Immunogenicity of recombinant VP2 proteins of all nive serotypes of African horse sickness virus

Autor: Yuki Kaname, Polly Roy, Mieke A. Maris-Veldhuis, Piet A. van Rijn, T.N. Athmaram, Yuta Kanai
Jazyk: angličtina
Rok vydání: 2014
Předmět:
Serotype
viruses
African Horse Sickness Virus
Antibodies
Viral

baculovirus
vaccine
biology
horsesickness-virus
Immunogenicity
Antibody titer
virus diseases
Recombinant Proteins
3. Good health
Virology & Molecular Biology
Titer
Infectious Diseases
Vaccines
Subunit

Molecular Medicine
African horse sickness
Female
Capsid protein VP2
Antibody
Baculoviridae
outer capsid proteins
sheep
Recombinant protein
Guinea Pigs
Reoviridae
Serogroup
Subunit vaccine
Article
bluetongue virus
Neutralization Tests
Immunology and Microbiology(all)
expression
Animals
protective efficacy
General Veterinary
General Immunology and Microbiology
Public Health
Environmental and Occupational Health

Viral Vaccines
biochemical phenomena
metabolism
and nutrition

biology.organism_classification
Antibodies
Neutralizing

veterinary(all)
Virology
Virologie & Moleculaire Biologie
biology.protein
challenge
responses
Capsid Proteins
Zdroj: Vaccine 32 (2014) 39
Vaccine, 32(39), 4932-4937
Vaccine
ISSN: 0264-410X
Popis: African horse sickness (AHS) is an equine disease with a mortality of up to 90% for susceptible horses. The causative agent AHS virus (AHSV) is transmitted by species of Culicoides. AHSV serogroup within the genus Orbivirus of the Reoviridae family consists of nine serotypes that show no or very limited cross-neutralization. Of the seven structural proteins (VP1-VP7) of AHSV, VP2 is the serotype specific protein, and the major target for neutralizing antibodies. In this report, recombinant VP2 proteins of all nine serotypes were expressed individually by the baculovirus expression system and the immunogenicity of each was studied by immunization of guinea pigs with single VP2 as well as with cocktails of VP2 proteins. Homologous neutralizing antibodies measured by 50% plaque reduction assay showed varying degrees (from 37 to 1365) of titers for different VP2 proteins. A low cross-neutralizing antibody titer was found for genetically related AHSV serotypes. Immunization with VP2 cocktails containing equal amounts of each of the VP2 proteins also triggered neutralizing antibodies albeit to lower titers (4-117) to each of the serotypes in the cocktail. This study is a first step to develop a VP2 subunit vaccine for AHS and our results indicate that VP2 subunit vaccines are feasible individually or in a multi-serotype cocktail.
Databáze: OpenAIRE