Rapid and Technically Simple Detection of SARS-CoV-2 Variants Using CRISPR Cas12 and Cas13

被引:0
|
作者
Lamothe, Gabriel [1 ,2 ]
Carbonneau, Julie [1 ,3 ,4 ]
Beauparlant, Charles Joly [1 ,2 ]
Vincent, Thierry [5 ,6 ]
Quessy, Patrik [7 ,8 ]
Guedon, Anthony [7 ,8 ]
Kobinger, Gary [9 ]
Lemay, Jean-Francois [7 ,8 ]
Boivin, Guy [1 ,3 ,4 ]
Droit, Arnaud [1 ,2 ]
Turgeon, Nathalie [1 ,10 ]
Tremblay, Jacques P. [1 ,2 ,11 ]
机构
[1] Ctr Rech CHU Quebec, Quebec City, PQ, Canada
[2] Laval Univ, Fac Med, Dept Mol Med, Quebec City, PQ, Canada
[3] Univ Laval, CHU Quebec, Infectiol Res Ctr, Quebec City, PQ, Canada
[4] Univ Laval, Fac Med, Dept Pediat, Quebec City, PQ, Canada
[5] Ctr Rech Fonct, Struct & Ingn Prot, Quebec City, PQ, Canada
[6] Univ Laval, Fac Sci, Dept Genie Chim, Quebec City, PQ, Canada
[7] CNETE, Shawinigan, PQ, Canada
[8] PROTEO, Quebec City, PQ, Canada
[9] Univ Texas Med Branch, Galveston Natl Lab, Galveston, TX USA
[10] Inst Univ Cardiol & Pneumol Quebec, Quebec City, PQ, Canada
[11] Ctr Rech CHU Quebec, 2705 Bd Laurier, Quebec City, PQ G1V 4G2, Canada
来源
CRISPR JOURNAL | 2023年 / 6卷 / 04期
基金
加拿大健康研究院;
关键词
D O I
10.1089/crispr.2023.0007
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The worldwide proliferation of the SARS-CoV-2 virus in the past 3 years has allowed the virus to accumulate numerous mutations. Dangerous lineages have emerged one after another, each leading to a new wave of the pandemic. In this study, we have developed the THRASOS pipeline to rapidly discover lineage-specific mutation signatures and thus advise the development of Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)-based diagnostic tests. We also optimized a strategy to modify loop-mediated isothermal amplification amplicons for downstream use with Cas12 and Cas13 for future multiplexing. The close ancestry of the BA.1 and BA.2 variants of SARS-CoV-2 (Omicron) made these excellent candidates for the development of a first test using this workflow. With a quick turnaround time and low requirements for laboratory equipment, the test we have created is ideally suited for settings such as mobile clinics lacking equipment such as Next-Generation Sequencers or Sanger Sequencers and the personnel to run these devices.
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页码:369 / 385
页数:17
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