Strong protection induced by an experimental DIVA subunit vaccine against bluetongue virus serotype 8 in cattle.

Archive ouverte

Anderson, Jenna | Hagglund, Sara | Breard, Emmanuel | Riou, Mickaël | Zohari, Siamak | Comtet, Loic | Olofson, Ann-Sophie | Gelineau, Robert | Martin, Guillaume | Elvander, Marianne | Blomqvist, Gunilla | Zientara, Stéphan | Valarcher, Jean François

Edité par CCSD ; Elsevier -

International audience. Bluetongue virus (BTV) infections in ruminants pose a permanent agricultural threat since new serotypes are constantly emerging in new locations. Clinical disease is mainly observed in sheep, but cattle were unusually affected during an outbreak of BTV seroype 8 (BTV-8) in Europe. We previously developed an experimental vaccine based on recombinant viral protein 2 (VP2) of BTV-8 and non-structural proteins 1 (NS1) and NS2 of BTV-2, mixed with an immunostimulating complex (ISCOM)-matrix adjuvant. We demonstrated that bovine immune responses induced by this vaccine were as good or superior to those induced by a classic commercial inactivated vaccine. In this study, we evaluated the protective efficacy of the experimental vaccine in cattle and, based on the detection of VP7 antibodies, assessed its DIVA compliancy following virus challenge. Two groups of BTV-seronegative calves were subcutaneously immunized twice at a 3-week interval with the subunit vaccine (n=6) or with adjuvant alone (n=6). Following BTV-8 challenge 3 weeks after second immunization, controls developed viremia and fever associated with other mild clinical signs of bluetongue disease, whereas vaccinated animals were clinically and virologically protected. The vaccine-induced protection was likely mediated by high virus-neutralizing antibody titers directed against VP2 and perhaps by cellular responses to NS1 and NS2. T lymphocyte responses were cross-reactive between BTV-2 and BTV-8, suggesting that NS1 and NS2 may provide the basis of an adaptable vaccine that can be varied by using VP2 of different serotypes. The detection of different levels of VP7 antibodies in vaccinated animals and controls after challenge suggested a compliancy between the vaccine and the DIVA companion test. This BTV subunit vaccine is a promising candidate that should be further evaluated and developed to protect against different serotypes.

Consulter en ligne

Suggestions

Du même auteur

Development and evaluation of a DIVA subunit vaccine against Bluetongue virus serotype 8 in cattle

Archive ouverte | Anderson, Jenna | CCSD

Session 3 : Antivirals & VaccinesSession 3 : Antivirals & Vaccines. The incursion and circulation of more than nine different serotypes of Bluetongue virus (BTV) in central and northern Europe over the past fifteen ...

Evaluation of the Immunogenicity of an Experimental Subunit Vaccine That Allows Differentiation between Infected and Vaccinated Animals against Bluetongue Virus Serotype 8 in Cattle

Archive ouverte | Anderson, Jenna | CCSD

International audience. Bluetongue virus (BTV), the causative agent of bluetongue in ruminants, is an emerging virus in northern Europe. The 2006 out-break of BTV serotype 8 (BTV-8) in Europe was marked by an unusua...

Purification, stability, and immunogenicity analyses of five bluetongue virus proteins for use in development of a subunit vaccine that allows differentiation of infected from vaccinated animals

Archive ouverte | Anderson, Jenna | CCSD

International audience. Bluetongue virus (BTV) causes bluetongue disease, a vector-borne disease of ruminants. The recent northerly spread of BTV serotype 8 in Europe resulted in outbreaks characterized by clinical ...

Chargement des enrichissements...