National HIV and Retrovirology Laboratory, National Microbiology Laboratory, JC Wilt Infectious Diseases Research Centre, Public Health Agency of Canada, Winnipeg, Canada.
Department of Medical Microbiology and Infectious Diseases, University of Manitoba, Winnipeg, Canada.
PLoS One. 2020 Nov 9;15(11):e0241959. doi: 10.1371/journal.pone.0241959. eCollection 2020.
The coronavirus disease 2019 (Covid-19) pandemic, caused by SARS-CoV-2, has resulted in a global testing supply shortage. In response, pooled testing has emerged as a promising strategy that can immediately increase testing capacity. In pooled sample testing, multiple samples are combined (or pooled) together and tested as a single unit. If the pool is positive, the individual samples can then be individually tested to identify the positive case(s). Here, we provide support for the adoption of sample pooling with the point-of-care Cepheid Xpert® Xpress SARS-CoV-2 molecular assay. Corroborating previous findings, the limit of detection of this assay was comparable to laboratory-developed reverse-transcription quantitative PCR SARS-CoV-2 tests, with observed detection below 100 copies/mL. The Xpert® Xpress assay detected SARS-CoV-2 after samples with minimum viral loads of 461 copies/mL were pooled in groups of six. Based on these data, we recommend the adoption of pooled testing with the Xpert® Xpress SARS-CoV-2 assay where warranted based on public health needs. The suggested number of samples per pool, or the pooling depth, is unique for each point-of-care testing site and can be determined by the positive test rates. To statistically determine appropriate pooling depth, we have calculated the pooling efficiency for numerous combinations of pool sizes and test rates. This information is included as a supplemental dataset that we encourage public health authorities to use as a guide to make recommendations that will maximize testing capacity and resource conservation.
2019 年冠状病毒病(COVID-19)大流行是由严重急性呼吸综合征冠状病毒 2 型(SARS-CoV-2)引起的,导致全球检测供应短缺。作为应对措施,合并检测已成为一种很有前途的策略,可以立即增加检测能力。在合并样本检测中,将多个样本合并(或合并)在一起并作为一个单元进行检测。如果该池为阳性,则可以单独测试各个样本以鉴定阳性病例。在这里,我们提供采用即时护理 Cepheid Xpert® Xpress SARS-CoV-2 分子检测的合并样本检测的支持。该检测方法的检测限与实验室开发的逆转录定量聚合酶链反应 SARS-CoV-2 检测相当,观察到的检测下限低于 100 拷贝/mL。在将病毒载量最低为 461 拷贝/mL 的样本以六份一组合并后,Xpert® Xpress 检测到 SARS-CoV-2。基于这些数据,我们建议在根据公共卫生需求有必要的情况下,采用 Xpert® Xpress SARS-CoV-2 检测进行合并检测。每个合并样本的建议数量(或合并深度)因每个即时护理检测点而异,可通过阳性检测率确定。为了统计确定适当的合并深度,我们已经计算了许多不同的合并大小和检测率组合的合并效率。该信息包含在一个补充数据集中,我们鼓励公共卫生当局将其作为指南来制定建议,以最大程度地提高检测能力和资源利用效率。