Bhamidipati Sravya V, Surathu Anil, Chao Hsu, Agustinho Daniel P, Xiang Qin, Kottapalli Kavya, Santhanam Abirami, Momin Zeineen, Walker Kimberly, Menon Vipin K, Weissenberger George, Emerick Nathanael, Mahjabeen Faria, Meng Qingchang, Hu Jianhong, Sucgang Richard, Henke David, Sedlazeck Fritz J, Khan Ziad M, Metcalf Ginger A, Avadhanula Vasanthi, Piedra Pedro A, Ramani Sasirekha, Atmar Robert L, Estes Mary K, Petrosino Joseph F, Gibbs Richard A, Muzny Donna M, Javornik Sara Cregeen, Doddapaneni Harsha
Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, 77030, USA.
Department of Molecular Virology & Microbiology, Baylor College of Medicine, Houston, TX, 77030, USA.
Sci Rep. 2025 Jul 1;15(1):20526. doi: 10.1038/s41598-025-03398-6.
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.
呼吸道合胞病毒(RSV)是全球儿童下呼吸道感染的主要病因,而人诺如病毒(HuNoV)是流行性和散发性急性胃肠炎的主要病因。生成这些病毒的全长基因组序列对于了解病毒多样性和追踪新出现的变异体至关重要。然而,由于病毒株的变异性、质量和低滴度,获得高质量的测序数据往往具有挑战性。在此,我们展示了一组基于GenBank中1570个RSV和1376个HuNoV分离株序列设计的综合寡核苷酸探针集。使用这些探针集和捕获富集测序工作流程,对85份RSV阳性鼻拭子样本和55份(49份粪便样本和6份人肠道类器官样本)HuNoV阳性样本进行了表征,这些样本涵盖了主要亚型和基因型。对RSV的Ct值在17.0至29.9之间、HuNoV的Ct值在20.2至34.8之间的样本进行了测序,其中一些HuNoV样本低于检测限。捕获后,映射到病毒基因组的 reads 百分比对于 RSV 为85.1%,对于 HuNoV 为40.8%,而在捕获前文库中分别为0.08%和1.15%。所有RSV阳性样本以及55份HuNoV阳性样本中的47份都获得了全长基因组,这比从捕获前文库中恢复基因组有了显著改进。还从这些数据中对RSV转录组(亚基因组mRNA)序列进行了表征。