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简易核酸扩增检测疟疾法:一种利用交叉引物扩增技术检测疟原虫种类的简单、快速方法。

EasyNAT Malaria: a simple, rapid method to detect species using cross-priming amplification technology.

作者信息

Dong Liu, Xu Qianqian, Shen Linjie, Cao Ruoshui, Deng Xuan, Chen Jian, Jiang Haoqin, Guan Ming

机构信息

Department of Laboratory Medicine, Huashan Hospital, Fudan University, Shanghai, China.

出版信息

Microbiol Spectr. 2024 Jun 13;12(8):e0058324. doi: 10.1128/spectrum.00583-24.

Abstract

UNLABELLED

Malaria infection remains a serious threat to human health worldwide. Rapid and accurate detection technology is crucial for preventing malaria transmission and minimizing damage. We aimed to establish and validate a new rapid molecular detection method for malaria, called EasyNAT Malaria Assay, targeting , , , and . The analytical performance of EasyNAT Malaria Assay was determined using positive materials. We identified 42 clinical samples as malaria positive and 95 negative samples. Each sample was examined by four methods: light microscopy, rapid diagnostic test, EasyNAT Malaria Assay, and digital PCR. Diagnostic accuracy and clinical performance were evaluated. The limit of detection (LOD) of EasyNAT Malaria was consistently 40 parasites/mL. It specifically amplified and performed with reliable repeatability and reproducibility. In 137 clinical samples, EasyNAT Malaria detected four more positive samples than microscopic examination and two more positive samples than rapid diagnostic test (RDT). One clinical sample was positive only under digital PCR. However, no significant differences statistically in sensitivity or specificity were observed. Compared with microscopy, the total, positive, and negative concordance rates of EasyNAT were 97.08%, 100%, and 95.79%, respectively. Enhanced diagnostic accuracy of EasyNAT Malaria in patients who had taken anti-malarial medication before their clinical appointment was observed. The EasyNAT Malaria Assay has good detection efficiency for clinical samples, presents a promising molecular detection tool in clinical practice, and is particularly suitable for rapid screening of high-risk populations in the emergency room.

IMPORTANCE

This study established and validated EasyNAT Malaria Assay as a promising molecular detection tool for malaria screening of high-risk populations in clinical practice. This novel isothermal amplification method may effectively facilitate the rapid diagnosis of malaria and prevent its transmission.

摘要

未标记

疟疾感染仍是全球人类健康的严重威胁。快速准确的检测技术对于预防疟疾传播和减少损害至关重要。我们旨在建立并验证一种新的疟疾快速分子检测方法,称为EasyNAT疟疾检测法,其靶向……、……、……和……。使用阳性材料确定EasyNAT疟疾检测法的分析性能。我们将42份临床样本鉴定为疟疾阳性,95份为阴性样本。每个样本通过四种方法进行检测:光学显微镜检查、快速诊断检测、EasyNAT疟疾检测法和数字PCR。评估诊断准确性和临床性能。EasyNAT疟疾检测法的检测限始终为每毫升40个疟原虫。它能特异性扩增……,并且具有可靠的重复性和再现性。在137份临床样本中,EasyNAT疟疾检测法比显微镜检查多检测出4份阳性样本,比快速诊断检测(RDT)多检测出2份阳性样本。有一份临床样本仅在数字PCR检测下呈阳性。然而,在敏感性或特异性方面未观察到统计学上的显著差异。与显微镜检查相比,EasyNAT的总符合率、阳性符合率和阴性符合率分别为97.08%、100%和95.79%。观察到EasyNAT疟疾检测法在临床就诊前服用过抗疟药物的患者中提高了诊断准确性。EasyNAT疟疾检测法对临床样本具有良好的检测效率,是临床实践中一种有前景的分子检测工具,尤其适用于急诊室高危人群的快速筛查。

重要性

本研究建立并验证了EasyNAT疟疾检测法,作为临床实践中对高危人群进行疟疾筛查的一种有前景的分子检测工具。这种新型等温扩增方法可能有效地促进疟疾的快速诊断并预防其传播。

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本文引用的文献

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A rapid multiplex assay of human malaria parasites by digital PCR.通过数字PCR对人类疟原虫进行快速多重检测。
Clin Chim Acta. 2023 Jan 15;539:70-78. doi: 10.1016/j.cca.2022.12.001. Epub 2022 Dec 7.
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Malaria rapid diagnostic tests: challenges and prospects.疟疾快速诊断检测:挑战与展望。
J Med Microbiol. 2013 Oct;62(Pt 10):1491-1505. doi: 10.1099/jmm.0.052506-0.

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