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基于结构的引物设计可最大程度降低由 SARS-CoV-2 突变引起的 PCR 失败风险。

Structure-Based Primer Design Minimizes the Risk of PCR Failure Caused by SARS-CoV-2 Mutations.

机构信息

State Key Laboratory of Microbial Technology, Shandong University, Qingdao, China.

Research and Development Department, Shandong Shtars Medical Technology Co., Ltd, Jinan, China.

出版信息

Front Cell Infect Microbiol. 2021 Oct 25;11:741147. doi: 10.3389/fcimb.2021.741147. eCollection 2021.

DOI:10.3389/fcimb.2021.741147
PMID:34760717
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8573093/
Abstract

The coronavirus disease 2019 (COVID-19) has caused and is still causing tremendous damage to the global economy and human health. Qualitative reverse transcription-PCR (RT-qPCR) is the golden standard for COVID-19 test. However, the SARS-CoV-2 variants may not only make vaccine less effective but also evade RT-qPCR test. Here we suggest an innovative primer design strategy for the RT-qPCR test of SARS-CoV-2. The principle is that the primers should be designed based on both the nucleic acid sequence and the structure of the protein encoded. The three nucleotides closest to the 3' end of the primer should be the codon which encodes the tryptophan in the structure core. Based on this principle, we designed a pair of primers targeting the () gene. Since tryptophan is encoded by only one codon, any mutation that occurs at this position would change the amino acid residue, resulting in an unstable N protein. This means that this kind of SARS-CoV-2 variant could not survive. In addition, both our data and previous reports all indicate that the mutations occurring at other places in the primers do not significantly affect the RT-qPCR result. Consequently, no SARS-CoV-2 variant can escape detection by the RT-qPCR kit containing the primers designed based on our strategy.

摘要

新型冠状病毒病(COVID-19)对全球经济和人类健康造成了巨大的破坏。定性逆转录聚合酶链反应(RT-qPCR)是 COVID-19 检测的金标准。然而,SARS-CoV-2 的变异不仅会使疫苗效果降低,还可能逃避 RT-qPCR 检测。在这里,我们建议一种用于 SARS-CoV-2 的 RT-qPCR 检测的创新引物设计策略。其原理是基于核酸序列和编码蛋白的结构设计引物。引物 3' 端最接近的三个核苷酸应该是编码结构核心色氨酸的密码子。基于这一原则,我们设计了一对针对 () 基因的引物。由于色氨酸仅由一个密码子编码,因此该位置发生的任何突变都会改变氨基酸残基,导致不稳定的 N 蛋白。这意味着这种 SARS-CoV-2 变体无法存活。此外,我们的数据和以前的报告都表明,引物中其他位置的突变不会显著影响 RT-qPCR 结果。因此,任何 SARS-CoV-2 变体都无法逃避基于我们策略设计的 RT-qPCR 试剂盒的检测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7564/8573093/87eb42ee2b0c/fcimb-11-741147-g007.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7564/8573093/87eb42ee2b0c/fcimb-11-741147-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7564/8573093/56c34251b3af/fcimb-11-741147-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7564/8573093/d2258ca058b0/fcimb-11-741147-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7564/8573093/932096c925f9/fcimb-11-741147-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7564/8573093/35d550131fa5/fcimb-11-741147-g004.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7564/8573093/907c052e93e1/fcimb-11-741147-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7564/8573093/87eb42ee2b0c/fcimb-11-741147-g007.jpg

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