SARS-CoV-2 whole-genome sequencing using reverse complement PCR: For easy, fast and accurate outbreak and variant analysis.

被引:18
作者
Coolen, Jordy P. M. [1 ]
Wolters, Femke [1 ]
Tostmann, Alma [1 ]
van Groningen, Lenneke F. J. [2 ]
Bleeker-Rovers, Chantal P. [3 ]
Tan, Edward C. T. H. [4 ,5 ]
Van der Geest-Blankert, Nannet [6 ]
Hautvast, Jeannine L. A. [7 ]
Hopman, Joost [1 ]
Wertheim, Heiman F. L. [1 ]
Rahamat-Langendoen, Janette C. [1 ]
Storch, Marko [8 ]
Melchers, Willem J. G. [1 ]
机构
[1] Radboud Univ Nijmegen, Dept Med Microbiol, Med Ctr, Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Dept Haematol, Med Ctr, Nijmegen, Netherlands
[3] Radboud Univ Nijmegen, Dept Internal Med, Div Infect Dis, Med Ctr, Nijmegen, Netherlands
[4] Radboud Univ Nijmegen, Dept Emergency Med, Med Ctr, Nijmegen, Netherlands
[5] Radboud Univ Nijmegen, Dept Surg, Med Ctr, Nijmegen, Netherlands
[6] Radboud Univ Nijmegen, Dept Occupat Hlth, Med Ctr, Nijmegen, Netherlands
[7] Reg Publ Hlth Serv, Nijmegen, Netherlands
[8] Imperial Coll Translat & Innovat Hub, London Biofoundry, White City Campus,84 Wood Lane, London W12 0BZ, England
关键词
COVID-19; SARS-CoV-2; WGS; RC-PCR; Mutation; Lineage;
D O I
10.1016/j.jcv.2021.104993
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
During the course of the SARS-CoV-2 pandemic reports of mutations with effects on spreading and vaccine effectiveness emerged. Large scale mutation analysis using rapid SARS-CoV-2 Whole Genome Sequencing (WGS) is often unavailable but could support public health organizations and hospitals in monitoring transmission and rising levels of mutant strains. Here we report a novel WGS technique for SARS-CoV-2, the EasySeqTM RC-PCR SARS-CoV-2 WGS kit. By applying a reverse complement polymerase chain reaction (RC-PCR), an Illumina library preparation is obtained in a single PCR, thereby saving time, resources and facilitating high-throughput screening. Using this WGS technique, we evaluated SARS-CoV-2 diversity and possible transmission within a group of 173 patients and healthcare workers (HCW) of the Radboud university medical center during 2020. Due to the emergence of variants of concern, we screened SARS-CoV-2 positive samples in 2021 for identification of mutations and lineages. With use of EasySeqTM RC-PCR SARS-CoV-2 WGS kit we were able to obtain reliable results to confirm outbreak clusters and additionally identify new previously unassociated links in a considerably easier workaround compared to current methods. Furthermore, various SARS-CoV-2 variants of interest were detected among samples and validated against an Oxford Nanopore sequencing amplicon strategy which illustrates this technique is suitable for surveillance and monitoring current circulating variants.
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页数:9
相关论文
共 39 条
[1]  
[Anonymous], 2020, NCOV 2019 SEQUENCING
[2]   BAMClipper: removing primers from alignments to minimize false-negative mutations in amplicon next-generation sequencing [J].
Au, Chun Hang ;
Ho, Dona N. ;
Kwong, Ava ;
Chan, Tsun Leung ;
Ma, Edmond S. K. .
SCIENTIFIC REPORTS, 2017, 7
[3]   CoronaHiT: high-throughput sequencing of SARS-CoV-2 genomes [J].
Baker, Dave J. ;
Aydin, Alp ;
Le-Viet, Thanh ;
Kay, Gemma L. ;
Rudder, Steven ;
Martins, Leonardo de Oliveira ;
Tedim, Ana P. ;
Kolyva, Anastasia ;
Diaz, Maria ;
Alikhan, Nabil-Fareed ;
Meadows, Lizzie ;
Bell, Andrew ;
Gutierrez, Ana Victoria ;
Trotter, Alexander J. ;
Thomson, Nicholas M. ;
Gilroy, Rachel ;
Griffith, Luke ;
Adriaenssens, Evelien M. ;
Stanley, Rachael ;
Charles, Ian G. ;
Elumogo, Ngozi ;
Wain, John ;
Prakash, Reenesh ;
Meader, Emma ;
Mather, Alison E. ;
Webber, Mark A. ;
Dervisevic, Samir ;
Page, Andrew J. ;
O'Grady, Justin .
GENOME MEDICINE, 2021, 13 (01)
[4]  
Batty E.M., 2020, COMP LIB PREPARATION
[5]   From PREDICT to prevention, one pandemic later Comment [J].
Carlson, Colin J. .
LANCET MICROBE, 2020, 1 (01) :E6-E7
[6]   fastp: an ultra-fast all-in-one FASTQ preprocessor [J].
Chen, Shifu ;
Zhou, Yanqing ;
Chen, Yaru ;
Gu, Jia .
BIOINFORMATICS, 2018, 34 (17) :884-890
[7]   A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3 [J].
Cingolani, Pablo ;
Platts, Adrian ;
Wang, Le Lily ;
Coon, Melissa ;
Tung Nguyen ;
Wang, Luan ;
Land, Susan J. ;
Lu, Xiangyi ;
Ruden, Douglas M. .
FLY, 2012, 6 (02) :80-92
[8]   Rapid and precise alignment of raw reads against redundant databases with KMA [J].
Clausen, Philip T. L. C. ;
Aarestrup, Frank M. ;
Lund, Ole .
BMC BIOINFORMATICS, 2018, 19
[9]   Detection of 2019 novel coronavirus (2019-nCoV) by real-time RT-PCR (Publication with Expression of Concern) [J].
Corman, Victor M. ;
Landt, Olfert ;
Kaiser, Marco ;
Molenkamp, Richard ;
Meijer, Adam ;
Chu, Daniel K. W. ;
Bleicker, Tobias ;
Bruenink, Sebastian ;
Schneider, Julia ;
Schmidt, Marie Luisa ;
Mulders, Daphne G. J. C. ;
Haagmans, Bart L. ;
van der Veer, Bas ;
van den Brink, Sharon ;
Wijsman, Lisa ;
Goderski, Gabriel ;
Romette, Jean-Louis ;
Ellis, Joanna ;
Zambon, Maria ;
Peiris, Malik ;
Goossens, Herman ;
Reusken, Chantal ;
Koopmans, Marion P. G. ;
Drosten, Christian .
EUROSURVEILLANCE, 2020, 25 (03) :23-30
[10]   Powerful differential expression analysis incorporating network topology for next-generation sequencing data [J].
Dona, Malathi S. I. ;
Prendergast, Luke A. ;
Mathivanan, Suresh ;
Keerthikumar, Shivakumar ;
Salim, Agus .
BIOINFORMATICS, 2017, 33 (10) :1505-1513