Rapid Identification of SARS-CoV-2 Variants of Concern Using a Portable peakPCR Platform

被引:17
|
作者
Bechtold, Philippe [1 ,2 ]
Wagner, Philipp [3 ,4 ]
Hosch, Salome [3 ,4 ]
Siegrist, Denise [5 ]
Ruiz-Serrano, Amalia [1 ,2 ]
Gregorini, Michele [1 ,2 ]
Mpina, Maxmillian [3 ,4 ,6 ]
Ondo, Florentino Abaga [7 ]
Obama, Justino [7 ]
Ayekaba, Mitoha Ondo'o [7 ]
Engler, Olivier [5 ]
Stark, Wendelin J. [1 ,2 ]
Daubenberger, Claudia A. [3 ,4 ]
Schindler, Tobias [3 ,4 ]
机构
[1] Swiss Fed Inst Technol, Inst Chem & Bioengn, CH-8093 Zurich, Switzerland
[2] Diaxxo AG, CH-8093 Zurich, Switzerland
[3] Swiss Trop & Publ Hlth Inst, CH-4051 Basel, Switzerland
[4] Univ Basel, CH-4051 Basel, Switzerland
[5] Spiez Lab, CH-3700 Spiez, Switzerland
[6] Lab Invest Baney, Baney, Equat Guinea
[7] Minist Hlth & Social Welf, Malabo, Equat Guinea
基金
瑞士国家科学基金会;
关键词
D O I
10.1021/acs.analchem.1c02368
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The need for tools that facilitate rapid detection and continuous monitoring of SARS-CoV-2 variants of concern (VOCs) is greater than ever, as these variants are more transmissible and therefore increase the pressure of COVID-19 on healthcare systems. To address this demand, we aimed at developing and evaluating a robust and fast diagnostic approach for the identification of SARSCoV-2 VOC-associated spike gene mutations. Our diagnostic assays detect the E484K and N501Y single-nucleotide polymorphisms (SNPs) as well as a spike gene deletion (HV69/70) and can be run on standard laboratory equipment or on the portable rapid diagnostic technology platform peakPCR. The assays achieved excellent diagnostic performance when tested with RNA extracted from culture-derived SARS-CoV-2 VOC lineages and clinical samples collected in Equatorial Guinea, Central-West Africa. Simplicity of usage and the relatively low cost are advantages that make our approach well suitable for decentralized and rapid testing, especially in resource-limited settings.
引用
收藏
页码:16350 / 16359
页数:10
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