A divergent hepatitis A virus lineage in wild western lowland gorillas and central chimpanzees supports localized circulation and expands HAV diversity.

IF 3.8 2区 医学 Q1 VIROLOGY
Virus Evolution Pub Date : 2026-09-21 eCollection Date: 2026-01-01 DOI:10.1093/ve/veag060
Charles Sanctorum, Matheus A C Cosentino, Amandine Esteban, Christelle Butel, Innocent Ndong Bass, Simon-Pierre Ndimbo-Kumugo, Steve Ahuka-Mundeke, Eric Leroy, Charles Kouanfack, Ahidjo Ayouba, Martine Peeters
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引用次数: 0

Abstract

Hepatitis A virus (HAV) is a ubiquitous human pathogen that may cause acute liver disease. Despite the availability of effective vaccines, high prevalence rates are still reported in Southeast Asia and Africa, where sanitation conditions are poor. Although seven genotypes are known, including three in humans, three in non-human primates (NHP), and one recently identified in alpacas, the diversity, ecology, and evolutionary history of HAV remain poorly understood. In a pilot study of virome molecular characterization of wild African apes by using oligonucleotide probes enrichment, HAV sequences were detected in two animals (2/105; 1.9%): one from a western lowland gorilla (Gorilla gorilla gorilla) from southern Cameroon, sampled in 2006, and another from a central chimpanzee (Pan troglodytes troglodytes) in northeastern Gabon, sampled in 2011, approximately 450 km apart. Two near-full-length viral genomes were successfully reconstructed using specific primer sets that were developed. Phylogenetic analyses revealed that these sequences cluster within the simian HAV clade, forming a distinct cluster closely related to environmental strains from the Sanaga River in Cameroon and South Africa, yet clearly divergent from genotype V sequences (≥15.8% nucleotide divergence in the VP1 protein). Amino acid comparisons identified residues conserved in simian HAVs and, subsequently, only in African HAV strains. These results support the classification of a supplementary African simian genotype, provisionally designated HAV-VIII. HAV-positive samples (13/227; 5.7%) were detected in the same field sites, suggesting localized viral circulation in these populations. Bayesian time-scaled phylogenetic analysis estimated the most recent common ancestor of the human and simian HAV lineages at ~ 2 291 years ago and that of simian lineages at ~ 1900 years ago, with a more recent diversification (~100 years ago) within the identified lineage. This study highlights the presence of HAV in wild ape populations for the first time and also the first HAV detection among NHP species in Central Africa. These findings contribute to our current understanding of the diversity and evolution of HAV and highlight the need to extend surveillance across NHP species to better assess potential zoonotic risks.

西部低地野生大猩猩和中部黑猩猩的A型肝炎病毒分化谱系支持局部循环,扩大了甲肝病毒的多样性。
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来源期刊
Virus Evolution
Virus Evolution Immunology and Microbiology-Microbiology
CiteScore
10.50
自引率
5.70%
发文量
108
审稿时长
14 weeks
期刊介绍: Virus Evolution is a new Open Access journal focusing on the long-term evolution of viruses, viruses as a model system for studying evolutionary processes, viral molecular epidemiology and environmental virology. The aim of the journal is to provide a forum for original research papers, reviews, commentaries and a venue for in-depth discussion on the topics relevant to virus evolution.
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