# Unveiling Inter- and Intra-Patient Sequence Variability with a Multi-Sample Coronavirus Target Enrichment Approach

**Authors:** Sara Lado, Jakob Thannesberger, Kathrin Spettel, Jurica Arapović, Bibiana I. Ferreira, Marialuisa Lavitrano, Christoph Steininger

PMC · DOI: 10.3390/v16050786 · 2024-05-15

## TL;DR

This study uses a new sequencing method to track SARS-CoV-2 mutations across patients and regions, highlighting the virus's evolution and host interactions.

## Contribution

A novel multi-sample, high-throughput NGS approach for detecting SARS-CoV-2 sequence variability with high sensitivity.

## Key findings

- Envelope, Nucleocapsid, and Open Reading Frame 8 genes showed the highest mutation rates.
- Spike and Nucleocapsid genes exhibited signs of positive selection.
- The pooling strategy enabled detection of subtle sequence variability across viral populations.

## Abstract

Amid the global challenges posed by the COVID-19 pandemic, unraveling the genomic intricacies of SARS-CoV-2 became crucial. This study explores viral evolution using an innovative high-throughput next-generation sequencing (NGS) approach. By taking advantage of nasal swab and mouthwash samples from patients who tested positive for COVID-19 across different geographical regions during sequential infection waves, our study applied a targeted enrichment protocol and pooling strategy to increase detection sensitivity. The approach was extremely efficient, yielding a large number of reads and mutations distributed across 10 distinct viral gene regions. Notably, the genes Envelope, Nucleocapsid, and Open Reading Frame 8 had the highest number of unique mutations per 1000 nucleotides, with both spike and Nucleocapsid genes showing evidence for positive selection. Focusing on the spike protein gene, crucial in virus replication and immunogenicity, our findings show a dynamic SARS-CoV-2 evolution, emphasizing the virus–host interplay. Moreover, the pooling strategy facilitated subtle sequence variability detection. Our findings painted a dynamic portrait of SARS-CoV-2 evolution, emphasizing the intricate interplay between the virus and its host populations and accentuating the importance of continuous genomic surveillance to understand viral dynamics. As SARS-CoV-2 continues to evolve, this approach proves to be a powerful, versatile, fast, and cost-efficient screening tool for unraveling emerging variants, fostering understanding of the virus’s genetic landscape.

## Linked entities

- **Genes:** LOC124901580 (endogenous retrovirus group K member 6 Env polyprotein) [NCBI Gene 124901580], CHMP5 (charged multivesicular body protein 5) [NCBI Gene 51510]
- **Diseases:** COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** S (surface glycoprotein) [NCBI Gene 43740568] {aka spike glycoprotein}
- **Diseases:** COVID-19 (MESH:D000086382), infection (MESH:D007239), Coronavirus (MESH:D018352)
- **Species:** Homo sapiens (human, species) [taxon 9606], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11125942/full.md

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Source: https://tomesphere.com/paper/PMC11125942