Rapid and Flexible RT-qPCR Surveillance Platforms To Detect SARS-CoV-2 Mutations

被引:7
|
作者
Spiess, Katja [1 ]
Gunalan, Vithiagaran [1 ]
Marving, Ellinor [1 ]
Nielsen, Sofie Holdflod [2 ]
Jorgensen, Michelle G. P. [2 ]
Fomsgaard, Anna S. [1 ]
Nielsen, Line [2 ]
Alfaro-Nunez, Alonzo [1 ,4 ]
Karst, Soren M. [1 ]
Mortensen, Shila [1 ]
Rasmussen, Morten [1 ]
Lassauniere, Ria [1 ]
Rosenstierne, Maiken Worsoe [3 ]
Polacek, Charlotta [1 ]
Fonager, Jannik [1 ]
Cohen, Arieh S. [2 ]
Nielsen, Claus [1 ]
Fomsgaard, Anders [1 ]
Jacobs, Jonathan L.
Bereguiain, Miguel Angel Garcia
机构
[1] Statens Serum Inst, Dept Virus & Microbiol Special Diagnost, Copenhagen, Denmark
[2] Statens Serum Inst, Test Ctr Denmark, Copenhagen, Denmark
[3] Qlife ApS Symb, Copenhagen, Denmark
[4] Naestved Hosp, Dept Clin Biochem, Naestved, Denmark
来源
MICROBIOLOGY SPECTRUM | 2023年 / 11卷 / 01期
关键词
SARS-CoV-2; signature mutations; variant of concern; variant PCR; large-scale screening; whole-genome sequencing; national surveillance program; RT-qPCR platforms; variants of concern; national surveillance system; MAFFT;
D O I
10.1128/spectrum.03591-22
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Multiple mutations in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants of concern (VOCs) increase transmission, disease severity, and immune evasion and facilitate zoonotic or anthropozoonotic infections. Four such mutations, Delta H69/V70, L452R, E484K, and N501Y, occurred in the SARS-CoV-2 spike glycoprotein in combinations that allow the simultaneous detection of VOCs. Here, we present two flexible reverse transcription-quantitative PCR (RT-qPCR) platforms for small- and large-scale screening (also known as variant PCR) to detect these mutations and schemes for adapting the platforms to future mutations. The large-scale RT-qPCR platform was validated by pairwise matching of RT-qPCR results with whole-genome sequencing (WGS) consensus genomes, showing high specificity and sensitivity. Both platforms are valuable examples of complementing WGS to support the rapid detection of VOCs. Our mutational signature approach served as an important intervention measure for the Danish public health system to detect and delay the emergence of new VOCs.IMPORTANCE Denmark weathered the SARS-CoV-2 crisis with relatively low rates of infection and death. Intensive testing strategies with the aim of detecting SARS-CoV-2 in symptomatic and nonsymptomatic individuals were available by establishing a national test system called TestCenter Denmark. This testing regime included the detection of SARS-CoV-2 signature mutations, with referral to the national health system, thereby delaying outbreaks of variants of concern. Our study describes the design of the large-scale RT-qPCR platform established at TestCenter Denmark in conjunction with whole-genome sequencing to report mutations of concern to the national health system. Validation of the large-scale RT-qPCR platform using paired WGS consensus genomes showed high sensitivity and specificity. For smaller laboratories with limited infrastructure, we developed a flexible small-scale RT-qPCR platform to detect three signature mutations in a single run. The RT-qPCR platforms are important tools to support the control of the SARS-CoV-2 endemic in Denmark. Denmark weathered the SARS-CoV-2 crisis with relatively low rates of infection and death. Intensive testing strategies with the aim of detecting SARS-CoV-2 in symptomatic and nonsymptomatic individuals were available by establishing a national test system called TestCenter Denmark.
引用
收藏
页数:17
相关论文
共 50 条
  • [1] RT-qPCR Testing of SARS-CoV-2: A Primer
    Bustin, Stephen A.
