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实施高效的 SARS-CoV-2 标本汇集策略,以实现高通量诊断检测。

Implementation of an efficient SARS-CoV-2 specimen pooling strategy for high throughput diagnostic testing.

机构信息

KwaZulu-Natal Research Innovation and Sequencing Platform (KRISP), School of Laboratory Medicine & Medical Sciences, University of KwaZulu-Natal, Durban, South Africa.

African Institute for Mathematical Sciences, The Next Einstein Initiative, Kigali, Rwanda.

出版信息

Sci Rep. 2021 Sep 7;11(1):17793. doi: 10.1038/s41598-021-96934-z.

DOI:10.1038/s41598-021-96934-z
PMID:34493744
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8423848/
Abstract

The rapid identification and isolation of infected individuals remains a key strategy for controlling the spread of SARS-CoV-2. Frequent testing of populations to detect infection early in asymptomatic or presymptomatic individuals can be a powerful tool for intercepting transmission, especially when the viral prevalence is low. However, RT-PCR testing-the gold standard of SARS-CoV-2 diagnosis-is expensive, making regular testing of every individual unfeasible. Sample pooling is one approach to lowering costs. By combining samples and testing them in groups the number of tests required is reduced, substantially lowering costs. Here we report on the implementation of pooling strategies using 3-d and 4-d hypercubes to test a professional sports team in South Africa. We have shown that infected samples can be reliably detected in groups of 27 and 81, with minimal loss of assay sensitivity for samples with individual Ct values of up to 32. We report on the automation of sample pooling, using a liquid-handling robot and an automated web interface to identify positive samples. We conclude that hypercube pooling allows for the reliable RT-PCR detection of SARS-CoV-2 infection, at significantly lower costs than lateral flow antigen (LFA) tests.

摘要

快速识别和隔离感染者仍然是控制 SARS-CoV-2 传播的关键策略。对人群进行频繁的检测,以早期发现无症状或症状前个体的感染,可以成为阻断传播的有力工具,尤其是在病毒流行率较低的情况下。然而,实时聚合酶链式反应(RT-PCR)检测——SARS-CoV-2 诊断的金标准——费用昂贵,使得对每个个体进行常规检测变得不切实际。样本合并是降低成本的一种方法。通过将样本合并并分组进行检测,可以减少所需的检测数量,从而大幅降低成本。在这里,我们报告了使用 3 维和 4 维超立方体来检测南非一支职业运动队的合并策略的实施情况。我们已经表明,在每组 27 个和 81 个样本中可以可靠地检测到感染样本,对于 Ct 值高达 32 的单个样本,检测灵敏度的损失最小。我们报告了使用液体处理机器人和自动化网络界面进行样本合并的自动化,以识别阳性样本。我们得出结论,超立方体合并允许可靠地进行 RT-PCR 检测 SARS-CoV-2 感染,成本明显低于侧向流动抗原(LFA)检测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad2f/8423848/2fab59bba50d/41598_2021_96934_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad2f/8423848/0daa394769fa/41598_2021_96934_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad2f/8423848/663f07e77d32/41598_2021_96934_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad2f/8423848/2fab59bba50d/41598_2021_96934_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad2f/8423848/0daa394769fa/41598_2021_96934_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad2f/8423848/663f07e77d32/41598_2021_96934_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad2f/8423848/2fab59bba50d/41598_2021_96934_Fig3_HTML.jpg

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