Determination of serotypes of red clover necrotic mosaic virus by enzyme-linked immunosorbent assay
Language English Country Switzerland Media print
Document type Journal Article
PubMed
1705747
Knihovny.cz E-resources
- MeSH
- Antigens, Viral analysis MeSH
- Enzyme-Linked Immunosorbent Assay methods MeSH
- Epitopes MeSH
- Immunoglobulin G MeSH
- Antibodies, Viral MeSH
- Serotyping methods MeSH
- Mosaic Viruses classification immunology MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Antigens, Viral MeSH
- Epitopes MeSH
- Immunoglobulin G MeSH
- Antibodies, Viral MeSH
The direct double antibody sandwich (DAS) type of enzyme-linked immunosorbent assay (ELISA) was used to determine the degree of serological and antigenic differences, among the three serotypes (A, B, C) of red clover necrotic mosaic virus (RCNMV). Homologous and heterologous antibody titres in the used IgGs to isolates TpM34 (serotype A), TpM48 (serotype B) and isolate No. 6 (serotype C) as determined by ELISA were 100- to 200-fold higher than by ring precipitation test. Intensity of homologous and heterologous reactions in ELISA depended on the concentration of antigen, of the IgG used for coating and of the labelled IgG. The IgG preparations used contained 50 to 100 times higher concentration of homologous (serotype-specific) than heterologous (interserotype-specific) antibodies. Such a great difference between the two antibody types accounts for a comparatively high degree of selectivity of the homologous reactions.