Language

English

Publication Date

7-1-2025

Journal

Scientific Reports

DOI

10.1038/s41598-025-03398-6

PMID

40594045

PMCID

PMC12216758

PubMedCentral® Posted Date

7-1-2025

PubMedCentral® Full Text Version

Post-print

Abstract

Respiratory syncytial virus (RSV) is the leading cause of lower respiratory tract infections in children worldwide, while human noroviruses (HuNoV) are a leading cause of epidemic and sporadic acute gastroenteritis. Generating full-length genome sequences for these viruses is crucial for understanding viral diversity and tracking emerging variants. However, obtaining high-quality sequencing data is often challenging due to viral strain variability, quality, and low titers. Here, we present a set of comprehensive oligonucleotide probe sets designed from 1,570 RSV and 1,376 HuNoV isolate sequences in GenBank. Using these probe sets and a capture enrichment sequencing workflow, 85 RSV positive nasal swab samples and 55 (49 stool and six human intestinal enteroids) HuNoV positive samples encompassing major subtypes and genotypes were characterized. Samples with Ct values 17.0-29.9 for RSV, and 20.2-34.8 for HuNoV, with some HuNoV below the detection limit were sequenced. The percentage of reads mapped to viral genomes was 85.1% for RSV and 40.8% for HuNoV post-capture, compared to 0.08% and 1.15% in pre-capture libraries. Full-length genomes were obtained for all RSV positive samples and in 47/55 HuNoV positive samples-a significant improvement over genome recovery from pre-capture libraries. RSV transcriptome (subgenomic mRNAs) sequences were also characterized from this data.

Keywords

Humans, Norovirus, Genome, Viral, Respiratory Syncytial Virus, Human, Caliciviridae Infections, Genomics, Respiratory Syncytial Virus Infections, Genotype, Phylogeny, Gastroenteritis, Oligonucleotide Probes, Respiratory syncytial virus (RSV), Human norovirus (HuNoV), Capture enrichment, Genome sequencing, Biological techniques, Biotechnology, Computational biology and bioinformatics, Genetics, Molecular biology, Diseases

Published Open-Access

yes

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