Institute of Diagnostic Virology, Friedrich-Loeffler-Institut, Südufer 10, 17493 Greifswald-Insel Riems, Germany.
Friedrich-Loeffler-Institut, Südufer 10, 17493 Greifswald-Insel Riems, Germany.
Viruses. 2020 Oct 29;12(11):1227. doi: 10.3390/v12111227.
To assist the global eradication of peste des petits ruminants virus (PPRV), a molecular test for the rapid and reliable detection of PPRV was developed which additionally enables the detection of pathogens relevant for differential diagnostics. For this purpose, the necessary time frame of a magnetic bead-based nucleic acid extraction protocol was markedly shortened to 7 min and 13 s. The optimized extraction was run on a BioSprint 15 platform. Furthermore, a high-speed multi-well RT-qPCR for the genome detection of PPRV and additional important pathogens such as Foot-and-mouth disease virus, Parapoxvirus ovis, Goatpox virus, and was established and combined with suitable internal control assays. The here-described qPCR is based on a lyophilized master mix and takes only around 30 to 40 min. Several qPCR cyclers were evaluated regarding their suitability for fast-cycling approaches and for their diagnostic performance in a high-speed RT-qPCR. The final evaluation was conducted on the BioRad CFX96 and also on a portable Liberty16 qPCR cycler. The new molecular test designated as "FastCheck PPR-like", which is based on rapid nucleic acid extraction and high-speed RT-qPCR, delivered reliable results in less than one hour, allowing its use also in a pen-side scenario.
为了协助全球消灭小反刍兽疫病毒(PPRV),我们开发了一种用于快速可靠检测 PPRV 的分子检测方法,该方法还能检测到用于鉴别诊断的相关病原体。为此,我们显著缩短了基于磁珠的核酸提取方案的必要时间框架,使其达到 7 分 13 秒。优化后的提取在 BioSprint 15 平台上进行。此外,我们还建立了一种高通量多孔 RT-qPCR,用于检测 PPRV 基因组和其他重要病原体,如口蹄疫病毒、羊口疮病毒、山羊痘病毒和,同时结合了合适的内参检测方法。这里描述的 qPCR 基于冻干的主混合物,仅需约 30 到 40 分钟。我们评估了几种 qPCR 循环仪,以确定它们是否适合快速循环方法以及在高通量 RT-qPCR 中的诊断性能。最终的评估分别在 BioRad CFX96 和便携式 Liberty16 qPCR 循环仪上进行。新的分子检测方法被命名为“FastCheck PPR-like”,它基于快速核酸提取和高通量 RT-qPCR,在不到一个小时内就能提供可靠的结果,允许在笔式检测场景中使用。