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A novel group A rotavirus G serotype: serological and genomic characterization of equine isolate FI23
G F Browning1, T A Fitzgerald, R M Chalmers
1Moredun Research Institute, Edinburgh, Scotland.
Journal of Clinical Microbiology
|September 1, 1991
Abstract:
Equine rotavirus FI23 was shown to be prototypic of a novel G serotype, provisionally G14, by cross-neutralization and VP7 sequence determination. Although distinct, there are as few as six differing amino acid residues (92, 94, 96, 146, 147, and 221) in the VP7 antigenic regions of FI23 and G3 rotaviruses.
Insights
Equine rotavirus FI23 represents a new G serotype, G14. This equine rotavirus strain shows only six amino acid differences in its VP7 protein compared to G3 rotaviruses.
Area of Science:
- Veterinary Virology
- Microbiology
- Animal Health
Background:
- Equine rotaviruses cause significant gastrointestinal disease in foals.
- Rotavirus G serotypes are classified based on the VP7 outer capsid protein.
- Previous studies have identified various G serotypes in equine rotavirus strains.
Purpose of the Study:
- To characterize the novel equine rotavirus strain FI23.
- To determine the G serotype of the equine rotavirus FI23 strain.
- To compare the VP7 protein of FI23 with other known rotavirus strains.
Main Methods:
- Cross-neutralization assays were performed to assess serological relationships.
- VP7 gene sequencing was utilized for genetic characterization.
- Amino acid sequence comparison of VP7 proteins was conducted.
Main Results:
- Equine rotavirus FI23 was identified as prototypic of a novel G serotype, provisionally designated G14.
- Sequence analysis revealed that the VP7 protein of FI23 differs from G3 rotaviruses by only six amino acid residues.
- These differences are located within the VP7 antigenic regions.
Conclusions:
- Equine rotavirus FI23 represents a distinct and novel G serotype (G14).
- The close genetic relationship between FI23 (G14) and G3 rotaviruses is highlighted by minimal amino acid variations in VP7.
- Further research is warranted to understand the full antigenic and epidemiological implications of this new equine rotavirus G serotype.