Title | SARS-CoV-2 genomic diversity and the implications for qRT-PCR diagnostics and transmission. |
Publication Type | Journal Article |
Year of Publication | 2021 |
Authors | Sapoval, N, Mahmoud, M, Jochum, MD, Liu, Y, Elworth, RALeo, Wang, Q, Albin, D, Ogilvie, HA, Lee, MD, Villapol, S, Hernandez, KM, Berry, IMaljkovic, Foox, J, Beheshti, A, Ternus, K, Aagaard, KM, Posada, D, Mason, CE, Sedlazeck, FJ, Treangen, TJ |
Journal | Genome Res |
Volume | 31 |
Issue | 4 |
Pagination | 635-644 |
Date Published | 2021 Apr |
ISSN | 1549-5469 |
Keywords | COVID-19, Genetic Variation, Genome, Viral, Host-Pathogen Interactions, Humans, Polymorphism, Single Nucleotide, Real-Time Polymerase Chain Reaction, SARS-CoV-2 |
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 data sets and 6928 consensus genomes to contrast the intra-host and inter-host diversity of SARS-CoV-2. Our analyses yielded three major observations. First, the mutational profile of SARS-CoV-2 highlights intra-host single nucleotide variant (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. |
DOI | 10.1101/gr.268961.120 |
Alternate Journal | Genome Res |
PubMed ID | 33602693 |
PubMed Central ID | PMC8015855 |
Grant List | R01 HD091731 / HD / NICHD NIH HHS / United States R21 NS106640 / NS / NINDS NIH HHS / United States U19 AI144297 / AI / NIAID NIH HHS / United States |