Direct Testing of Blood Samples to Diagnose Bloodstream Infections.

IF 4 2区 医学 Q2 CHEMISTRY, MEDICINAL
Xiaoyi Yang, Yiyang Fan, Xin Xu, Tong Shen, Xiaohui An, Yuting Zhang, Ze Zhang, Hongzhi Pan, Dong Chang
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Abstract

Bloodstream infection (BSI) is a critical condition with extremely high mortality. Rapid and accurate diagnosis is crucial for effective treatment. The traditional blood culture (BC) method has issues, such as long testing times and limited sensitivity, making it challenging to meet the need for timely diagnosis. To address this problem, various molecular biology methods for directly detecting blood samples (whole blood, plasma, serum, and positive BC samples) have emerged. These include Raman spectroscopy, mass spectrometry, nucleic acid amplification, and hybridization techniques (such as the CRISPR/Cas system, digital droplet PCR (ddPCR), and T2 magnetic resonance (T2MR)), biosensors, and next-generation sequencing (NGS). These methods can quickly identify pathogens and their drug-resistant markers, significantly reducing diagnostic delays and helping to provide earlier targeted treatment. This article systematically analyzes the principles, advantages, and disadvantages of these advanced techniques, explores their value in revolutionizing the BSI diagnostic model, and looks ahead to future development directions, providing a reference for research and clinical applications in this field.

直接检测血液样本诊断血流感染。
血流感染(BSI)是一种死亡率极高的危重疾病。快速准确的诊断对有效治疗至关重要。传统的血培养(BC)方法存在检测时间长、灵敏度有限等问题,难以满足及时诊断的需要。为了解决这个问题,出现了各种直接检测血液样本(全血、血浆、血清和阳性BC样本)的分子生物学方法。这些技术包括拉曼光谱、质谱、核酸扩增和杂交技术(如CRISPR/Cas系统、数字液滴PCR (ddPCR)和T2磁共振(T2MR))、生物传感器和下一代测序(NGS)。这些方法可以快速识别病原体及其耐药标记物,显著减少诊断延误,并有助于提供更早的靶向治疗。本文系统分析了这些先进技术的原理、优缺点,探讨了它们在彻底改变BSI诊断模式方面的价值,并展望了未来的发展方向,为该领域的研究和临床应用提供参考。
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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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