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Archives of virology2005; 150(12); 2583-2592; doi: 10.1007/s00705-005-0607-9

Glycoprotein G deletion mutants of equine herpesvirus 1 (EHV1; equine abortion virus) and EHV4 (equine rhinopneumonitis virus).

Abstract: Glycoprotein G (gG) deletion mutants of EHV1 and EHV4, designated EHV1DeltagG and EHV4DeltagG, were constructed. The growth characteristics of the EHV1DeltagG mutants were similar to the parent virus. All of the EHV4DeltagG mutants grew more slowly in cell culture and produced plaques of different morphology including smaller size. The yields of both gG deletion mutant viruses in cell culture were similar to the parent viruses. Sequencing of the genes flanking gG, Southern blot, PCR and western blot analyses of the mutant viruses demonstrated that the deletions were as expected, except for EHV4DeltagG mutants, which in addition to deletion of gG contained unexpected deletions in the adjacent down stream gene ORF 71 (glycoprotein 2). Antisera to EHV1DeltagG and EHV4DeltagG neutralised the respective mutant and the parent viruses to the same titre and these antisera could be distinguished from antisera to the wild type viruses in a gG antibody detection ELISA. The mutant viruses may be useful as vaccine candidates and the deletion of gG may act as a marker to distinguish vaccinated from the naturally infected horses.
Publication Date: 2005-08-01 PubMed ID: 16052277DOI: 10.1007/s00705-005-0607-9Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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This research focuses on the creation and examination of Glycoprotein G deletion mutants for equine herpesvirus 1 (EHV1) and 4 (EHV4), and suggests that these mutations could potentially serve as vaccines for these viruses in horses.

Construction of Deletion Mutants

  • The study details the development of Glycoprotein G (gG) deletion mutants for two equine herpesviruses – EHV1 and EHV4.
  • These “edited” viruses are referred to as EHV1DeltagG and EHV4DeltagG.
  • The growth characteristics of these mutants were compared with the parent viruses, with the aim of determining any differences in proliferation and morphology due to the deletion.

Growth Characteristics and Mutations

  • It was found that the growth characteristics of EHV1DeltagG were similar to the original EHV1 virus, indicating that the gG deletion did not significantly alter its growth.
  • In contrast, all EHV4DeltagG mutants grew at a slower rate in cell culture and exhibited different morphological characteristics, such as smaller plaque sizes.
  • Upon further investigation, it was discovered that in addition to the gG deletion, the EHV4DeltagG mutants also had unexpected deletions in the adjacent downstream gene, ORF 71.

Antibodies and Potential Vaccines

  • Antibodies produced in response to the mutant viruses were able to neutralize both the mutant and parent viruses. This could suggest potential use of these mutants as vaccines.
  • The antisera, or blood serum containing these antibodies, could also be distinguished from antisera to the wild type viruses, particularly using a gG antibody detection ELISA (enzyme-linked immunosorbent assay).
  • This ability to distinctly identify gG-deletion mutants from wild type viruses could also make these mutants useful as a marker to differentiate vaccinated horses from those that are naturally infected.

Cite This Article

APA
Huang J, Hartley CA, Ficorilli NP, Crabb BS, Studdert MJ. (2005). Glycoprotein G deletion mutants of equine herpesvirus 1 (EHV1; equine abortion virus) and EHV4 (equine rhinopneumonitis virus). Arch Virol, 150(12), 2583-2592. https://doi.org/10.1007/s00705-005-0607-9

Publication

ISSN: 0304-8608
NlmUniqueID: 7506870
Country: Austria
Language: English
Volume: 150
Issue: 12
Pages: 2583-2592

Researcher Affiliations

Huang, J
  • Centre for Equine Virology, School of Veterinary Science, The University of Melbourne, Melbourne, Australia.
Hartley, C A
    Ficorilli, N P
      Crabb, B S
        Studdert, M J

          MeSH Terms

          • Animals
          • Antibodies, Viral / analysis
          • Blotting, Southern
          • Blotting, Western
          • Cell Line
          • Enzyme-Linked Immunosorbent Assay
          • Gene Deletion
          • Herpesvirus 1, Equid / genetics
          • Herpesvirus 1, Equid / growth & development
          • Herpesvirus 1, Equid / immunology
          • Herpesvirus 4, Equid / genetics
          • Herpesvirus 4, Equid / growth & development
          • Herpesvirus 4, Equid / immunology
          • Neutralization Tests
          • Rabbits
          • Sequence Analysis, DNA
          • Sequence Deletion
          • Viral Envelope Proteins / genetics
          • Viral Plaque Assay

          Citations

          This article has been cited 3 times.
          1. Azab W, El-Sheikh A, Abdel-Gawad A. In vitro characterization of EHV-4 gG-deleted mutant. Virus Genes 2012 Feb;44(1):109-11.
            doi: 10.1007/s11262-011-0677-6pubmed: 21960433google scholar: lookup
          2. Van de Walle GR, Sakamoto K, Osterrieder N. CCL3 and viral chemokine-binding protein gg modulate pulmonary inflammation and virus replication during equine herpesvirus 1 infection. J Virol 2008 Feb;82(4):1714-22.
            doi: 10.1128/JVI.02137-07pubmed: 18077722google scholar: lookup
          3. Hu Y, Wu G, Jia Q, Zhang B, Sun W, Sa R, Zhang S, Cai W, Jarhen, Ran D, Liu J. Development of a live attenuated vaccine candidate for equid alphaherpesvirus 1 control: a step towards efficient protection. Front Immunol 2024;15:1408510.
            doi: 10.3389/fimmu.2024.1408510pubmed: 39021566google scholar: lookup