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A Synthetic Modified Live Chimeric Marker Vaccine against BVDV-1 and BVDV-2

Bovine viral diarrhea virus (BVDV), a pestivirus which exists in the two distinct species BVDV-1 (syn. Pestivirus A) and BVDV-2 (syn. Pestivirus B), is the causative agent of one of the most widespread and economically important virus infections in cattle. For economic as well as for animal health r...

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Autores principales: Koethe, Susanne, König, Patricia, Wernike, Kerstin, Pfaff, Florian, Schulz, Jana, Reimann, Ilona, Makoschey, Birgit, Beer, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7712951/
https://www.ncbi.nlm.nih.gov/pubmed/33023099
http://dx.doi.org/10.3390/vaccines8040577
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author Koethe, Susanne
König, Patricia
Wernike, Kerstin
Pfaff, Florian
Schulz, Jana
Reimann, Ilona
Makoschey, Birgit
Beer, Martin
author_facet Koethe, Susanne
König, Patricia
Wernike, Kerstin
Pfaff, Florian
Schulz, Jana
Reimann, Ilona
Makoschey, Birgit
Beer, Martin
author_sort Koethe, Susanne
collection PubMed
description Bovine viral diarrhea virus (BVDV), a pestivirus which exists in the two distinct species BVDV-1 (syn. Pestivirus A) and BVDV-2 (syn. Pestivirus B), is the causative agent of one of the most widespread and economically important virus infections in cattle. For economic as well as for animal health reasons, an increasing number of national BVDV control programs were recently implemented. The main focus lies on the detection and removal of persistently infected cattle. The application of efficient marker or DIVA (differentiation of infected from vaccinated animals) vaccines would be beneficial for the eradication success in regions with a high BVDV prevalence to prevent fetal infection and it would allow serological monitoring of the BVDV status also in vaccinated farms. Therefore, a marker vaccine based on the cytopathic (cp) BVDV-1b strain CP7 was constructed as a synthetic backbone (BVDV-1b_synCP7). For serological discrimination of vaccinated from infected animals, the viral protein E(rns) was substituted by the heterologous E(rns) of Bungowannah virus (BuPV, species Pestivirus F). In addition, the vaccines were attenuated by a deletion within the type I interferon inhibitor N(pro) protein encoding sequence. The BVDV-2 vaccine candidate is based on the genetic sequence of the glycoproteins E1 and E2 of BVDV-2 strain CS8644 (CS), which were introduced into the backbone of BVDV-1b_synCP7_ΔN(pro)_E(rns) Bungo in substitution of the homologous glycoproteins. Vaccine virus recovery resulted in infectious cytopathic virus chimera that grew to titers of up to 10(6) TCID(50)/mL. Both synthetic chimera BVDV-1b_synCP7_ΔN(pro)_E(rns) Bungo and BVDV-1b_synCP7_ΔN(pro)_E(rns) Bungo_E1E2 BVDV-2 CS were avirulent in cattle, provided a high level of protection in immunization and challenge experiments against both BVDV species and allowed differentiation of infected from vaccinated cattle. Our study presents the first report on an efficient BVDV-1 and -2 modified live marker vaccine candidate and the accompanying commercially available serological marker ELISA system.
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spelling pubmed-77129512020-12-04 A Synthetic Modified Live Chimeric Marker Vaccine against BVDV-1 and BVDV-2 Koethe, Susanne König, Patricia Wernike, Kerstin Pfaff, Florian Schulz, Jana Reimann, Ilona Makoschey, Birgit Beer, Martin Vaccines (Basel) Article Bovine viral diarrhea virus (BVDV), a pestivirus which exists in the two distinct species BVDV-1 (syn. Pestivirus A) and BVDV-2 (syn. Pestivirus B), is the causative agent of one of the most widespread and economically important virus infections in cattle. For economic as well as for animal health reasons, an increasing number of national BVDV control programs were recently implemented. The main focus lies on the detection and removal of persistently infected cattle. The application of efficient marker or DIVA (differentiation of infected from vaccinated animals) vaccines would be beneficial for the eradication success in regions with a high BVDV prevalence to prevent fetal infection and it would allow serological monitoring of the BVDV status also in vaccinated farms. Therefore, a marker vaccine based on the cytopathic (cp) BVDV-1b strain CP7 was constructed as a synthetic backbone (BVDV-1b_synCP7). For serological discrimination of vaccinated from infected animals, the viral protein E(rns) was substituted by the heterologous E(rns) of Bungowannah virus (BuPV, species Pestivirus F). In addition, the vaccines were attenuated by a deletion within the type I interferon inhibitor N(pro) protein encoding sequence. The BVDV-2 vaccine candidate is based on the genetic sequence of the glycoproteins E1 and E2 of BVDV-2 strain CS8644 (CS), which were introduced into the backbone of BVDV-1b_synCP7_ΔN(pro)_E(rns) Bungo in substitution of the homologous glycoproteins. Vaccine virus recovery resulted in infectious cytopathic virus chimera that grew to titers of up to 10(6) TCID(50)/mL. Both synthetic chimera BVDV-1b_synCP7_ΔN(pro)_E(rns) Bungo and BVDV-1b_synCP7_ΔN(pro)_E(rns) Bungo_E1E2 BVDV-2 CS were avirulent in cattle, provided a high level of protection in immunization and challenge experiments against both BVDV species and allowed differentiation of infected from vaccinated cattle. Our study presents the first report on an efficient BVDV-1 and -2 modified live marker vaccine candidate and the accompanying commercially available serological marker ELISA system. MDPI 2020-10-02 /pmc/articles/PMC7712951/ /pubmed/33023099 http://dx.doi.org/10.3390/vaccines8040577 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Koethe, Susanne
König, Patricia
Wernike, Kerstin
Pfaff, Florian
Schulz, Jana
Reimann, Ilona
Makoschey, Birgit
Beer, Martin
A Synthetic Modified Live Chimeric Marker Vaccine against BVDV-1 and BVDV-2
title A Synthetic Modified Live Chimeric Marker Vaccine against BVDV-1 and BVDV-2
title_full A Synthetic Modified Live Chimeric Marker Vaccine against BVDV-1 and BVDV-2
title_fullStr A Synthetic Modified Live Chimeric Marker Vaccine against BVDV-1 and BVDV-2
title_full_unstemmed A Synthetic Modified Live Chimeric Marker Vaccine against BVDV-1 and BVDV-2
title_short A Synthetic Modified Live Chimeric Marker Vaccine against BVDV-1 and BVDV-2
title_sort synthetic modified live chimeric marker vaccine against bvdv-1 and bvdv-2
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7712951/
https://www.ncbi.nlm.nih.gov/pubmed/33023099
http://dx.doi.org/10.3390/vaccines8040577
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