Rapid detection and tracking of Omicron variant of SARS-CoV-2 using CRISPR-Cas12a-based assay

被引:39
|
作者
Liang, Yuanhao [1 ]
Lin, Hongqing [1 ]
Zou, Lirong [2 ]
Deng, Xiaoling [2 ]
Tang, Shixing [1 ,3 ]
机构
[1] Southern Med Univ, Sch Publ Hlth, Dept Epidemiol, Guangzhou 510515, Peoples R China
[2] Chinese Acad Med Sci, Guangdong Prov Ctr Dis Control & Prevent, Inst Pathogen Microbiol, Guangdong Workstn Emerging Infect Dis Control & P, Guangzhou 511430, Peoples R China
[3] Southern Med Univ, Nanfang Hosp, Dept Infect Dis, Guangzhou 510515, Peoples R China
来源
关键词
SARS-CoV-2; Variants of concern; Omicron; Variant genotyping; CRISPR-Cas12a system;
D O I
10.1016/j.bios.2022.114098
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Background: The newly emerged SARS-CoV-2 variant of concern (VOC) Omicron is spreading quickly worldwide, which manifests an urgent need of simple and rapid assay to detect and diagnose Omicron infection and track its spread. Methods: To design allele-specific CRISPR RNAs (crRNAs) targeting the signature mutations in the spike protein of Omicron variant, and to develop a CRISPR-Cas12a-based assay to specifically detect Omicron variant. Results: Our system showed a low limit of detection of 2 copies per reaction for the plasmid DNA of Omicron variant, and could readily detect Omicron variant in 5 laboratory-confirmed clinical samples and distinguish them from 57 SARS-CoV-2 positive clinical samples (4 virus isolates and 53 oropharyngeal swab specimens) infected with wild-type (N = 8) and the variants of Alpha (N = 17), Beta (N = 17) and Delta (N = 15). The testing results could be measured by fluorescent detector or judged by naked eyes. In addition, no cross-reaction was observed when detecting 16 clinical samples infected with 9 common respiratory pathogens. Conclusions: The rapid assay could be easily set up in laboratories already conducting SARS-CoV-2 nucleic acid amplification tests and implemented routinely in resource-limited settings to monitor and track the spread of Omicron variant.
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页数:5
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