Ramani Sasirekha, Javornik Cregeen Sara J, Surathu Anil, Neill Frederick H, Muzny Donna M, Doddapaneni Harsha, Menon Vipin K, Hoffman Kristi L, Ross Matthew C, Metcalf Ginger, Opekun Antone R, Graham David Y, Gibbs Richard A, Petrosino Joseph F, Estes Mary K, Atmar Robert L
Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, TX, 77030, USA.
The Alkek Center for Metagenomics and Microbiome Research, Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, TX, 77030, USA.
bioRxiv. 2024 Sep 5:2023.05.30.542907. doi: 10.1101/2023.05.30.542907.
Human noroviruses are a leading cause of acute and sporadic gastroenteritis worldwide. The evolution of human noroviruses in immunocompromised persons has been evaluated in many studies. Much less is known about the evolutionary dynamics of human norovirus in healthy adults.
We used sequential samples collected from a controlled human infection study with GI.1/Norwalk/US/68 virus to evaluate intra- and inter-host evolution of a human norovirus in healthy adults. Up to 12 samples from day 1 to day 56 post-challenge were sequenced using a norovirus-specific capture probe method.
Complete genomes were assembled, even in samples that were below the limit of detection of standard RT-qPCR assays, up to 28 days post-challenge. Analysis of 123 complete genomes showed changes in the GI.1 genome in all persons, but there were no conserved changes across all persons. Single nucleotide variants resulting in non-synonymous amino acid changes were observed in all proteins, with the capsid VP1 and nonstructural protein NS3 having the largest numbers of changes.
These data highlight the potential of a new capture-based sequencing approach to assemble human norovirus genomes with high sensitivity and demonstrate limited conserved immune pressure-driven evolution of GI.1 virus in healthy adults.
人诺如病毒是全球急性散发性胃肠炎的主要病因。许多研究评估了免疫功能低下人群中人诺如病毒的进化情况。而关于健康成年人中人诺如病毒的进化动态,人们了解得要少得多。
我们使用从一项针对GI.1/诺沃克/美国/68病毒的人体对照感染研究中收集的连续样本,来评估健康成年人中人诺如病毒在宿主内和宿主间的进化情况。使用诺如病毒特异性捕获探针方法对攻毒后第1天至第56天的多达12个样本进行测序。
即使在攻毒后长达28天的样本中,标准逆转录定量聚合酶链反应(RT-qPCR)检测限以下的样本也成功组装出了完整基因组。对123个完整基因组的分析表明,所有人的GI.1基因组均有变化,但并非所有人都有保守变化。在所有蛋白质中均观察到导致非同义氨基酸变化的单核苷酸变异,衣壳蛋白VP1和非结构蛋白NS3的变化数量最多。
这些数据凸显了一种基于捕获的新测序方法在高灵敏度组装人诺如病毒基因组方面的潜力,并证明了在健康成年人中GI.1病毒受免疫压力驱动的保守进化有限。