Center for Research and Innovation, Faculty of Medical Technology, Mahidol University, Bangkok 10700, Thailand.
Graduate Program in Biomedical Sciences, Faculty of Allied Health Sciences, Thammasat University, Pathum Thani 12120, Thailand.
Talanta. 2017 Mar 1;164:645-650. doi: 10.1016/j.talanta.2016.10.106. Epub 2016 Nov 5.
The highly sensitive and specific detection of Pfg377 gene of Plasmodium falciparum gametocyte using Magnetic Nanoparticles PCR Enzyme-Linked Gene Assay (MELGA) was successfully developed. The MELGA included amplification of the Pfg377 gene by polymerase chain reaction (PCR) using magnetic nanoparticles (MNPs)-conjugated forward primer and biotinylated reverse primer, followed by post-analytical process using horseradish peroxidase (HRP)-conjugated streptavidin (SA). The complexes of MELGA product were incubated with the peroxidase substrate and hydrogen peroxide to produce the signal for colorimetric measurement. Altogether, the MELGA technique provided a highly sensitive and specific detection at 1 P. falciparum gametocyte/µL, which was more efficient than that of microscopic examination and rapid diagnostic tests (RDTs). Additionally, the MELGA could detect target gene at femtogram level, which was greater sensitive than the conventional PCR, nested PCR and loop-mediated isothermal amplification (LAMP). The MELGA technique could become a novel and practical method that overcome limitation of traditional gametocyte detection.
利用磁性纳米颗粒聚合酶链反应酶联基因检测(MELGA)成功开发了对恶性疟原虫配子体 Pfg377 基因的高敏感和特异性检测方法。MELGA 包括使用磁性纳米颗粒(MNPs)偶联的正向引物和生物素化的反向引物通过聚合酶链反应(PCR)扩增 Pfg377 基因,然后通过辣根过氧化物酶(HRP)偶联的链霉亲和素(SA)进行后分析处理。MELGA 产物的复合物与过氧化物酶底物和过氧化氢孵育,产生比色测量的信号。总之,MELGA 技术在 1 个恶性疟原虫配子体/μL 时提供了高敏感和特异性的检测,比显微镜检查和快速诊断测试(RDT)更有效。此外,MELGA 可以在飞克级水平检测靶基因,比常规 PCR、巢式 PCR 和环介导等温扩增(LAMP)更灵敏。MELGA 技术可能成为一种新颖实用的方法,可以克服传统配子体检测的局限性。