Safety and immunogenicity of a novel cold-adapted modified-live equine influenza virus vaccine.
Abstract: To design and evaluate the safety and immunogenicity of a modified-live vaccine to prevent equine influenza virus (EIV) infection based on the novel reassortant cold-adapted strain A/HK/Otar/6:2/2010. Methods: Surface proteins (HA, NA) from the wild-type strain A/equine/Otar/764/2007 (H3N8) and internal proteins (PB2, PB1, PA, NP, M, NS) from the attenuated cold-adapted donor strain A/Hong Kong/1/68/162/35CA (H3N2) were included in the vaccine. Horses were administered 10(9.2) EID50 /mL of the modified-live vaccine or saline solution using a nasal spray. The clinical condition of the animals was assessed throughout the study and nasopharyngeal swabs were collected for virus titration. Two yearlings in each group were euthanased on day 5 post vaccination (PV) for histological examination and measurement of viral titres in the organs. Serum samples and nasal secretions were collected to evaluate serological response. Lymphoproliferation after restimulation in vitro was determined to evaluate cell-mediated immunity. To evaluate the protective capacity of the vaccine, the yearlings in both groups were challenged with the wild-type virus at 28 days PV and their clinical condition and serological response was evaluated. Nasal swabs were collected to assess viral shedding from the upper respiratory tract. Results: Single intranasal administration of a modified-live EIV vaccine caused no adverse effects and vaccinated yearlings and pregnant mares did not form detectable levels of antibodies by days 7, 14 and 28 PV, as indicated by the HI reaction and ELISA. Secretory antibodies could be detected on day 7 and reached maximal levels on day 14 PV. In vitro studies showed that the yearlings and pregnant mares both formed a cell-mediated immune response by day 14 PV. The vaccine protected yearlings against challenge with wild-type virus. We conclude that single intranasal administration of the modified-live EIV vaccine was safe in the yearlings and pregnant mares that we treated, and was immunogenic and protective in the yearlings.
© 2014 Australian Veterinary Association.
Publication Date: 2014-10-29 PubMed ID: 25348146DOI: 10.1111/avj.12248Google Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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The research focuses on the development and assessment of a new live vaccine to prevent equine influenza virus (EIV) in horses. The vaccine, which is derived from a new cold-adapted strain, was found to be safe and capable of inducing an immune response without causing any notable side effects.
Study Methodology
- This study involved the creation of a modified-live vaccine for the prevention of EIV based on a newly-identified cold-adapted strain. This virus strain was made to include surface proteins (HA, NA) from a wild-type strain and internal proteins from an already-attenuated cold-adapted donor strain.
- The vaccine was administered to horses via a nasal spray at a certain dosage. Their health conditions were monitored throughout the experiment, and samples were taken for virus titration.
- For further exploration of the vaccine’s safety and impact, a couple of horses in each group were euthanized for histological examination and viral titre measurements in their organs.
- The serum samples and nasal secretions were gathered from the horses to assess their serological response to the vaccine. Cell-mediated immunity was evaluated via lymphocyte proliferation after restimulation in vitro.
- The vaccinated horses were exposed to the wild-type virus after 28 days to assess the vaccine’s protective capabilities. Any variations in their clinical conditions and serological responses were observed, along with the viral load in their nasal swabs.
Results and Conclusion
- The results revealed that the vaccine, when delivered in a single intranasal dose, had no adverse consequences. The vaccinated horses and pregnant mares did not produce detectable antibody levels by notable post-vaccination days, as per the HI reaction and ELISA.
- Secretory antibodies were found on day 7 and reached their highest levels on day 14.
- The vaccinated horses also showed a cell-mediated immune response by day 14, as seen in vitro.
- Post-exposure to the wild-type virus, the yearlings were seen to be protected, suggesting that the vaccine was effective.
- The researchers concluded that the single intranasal administration of this vaccine is safe and effectively stimulates an immune response in yearlings and pregnant mares, besides offering protection against EIV.
Cite This Article
APA
Tabynov K, Kydyrbayev Z, Ryskeldinova S, Assanzhanova N, Kozhamkulov Y, Inkarbekov D, Sansyzbay A.
(2014).
Safety and immunogenicity of a novel cold-adapted modified-live equine influenza virus vaccine.
Aust Vet J, 92(11), 450-457.
https://doi.org/10.1111/avj.12248 Publication
Researcher Affiliations
- Research Institute for Biological Safety Problems, Science Committee of the Ministry of Education and Science of the Republic of Kazakhstan, Gvardeiskiy, Republic of Kazakhstan. tabynov_81@biosafety.kz.
MeSH Terms
- Administration, Intranasal / veterinary
- Animals
- Antibodies, Viral / blood
- Chick Embryo
- Enzyme-Linked Immunosorbent Assay / veterinary
- Euthanasia, Animal
- Female
- Horse Diseases / blood
- Horse Diseases / prevention & control
- Horses
- Immunity, Cellular
- Immunity, Humoral
- Influenza A Virus, H3N8 Subtype / immunology
- Influenza Vaccines / immunology
- Influenza Vaccines / standards
- Male
- Nasopharynx / virology
- Orthomyxoviridae Infections / prevention & control
- Orthomyxoviridae Infections / veterinary
- Pregnancy
- Specific Pathogen-Free Organisms
- Virus Shedding
Citations
This article has been cited 5 times.- Tabynov K, Solomadin M, Turebekov N, Babayeva M, Fomin G, Yadagiri G, Renu S, Yerubayev T, Petrovsky N, Renukaradhya GJ, Tabynov K. An intranasal vaccine comprising SARS-CoV-2 spike receptor-binding domain protein entrapped in mannose-conjugated chitosan nanoparticle provides protection in hamsters.. Sci Rep 2023 Jul 26;13(1):12115.
- Pavulraj S, Bergmann T, Trombetta CM, Marchi S, Montomoli E, Alami SSE, Ragni-Alunni R, Osterrieder N, Azab W. Immunogenicity of Calvenza-03 EIV/EHV(®) Vaccine in Horses: Comparative In Vivo Study.. Vaccines (Basel) 2021 Feb 17;9(2).
- Blanco-Lobo P, Rodriguez L, Reedy S, Oladunni FS, Nogales A, Murcia PR, Chambers TM, Martinez-Sobrido L. A Bivalent Live-Attenuated Vaccine for the Prevention of Equine Influenza Virus.. Viruses 2019 Oct 11;11(10).
- Singh RK, Dhama K, Karthik K, Khandia R, Munjal A, Khurana SK, Chakraborty S, Malik YS, Virmani N, Singh R, Tripathi BN, Munir M, van der Kolk JH. A Comprehensive Review on Equine Influenza Virus: Etiology, Epidemiology, Pathobiology, Advances in Developing Diagnostics, Vaccines, and Control Strategies.. Front Microbiol 2018;9:1941.
- Mailybayeva A, Yespembetov B, Ryskeldinova S, Zinina N, Sansyzbay A, Renukaradhya GJ, Petrovsky N, Tabynov K. Improved influenza viral vector based Brucella abortus vaccine induces robust B and T-cell responses and protection against Brucella melitensis infection in pregnant sheep and goats.. PLoS One 2017;12(10):e0186484.
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