Altered Subgenomic RNA Expression in SARS-CoV-2 B.1.1.7 Infections

Matthew Parker(Neuroscience Institute), Benjamin B. Lindsey(Sheffield Teaching Hospitals NHS Foundation Trust), Dhruv R. Shah(University of Sheffield), Sharon Hsu(University of Sheffield), Alexander J. Keeley(Sheffield Teaching Hospitals NHS Foundation Trust), David G. Partridge(Sheffield Teaching Hospitals NHS Foundation Trust), Shay Leary(Murdoch University), Alison Cope(Sheffield Teaching Hospitals NHS Foundation Trust), Amy State(Sheffield Teaching Hospitals NHS Foundation Trust), Katie Johnson(Sheffield Teaching Hospitals NHS Foundation Trust), Nasar Ali(Sheffield Teaching Hospitals NHS Foundation Trust), Rasha Raghei(Sheffield Teaching Hospitals NHS Foundation Trust), Joe Heffer(University of Sheffield), Darren Smith(University of Sheffield), Peijun Zhang(University of Sheffield), Marta Gallis(University of Sheffield), Stavroula F. Louka(University of Sheffield), Hailey Hornsby(University of Sheffield), Max Whiteley(University of Sheffield), Benjamin H. Foulkes(University of Sheffield), Stella Christou(University of Sheffield), Paige Wolverson(University of Sheffield), Manoj Baliram Pohare(University of Sheffield), Samantha E. Hansford(University of Sheffield), Luke R. Green(University of Sheffield), Cariad Evans(Sheffield Teaching Hospitals NHS Foundation Trust), Mohammad Raza(Sheffield Teaching Hospitals NHS Foundation Trust), Dennis Wang(Neuroscience Institute), Silvana Gaudieri(Murdoch University), S. Mallal(The University of Western Australia), Thushan I. de Silva(Sheffield Teaching Hospitals NHS Foundation Trust)
bioRxiv (Cold Spring Harbor Laboratory)
March 3, 2021
Cited by 34Open Access
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Abstract

Abstract SARS-CoV-2 lineage B.1.1.7 viruses are more transmissible, may lead to greater clinical severity, and result in modest reductions in antibody neutralization. subgenomic RNA (sgRNA) is produced by discontinuous transcription of the SARS-CoV-2 genome and is a crucial step in the SARS-CoV-2 life cycle. Applying our tool (periscope) to ARTIC Network Oxford Nanopore genomic sequencing data from 4400 SARS-CoV-2 positive clinical samples, we show that normalised sgRNA expression profiles are significantly increased in B.1.1.7 infections (n=879). This increase is seen over the previous dominant circulating lineage in the UK, B.1.177 (n=943), which is independent of genomic reads, E gene cycle threshold and days since symptom onset at sampling. A noncanonical sgRNA which could represent ORF9b is found in 98.4% of B.1.1.7 SARS-CoV-2 infections compared with only 13.8% of other lineages, with a 16-fold increase in median expression. We hypothesise that this is a direct consequence of a triple nucleotide mutation in nucleocapsid (28280:GAT>CAT, D3L) creating a transcription regulatory-like sequence complementary to a region 3’ of the genomic leader. These findings provide a unique insight into the biology of B.1.1.7 and support monitoring of sgRNA profiles in sequence data to evaluate emerging potential variants of concern. One Sentence Summary The recently emerged and more transmissible SARS-CoV-2 lineage B.1.1.7 shows greater subgenomic RNA expression in clinical infections and enhanced expression of a noncanonical subgenomic RNA near ORF9b.


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