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A protective bivalent vaccine against Rift Valley fever and bluetongue

Eva Calvo-Pinilla, Alejandro Marín-López, Sandra Moreno, Gema Lorenzo, Sergio Utrilla-Trigo, Luís Jiménez-Cabello, Júlio Benavides, Aitor Nogales, Rafael Blasco, Alejandro Brun, Javier Ortego

2020npj Vaccines36 citationsDOIOpen Access PDF

Abstract

Abstract Rift Valley fever (RVF) and bluetongue (BT) are two important ruminant diseases transmitted by arthropods. Both viruses have shown important geographic spread leading to endemicity of BT virus (BTV) in Africa and Europe. In this work, we report a dual vaccine that simultaneously induces protective immune responses against BTV and RVFV based on modified vaccinia Ankara virus (MVA) expressing BTV proteins VP2, NS1, or a truncated form of NS1 (NS1-Nt), and RVFV Gn and Gc glycoproteins. IFNAR (−/−) mice immunized with two doses of MVA-GnGc-VP2 developed a significant neutralizing antibody response against BTV-4 and RVFV. Furthermore, the homologous prime-boost immunization with MVA-GnGc-NS1 or MVA-GnGc-NS1-Nt triggered neutralizing antibodies against RVFV and NS1-specific cytotoxic CD8+ T cells in mice. Moreover, all mice immunized with MVA-GnGc-NS1 or MVA-GnGc-NS1-Nt remained healthy after lethal challenge with RVFV or BTV-4. The homologous prime-boost vaccination with MVA-GnGc-NS1, which was the best immunization strategy observed in mice, was assayed in sheep. Clinical signs and viremia were absent or highly reduced in vaccinated sheep after challenge with BTV-4 or RVFV. These results indicate that MVA-GnGc-NS1 vaccination elicits immune protection against RVFV and BTV in sheep.

Topics & Concepts

VirologyRift Valley feverBiologyModified vaccinia AnkaraVacciniaViremiaVaccinationNeutralizing antibodyImmunizationAntibodyImmune systemVirusCytotoxic T cellImmunologyRecombinant DNAIn vitroBiochemistryGeneVector-Borne Animal DiseasesViral Infections and VectorsAnimal Disease Management and Epidemiology
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