Multiplexed RT-qPCR Coupled with Whole-Genome Sequencing to Monitor a SARS-CoV-2 Omicron Variant of Concern in a Hospital Laboratory Setting in Latvia

被引:1
作者
Niedre-Otomere, Baiba [1 ]
Kampenusa, Inara [1 ]
Trofimova, Julija [1 ]
Bodrenko, Jevgenijs [1 ]
Vangravs, Reinis [1 ]
Skenders, Girts [1 ]
Nikisins, Sergejs [1 ]
Savicka, Oksana [1 ]
机构
[1] Riga East Univ Hosp, Lab Latvian Ctr Infect Dis, Lab Serv, Natl Microbiol Reference Lab Latvia, Linezera St 3, LV-1006 Riga, Latvia
关键词
multiplexed RT-qPCR; whole-genome sequencing; SARS-CoV-2 Omicron variant of concern; SARS-CoV-2 signature mutations: Delta H69/V70; E484A; N501Y; IMMUNE ESCAPE;
D O I
10.3390/diagnostics13223467
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
At the end of 2021, the SARS-CoV-2 Omicron variant of concern (VOC) displaced the previously dominant Delta VOC and enhanced diagnostic and therapeutic challenges worldwide. Respiratory specimens submitted to the Riga East University Hospital Laboratory Service by the central and regional hospitals of Latvia from January to March 2022 that were positive for SARS-CoV-2 RNA were tested by commercial multiplexed RT-qPCR targeting three of the Omicron VOC signature mutations: Delta H69/V70, E484A, and N501Y. Of the specimens tested and analyzed in parallel by whole-genome sequencing (WGS), 964 passed the internal quality criteria (genome coverage >= 90%, read depth >= 400x) and the Nextstrain's quality threshold for "good". We validated the detection accuracy of RT-qPCR for each target individually by using WGS as a control. The results were concordant with both approaches for 938 specimens, with the correct classification rate exceeding 96% for each target (CI 95%); however, the presumptive WHO label was misassigned for 21 specimens. The RT-qPCR genotyping provided an acceptable means to pre-monitor the prevalence of the two presumptive Omicron VOC sublineages, BA.1 and BA.2.
引用
收藏
页数:11
相关论文
共 49 条
[1]  
[Anonymous], 2023, Nat Commun
[2]  
[Anonymous], US
[3]  
[Anonymous], Mutation Report
[4]  
[Anonymous], TaqMan SARS-CoV-2 Mutation Research Panel-LV
[5]  
[Anonymous], Classification of Omicron (B.1.1.529): SARS-CoV-2 Variant of Concern
[6]  
[Anonymous], METHODS DETECTION CH
[7]   Development of a simple genotyping method based on indel mutations to rapidly screen SARS-CoV-2 circulating variants: Delta, Omicron BA.1 and BA.2 [J].
Ayadi, Wajdi ;
Taktak, Awatef ;
Gargouri, Saba ;
Smaoui, Fahmi ;
Chtourou, Amel ;
Skouri-Gargouri, Houda ;
Derbel, Rihab ;
Sassi, Azza Hadj ;
Gargouri, Ali ;
Hammami, Adnene ;
Karray-Hakim, Hela ;
Mokdad-Gargouri, Raja ;
Fki-Berrajah, Lamia .
JOURNAL OF VIROLOGICAL METHODS, 2022, 307
[8]   SARS-CoV-2 Variants Identification: Overview of Molecular Existing Methods [J].
Berno, Giulia ;
Fabeni, Lavinia ;
Matusali, Giulia ;
Gruber, Cesare Ernesto Maria ;
Rueca, Martina ;
Giombini, Emanuela ;
Garbuglia, Anna Rosa .
PATHOGENS, 2022, 11 (09)
[9]   Rapid and Accurate Identification of SARS-CoV-2 Variants Using Real Time PCR Assays [J].
Borillo, Gwynngelle A. ;
Kagan, Ron M. ;
Marlowe, Elizabeth M. .
FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY, 2022, 12
[10]   S-Gene Target Failure as a Marker of Variant B.1.1.7 Among SARS-CoV-2 Isolates in the Greater Toronto Area, December 2020 to March 2021 [J].
Brown, Kevin A. ;
Gubbay, Jonathan ;
Hopkins, Jessica ;
Patel, Samir ;
Buchan, Sarah A. ;
Daneman, Nick ;
Goneau, Lee William .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2021, 325 (20) :2115-2116