Oligonucleotide capture sequencing of the SARS-CoV-2 genome and subgenomic fragments from COVID-19 individuals

The newly emerged and rapidly spreading SARS-CoV-2 causes coronavirus disease 2019 (COVID-19). To facilitate a deeper understanding of the viral biology we developed a capture sequencing methodology to generate SARS-CoV-2 genomic and transcriptome sequences from infected patients. We utilized an oli...

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Veröffentlicht in:PloS one 2021-08, Vol.16 (8), p.e0244468-e0244468
Hauptverfasser: Doddapaneni, Harsha, Cregeen, Sara Javornik, Sucgang, Richard, Meng, Qingchang, Qin, Xiang, Avadhanula, Vasanthi, Chao, Hsu, Menon, Vipin, Nicholson, Erin, Henke, David, Piedra, Felipe-Andres, Rajan, Anubama, Momin, Zeineen, Kottapalli, Kavya, Hoffman, Kristi L, Sedlazeck, Fritz J, Metcalf, Ginger, Piedra, Pedro A, Muzny, Donna M, Petrosino, Joseph F, Gibbs, Richard A
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Sprache:eng
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Zusammenfassung:The newly emerged and rapidly spreading SARS-CoV-2 causes coronavirus disease 2019 (COVID-19). To facilitate a deeper understanding of the viral biology we developed a capture sequencing methodology to generate SARS-CoV-2 genomic and transcriptome sequences from infected patients. We utilized an oligonucleotide probe-set representing the full-length genome to obtain both genomic and transcriptome (subgenomic open reading frames [ORFs]) sequences from 45 SARS-CoV-2 clinical samples with varying viral titers. For samples with higher viral loads (cycle threshold value under 33, based on the CDC qPCR assay) complete genomes were generated. Analysis of junction reads revealed regions of differential transcriptional activity among samples. Mixed allelic frequencies along the 20kb ORF1ab gene in one sample, suggested the presence of a defective viral RNA species subpopulation maintained in mixture with functional RNA in one sample. The associated workflow is straightforward, and hybridization-based capture offers an effective and scalable approach for sequencing SARS-CoV-2 from patient samples.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0244468