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Novel techniques and future directions in molecular diagnosis of malaria in resource-limited settings.在资源有限的环境中,疟疾分子诊断的新方法和未来方向。
Expert Rev Mol Diagn. 2015;15(11):1419-26. doi: 10.1586/14737159.2015.1090878. Epub 2015 Sep 28.
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Comparison of three molecular methods for the detection and speciation of five human Plasmodium species.三种分子方法用于检测五种人类疟原虫物种及进行物种鉴定的比较
Am J Trop Med Hyg. 2015 Jan;92(1):28-33. doi: 10.4269/ajtmh.14-0309. Epub 2014 Nov 10.
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Rapid detection of Plasmodium falciparum with isothermal recombinase polymerase amplification and lateral flow analysis.应用等温重组酶聚合酶扩增和侧流分析技术快速检测恶性疟原虫。
Malar J. 2014 Mar 15;13:99. doi: 10.1186/1475-2875-13-99.
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Detection and species identification of malaria parasites by isothermal tHDA amplification directly from human blood without sample preparation.无需样品制备,通过等温 tHDA 扩增直接从人血中检测和鉴定疟原虫。
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Laboratory markers of disease severity in Plasmodium knowlesi infection: a case control study.伯氏疟原虫感染疾病严重程度的实验室标志物:病例对照研究。
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Evaluation of a loop-mediated isothermal amplification method as a tool for diagnosis of infection by the zoonotic simian malaria parasite Plasmodium knowlesi.评估环介导等温扩增法作为诊断动物源疟原虫感染的工具。
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重组酶聚合酶扩增联合侧向流层析检测 。

Recombinase Polymerase Amplification Combined with a Lateral Flow Strip for the Detection of .

机构信息

Department of Parasitology, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.

Sarawak State Health Department, Kuching, Sarawak, Malaysia.

出版信息

Am J Trop Med Hyg. 2018 Mar;98(3):700-703. doi: 10.4269/ajtmh.17-0738. Epub 2017 Dec 14.

DOI:10.4269/ajtmh.17-0738
PMID:29260656
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5930912/
Abstract

The aim of this study was to develop a recombinase polymerase amplification (RPA) combined with a lateral flow (LF) strip method for specific diagnosis of . With incubation at 37°C, the gene of was successfully amplified within 12 minutes. By adding a specifically designed probe to the reaction solution, the amplified RPA product can be visualized on a LF strip. The RPA assay exhibited high sensitivity with limits of detection down to 10 parasites/μL of . Nonetheless, it was demonstrated that all ( = 41) and other sp. ( = 25) were positive while negative samples ( = 8) were negative. Therefore, a combination of RPA and LF strip detection is a highly promising approach with the potential to be suitable for use in resource-limited settings.

摘要

本研究旨在开发一种重组酶聚合酶扩增(RPA)与侧向流动(LF)条带方法相结合,用于 的特异性诊断。在 37°C 孵育下, 基因在 12 分钟内成功扩增。通过在反应溶液中添加特异性设计的探针,可以在 LF 条带中可视化扩增的 RPA 产物。RPA 检测法具有较高的灵敏度,检测下限低至 10 个寄生虫/μL 的 。然而,结果表明所有 (=41)和其他 sp.(=25)均为阳性,而阴性样本(=8)均为阴性。因此,RPA 和 LF 条带检测的组合是一种很有前途的方法,有可能适用于资源有限的环境。