Hu Mingda, Lin Yixiong, Zhang Rui, Wang Xin, He Yaqing, Huang Huitao, Wang Boqian, Liu Wanqiu, Li Kexin, Fu Jingjing, Zhao Xinru, Aimaiti Buaijier, Yang Wensheng, Song Hongbin, Ren Hongguang, Hu Xiaofeng
Laboratory of Advanced Biotechnology, Beijing Institute of Biotechnology, Beijing, China.
Institute of Pathogen Biology, Zhuhai Center for Disease Control and Prevention, Zhuhai, China.
BMC Genomics. 2025 Aug 18;26(1):752. doi: 10.1186/s12864-025-11953-8.
Rotavirus A group (RVA) is a leading cause of viral diarrhea, posing a substantial economic and public health burden. Compared to other enteric viruses, RVA possesses diverse genetic mechanisms, making it more challenging to control and prevent. Moreover, surveillance and evolutionary studies on RVA remain limited in Southern China.
We collected diarrheal stool samples from sentinel hospitals in Shenzhen and Zhuhai between 2020 and 2023. RVA-positive samples were identified via RT-PCR, followed by RNA extraction, sequencing, and genome assembly, yielding 57 RVA strains, comprising 604 sequences. Genotype trends were analyzed statistically. For phylogenetic analysis, global sequences were curated by CD-HIT, aligned with contributed sequences by MAFFT, and analyzed using IQ-TREE. Recombination and reassortment events were detected via RDP4.
We analyzed the temporal distribution and genetic diversity of 57 newly sequenced strains from Shenzhen and Zhuhai in the context of global sequences. Our findings reveal that the prevalent genotypes of RVA in China have undergone changes over time with the decreasing of G9P[8] and the rising of G8P[8]. Phylogenetic analysis focusing on the VP7 and VP4 genes revealed distinct evolutionary patterns among different genotypes across temporal and geographical dimensions. Additionally, we discovered one reassortment event in the VP7 gene and two recombination events in the NSP1 and NSP5/6 gene.
we observed significant variability and complexity in the evolutionary characteristics of RVA in Shenzhen and Zhuhai. These insights enhance our understanding of global evolution and transmission of RVA and provide guidance for future research and vaccine development.
A组轮状病毒(RVA)是病毒性腹泻的主要病因,造成了巨大的经济和公共卫生负担。与其他肠道病毒相比,RVA具有多样的遗传机制,使其控制和预防更具挑战性。此外,中国南方对RVA的监测和进化研究仍然有限。
我们收集了2020年至2023年期间深圳和珠海哨点医院的腹泻粪便样本。通过逆转录聚合酶链反应(RT-PCR)鉴定出RVA阳性样本,随后进行RNA提取、测序和基因组组装,获得了57株RVA毒株,包含604个序列。对基因型趋势进行了统计分析。对于系统发育分析,通过CD-HIT整理全球序列,使用MAFFT将其与贡献的序列进行比对,并使用IQ-TREE进行分析。通过RDP4检测重组和重配事件。
我们在全球序列的背景下分析了深圳和珠海57株新测序毒株的时间分布和遗传多样性。我们的研究结果表明,中国RVA的流行基因型随时间发生了变化,G9P[8]减少,G8P[8]增加。聚焦于VP7和VP4基因的系统发育分析揭示了不同基因型在时间和地理维度上的不同进化模式。此外,我们在VP7基因中发现了一个重配事件,在NSP1和NSP5/6基因中发现了两个重组事件。
我们观察到深圳和珠海RVA进化特征存在显著变异性和复杂性。这些见解增强了我们对RVA全球进化和传播的理解,并为未来研究和疫苗开发提供了指导。