Center for Fundamental and Applied Microbiomics, Biodesign Institute, Arizona State University, Tempe, AZ 85287, USA.
Center for Personalized Diagnostics, Biodesign Institute, Arizona State University, Tempe, AZ 85287, USA.
Viruses. 2022 Jun 16;14(6):1316. doi: 10.3390/v14061316.
As the SARS-CoV-2 virus evolves, mutations may result in diminished sensitivity to qRT-PCR diagnostic assays. We investigated four polymorphisms circulating in the SARS-CoV-2 Delta lineage that result in gene target failure (NGTF) on the TaqPath COVID-19 Combo Kit. These mutations were detected from the SARS-CoV-2 genome sequences that matched with the diagnostic assay results of saliva specimens. Full length genes from the samples displaying NGTF were cloned into plasmids and assayed using three SARS-CoV-2 qRT-PCR assays. These constructs resulted in reduced sensitivity to the TaqPath COVID-19 Combo Kit compared to the controls (mean C differences of 3.06, 7.70, 12.46, and 14.12), but were detected equivalently on the TaqPath COVID-19 Fast PCR Combo 2.0 or CDC 2019_nCoV_N2 assays. This work highlights the importance of genomic sequencing to monitor circulating mutations and provide guidance in improving diagnostic assays.
随着 SARS-CoV-2 病毒的进化,突变可能导致实时荧光定量 RT-PCR(qRT-PCR)诊断检测的敏感性降低。我们研究了在 SARS-CoV-2 德尔塔谱系中循环的四个导致 TaqPath COVID-19 Combo Kit 基因目标失败(NGTF)的多态性。这些突变是从与唾液标本诊断检测结果匹配的 SARS-CoV-2 基因组序列中检测到的。来自显示 NGTF 的样本的全长基因被克隆到质粒中,并使用三种 SARS-CoV-2 qRT-PCR 检测进行检测。与对照相比,这些构建体对 TaqPath COVID-19 Combo Kit 的敏感性降低(平均 C 差异分别为 3.06、7.70、12.46 和 14.12),但在 TaqPath COVID-19 Fast PCR Combo 2.0 或 CDC 2019_nCoV_N2 检测中同样可以检测到。这项工作强调了基因组测序监测循环突变的重要性,并为改进诊断检测提供了指导。