Identifying SARS-CoV-2 Variants of Concern through Saliva-Based RT-qPCR by Targeting Recurrent Mutation Sites

被引:5
作者
Ham, Rachel E. [1 ]
Smothers, Austin R. [1 ,2 ]
Che, Rui [1 ,3 ]
Sell, Keegan J. [1 ]
Peng, Congyue Annie [1 ]
Dean, Delphine [1 ,2 ]
机构
[1] Clemson Univ, Ctr Innovat Med Devices & Sensors, REDDI Lab, Clemson, SC 29634 USA
[2] Clemson Univ, Dept Bioengn, Clemson, SC 29634 USA
[3] Clemson Univ, Dept Genet & Biochem, Clemson, SC USA
来源
MICROBIOLOGY SPECTRUM | 2022年 / 10卷 / 03期
基金
美国国家科学基金会;
关键词
COVID-19; RT-qPCR; SARS-CoV-2; variants of concern; clinical methods; diagnostics; REAL-TIME PCR;
D O I
10.1128/spectrum.00797-22
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
SARS-CoV-2 variants of concern and their many sublineages can be characterized by mutations present within their genetic sequences. These mutations can provide selective advantages such as increased transmissibility and antibody evasion, which influences public health recommendations such as mask mandates, quarantine requirements, and treatment regimens. SARS-CoV-2 variants of concern (VOCs) continue to pose a public health threat which necessitates a real-time monitoring strategy to complement whole genome sequencing. Thus, we investigated the efficacy of competitive probe RT-qPCR assays for six mutation sites identified in SARS-CoV-2 VOCs and, after validating the assays with synthetic RNA, performed these assays on positive saliva samples. When compared with whole genome sequence results, the S Delta 69-70 and ORF1a Delta 3675-3677 assays demonstrated 93.60 and 68.00% accuracy, respectively. The SNP assays (K417T, E484K, E484Q, L452R) demonstrated 99.20, 96.40, 99.60, and 96.80% accuracies, respectively. Lastly, we screened 345 positive saliva samples from 7 to 22 December 2021 using Omicron-specific mutation assays and were able to quickly identify rapid spread of Omicron in Upstate South Carolina. Our workflow demonstrates a novel approach for low-cost, real-time population screening of VOCs. IMPORTANCE SARS-CoV-2 variants of concern and their many sublineages can be characterized by mutations present within their genetic sequences. These mutations can provide selective advantages such as increased transmissibility and antibody evasion, which influences public health recommendations such as mask mandates, quarantine requirements, and treatment regimens. Our RT-qPCR workflow allows for strain identification of SARS-CoV-2 positive saliva samples by targeting common mutation sites shared between variants of concern and detecting single nucleotides present at the targeted location. This differential diagnostic system can quickly and effectively identify a wide array of SARS-CoV-2 strains, which can provide more informed public health surveillance strategies in the future.
引用
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页数:12
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