂。然而,靶向NGS (tNGS)侧重于临床相关病原体的关键区域,在保持高灵敏度的同时降低了成本并简化了工作流程,使其更适用于常规诊断。在这项研究中,我们介绍了一种结合人类细胞特异性过滤膜和多路tNGS面板的新方法来克服这些挑战。该过滤膜具有表面电荷特性,对白细胞具有静电吸引力,可选择性捕获特定细胞,在去除宿主细胞和核酸方面表现出高效率,使宿主DNA减少98%以上,从而最大限度地减少病原体检测中的背景干扰。此外,我们开发了一种针对330多种临床相关病原体的有效的多重tNGS面板,并验证了其与mNGS和血培养结果的一致性,显示出检测灵敏度的显着提高。通过整合这两种方法,我们实现了诊断能力的协同增强,将病原体读数提高了6- 8倍,即使在低丰度病原体的情况下也能进行可靠的鉴定。这种方法提供了更快、更准确、更敏感的bsi检测,从而能够更早地识别感染。这有助于及时和有针对性的治疗,最终改善重症监护环境中的患者预后。考虑到过滤膜的独特特性和tNGS面板的优势,这种方法在产前和遗传健康支持以及推进早期癌症筛查策略方面显示出有希望的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhancing bloodstream infection diagnostics: a novel filtration and targeted next-generation sequencing approach for precise pathogen identification.

Bloodstream infections (BSIs) pose a significant diagnostic challenge, largely due to the limitations of traditional methods such as blood cultures. These methods often yield low positive rates, have lengthy processing times that delay treatment, and are limited in detecting only a narrow range of pathogens. Such delays and inaccuracies can critically impede timely clinical interventions, potentially compromising patient outcomes. Next-generation sequencing (NGS) is a powerful tool for rapid, precise pathogen identification. While metagenomic NGS (mNGS) offers broad pathogen coverage, it is often costly and complex. Targeted NGS (tNGS), however, focuses on key regions of clinically relevant pathogens, reducing costs and simplifying workflows while maintaining high sensitivity, making it more practical for routine diagnostics. In this study, we introduce a novel approach combining a human cell-specific filtration membrane with a multiplex tNGS panel to overcome these challenges. The filtration membrane, designed with surface charge properties to be electrostatically attractive to leukocytes for the selective capture of specific cells, demonstrated high efficiency in removing host cells and nucleic acids, achieving over a 98% reduction in host DNA and thereby minimizing background interference in pathogen detection. Additionally, we developed an effective multiplex tNGS panel targeting over 330 clinically relevant pathogens and verified its consistency with mNGS and blood culture results, demonstrating a significant improvement in detection sensitivity. By integrating these two methods, we achieved a synergistic enhancement in diagnostic capability, boosting pathogen reads by 6- to 8-fold, which enabled reliable identification even in cases of low-abundance pathogens. This approach provides faster, more accurate, and more sensitive detection of BSIs, enabling earlier identification of infections. This facilitates timely and targeted treatment, ultimately improving patient outcomes in critical care settings. Given the unique properties of the filtration membrane and the strengths of the tNGS panel, this approach shows promising applications in prenatal and genetic health support, as well as in advancing early cancer screening strategies.

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来源期刊
CiteScore
7.70
自引率
9.60%
发文量
4837
审稿时长
14 weeks
期刊介绍: Frontiers in Microbiology is a leading journal in its field, publishing rigorously peer-reviewed research across the entire spectrum of microbiology. Field Chief Editor Martin G. Klotz at Washington State University is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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