SARS-CoV-2 variant detection with ADSSpike

被引:4
|
作者
Castaneda-Mogollon, Daniel [1 ,2 ,3 ]
Kamaliddin, Claire [1 ,2 ,3 ]
Fine, Laura [1 ,2 ,3 ]
Oberding, Lisa K. [1 ,2 ,3 ]
Pillai, Dylan R. [1 ,2 ,3 ,4 ]
机构
[1] Univ Calgary, Cumming Sch Med, Dept Pathol & Lab Med, Calgary, AB, Canada
[2] Univ Calgary, Cumming Sch Med, Dept Microbiol Immunol & Infect Dis, Calgary, AB, Canada
[3] Univ Calgary, Calvin Phoebe & Joan Snyder Inst Chron Dis, Calgary, AB, Canada
[4] Alberta Precis Labs, Diagnost & Sci Ctr, Calgary, AB, Canada
基金
加拿大健康研究院;
关键词
SARS-CoV-2; Amplicon deep sequencing; Variants of concern; Variants of interest; S gene;
D O I
10.1016/j.diagmicrobio.2021.115606
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The SARS-CoV-2 coronavirus pandemic has been an unprecedented challenge to global pandemic response and preparedness. With the continuous appearance of new SARS-CoV-2 variants, it is imperative to implement tools for genomic surveillance and diagnosis in order to decrease viral transmission and prevalence. The ADSSpike workflow was developed with the goal of identifying signature SNPs from the S gene associated with SARS-CoV-2 variants through amplicon deep sequencing. Seventy-two samples were sequenced, and 30 mutations were identified. Among those, signature SNPs were linked to 2 Zeta-VOI (P.2) samples and one to the Alpha-VOC (B.1.17). An average depth of 700 reads was found to properlycorrectly identify all SNPs and deletions pertinent to SARS-CoV-2 mutants. ADSSpike is the first workflow to provide a practical, cost-effective, and scalable solution to diagnose SARS-CoV-2 VOC/VOI in the clinical laboratory, adding a valuable tool to public health measures to fight the COVID-19 pandemic for approximately $41.85 USD/reaction. (C) 2021 The Author( s). Published by Elsevier Inc.
引用
收藏
页数:7
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