Yeo Daseul, Jung Soontag, Yoon Danbi, Hwang Seongwon, Lim Dong Jae, Jin Songfeng, Choi Jinho, Hong Ki Ho, Choi Changsun
Department of Food and Nutrition, School of Food Science and Technology, College of Biotechnology and Natural Resources, Chung-Ang University, 4726 Seodongdaero, Daeduck-myeon, Anseong-si, Gyeonggi-do, 17546, Republic of Korea.
Sanigen, 16 Heungan-daero, Dongan-gu, Anyang-si, Gyeonggi-do, 14059, Republic of Korea.
Sci Rep. 2025 Jul 11;15(1):25005. doi: 10.1038/s41598-025-09812-3.
Hepatitis A virus (HAV) is transmitted via the fecal-oral route, including through person-to-person contact and consumption of contaminated food. In 2019, 17,638 cases of HAV infection were reported in South Korea. The use of whole-genome sequencing (WGS) for rapid and accurate epidemiological investigation of HAV remains challenging due to the low viral titers and the lack of a cell culture system. Here, we developed a multiplex PCR (mPCR)-based next generation sequencing (NGS) method for direct WGS of HAV from serum using the Illumina platform. Overlapping primers were designed to generate amplicons covering the entire HAV genome, enabling successful sequencing from samples with viral titers as low as 3.0 log copies/µL. The method achieved a mapping rate of 98.95% and 98.32% genome coverage. All nine HAV strains analyzed were classified as genotype IA and showed > 99% sequence homology. Phylogenetic analysis of the whole genome, structural, and non-structural regions demonstrated clustering with HAV strains previously isolated in Japan. Correlation coefficients between WGS and individual gene regions approached 1.0, confirming the method's reliability for molecular epidemiology. This mPCR-based NGS approach provides a robust tool for HAV surveillance and facilitates high-resolution genomic analysis from non-culturable clinical samples.
甲型肝炎病毒(HAV)通过粪-口途径传播,包括人与人之间的接触以及食用受污染的食物。2019年,韩国报告了17638例HAV感染病例。由于病毒滴度低且缺乏细胞培养系统,使用全基因组测序(WGS)对HAV进行快速准确的流行病学调查仍然具有挑战性。在此,我们开发了一种基于多重PCR(mPCR)的下一代测序(NGS)方法,用于使用Illumina平台直接从血清中对HAV进行全基因组测序。设计了重叠引物以生成覆盖整个HAV基因组的扩增子,从而能够从病毒滴度低至3.0 log拷贝/µL的样本中成功测序。该方法的映射率为98.95%,基因组覆盖率为98.32%。分析的所有9株HAV毒株均被归类为IA基因型,序列同源性>99%。对全基因组、结构和非结构区域的系统发育分析表明,它们与先前在日本分离的HAV毒株聚类。WGS与各个基因区域之间的相关系数接近1.0,证实了该方法在分子流行病学方面的可靠性。这种基于mPCR的NGS方法为HAV监测提供了一个强大的工具,并有助于对不可培养的临床样本进行高分辨率基因组分析。