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通过双重通用PCR和高分辨率熔解曲线进行跨物种病原体检测

Cross-kingdom pathogen detection via duplex universal PCR and high-resolution melt.

作者信息

Lee Pei-Wei, Totten Marissa, Traylor Amelia, Zhang Sean X, Wang Tza-Huei, Hsieh Kuangwen

机构信息

Department of Mechanical Engineering, Johns Hopkins University, Baltimore, MD, United States.

Division of Microbiology, Department of Pathology, Johns Hopkins School of Medicine, Baltimore, MD, United States.

出版信息

Biosens Bioelectron. 2025 Feb 15;270:116922. doi: 10.1016/j.bios.2024.116922. Epub 2024 Nov 13.

Abstract

Infectious diseases caused by pathogenic bacteria and fungi continuously pose a significant threat worldwide. The occurrence of polymicrobial infections, including polybacterial, polyfungal or bacteria-fungal co-infections further complicates diagnosis and treatment. Current diagnostic methods, heavily reliant on culture methods, are slow and often inefficient. This inefficiency underscores the urgent need for new diagnostic approaches that can swiftly identify a wide array of pathogens across both the bacterial and fungal kingdoms. In response to this need, our study introduces a duplex universal PCR and high-resolution melt (HRM) method that enables the detection of both bacterial and fungal pathogens within a single PCR-HRM procedure. This method uses two universal primer sets designed to target bacterial and fungal genomic DNA respectively, facilitating broad-range detection of 16 pathogens flagged by the World Health Organization (WHO). Moreover, this assay can be adapted in microfluidic-based digital reaction format and when analyzed via a one-versus-one support vector machine classifier achieved a detection accuracy exceeding 99.9%. This digital duplex PCR-HRM method has the capacity to quantitatively detect co-infections with varying pathogen ratios in simulated samples, demonstrating its versatility and multiplexed capacity. When applied to clinical bronchoalveolar lavage (BAL) samples, digital duplex PCR-HRM successfully identified both monomicrobial and polymicrobial infections. This development marks a significant advancement in the field of infectious disease diagnostics, offering a rapid, accurate, and comprehensive method for identifying a broad spectrum of bacterial and fungal pathogens, thus potentially improving patient management and outcomes.

摘要

由致病细菌和真菌引起的传染病在全球范围内持续构成重大威胁。包括多细菌、多真菌或细菌 - 真菌混合感染在内的多重微生物感染的发生,进一步使诊断和治疗复杂化。目前严重依赖培养方法的诊断方法速度慢且效率低下。这种低效率凸显了对新诊断方法的迫切需求,这些新方法能够快速识别细菌和真菌界的多种病原体。为满足这一需求,我们的研究引入了一种双重通用PCR和高分辨率熔解(HRM)方法,该方法能够在单个PCR - HRM程序中检测细菌和真菌病原体。该方法使用分别针对细菌和真菌基因组DNA设计的两套通用引物,便于对世界卫生组织(WHO)标记的16种病原体进行广泛检测。此外,该检测方法可采用基于微流控的数字反应形式,通过一对一支持向量机分类器分析时,检测准确率超过99.9%。这种数字双重PCR - HRM方法能够定量检测模拟样本中不同病原体比例的混合感染,展示了其多功能性和多重检测能力。当应用于临床支气管肺泡灌洗(BAL)样本时,数字双重PCR - HRM成功识别了单一微生物感染和多重微生物感染。这一进展标志着传染病诊断领域的重大进步,为识别广泛的细菌和真菌病原体提供了一种快速、准确且全面的方法,从而有可能改善患者管理和治疗结果。

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