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An Equine Model for Vaccination against a Hepacivirus: Insights into Host Responses to E2 Recombinant Protein Vaccination and Subsequent Equine Hepacivirus Inoculation

Badenhorst, Marcha; Saalmüller, Armin; Daly, Janet M.; Ertl, Reinhard; Stadler, Maria; Puff, Christina; de le Roi, Madeleine; Baumgärtner, Wolfgang; Engelmann, Michael; Brandner, Sabine; Junge, Hannah K; Pratscher, Barbara; Volz, Asisa; Saunier, Bertrand; Krey, Thomas; Wittmann, Johannes; Heelemann, Steffen; Delarocque, Julien; Wagner, Bettina; Todt, Daniel; Steinmann, Eike; Cavalleri, Jessika-M V

An Equine Model for Vaccination against a Hepacivirus: Insights into Host Responses to E2 Recombinant Protein Vaccination and Subsequent Equine Hepacivirus Inoculation Thumbnail


Authors

Marcha Badenhorst

Armin Saalmüller

JANET DALY janet.daly@nottingham.ac.uk
Professor of Viral Zoonoses

Reinhard Ertl

Maria Stadler

Christina Puff

Madeleine de le Roi

Wolfgang Baumgärtner

Michael Engelmann

Sabine Brandner

Hannah K Junge

Barbara Pratscher

Asisa Volz

Bertrand Saunier

Thomas Krey

Johannes Wittmann

Steffen Heelemann

Julien Delarocque

Bettina Wagner

Daniel Todt

Eike Steinmann

Jessika-M V Cavalleri



Abstract

Equine hepacivirus (EqHV) is the closest known genetic homologue of hepatitis C virus. An effective prophylactic vaccine is currently not available for either of these hepaciviruses. The equine as potential surrogate model for hepacivirus vaccine studies was investigated, while equine host responses following vaccination with EqHV E2 recombinant protein and subsequent EqHV inoculation were elucidated. Four ponies received prime and booster vaccinations (recombinant protein, adjuvant) four weeks apart (day −55 and −27). Two control ponies received adjuvant only. Ponies were inoculated with EqHV RNA-positive plasma on day 0. Blood samples and liver biopsies were collected over 26 weeks (day −70 to +112). Serum analyses included detection of EqHV RNA, isotypes of E2-specific immunoglobulin G (IgG), nonstructural protein 3-specific IgG, haematology, serum biochemistry, and metabolomics. Liver tissue analyses included EqHV RNA detection, RNA sequencing, histopathology, immunohistochemistry, and fluorescent in situ hybridization. Al-though vaccination did not result in complete protective immunity against experimental EqHV inoculation, the majority of vaccinated ponies cleared the serum EqHV RNA earlier than the control ponies. The majority of vaccinated ponies appeared to recover from the EqHV-associated liver insult earlier than the control ponies. The equine model shows promise as a surrogate model for future hepacivirus vaccine research.

Citation

Badenhorst, M., Saalmüller, A., Daly, J. M., Ertl, R., Stadler, M., Puff, C., …Cavalleri, J. V. (2022). An Equine Model for Vaccination against a Hepacivirus: Insights into Host Responses to E2 Recombinant Protein Vaccination and Subsequent Equine Hepacivirus Inoculation. Viruses, 14(7), Article 1401. https://doi.org/10.3390/v14071401

Journal Article Type Article
Acceptance Date Jun 15, 2022
Online Publication Date Jun 27, 2022
Publication Date Jul 1, 2022
Deposit Date Jun 17, 2022
Publicly Available Date Jun 17, 2022
Journal Viruses
Electronic ISSN 1999-4915
Publisher MDPI
Peer Reviewed Peer Reviewed
Volume 14
Issue 7
Article Number 1401
DOI https://doi.org/10.3390/v14071401
Keywords Virology; Infectious Diseases
Public URL https://nottingham-repository.worktribe.com/output/8500467
Publisher URL https://www.mdpi.com/1999-4915/14/7/1401

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