    Nolan, Tania
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2020, 21 (08)
  • [2] SARS-CoV-2 Surveillance in Hospital Wastewater: CLEIA vs. RT-qPCR
    Thongpradit, Supranee
    Chanprasertyothin, Suwannee
    Pasomsub, Ekawat
    Ongphiphadhanakul, Boonsong
    Prasongtanakij, Somsak
    WATER, 2023, 15 (13)
  • [3] Variant-specific RT-qPCR for rapid screening of B.1.617 mutations in SARS-CoV-2
    Jallul, Mwada
    Ibrahim, Khaled
    Zaghdani, Ahmed
    Abdusalam, Mohamed Musbah
    Al Dwigen, Samira M.
    Atwair, Wafya S.
    Elbasir, Mohamed
    Alhudiri, Inas
    El Meshri, Salah Edin
    Elzagheid, Adam
    LIBYAN JOURNAL OF MEDICINE, 2022, 17 (01)
  • [4] Detection of SARS-CoV-2 RNA by multiplex RT-qPCR
    Kudo, Eriko
    Israelow, Benjamin
    Vogels, Chantal B. F.
    Lu, Peiwen
    Wyllie, Anne L.
    Tokuyama, Maria
    Venkataraman, Arvind
    Brackney, Doug E.
    Ott, Isabel M.
    Petrone, Mary E.
    Earnest, Rebecca
    Lapidus, Sarah
    Muenker, M. Catherine
    Moore, Adam J.
    Casanovas-Massana, Arnau
    Omer, Saad B.
    Dela Cruz, Charles S.
    Farhadian, Shelli F.
    Ko, Albert I.
    Grubaugh, Nathan D.
    Iwasaki, Akiko
    PLOS BIOLOGY, 2020, 18 (10)
  • [5] Comparison of RT-qPCR and RT-dPCR Platforms for the Trace Detection of SARS-CoV-2 RNA in Wastewater
    Ahmed, Warish
    Smith, Wendy J. M.
    Metcalfe, Suzanne
    Jackson, Greg
    Choi, Phil M.
    Morrison, Mary
    Field, Daniel
    Gyawali, Pradip
    Bivins, Aaron
    Bibby, Kyle
    Simpson, Stuart L.
    ACS ES&T WATER, 2022, : 1871 - 1880
  • [6] RT-qPCR and ATOPlex sequencing for the sensitive detection of SARS-CoV-2 RNA for wastewater surveillance
    Ahmed, Warish
    Bivins, Aaron
    Metcalfe, Suzanne
    Smith, Wendy J. M.
    Ziels, Ryan
    Korajkic, Asja
    McMinn, Brian
    Graber, Tyson E.
    Simpson, Stuart L.
    WATER RESEARCH, 2022, 220
  • [7] Influence of storage solution, temperature, assay time and concentration on RT-qPCR nucleic acid detection for SARS-CoV-2 detection of SARS-CoV-2 by the RT-qPCR
    Su, Lingxuan
    Lou, Yihan
    Li, Jiaxuan
    Mao, Haiyan
    Li, Jianhua
    Sun, Yi
    Zhou, Biaofeng
    Wu, Guangshang
    Huang, Chen
    Zhang, Yanjun
    Chen, Keda
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2024, 707
  • [8] RT-qPCR Diagnostics: The "Drosten" SARS-CoV-2 Assay Paradigm
    Bustin, Stephen
    Kirvell, Sara
    Huggett, Jim F.
    Nolan, Tania
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 (16)
  • [9] Rapid Detection SARS-CoV-2 Variants by Molecular Clamping Technology Based RT-qPCR
    Shen, S.
    Fu, A.
    Jamba, M.
    Li, J.
    Cui, Z.
    Pastor, L.
    Cataldi, D.
    Sun, Q.
    Pathakamuri, J.
    Kuebler, D.
    Rohall, M.
    Krohn, M.
    Kissinger, D.
    Neves, J.
    Archibeque, I.
    Powell, M.
    Zhang, A.
    Lu, C.
    Sha, M.
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2022, 24 (10): : S56 - S57
  • [10] Comparison of Rapid Nucleic Acid Extraction Methods for SARS-CoV-2 Detection by RT-qPCR
    Silva, Livia Mara
    Riani, Lorena Rodrigues
    Silverio, Marcelo Silva
    Pereira-Junior, Olavo dos Santos
    Pittella, Frederico
    DIAGNOSTICS, 2022, 12 (03)