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Vaccine2022; 40(44); 6362-6366; doi: 10.1016/j.vaccine.2022.09.047

Protective efficacy of a reverse genetics-derived inactivated vaccine against equine influenza virus in horses.

Abstract: Updating vaccine strains is essential to control equine influenza. We evaluated the protective efficacy of an inactivated equine influenza vaccine derived from viruses generated by reverse genetics (RG) in horses in an experimental viral challenge study. Wild-type (WT) virus (A/equine/Tipperary/1/2019) and virus generated by RG (consisting of hemagglutinin and neuraminidase genes from A/equine/Tipperary/1/2019 and six other genes from high-growth A/Puerto Rico/8/34) were inactivated by formalin for vaccine use. Twelve 1-year-old naïve horses with no antibodies against equine influenza virus were assigned to three groups (each n = 4): control, WT, and RG. They were vaccinated twice, 4 weeks apart, and were challenged with A/equine/Tipperary/1/2019 2 weeks after the second vaccination. All four horses in the control group and one horse in the WT group had pyrexia for multiple days and respiratory illness, and one horse in the RG group had pyrexia for 2 days without respiratory illness. The mean rectal temperatures and the mean concentrations of serum amyloid A in the WT and RG groups were significantly lower than those in the control group, with no significant differences between them. The WT and RG vaccines significantly reduced viral shedding relative to the control. The protective efficacy of the RG-derived inactivated vaccine against equine influenza virus is comparable to that of the vaccine derived from WT viruses in horses. The RG technique can make it easy to update equine influenza vaccine strains.
Publication Date: 2022-09-27 PubMed ID: 36175213DOI: 10.1016/j.vaccine.2022.09.047Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research article presents a study examining the effectiveness of a newly developed vaccine, based on reverse genetics, in protecting horses from the equine influenza virus. The findings indicate that this new vaccine, derived using reverse genetics, has comparable efficacy to that of traditional vaccines created from wild-type viruses and supports the use of reverse genetics in updating equine influenza vaccine strains.

Research Methodology

  • For the purpose of the research, a virus strain (A/equine/Tipperary/1/2019) was selected. Two versions of the virus, a wild-type (WT) version, and another created through reverse genetics (RG), were inactivated using formalin to prepare vaccines.
  • The RG virus was generated using hemagglutinin and neuraminidase genes from the selected strain, combined with six other genes from a high-growth virus (A/Puerto Rico/8/34).
  • Twelve horses, aged one year and without any existing antibodies against the equine influenza virus, were sorted into three groups: a control group, a group for WT vaccination, and a group for RG vaccination.
  • The horses received two doses of their respective vaccines, four weeks apart, and were then exposed to the selected virus strain two weeks after the second vaccination.

Findings and Analysis

  • The researchers monitored pyrexia (fever) and respiratory illness as indicators of infection. All horses in the control group and one in the WT group showed these symptoms for multiple days, while one RG vaccinated horse exhibited pyrexia but no respiratory illness.
  • The mean rectal temperatures and concentrations of serum amyloid A (an inflammation marker) were significantly lower in the WT and RG groups compared to the control group, with no significant differences observed between the WT and RG groups.
  • Both the WT and RG vaccines were found to greatly decrease viral shedding compared to the control group.

Conclusions

  • The results suggest that the equine influenza vaccine developed using reverse genetics is as effective in protecting against the disease as a vaccine utilizing traditional wild-type viruses.
  • The researchers concluded that the RG technique has potential in simplifying the process of updating equine influenza vaccine strains, proving to be a promising avenue for future vaccine developments.

Cite This Article

APA
Ohta M, Kambayashi Y, Mita H, Kuroda T, Bannai H, Tsujimura K, Yamanaka T, Garvey M, Cullinane A, Yamayoshi S, Kawaoka Y, Nemoto M. (2022). Protective efficacy of a reverse genetics-derived inactivated vaccine against equine influenza virus in horses. Vaccine, 40(44), 6362-6366. https://doi.org/10.1016/j.vaccine.2022.09.047

Publication

ISSN: 1873-2518
NlmUniqueID: 8406899
Country: Netherlands
Language: English
Volume: 40
Issue: 44
Pages: 6362-6366
PII: S0264-410X(22)01155-0

Researcher Affiliations

Ohta, Minoru
  • Equine Research Institute, Japan Racing Association, Tochigi, Japan.
Kambayashi, Yoshinori
  • Equine Research Institute, Japan Racing Association, Tochigi, Japan.
Mita, Hiroshi
  • Equine Research Institute, Japan Racing Association, Tochigi, Japan.
Kuroda, Taisuke
  • Equine Research Institute, Japan Racing Association, Tochigi, Japan.
Bannai, Hiroshi
  • Equine Research Institute, Japan Racing Association, Tochigi, Japan.
Tsujimura, Koji
  • Equine Research Institute, Japan Racing Association, Tochigi, Japan.
Yamanaka, Takashi
  • Equine Research Institute, Japan Racing Association, Tochigi, Japan.
Garvey, Marie
  • Virology Unit, Irish Equine Centre, Kildare, Ireland.
Cullinane, Ann
  • Virology Unit, Irish Equine Centre, Kildare, Ireland.
Yamayoshi, Seiya
  • Division of Virology, Institute of Medical Science, University of Tokyo, Tokyo, Japan; The Research Center for Global Viral Diseases, National Center for Global Health and Medicine Research Institute, Tokyo, Japan.
Kawaoka, Yoshihiro
  • Division of Virology, Institute of Medical Science, University of Tokyo, Tokyo, Japan; The Research Center for Global Viral Diseases, National Center for Global Health and Medicine Research Institute, Tokyo, Japan; Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, WI, USA.
Nemoto, Manabu
  • Equine Research Institute, Japan Racing Association, Tochigi, Japan. Electronic address: nemoto_manabu@equinst.go.jp.

MeSH Terms

  • Horses
  • Animals
  • Vaccines, Inactivated
  • Influenza Vaccines
  • Reverse Genetics
  • Hemagglutinins
  • Neuraminidase / genetics
  • Serum Amyloid A Protein / genetics
  • Horse Diseases
  • Influenza A virus
  • Orthomyxoviridae Infections / prevention & control
  • Orthomyxoviridae Infections / veterinary
  • Fever
  • Formaldehyde
  • Antibodies, Viral
  • Influenza A Virus, H3N8 Subtype / genetics
  • Vaccination / veterinary

Conflict of Interest Statement

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Citations

This article has been cited 2 times.
  1. Nemoto M, Kawanishi N, Kambayashi Y, Bannai H, Yamanaka T, Garvey M, Cullinane A, Yamayoshi S, Kawaoka Y, Tsujimura K. Growth properties of recombinant equine influenza viruses with different backbones generated by reverse genetics in embryonated chicken eggs. Arch Virol 2025 Jul 12;170(8):181.
    doi: 10.1007/s00705-025-06368-5pubmed: 40646296google scholar: lookup
  2. Atwa AS, Gomaa L, Elmenofy W, Amer HM, Ahmed BM. Expression of recombinant Florida clade 2 hemagglutinin in baculovirus expression system: A step for subunit vaccine development against H3N8 equine influenza virus. Open Vet J 2024 Jan;14(1):350-359.
    doi: 10.5455/OVJ.2024.v14.i1.32pubmed: 38633177google scholar: lookup