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用于快速灵敏检测前病毒HIV-1 DNA的重组酶聚合酶扩增检测的非仪器孵育法

Non-instrumented incubation of a recombinase polymerase amplification assay for the rapid and sensitive detection of proviral HIV-1 DNA.

作者信息

Lillis Lorraine, Lehman Dara, Singhal Mitra C, Cantera Jason, Singleton Jered, Labarre Paul, Toyama Anthony, Piepenburg Olaf, Parker Mathew, Wood Robert, Overbaugh Julie, Boyle David S

机构信息

PATH, Seattle, Washington, United States of America.

Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.

出版信息

PLoS One. 2014 Sep 29;9(9):e108189. doi: 10.1371/journal.pone.0108189. eCollection 2014.

Abstract

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.

摘要

传染病的灵敏诊断测试通常采用核酸扩增技术(NAATs)。然而,大多数NAAT检测方法,包括许多等温扩增方法,都需要依赖电力的仪器进行孵育。对于在资源匮乏地区(LRS)使用而言,不需要持续电力供应的诊断方法将是理想之选。重组酶聚合酶扩增(RPA)是一种等温扩增技术,已证明其通常在25 - 43°C的温度范围内工作,并且不需要严格的孵育温度即可实现最佳性能。在此,我们评估了在环境温度下或使用简单的无仪器加热源孵育用于LRS婴儿HIV诊断的HIV-1 RPA检测的能力。为了确定HIV-1婴儿诊断最有用的环境温度范围,分析了撒哈拉以南非洲每日温度的季节性范围数据集,结果显示环境温度低至10°C,很少高于43°C。当在31°C至43°C之间孵育20分钟时,24个HIV-1 RPA反应全部(100%)扩增。在30°C以下温度下,所研究的HIV-1 RPA检测的扩增一致性较差。因此,我们开发了一种化学加热器,用于在环境温度为10°C至30°C时孵育HIV-1 RPA检测。在15°C、20°C、25°C和30°C的环境温度下,所有12/12(100%)反应通过化学加热孵育均实现扩增。我们还观察到,在较低温度下孵育30分钟可提高检测性能,在20分钟孵育时检测结果零星出现的较低温度下尤其如此。我们已经证明,通过环境温度或使用化学加热器孵育RPA HIV-1检测,其结果与使用电动设备相似。我们提出,这种RPA HIV-1检测可能无需专用设备即可成为在LRS诊断婴儿HIV-1的高灵敏度工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41d8/4180440/6370d97000b6/pone.0108189.g001.jpg

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