Department of Pathogen Biology and Immunology, Jiangsu Key Laboratory of Immunity and Metabolism, Jiangsu International Laboratory of Immunity and Metabolism, Xuzhou Medical University, Xuzhou, China.
Department of Pathogen Biology and Immunology, Jiangsu Key Laboratory of Immunity and Metabolism, Jiangsu International Laboratory of Immunity and Metabolism, Xuzhou Medical University, Xuzhou, China.
Mol Phylogenet Evol. 2024 Aug;197:108114. doi: 10.1016/j.ympev.2024.108114. Epub 2024 May 31.
Chronic infection of hepatitis B virus (HBV) and hepatitis D virus (HDV) causes the most severe form of viral hepatitis. Due to the dependence on HBV, HDV was deemed to co-evolve and co-migrate with HBV. However, we previously found that the naturally occurred HDV/HBV combinations do not always reflect the most efficient virological adaptation (Wang et al., 2021). Moreover, regions with heavy HBV burden do not always correlate with high HDV prevalence (e.g., East Asia), and vice versa (e.g., Central Asia). Herein, we systematically elucidated the spatiotemporal evolutionary landscape of HDV to understand the unique epidemic features of HDV. We found that the MRCA of HDV was from South America around the late 13th century, was globally dispersed mainly via Central Asia, and evolved into eight genotypes from the 19th to 20th century. In contrast, the MRCA of HBV was from Europe ∼23.7 thousand years ago (Kya), globally dispersed mainly via Africa and East Asia, and evolved into eight genotypes ∼1100 years ago. When HDV stepped in, all present-day HBV genotypes had already formed and its global genotypic distribution had stayed stable geographically. Nevertheless, regionalized HDV adapted to local HBV genotypes and human lineages, contributing to the global geographical separation of HDV genotypes. Additionally, a sharp increase in HDV infections was observed after the 20th century. In conclusion, HDV exhibited a distinct spatiotemporal distribution path compared with HBV. This unique evolutionary relationship largely fostered the unique epidemic features we observe nowadays. Moreover, HDV infections may continue to ramp up globally, thus more efforts are urgently needed to combat this disease.
慢性乙型肝炎病毒 (HBV) 和丁型肝炎病毒 (HDV) 感染可导致最严重的病毒性肝炎。由于依赖 HBV,HDV 被认为是与 HBV 共同进化和共同迁移的。然而,我们之前发现,自然发生的 HDV/HBV 组合并不总是反映最有效的病毒学适应性(Wang 等人,2021 年)。此外,HBV 负担较重的地区并不总是与 HDV 高流行率相关(例如东亚),反之亦然(例如中亚)。在此,我们系统地阐明了 HDV 的时空进化景观,以了解 HDV 的独特流行特征。我们发现 HDV 的 MRCA 来自 13 世纪后期的南美洲,主要通过中亚在全球传播,并在 19 至 20 世纪演变成八个基因型。相比之下,HBV 的 MRCA 来自欧洲约 23700 年前,主要通过非洲和东亚在全球传播,并在约 1100 年前演变成八个基因型。当 HDV 出现时,所有现今的 HBV 基因型已经形成,其全球基因型分布在地理上保持稳定。然而,区域性的 HDV 适应了当地的 HBV 基因型和人类谱系,导致了 HDV 基因型在全球的地理分离。此外,在 20 世纪后观察到 HDV 感染急剧增加。总之,HDV 与 HBV 相比表现出明显的时空分布路径。这种独特的进化关系在很大程度上促成了我们现今观察到的独特流行特征。此外,HDV 感染可能会在全球范围内继续增加,因此迫切需要更多的努力来对抗这种疾病。