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采用 Seegene Allplex™ 2019-nCoV assay 对未经提取的口咽鼻拭子标本进行实时 RT-PCR 检测 SARS-CoV-2 的高效性。

Efficient SARS-CoV-2 detection in unextracted oro-nasopharyngeal specimens by rRT-PCR with the Seegene Allplex™ 2019-nCoV assay.

机构信息

Institut national de la recherche scientifique, Centre Armand-Frappier Santé Biotechnologie, Laval, QC, H7V 1B7, Canada.

Département de chimie, biochimie et physique, Université du Québec à Trois-Rivières, Trois-Rivières, QC, Canada.

出版信息

Virol J. 2020 Dec 18;17(1):196. doi: 10.1186/s12985-020-01468-x.

Abstract

BACKGROUND

The fight against the COVID-19 pandemic has created an urgent need to rapidly detect infected people. The challenge for clinical laboratories has been finding a high throughput, cost-efficient, and accurate testing method in the context of extraction reagents shortage on a global scale. To answer this need, we studied SARS-CoV-2 detection in oro-nasopharyngeal (ONP) swabs stored in Universal Transport Media (UTM) or in RNase-free water by rRT-PCR with Seegene Allplex™ 2019-nCoV assay without RNA extraction.

RESULTS

Optimal results were obtained when swabs stored in UTM were diluted 1/5 and 1/2 in RNase-free water. Thermal lysis before rRT-PCR testing slightly improved detection rate. In addition, proteinase K (PK) treatment allowed for a significant reduction of invalid results and increased sensitivity for detection of low viral load specimens. In a panel of positive samples with all 3 viral genes amplified and N gene Cycle threshold values (C values) from 15 to 40, our detection rate was 98.9% with PK and 94.4% without. In a challenging panel of low positive samples with only the N gene being detectable at C values > 30, detection rate was increased from 53.3 to 76.7% with the addition of PK, and invalid rate fell off from 18.3 to 0%. Furthermore, we demonstrated that our method reliably detects specimens with C values up to 35, whereas false negative samples become frequent above this range. Finally, we show that swabs should be stored at - 70 °C rather than 4 °C when testing cannot be performed within 72 h of collection.

CONCLUSION

We successfully optimized the unextracted rRT-PCR process using the Seegene Allplex™ 2019-nCoV assay to detect SARS-CoV-2 RNAs in nasopharyngeal swabs. This improved method offers cost savings and turnaround time advantages compared to automated extraction, with high efficiency of detection that could play an important role in the surveillance of Covid-19.

摘要

背景

抗击 COVID-19 大流行的斗争迫切需要快速检测感染者。临床实验室面临的挑战是在全球范围内提取试剂短缺的情况下,找到一种高通量、具有成本效益且准确的检测方法。为了满足这一需求,我们研究了在没有 RNA 提取的情况下,使用 Seegene Allplex™ 2019-nCoV 检测试剂盒,通过 rRT-PCR 检测储存在通用运输介质(UTM)或无 RNA 酶水中的口咽(ONP)拭子中的 SARS-CoV-2。

结果

当 UTM 中的拭子在无 RNA 酶水中稀释 1/5 和 1/2 时,可获得最佳结果。rRT-PCR 检测前的热裂解略微提高了检测率。此外,蛋白酶 K(PK)处理可显著减少无效结果,并提高对低病毒载量标本的检测灵敏度。在一组阳性样本中,所有 3 个病毒基因均扩增,N 基因循环阈值(C 值)为 15 至 40,我们的检测率为 98.9%,PK 处理组为 94.4%,无 PK 处理组为 94.4%。在一组具有挑战性的低阳性样本中,仅 N 基因可在 C 值>30 时检测到,添加 PK 后,检测率从 53.3%提高到 76.7%,无效率从 18.3%下降到 0%。此外,我们证明我们的方法可以可靠地检测 C 值高达 35 的标本,而在该范围以上,假阴性样本变得频繁。最后,我们表明,当不能在采集后 72 小时内进行检测时,拭子应储存在-70°C 而不是 4°C。

结论

我们成功优化了使用 Seegene Allplex™ 2019-nCoV 检测试剂盒检测鼻咽拭子中 SARS-CoV-2 RNA 的未提取 rRT-PCR 流程。与自动化提取相比,这种改进的方法具有成本节约和周转时间优势,检测效率高,在新冠病毒监测中可能发挥重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51a6/7747408/925aee3165c7/12985_2020_1468_Fig1_HTML.jpg

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