Arslan Nurhan, Reuter Bernhard, Buech Joachim, Lengauer Thomas, Obermeier Martin, Kaiser Rolf, Pfeifer Nico
Department of Computer Science, Methods in Medical Informatics, University of Tuebingen, Tübingen, Germany.
Departments Computational Biology & Applied Algorithmics, Max Planck Institute for Informatics, Saarbruecken, Germany.
J Med Virol. 2025 Feb;97(2):e70169. doi: 10.1002/jmv.70169.
Hepatitis C virus infection is a significant global health concern, affecting millions worldwide. Although direct-acting antivirals achieve over 90% success rate, treatment failures still occur, particularly when pan-genotypic DAAs are unavailable, and drugs need to be chosen based on the present HCV genotype. Genotyping tests can be misleading, especially in cases involving the 2k/1b recombinant variant. The 2k/1b variant was first discovered in Saint Petersburg in 2002 and is most commonly observed in Eastern European countries, including Russia, Georgia, and Ukraine. Due to migration, the 2k/1b variant has spread to Western Europe and other regions, potentially increasing HCV transmission and changing the virus's epidemiological landscape. The situation highlights the importance of molecular epidemiology in monitoring the spread of the 2k/1b variant. Accurate detection and characterization of the 2k/1b variant are crucial for an effective treatment if no pan-genotypic DAAs are available. To address this need, machine learning models were developed to predict the 2k/1b variant based on 1b and 2k/1b sequence data from nonstructural proteins. They were integrated into the tool, providing physicians and researchers with an open-access resource for determining HCV genotypes, including the 2k/1b variant.
丙型肝炎病毒感染是一个重大的全球健康问题,影响着全球数百万人。尽管直接抗病毒药物的成功率超过90%,但治疗失败仍会发生,尤其是在没有泛基因型直接抗病毒药物可用,且需要根据当前的丙型肝炎病毒基因型选择药物时。基因分型检测可能会产生误导,特别是在涉及2k/1b重组变体的情况下。2k/1b变体于2002年在圣彼得堡首次发现,最常见于东欧国家,包括俄罗斯、格鲁吉亚和乌克兰。由于移民,2k/1b变体已传播到西欧和其他地区,可能会增加丙型肝炎病毒的传播,并改变该病毒的流行病学格局。这种情况凸显了分子流行病学在监测2k/1b变体传播方面的重要性。如果没有泛基因型直接抗病毒药物可用,准确检测和鉴定2k/1b变体对于有效治疗至关重要。为满足这一需求,开发了机器学习模型,以根据非结构蛋白的1b和2k/1b序列数据预测2k/1b变体。这些模型被整合到该工具中,为医生和研究人员提供了一个开放获取的资源,用于确定丙型肝炎病毒基因型,包括2k/1b变体。