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Peptide Scanning-assisted Identification of a Monoclonal Antibody-recognized Linear B-cell Epitope
Published on: March 24, 2017
Antigenic relationships between six genotypes of the small hydrophobic protein gene of mumps virus
Claes Örvell1, Tesfaldet Tecle1, Bo Johansson1
1Huddinge University Hospital, Department of Clinical Virology, Karolinska Institutet, SE-141 86 Stockholm, Sweden1.
Abstract:
Six different genotypes of mumps virus, A, C, D, G, H and I, genotyped on the basis of the small hydrophobic protein gene sequence, were subjected to antigenic comparison. Monoclonal antibodies directed against the haemagglutinin-neuraminidase protein of the SBL-1 strain of genotype A were used in immunofluorescence tests with different mumps virus strains. In addition, the six virus genotypes were compared by cross-neutralization tests with human post-vaccination sera after vaccination with the Jeryl Lynn (JL) strain of mumps virus and with rabbit hyperimmune sera directed against the A or D genotypes of mumps virus. Genotypes C, D, G, H and I could not be antigenically separated. In contrast, three different virus strains of genotype A, SBL-1, JL and Kilham, were distinct and were found to represent three different serotypes within the A genotype of mumps virus. Vaccination of Swedish children with the JL strain of mumps virus resulted in clearly lower neutralization titres against the SBL-1 strain, which is endemic in Sweden, compared to the homologous vaccine titres.
Insights
Mumps virus genotypes C, D, G, H, and I are antigenically indistinguishable. However, genotype A comprises three distinct serotypes, indicating potential challenges for mumps virus vaccines in providing broad protection.
Area of Science:
- Virology
- Immunology
- Molecular Biology
Background:
- Mumps virus exhibits genetic diversity with multiple genotypes identified.
- Antigenic characterization is crucial for understanding mumps virus evolution and vaccine efficacy.
Purpose of the Study:
- To compare the antigenicity of six mumps virus genotypes (A, C, D, G, H, I).
- To investigate the antigenic relationship between different strains within genotype A.
- To assess the cross-neutralization capacity of vaccines against endemic strains.
Main Methods:
- Immunofluorescence assays using monoclonal antibodies against the haemagglutinin-neuraminidase protein.
- Cross-neutralization tests with human post-vaccination sera and rabbit hyperimmune sera.
- Genotyping based on the small hydrophobic protein gene sequence.
Main Results:
- Mumps virus genotypes C, D, G, H, and I could not be antigenically differentiated.
- Three distinct serotypes were identified within genotype A: SBL-1, Jeryl Lynn (JL), and Kilham strains.
- Vaccination with the JL strain showed lower neutralization titers against the endemic SBL-1 strain compared to homologous titers.
Conclusions:
- Mumps virus genotypes C, D, G, H, and I represent a single serological group.
- Genotype A contains at least three distinct serotypes, suggesting limited cross-protection.
- Current mumps virus vaccines may offer suboptimal protection against circulating endemic strains like SBL-1.
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