Bykov Roman, Itani Tarek, Pletenchuk Daria, Ohlopkova Olesia, Moshkin Alexey, Stepanyuk Marina, Semenov Aleksandr
Federal Budgetary Institution of Science, «Federal Scientific Research Institute of Viral Infections «Virome»», Federal Service for Surveillance on Consumer Rights Protection and Human Wellbeing, Ekaterinburg 620030, Russia.
Research Institute of Virology, Federal State Budgetary Scientific Institution «Federal Research Center for Fundamental and Translational Medicine», Novosibirsk 630060, Russia.
Viruses. 2025 Sep 15;17(9):1243. doi: 10.3390/v17091243.
Human noroviruses (HuNoVs) stand as the primary cause of acute viral gastroenteritis outbreaks worldwide, particularly impacting children under the age of five. In Russia, reports of norovirus gastroenteritis have surged, especially in the post-COVID-19 era starting in 2022, with elevated infection rates reported into 2024. These viruses exhibit significant mutational variability, leading to the emergence of recombinant strains that can evade immune responses. A comprehensive examination of the complete genome is crucial for understanding the evolution of norovirus genes and for predicting potential outbreaks. This research focuses on analyzing the genotypic composition of HuNoVs circulating in the Sverdlovsk region during 2024, using Sanger sequencing and next-generation sequencing (NGS). Biological samples were collected (n = 384) from patients diagnosed with norovirus infection within the region. Bioinformatics analysis targeted the nucleotide sequences of the ORF1/ORF2 fragment and the assembly of complete genomes for the GII.4 and GII.7 genotypes. In total, 220 HuNoVs were characterized, representing 57.3% of the collected samples. The main capsid variants forming the predominant genotypic profile included GII.4 (n = 88, 40%), GII.7 (n = 86, 39%), and GII.17 (n = 14, 6%). Using NGS, we successfully assembled 8 out of 10 complete genomes for noroviruses GII.4[P16] and GII.7[P7]. Non-synonymous substitutions appeared at amino acid sites corresponding to the subdomains of VP1 in these strains. This molecular-genetic analysis provides contemporary insights into the genotypic composition, circulation patterns, and evolutionary dynamics associated with the dominant genovariants GII.4[P16] and GII.7[P7].
人诺如病毒(HuNoVs)是全球急性病毒性肠胃炎暴发的主要原因,对五岁以下儿童影响尤甚。在俄罗斯,诺如病毒肠胃炎的报告激增,特别是在2022年开始的新冠疫情后时代,2024年感染率仍居高不下。这些病毒具有显著的突变变异性,导致能够逃避免疫反应的重组毒株出现。全面检查完整基因组对于理解诺如病毒基因的进化以及预测潜在暴发至关重要。本研究聚焦于利用桑格测序和下一代测序(NGS)分析2024年斯维尔德洛夫斯克地区流行的HuNoVs的基因型组成。从该地区被诊断为诺如病毒感染的患者中收集了生物样本(n = 384)。生物信息学分析针对ORF1/ORF2片段的核苷酸序列以及GII.4和GII.7基因型的完整基因组组装。总共鉴定出220株HuNoVs,占所收集样本的57.3%。构成主要基因型谱的主要衣壳变体包括GII.4(n = 88,40%)、GII.7(n = 86,39%)和GII.17(n = 14,6%)。利用NGS,我们成功组装了10株诺如病毒GII.4[P16]和GII.7[P7]中的8个完整基因组。这些毒株在与VP1亚结构域相对应的氨基酸位点出现了非同义替换。这种分子遗传学分析为与优势基因变体GII.4[P16]和GII.7[P7]相关的基因型组成、传播模式和进化动态提供了当代见解。