Journal article

Natural co-infection of divergent hepatitis B and C virus homologues in carnivores


Authors listJo, Wendy K.; Alfonso-Toledo, Jorge A.; Salas-Rojas, Monica; Almazan-Marin, Cenia; Galvez-Romero, Guillermo; Garcia-Baltazar, Anahi; Obregon-Morales, Cirani; Rendon-Franco, Emilio; Kuhne, Arne; Carvalho-Urbieta, Victor; Rasche, Andrea; Brunink, Sebastian; Glebe, Dieter; Aguilar-Setien, Alvaro; Drexler, Jan Felix

Publication year2022

Pages195-203

JournalTransboundary and Emerging Diseases

Volume number69

Issue number2

ISSN1865-1674

eISSN1865-1682

Open access statusGold

DOI Linkhttps://doi.org/10.1111/tbed.14340

PublisherWiley


Abstract
In humans, co-infection of hepatitis B and C viruses (HBV, HCV) is common and aggravates disease outcome. Infection-mediated disease aggravation is poorly understood, partly due to lack of suitable animal models. Carnivores are understudied for hepatitis virus homologues. We investigated Mexican carnivores (ringtails, Bassariscus astutus) for HBV and HCV homologues. Three out of eight animals were infected with a divergent HBV termed ringtail HBV (RtHBV) at high viral loads of 5 x 10(9) -1.4 x 10(10) copies/ml serum. Two of the RtHBV-infected animals were co-infected with a divergent hepacivirus termed ringtail hepacivirus (RtHV) at 4 x 10(6)-7.5 x 10(7) copies/ml in strain-specific qRT-PCR assays. Immunofluorescence assays relying on HBV core and RtHV NS3/4a proteins indicated that none of the animals had detectable hepadnavirus core-specific antibodies, whereas one RtHV-infected animal had concomitant RtHV-specific antibodies at 1:800 end-point titre. RtHBV and RtHV complete genomes showed typical HBV and HCV structure and length. All RtHBV genomes were identical, whereas RtHV genomes showed four amino acid substitutions located predominantly in the E1/E2-encoding genomic regions. Both RtHBV (>28% genomic nucleotide sequence distance) and RtHV (>30% partial NS3/NS5B amino acid sequence distance) formed new species within their virus families. Evolutionary analyses showed that RtHBV grouped with HBV homologues from different laurasiatherian hosts (carnivores, bats, and ungulates), whereas RtHV grouped predominantly with rodent-borne viruses. Ancestral state reconstructions showed that RtHV, but not RtHBV, likely emerged via a non-recent host switch involving rodent-borne hepacivirus ancestors. Conserved hepatitis virus infection patterns in naturally infected ringtails indicate that carnivores may be promising animal models to understand HBV/HCV co-infection.



Citation Styles

Harvard Citation styleJo, W., Alfonso-Toledo, J., Salas-Rojas, M., Almazan-Marin, C., Galvez-Romero, G., Garcia-Baltazar, A., et al. (2022) Natural co-infection of divergent hepatitis B and C virus homologues in carnivores, Transboundary and Emerging Diseases, 69(2), pp. 195-203. https://doi.org/10.1111/tbed.14340

APA Citation styleJo, W., Alfonso-Toledo, J., Salas-Rojas, M., Almazan-Marin, C., Galvez-Romero, G., Garcia-Baltazar, A., Obregon-Morales, C., Rendon-Franco, E., Kuhne, A., Carvalho-Urbieta, V., Rasche, A., Brunink, S., Glebe, D., Aguilar-Setien, A., & Drexler, J. (2022). Natural co-infection of divergent hepatitis B and C virus homologues in carnivores. Transboundary and Emerging Diseases. 69(2), 195-203. https://doi.org/10.1111/tbed.14340



Keywords


CARNIVORESco-infection

Last updated on 2025-10-06 at 11:31