Journal article
Authors list: Jo, 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 year: 2022
Pages: 195-203
Journal: Transboundary and Emerging Diseases
Volume number: 69
Issue number: 2
ISSN: 1865-1674
eISSN: 1865-1682
Open access status: Gold
DOI Link: https://doi.org/10.1111/tbed.14340
Publisher: Wiley
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 style: Jo, 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 style: Jo, 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
CARNIVORES; co-infection