University Medical Center, Department of Virology, Göttingen, Germany.
J Clin Microbiol. 2013 Apr;51(4):1110-7. doi: 10.1128/JCM.02704-12. Epub 2013 Jan 23.
Syndromic panels for infectious disease have been suggested to be of value in point-of-care diagnostics for developing countries and for biodefense. To test the performance of isothermal recombinase polymerase amplification (RPA) assays, we developed a panel of 10 RPAs for biothreat agents. The panel included RPAs for Francisella tularensis, Yersinia pestis, Bacillus anthracis, variola virus, and reverse transcriptase RPA (RT-RPA) assays for Rift Valley fever virus, Ebola virus, Sudan virus, and Marburg virus. Their analytical sensitivities ranged from 16 to 21 molecules detected (probit analysis) for the majority of RPA and RT-RPA assays. A magnetic bead-based total nucleic acid extraction method was combined with the RPAs and tested using inactivated whole organisms spiked into plasma. The RPA showed comparable sensitivities to real-time RCR assays in these extracts. The run times of the assays at 42°C ranged from 6 to 10 min, and they showed no cross-detection of any of the target genomes of the panel nor of the human genome. The RPAs therefore seem suitable for the implementation of syndromic panels onto microfluidic platforms.
用于传染病的综合征检测面板被认为对发展中国家的即时护理诊断和生物防御具有重要价值。为了测试等温重组酶聚合酶扩增(RPA)检测的性能,我们开发了针对生物威胁剂的 10 个 RPA 检测面板。该面板包括弗朗西斯菌、鼠疫杆菌、炭疽杆菌、天花病毒以及裂谷热病毒、埃博拉病毒、苏丹病毒和马尔堡病毒的逆转录酶 RPA(RT-RPA)检测。大多数 RPA 和 RT-RPA 检测的分析灵敏度范围为检测到的 16 至 21 个分子(概率分析)。基于磁珠的总核酸提取方法与 RPA 相结合,并使用掺入血浆中的灭活全生物体进行测试。在这些提取物中,RPA 与实时 RT-PCR 检测具有相当的灵敏度。在 42°C 下,检测的运行时间为 6 至 10 分钟,并且它们没有对面板的任何目标基因组或人类基因组进行交叉检测。因此,RPA 似乎适合将综合征检测面板实施到微流控平台上。