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在食蟹猴中发现的一种新型乙型肝炎病毒为灵长类动物嗜肝 DNA 病毒的进化提供了新的线索。

A novel hepatitis B virus species discovered in capuchin monkeys sheds new light on the evolution of primate hepadnaviruses.

机构信息

Institute of Virology, University of Bonn Medical Centre, Bonn, Germany; University Hospital Prof. Edgard Santos, Infectious Diseases Research Laboratory, Federal University of Bahia, Salvador, Brazil.

Institute of Medical Virology, National Reference Center for Hepatitis B and D Viruses, Justus Liebig University, Giessen, Germany; German Centre for Infection Research (Deutsches Zentrum für Infektionsforschung), Berlin, Germany.

出版信息

J Hepatol. 2018 Jun;68(6):1114-1122. doi: 10.1016/j.jhep.2018.01.029. Epub 2018 Feb 8.

Abstract

BACKGROUND & AIMS: All known hepatitis B virus (HBV) genotypes occur in humans and hominoid Old World non-human primates (NHPs). The divergent woolly monkey HBV (WMHBV) forms another orthohepadnavirus species. The evolutionary origins of HBV are unclear.

METHODS

We analysed sera from 124 Brazilian monkeys collected during 2012-2016 for hepadnaviruses using molecular and serological tools, and conducted evolutionary analyses.

RESULTS

We identified a novel orthohepadnavirus species in capuchin monkeys (capuchin monkey hepatitis B virus [CMHBV]). We found CMHBV-specific antibodies in five animals and high CMHBV concentrations in one animal. Non-inflammatory, probably chronic infection was consistent with an intact preCore domain, low genetic variability, core deletions in deep sequencing, and no elevated liver enzymes. Cross-reactivity of antisera against surface antigens suggested antigenic relatedness of HBV, CMHBV, and WMHBV. Infection-determining CMHBV surface peptides bound to the human HBV receptor (human sodium taurocholate co-transporting polypeptide), but preferentially interacted with the capuchin monkey receptor homologue. CMHBV and WMHBV pseudotypes infected human hepatoma cells via the human sodium taurocholate co-transporting polypeptide, and were poorly neutralised by HBV vaccine-derived antibodies, suggesting that cross-species infections may be possible. Ancestral state reconstructions and sequence distance comparisons associated HBV with humans, whereas primate hepadnaviruses as a whole were projected to NHP ancestors. Co-phylogenetic analyses yielded evidence for co-speciation of hepadnaviruses and New World NHP. Bayesian hypothesis testing yielded strong support for an association of the HBV stem lineage with hominoid ancestors. Neither CMHBV nor WMHBV was likely the ancestor of the divergent human HBV genotypes F/H found in American natives.

CONCLUSIONS

Our data suggest ancestral co-speciation of hepadnaviruses and NHP, and an Old World origin of the divergent HBV genotypes F/H. The identification of a novel primate hepadnavirus offers new perspectives for urgently needed animal models of chronic hepatitis B.

LAY SUMMARY

The origins of HBV are unclear. The new orthohepadnavirus species from Brazilian capuchin monkeys resembled HBV in elicited infection patterns and could infect human liver cells using the same receptor as HBV. Evolutionary analyses suggested that primate HBV-related viruses might have emerged in African ancestors of New World monkeys millions of years ago. HBV was associated with hominoid primates, including humans and apes, suggesting evolutionary origins of HBV before the formation of modern humans. HBV genotypes found in American natives were divergent from those found in American monkeys, and likely introduced along prehistoric human migration. Our results elucidate the evolutionary origins and dispersal of primate HBV, identify a new orthohepadnavirus reservoir, and enable new perspectives for animal models of hepatitis B.

摘要

背景与目的

所有已知的乙型肝炎病毒(HBV)基因型都存在于人类和旧世界灵长类动物(NHPs)中。分化的毛猴 HBV(WMHBV)形成了另一种正嗜肝 DNA 病毒物种。HBV 的进化起源尚不清楚。

方法

我们使用分子和血清学工具分析了 2012-2016 年期间收集的 124 只巴西猴子的血清,以检测肝病毒,并进行了进化分析。

结果

我们在卷尾猴中发现了一种新的正嗜肝 DNA 病毒物种(卷尾猴乙型肝炎病毒 [CMHBV])。我们在五只动物中发现了 CMHBV 特异性抗体,在一只动物中发现了高浓度的 CMHBV。非炎症性、可能是慢性感染与完整的前核心区、遗传变异性低、深度测序中的核心缺失以及没有升高的肝酶一致。针对表面抗原的抗血清的交叉反应性表明 HBV、CMHBV 和 WMHBV 具有抗原相关性。感染决定的 CMHBV 表面肽与人类乙型肝炎病毒受体(人钠牛磺胆酸盐共转运多肽)结合,但与卷尾猴受体同源物优先相互作用。CMHBV 和 WMHBV 假型通过人钠牛磺胆酸盐共转运多肽感染人肝癌细胞,并且 HBV 疫苗衍生的抗体对其的中和作用很差,表明跨种感染可能是可能的。祖先状态重建和序列距离比较将 HBV 与人类联系起来,而整个灵长类动物肝病毒被预测为 NHPs 的祖先。共进化分析为肝病毒与新世界 NHP 的共同进化提供了证据。贝叶斯假设检验强烈支持 HBV 茎系与同源人祖先的关联。CMHBV 和 WMHBV 都不太可能是在美洲原住民中发现的具有高度分化的人类 HBV 基因型 F/H 的祖先。

结论

我们的数据表明,肝病毒与 NHP 共同进化,并且具有高度分化的 HBV 基因型 F/H 的起源于旧世界。从巴西卷尾猴中鉴定出的新型灵长类动物肝病毒为慢性乙型肝炎急需的动物模型提供了新的视角。

要点总结

HBV 的起源尚不清楚。来自巴西卷尾猴的新型正嗜肝 DNA 病毒在诱发感染模式上与 HBV 相似,并且可以使用与 HBV 相同的受体感染人肝细胞。进化分析表明,灵长类动物 HBV 相关病毒可能在数百万年前出现在新世界猴子的非洲祖先中。HBV 与包括人类和类人猿在内的人科灵长类动物有关,这表明 HBV 的进化起源早于现代人类的形成。在美洲原住民中发现的 HBV 基因型与在美洲猴中发现的 HBV 基因型不同,可能是随着史前人类的迁移而引入的。我们的研究结果阐明了灵长类动物 HBV 的进化起源和传播,确定了一个新的正嗜肝 DNA 病毒储存库,并为乙型肝炎的动物模型提供了新的视角。

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