Malaria Branch, Division of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, Georgia, United States of America.
PLoS One. 2010 Oct 29;5(10):e13733. doi: 10.1371/journal.pone.0013733.
Molecular diagnostic methods can complement existing tools to improve the diagnosis of malaria. However, they require good laboratory infrastructure thereby restricting their use to reference laboratories and research studies. Therefore, adopting molecular tools for routine use in malaria endemic countries will require simpler molecular platforms. The recently developed loop-mediated isothermal amplification (LAMP) method is relatively simple and can be improved for better use in endemic countries. In this study, we attempted to improve this method for malaria diagnosis by using a simple and portable device capable of performing both the amplification and detection (by fluorescence) of LAMP in one platform. We refer to this as the RealAmp method.
Published genus-specific primers were used to test the utility of this method. DNA derived from different species of malaria parasites was used for the initial characterization. Clinical samples of P. falciparum were used to determine the sensitivity and specificity of this system compared to microscopy and a nested PCR method. Additionally, directly boiled parasite preparations were compared with a conventional DNA isolation method. The RealAmp method was found to be simple and allowed real-time detection of DNA amplification. The time to amplification varied but was generally less than 60 minutes. All human-infecting Plasmodium species were detected. The sensitivity and specificity of RealAmp in detecting P. falciparum was 96.7% and 91.7% respectively, compared to microscopy and 98.9% and 100% respectively, compared to a standard nested PCR method. In addition, this method consistently detected P. falciparum from directly boiled blood samples.
This RealAmp method has great potential as a field usable molecular tool for diagnosis of malaria. This tool can provide an alternative to conventional PCR based diagnostic methods for field use in clinical and operational programs.
分子诊断方法可以补充现有的工具,以提高疟疾的诊断。然而,它们需要良好的实验室基础设施,从而限制了它们在参考实验室和研究中的使用。因此,在疟疾流行国家采用分子工具进行常规使用将需要更简单的分子平台。最近开发的环介导等温扩增(LAMP)方法相对简单,可以进行改进,以便更好地在流行国家使用。在这项研究中,我们试图通过使用一种简单且便携式的设备来改进这种方法,该设备能够在一个平台上同时进行 LAMP 的扩增和检测(通过荧光)。我们将其称为 RealAmp 方法。
使用已发表的属特异性引物来测试该方法的实用性。使用不同疟原虫种的 DNA 进行初始表征。使用 P. falciparum 的临床样本来确定该系统与显微镜和巢式 PCR 方法相比的灵敏度和特异性。此外,还将直接煮沸的寄生虫制剂与常规 DNA 分离方法进行了比较。发现 RealAmp 方法简单,允许实时检测 DNA 扩增。扩增时间不同,但通常不到 60 分钟。所有感染人类的疟原虫种均被检测到。与显微镜相比,RealAmp 检测 P. falciparum 的灵敏度和特异性分别为 96.7%和 91.7%,与标准巢式 PCR 方法相比分别为 98.9%和 100%。此外,该方法一致地从直接煮沸的血液样本中检测到 P. falciparum。
这种 RealAmp 方法作为一种可在现场使用的疟疾分子诊断工具具有很大的潜力。该工具可以为现场使用的临床和运营计划提供替代传统基于 PCR 的诊断方法。