Department of Clinical Parasitology, Hospital for Tropical Diseases, London Hospitals University College NHS Foundation Trust, Mortimer Market, Capper Street, London WC1E 6JB, United Kingdom.
J Clin Microbiol. 2010 Aug;48(8):2866-71. doi: 10.1128/JCM.00355-10. Epub 2010 Jun 16.
Loop-mediated isothermal amplification (LAMP) of DNA offers the ability to detect very small quantities of pathogen DNA following minimal tissue sample processing and is thus an attractive methodology for point-of-care diagnostics. Previous attempts to diagnose malaria by the use of blood samples and LAMP have targeted the parasite small-subunit rRNA gene, with a resultant sensitivity for Plasmodium falciparum of around 100 parasites per microl. Here we describe the use of mitochondrial targets for LAMP-based detection of any Plasmodium genus parasite and of P. falciparum specifically. These new targets allow routine amplification from samples containing as few as five parasites per microl of blood. Amplification is complete within 30 to 40 min and is assessed by real-time turbidimetry, thereby offering rapid diagnosis with greater sensitivity than is achieved by the most skilled microscopist or antigen detection using lateral flow immunoassays.
环介导等温扩增 (LAMP) 可在对组织样本进行最小程度处理的情况下检测到极少量的病原体 DNA,因此非常适合用于即时诊断。之前曾尝试通过使用血液样本和 LAMP 来诊断疟疾,目标是寄生虫小亚基 rRNA 基因,结果对恶性疟原虫的灵敏度约为每微升 100 个寄生虫。在这里,我们描述了使用线粒体靶标进行基于 LAMP 的任何疟原虫属寄生虫的检测,特别是对恶性疟原虫的检测。这些新的靶标允许从每微升血液中含有低至 5 个寄生虫的样本中进行常规扩增。扩增在 30 到 40 分钟内完成,并通过实时浊度测定进行评估,从而提供了比最熟练的显微镜检查或使用侧流免疫分析的抗原检测更快的诊断,具有更高的灵敏度。