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Virology1987; 157(2); 488-496; doi: 10.1016/0042-6822(87)90291-1

An equine rotavirus (FI-14 strain) which bears both subgroup I and subgroup II specificities on its VP6.

Abstract: An equinine rotavirus FI-14 strain, originally isolated from a diarrheic foal in New York state, was shown to belong to serotype 3 by neutralization assay. In addition, it was found to react with both subgroup I and subgroup II monoclonal antibodies by enzyme-linked immunosorbent assay (ELISA), thus representing the first rotavirus strain to exhibit both subgroup specificities. By using hybridoma technology, we successfully produced monoclonal antibodies directed against the major inner capsid protein VP6 (the sixth gene product) of FI-14 virus. Such monoclonal antibodies reacted specifically with either subgroup I or subgroup II rotaviruses thus demonstrating that the VP6 of FI-14 virus has both subgroup I- and subgroup II-specific epitopes. Four additional monoclones directed to the VP6 of FI-14 demonstrated distinct reactivities by ELISA with a panel of 49 rotavirus strains derived from 11 different animal and avian species. Thus, at least six distinct antigenic sites were shown to exist on VP6 of FI-14 virus. When these 49 rotavirus strains were arranged based on their reactivity patterns with the six representative monoclones, they fell into one of eight reactivity groups. Analysis of the reactivity patterns of rotaviruses derived from various animal species suggested that human rotaviruses may have two ancestral lineages: one (subgroup II, serotype 1, 3, and 4) with pig-human lineage, and the other (subgroup I, serotype 2) with bovine-simian-human lineage. When analyzed by radioimmunoprecipitation, the molecular weight of the FI-14 virus VP6 (subgroups I and II) appeared to be larger (approx 45K) than those (approx 42K) of rhesus monkey MMU18006 virus VP6 (subgroup I) or human Wa virus VP6 (subgroup II). By RNA-RNA hybridization analysis, the FI-14 virus was shown not to share significant homology with viruses belonging to the four known human rotavirus serotypes.
Publication Date: 1987-04-01 PubMed ID: 2435059DOI: 10.1016/0042-6822(87)90291-1Google Scholar: Lookup
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  • Journal Article

Summary

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This study identified a new equine rotavirus strain (FI-14) which reacts with both subgroup I and II monoclonal antibodies, making it the first of its kind. The research involved producing antibodies and testing them on various animal species which suggest that human rotaviruses may have two ancestral lineages. The strain doesn’t show homology with known human rotavirus serotypes.

Research Methodology

In this study, students used different established methods to identify and understand the novel rotavirus strain.

  • An equine rotavirus strain, referred to as FI-14, was isolated from a foal diagnosed with diarrhea in New York. The neutralization assay determined that the strain belongs to serotype 3.
  • This FI-14 strain was then found to react with monoclonal antibodies from both subgroup I and subgroup II when tested through an enzyme-linked immunosorbent assay (ELISA), revealing the unique subgroup specificities of this strain.
  • Using hybridoma technology, the researchers generated monoclonal antibodies targeted toward the major inner capsid protein VP6 of the FI-14 virus.

Findings

Specific findings of the research were:

  • The antibodies were specific to either subgroup I or subgroup II rotaviruses. This validated that the VP6 of the FI-14 virus holds both subgroup I- and subgroup II-specific epitopes, which is a novel observation.
  • Additional monoclonal antibodies (monoclones) produced and tested with a panel of 49 rotavirus strains from different animal and avian species showed diverse reactions.
  • This diversity in reactions revealed at least six different antigenic sites on the VP6 of the FI-14 virus.
  • The rotaviruses, classified based on their reactivity patterns with the six representative monoclones, fell into one of eight reactivity groups.
  • To gain insight into the origin of rotaviruses, analysis of reactivity patterns of rotaviruses from various animal species was conducted. This suggested that human rotaviruses might have two ancestral lineages: one with pig-human lineage for subgroup II, serotype 1, 3, and 4; and another with bovine-simian-human lineage for subgroup I, serotype 2.
  • When analyzed by radioimmunoprecipitation, it was observed that the molecular weight of the FI-14 virus VP6 appeared to be more significant than those of the rhesus monkey MMU18006 virus VP6 or the human Wa virus VP6.
  • Using RNA-RNA hybridization analysis, it was determined that the FI-14 virus did not show significant homology with viruses from the known four human rotavirus serotypes, making it distinctly different.

Implication

This study’s outcomes contribute significant insights into the complexity of rotaviruses and their diverse nature. The unique dual specificity of the FI-14 strain to both subgroup I and II antibodies adds a new layer of understanding to rotavirus taxonomy. Furthermore, the possibility of two distinct ancestral lineages of human rotaviruses alludes to the multifaceted nature of rotaviral evolution. Hence, these findings can enrich future research into rotavirus diversity, evolution, and phylogenetics.

Cite This Article

APA
Hoshino Y, Gorziglia M, Valdesuso J, Askaa J, Glass RI, Kapikian AZ. (1987). An equine rotavirus (FI-14 strain) which bears both subgroup I and subgroup II specificities on its VP6. Virology, 157(2), 488-496. https://doi.org/10.1016/0042-6822(87)90291-1

Publication

ISSN: 0042-6822
NlmUniqueID: 0110674
Country: United States
Language: English
Volume: 157
Issue: 2
Pages: 488-496

Researcher Affiliations

Hoshino, Y
    Gorziglia, M
      Valdesuso, J
        Askaa, J
          Glass, R I
            Kapikian, A Z

              MeSH Terms

              • Animals
              • Antibodies, Monoclonal / immunology
              • Antibodies, Viral / immunology
              • Antigens, Viral / immunology
              • Capsid / immunology
              • Epitopes
              • Horses / microbiology
              • Humans
              • Nucleic Acid Hybridization
              • RNA, Viral / genetics
              • Rotavirus / classification
              • Rotavirus / immunology
              • Serotyping

              Citations

              This article has been cited 29 times.