Research

Hidden genomic diversity of SARS-CoV-2: implications for qRT-PCR diagnostics and transmission

    • 1 Rice University;
    • 2 Baylor College of Medicine;
    • 3 Baylor College of Medicine and Texas Children's Hospital;
    • 4 Systems, Synthetic, and Physical Biology (SSPB) Graduate Program;
    • 5 NASA Ames Research Center, Blue Marble Space Institute of Science;
    • 6 Houston Methodist Research Institute;
    • 7 University of Chicago;
    • 8 Walter Reed Army Institute of Research;
    • 9 Weill Cornell Medicine;
    • 10 NASA Ames Research Center;
    • 11 Signature Science, LLC;
    • 12 CINBIO, Universidade de Vigo, Galicia Sur Health Research Institute;
    • 13 Weill Cornell Medical College
Published February 18, 2021. https://doi.org/10.1101/gr.268961.120
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cover of Genome Research Vol 36 Issue 6
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Abstract

The COVID-19 pandemic has sparked an urgent need to uncover the underlying biology of this devastating disease. Though RNA viruses mutate more rapidly than DNA viruses, there are a relatively small number of single nucleotide polymorphisms (SNPs) that differentiate the main SARS-CoV-2 lineages that have spread throughout the world. In this study, we investigated 129 RNA-seq datasets and 6,928 consensus genomes to contrast the intrahost and interhost diversity of SARS-CoV-2. Our analyses yielded three major observations. First, the mutational profile of SARS-CoV-2 highlights iSNV and SNP similarity, albeit with differences in C>U changes. Second, iSNV and SNP patterns in SARS-CoV-2 are more similar to MERS-CoV than SARS-CoV-1. Third, a significant fraction of insertions and deletions contribute to the genetic diversity of SARS-CoV-2. Altogether, our findings provide insight into SARS-CoV-2 genomic diversity, inform the design of detection tests, and highlight the potential of iSNVs for tracking the transmission of SARS-CoV-2.

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