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开发一种高灵敏度 RT-PCR 检测方法,用于检测个体和混合鼻咽样本中的 SARS-CoV-2。

Development of a high sensitivity RT-PCR assay for detection of SARS-CoV-2 in individual and pooled nasopharyngeal samples.

机构信息

Erba Molecular, Ely, Cambridgeshire, UK.

Materials for Health Lab, Department of Chemical Engineering, University of Bath, Bath, UK.

出版信息

Sci Rep. 2022 Mar 30;12(1):5369. doi: 10.1038/s41598-022-09254-1.

Abstract

The COVID-19 pandemic requires sensitive detection of the SARS-CoV-2 virus from samples to ensure accurate detection of infected patients, an essential component of effective national track and trace programs. Due to the scaling challenges of large sample numbers, sample pooling is an attractive solution to reduce both extraction and amplification reagent costs, if high sensitivity can be maintained. We demonstrate that the Erba Molecular ErbaMDx SARS-CoV-2 RT-PCR Kit (EM kit) delivers high sensitivity, achieving analytical detection of 5 copies/reaction SARS-CoV-2 genomic RNA, and 200 copies/mL SARS-CoV-2 inactivated virus spiked into nasopharyngeal swab (NP) samples and extracted through workflow. Furthermore, the EM Kit demonstrates high sensitivity in both pooled (1 in 5) and non-pooled NP samples when compared to an FDA Emergency Use Authorization approved assay, following published FDA guidelines. These findings demonstrate that the EM Kit is suitable for sample pooling, with minimal impact on assay performance. As the COVID-19 pandemic progresses, high sensitivity assays such as the EM Kit will have an important role in ensuring high throughput and sensitive testing using pooled samples can be maintained, delivering the most cost-effective sample extraction and amplification option for national test and trace programs.

摘要

新冠疫情大流行要求从样本中灵敏检测 SARS-CoV-2 病毒,以确保准确检测感染患者,这是有效国家追踪和溯源计划的重要组成部分。由于样本数量庞大,因此如果能保持高灵敏度,样本混合是一种很有吸引力的降低提取和扩增试剂成本的解决方案。我们证明 Erba Molecular ErbaMDx SARS-CoV-2 RT-PCR 试剂盒(EM 试剂盒)具有高灵敏度,可实现分析检测 5 拷贝/反应 SARS-CoV-2 基因组 RNA,以及在鼻咽拭子(NP)样本中检测到 200 拷贝/mL 经灭活的 SARS-CoV-2 病毒,这些样本经过工作流程提取。此外,与经 FDA 紧急使用授权批准的检测方法相比,按照 FDA 发布的指南,EM 试剂盒在混合(1/5)和非混合 NP 样本中均具有高灵敏度。这些发现表明,EM 试剂盒适合样本混合,对检测性能的影响最小。随着新冠疫情的发展,高灵敏度检测方法(如 EM 试剂盒)将在使用混合样本进行高通量和灵敏检测方面发挥重要作用,为国家检测和溯源计划提供最具成本效益的样本提取和扩增选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1719/8969161/1bf93b8bdc12/41598_2022_9254_Fig1_HTML.jpg

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