Vaccination With Recombinant Adenoviruses Expressing the Bluetongue Virus Subunits VP7 and VP2 Provides Protection Against Heterologous Virus Challenge
Centro de Investigación en Sanidad Animal (CISA)
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Language: | English |
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Frontiers Media
2021-03-10
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Subjects: | IFNAR (−/−) mice, Orbivirus, T cell, Cytotoxic T lymphocytes, Vaccine, |
Online Access: | http://hdl.handle.net/10261/268889 http://dx.doi.org/10.13039/501100003329 http://dx.doi.org/10.13039/100012818 http://dx.doi.org/10.13039/501100000780 http://dx.doi.org/10.13039/501100004837 https://api.elsevier.com/content/abstract/scopus_id/85103067332 |
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dig-inia-es-10261-2688892024-05-15T20:39:04Z Vaccination With Recombinant Adenoviruses Expressing the Bluetongue Virus Subunits VP7 and VP2 Provides Protection Against Heterologous Virus Challenge Rojas, José Manuel Barba-Moreno, Diego Avia, Miguel Sevilla, Noemí Martín, Verónica Ministerio de Ciencia e Innovación (España) European Commission Comunidad de Madrid Ministerio de Economía y Competitividad (España) Rojas, José Manuel [0000-0002-4055-3967] Avia, Miguel [0000-0001-7661-4779] Sevilla, Noemí [0000-0003-0118-0376] IFNAR (−/−) mice Orbivirus T cell Cytotoxic T lymphocytes Vaccine Centro de Investigación en Sanidad Animal (CISA) Bluetongue virus (BTV) is the causative agent of a disease that affects domestic and wild ruminants and leads to critical economic losses. BTV is an arbovirus from the Reoviridae family that is typically transmitted by the bite of infected Culicoides midges. BTV possesses multiple serotypes (up to 28 have been described), and immunity to one serotype offers little cross-protection to other serotypes. The design of vaccines that provide protection across multiple serotypes is therefore highly desirable to control this disease. We previously reported that a recombinant replication-defective human adenovirus serotype 5 (Ad5) that expresses the VP7 inner core protein of BTV serotype 8 (Ad5VP7-8) induced T-cell responses and provided protection. In the present work, we evaluated as BTV vaccine the combination of Ad5VP7-8 with another recombinant Ad5 that expresses the outer core protein VP2 from BTV-1 (Ad5VP2-1). The combination of Ad5VP2-1 and Ad5VP7-8 protected against homologous BTV challenge (BTV-1 and BTV-8) and partially against heterologous BTV-4 in a murine model. Cross-reactive anti-BTV immunoglobulin G (IgG) were detected in immunized animals, but no significant titers of neutralizing antibodies were elicited. The Ad5VP7-8 immunization induced T-cell responses that recognized all three serotypes tested in this study and primed cytotoxic T lymphocytes specific for VP7. This study further confirms that targeting antigenic determinant shared by several BTV serotypes using cellular immunity could help develop multiserotype BTV vaccines. This work was funded by grants AGL2015-64290R and from the Ministerio de Ciencia (Spain), grant VetBioNet INFRAIA-731014 from the EU-H2020, and grant S2018/BAA-4370-PLATESA2 from Comunidad de Madrid (Fondo Europeo de Desarrollo Regional, FEDER). MA was funded by an FPI grant (BES-2013-066406). Peer reviewed 15 Pág. 2022-05-06T10:31:43Z 2022-05-06T10:31:43Z 2021-03-10 artículo http://purl.org/coar/resource_type/c_6501 Frontiers in Veterinary Science 8: 645561 (2021) http://hdl.handle.net/10261/268889 10.3389/fvets.2021.645561 2297-1769 http://dx.doi.org/10.13039/501100003329 http://dx.doi.org/10.13039/100012818 http://dx.doi.org/10.13039/501100000780 http://dx.doi.org/10.13039/501100004837 33778041 2-s2.0-85103067332 https://api.elsevier.com/content/abstract/scopus_id/85103067332 en #PLACEHOLDER_PARENT_METADATA_VALUE# #PLACEHOLDER_PARENT_METADATA_VALUE# #PLACEHOLDER_PARENT_METADATA_VALUE# #PLACEHOLDER_PARENT_METADATA_VALUE# info:eu-repo/grantAgreement/Ministerio de Ciencia//AGL2015-64290R info:eu-repo/grantAgreement/EH(2020)/NFRAIA-731014 S2018/BAA-4370-PLATESA2/CM info:eu-repo/grantAgreement/MINECO//BES-2013-066406/ES/BES-2013-066406/ Frontiers in veterinary science Publisher's version https://doi.org/10.3389/fvets.2021.645561 Sí open Frontiers Media |
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IFNAR (−/−) mice Orbivirus T cell Cytotoxic T lymphocytes Vaccine IFNAR (−/−) mice Orbivirus T cell Cytotoxic T lymphocytes Vaccine |
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IFNAR (−/−) mice Orbivirus T cell Cytotoxic T lymphocytes Vaccine IFNAR (−/−) mice Orbivirus T cell Cytotoxic T lymphocytes Vaccine Rojas, José Manuel Barba-Moreno, Diego Avia, Miguel Sevilla, Noemí Martín, Verónica Vaccination With Recombinant Adenoviruses Expressing the Bluetongue Virus Subunits VP7 and VP2 Provides Protection Against Heterologous Virus Challenge |
description |
Centro de Investigación en Sanidad Animal (CISA) |
author2 |
Ministerio de Ciencia e Innovación (España) |
author_facet |
Ministerio de Ciencia e Innovación (España) Rojas, José Manuel Barba-Moreno, Diego Avia, Miguel Sevilla, Noemí Martín, Verónica |
format |
artículo |
topic_facet |
IFNAR (−/−) mice Orbivirus T cell Cytotoxic T lymphocytes Vaccine |
author |
Rojas, José Manuel Barba-Moreno, Diego Avia, Miguel Sevilla, Noemí Martín, Verónica |
author_sort |
Rojas, José Manuel |
title |
Vaccination With Recombinant Adenoviruses Expressing the Bluetongue Virus Subunits VP7 and VP2 Provides Protection Against Heterologous Virus Challenge |
title_short |
Vaccination With Recombinant Adenoviruses Expressing the Bluetongue Virus Subunits VP7 and VP2 Provides Protection Against Heterologous Virus Challenge |
title_full |
Vaccination With Recombinant Adenoviruses Expressing the Bluetongue Virus Subunits VP7 and VP2 Provides Protection Against Heterologous Virus Challenge |
title_fullStr |
Vaccination With Recombinant Adenoviruses Expressing the Bluetongue Virus Subunits VP7 and VP2 Provides Protection Against Heterologous Virus Challenge |
title_full_unstemmed |
Vaccination With Recombinant Adenoviruses Expressing the Bluetongue Virus Subunits VP7 and VP2 Provides Protection Against Heterologous Virus Challenge |
title_sort |
vaccination with recombinant adenoviruses expressing the bluetongue virus subunits vp7 and vp2 provides protection against heterologous virus challenge |
publisher |
Frontiers Media |
publishDate |
2021-03-10 |
url |
http://hdl.handle.net/10261/268889 http://dx.doi.org/10.13039/501100003329 http://dx.doi.org/10.13039/100012818 http://dx.doi.org/10.13039/501100000780 http://dx.doi.org/10.13039/501100004837 https://api.elsevier.com/content/abstract/scopus_id/85103067332 |
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