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Non-Instrumented Incubation of a Recombinase Polymerase Amplification Assay for the Rapid and Sensitive Detection of Proviral HIV-1 DNA

机译:重组酶聚合酶扩增试验的非仪器温育用于快速和灵敏地检测原病毒HIV-1 DNA

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摘要

Sensitive diagnostic tests for infectious diseases often employ nucleic acid amplification technologies (NAATs). However, most NAAT assays, including many isothermal amplification methods, require power-dependent instrumentation for incubation. For use in low resource settings (LRS), diagnostics that do not require consistent electricity supply would be ideal. Recombinase polymerase amplification (RPA) is an isothermal amplification technology that has been shown to typically work at temperatures ranging from 25–43°C, and does not require a stringent incubation temperature for optimal performance. Here we evaluate the ability to incubate an HIV-1 RPA assay, intended for use as an infant HIV diagnostic in LRS, at ambient temperatures or with a simple non-instrumented heat source. To determine the range of expected ambient temperatures in settings where an HIV-1 infant diagnostic would be of most use, a dataset of the seasonal range of daily temperatures in sub Saharan Africa was analyzed and revealed ambient temperatures as low as 10°C and rarely above 43°C. All 24 of 24 (100%) HIV-1 RPA reactions amplified when incubated for 20 minutes between 31°C and 43°C. The amplification from the HIV-1 RPA assay under investigation at temperatures was less consistent below 30°C. Thus, we developed a chemical heater to incubate HIV-1 RPA assays when ambient temperatures are between 10°C and 30°C. All 12/12 (100%) reactions amplified with chemical heat incubation from ambient temperatures of 15°C, 20°C, 25°C and 30°C. We also observed that incubation at 30 minutes improved assay performance at lower temperatures where detection was sporadic using 20 minutes incubation. We have demonstrated that incubation of the RPA HIV-1 assay via ambient temperatures or using chemical heaters yields similar results to using electrically powered devices. We propose that this RPA HIV-1 assay may not need dedicated equipment to be a highly sensitive tool to diagnose infant HIV-1 in LRS.
机译:对传染病的敏感诊断测试通常采用核酸扩增技术(NAAT)。但是,大多数NAAT分析(包括许多等温扩增方法)都需要依赖功率的仪器进行孵育。对于在资源少的环境(LRS)中使用,不需要持续供电的诊断将是理想的。重组酶聚合酶扩增(RPA)是一种等温扩增技术,已显示通常在25-43°C的温度范围内工作,不需要严格的孵育温度即可获得最佳性能。在这里,我们评估了在室温或简单的非仪器热源条件下培养用于LRS的婴儿HIV诊断的HIV-1 RPA测定的能力。为了确定最需要使用HIV-1婴儿诊断仪的环境中的预期环境温度范围,对撒哈拉以南非洲每日温度的季节性范围数据集进行了分析,发现环境温度低至10°C,很少高于43°C。在31°C至43°C之间孵育20分钟时,24个(100%)HIV-1 RPA反应中的所有24个都扩增了。在低于30°C的温度下,正在研究的HIV-1 RPA分析的扩增不一致。因此,我们开发了一种化学加热器,用于在环境温度介于10°C至30°C之间时进行HIV-1 RPA分析。所有12/12(100%)反应都是通过化学热孵育从15°C,20°C,25°C和30°C的环境温度扩增而来的。我们还观察到,在较低温度下30分钟孵育可改善测定性能,在较低温度下使用20分钟孵育可进行零星检测。我们已经证明,通过环境温度或使用化学加热器对RPA HIV-1分析物进行培养可产生与使用电动设备相似的结果。我们建议,这种RPA HIV-1检测可能不需要专用设备即可成为诊断LRS中婴儿HIV-1的高度敏感的工具。

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