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SARS-CoV-2 变异株累积突变对 qPCR 检测效率的影响。

The Impact of Accumulated Mutations in SARS-CoV-2 Variants on the qPCR Detection Efficiency.

机构信息

Centre for Infection and Immunity Study (CIIS), School of Medicine, Sun Yat-sen University, Shenzhen, China.

出版信息

Front Cell Infect Microbiol. 2022 Jan 28;12:823306. doi: 10.3389/fcimb.2022.823306. eCollection 2022.

Abstract

SARS-CoV-2 is evolving with mutations throughout the genome all the time and a number of major variants emerged, including several variants of concern (VOC), such as Delta and Omicron variants. In this study, we demonstrated that mutations in the regions corresponding to the sequences of the probes and 3'-end of primers have a significant impact on qPCR detection efficiency. We also found that the G28916T mutation of the N gene accounts for 78.78% sequenced genomes of Delta variant. It was found that detection sensitivity of G28916T mutant was 2.35 and 1.74 times less than that of the wt sequence and detection limit was reduced from 1 copy/μl to 10 copies/μl for the commercially available CP3 and CP4 primer/probe sets. These results indicate that the detection probes and primers should be optimized to keep maximal detection efficiency in response to the emergence of new variants.

摘要

SARS-CoV-2 一直在基因组中发生突变和进化,出现了许多主要的变种,包括几种令人关注的变种(VOC),如德尔塔和奥密克戎变种。在这项研究中,我们证明了与探针序列和引物 3'-端相对应的区域中的突变对 qPCR 检测效率有显著影响。我们还发现,N 基因的 G28916T 突变占德尔塔变种测序基因组的 78.78%。结果发现,G28916T 突变体的检测灵敏度比 wt 序列低 2.35 倍和 1.74 倍,商用 CP3 和 CP4 引物/探针组的检测限从 1 拷贝/μl 降低到 10 拷贝/μl。这些结果表明,应优化检测探针和引物,以保持对新变种出现的最大检测效率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41e0/8834649/cccfd075a033/fcimb-12-823306-g001.jpg

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