Department of Parasitology, Faculty of Medicine, Universiti Malaya, Kuala Lumpur, Malaysia.
Vector Borne Disease Sector, Ministry of Health, Putrajaya, Malaysia.
Am J Trop Med Hyg. 2023 Mar 13;108(5):882-886. doi: 10.4269/ajtmh.22-0657. Print 2023 May 3.
This study highlights the development of two lateral flow recombinase polymerase amplification assays for the diagnosis of human malaria. The lateral flow cassettes contained test lines that captured biotin-, 6-carboxyfluorescein, digoxigenin-, cyanine 5-, and dinitrophenyl-labeled amplicons. The overall process can be completed in 30 minutes. Recombinase polymerase amplification coupled with lateral flow had a detection limit of 1 copy/µL for Plasmodium knowlesi, Plasmodium vivax, and Plasmodium falciparum. No cross-reactivity was observed among nonhuman malaria parasites such as Plasmodium coatneyi, Plasmodium cynomolgi, Plasmodium brasilanium, Plasmodium inui, Plasmodium fragile, Toxoplasma gondii, Sarcocystis spp., Brugia spp., and 20 healthy donors. It is rapid, highly sensitive, robust, and easy to use. The result can be read without the need for special equipment and thus has the potential to serve as an effective alternative to polymerase chain reaction methods for the diagnosis of malaria.
本研究开发了两种用于诊断人类疟疾的侧向流动重组酶聚合酶扩增检测方法。侧向流动盒包含了可捕获生物素、6-羧基荧光素、地高辛、Cy5 和二硝基苯标记的扩增子的检测线。整个过程可以在 30 分钟内完成。与侧向流动相结合的重组酶聚合酶扩增的检测限为 1 拷贝/μL,可检测间日疟原虫、卵形疟原虫和恶性疟原虫。在非人类疟原虫如库蚊疟原虫、猕猴疟原虫、巴西疟原虫、因纽特疟原虫、脆弱疟原虫、刚地弓形虫、肉孢子虫属、盘尾丝虫属和 20 名健康供体中未观察到交叉反应。它快速、高度敏感、稳健且易于使用。结果无需特殊设备即可读取,因此有可能成为聚合酶链反应方法的有效替代品,用于疟疾的诊断。