Vaccination of foals with a modified live, equid herpesvirus-1 gM deletion mutant (RacHΔgM) confers partial protection against infection.
Abstract: Equid herpesvirus-1 (EHV-1) causes respiratory and neurological disease and late gestation abortion in pregnant mares. Current vaccines contain either inactivated or live EHV-1, but fail to provide complete clinical or virological protection, namely prevention of nasopharyngeal shedding and cell-associated viraemia. Thus, the development of novel products, such as modified live virus (MLV) vaccines which stimulate virus-specific, humoral and cell mediated immune responses more effectively remains a priority. Two groups of weaned foals (n = 6 each group) were used in a longitudinal, prospective, experimental study to evaluate immune responses elicited by two vaccinations with a glycoprotein M (gM) deletion mutant of EHV-1 (RacHdeltagM). Following two concurrent intranasal and intramuscular inoculations six weeks apart, vaccinated (8.4 ± 0.2 months old) and control foals (6.2 ± 0.4 months) were challenge infected intranasally with EHV-1 Ab4/8 four weeks after the second vaccination and clinical signs and virological replication measured. Vaccination caused no adverse events, but did stimulate significantly higher complement fixing and virus neutralizing antibodies in serum compared with control foals at either equivalent or pre-vaccination time points. Virus-specific nasopharyngeal antibody levels and cytotoxic T lymphocyte responses were not significantly different between the groups. Following challenge infection, these immune responses were associated with a reduction in clinical signs and virological replication in the vaccinated foals, including a reduction in duration and magnitude of pyrexia, nasopharyngeal shedding and cell-associated viraemia. We conclude that the RacHΔgM MLV primed EHV-1-specific humoral immune responses in weaned foals. However, complete virological protection by vaccination against EHV-1 requires further research.
Copyright © 2019 Elsevier Ltd. All rights reserved.
Publication Date: 2019-10-16 PubMed ID: 31629571DOI: 10.1016/j.vaccine.2019.09.106Google Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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The researchers conducted a study using a modified live virus vaccine in foals to stimulate a stronger immune response to Equid herpesvirus-1 (EHV-1), a virus that can cause serious illness in horses. The vaccine didn’t completely prevent infection but resulted in less severe symptoms and less virus replication.
Research Context and Objectives
- This study was conducted in response to previous vaccines’ inability to provide full clinical or virological protection against the Equid herpesvirus-1 (EHV-1). EHV-1 is responsible for respiratory and neurological diseases, as well as late gestation abortion in pregnant mares.
- The primary objective was to investigate if a modified live virus (MLV) vaccine could stimulate a more effective immune response against the virus. For this, a glycoprotein M (gM) deletion mutant of EHV-1, known as RacHdeltagM, was used in the vaccine.
Research Methods
- A longitudinal, prospective, experimental study design was employed, involving two groups of weaned foals (six in each group).
- The foals received two intranasal and intramuscular vaccinations six weeks apart, then were exposed to the EHV-1 virus four weeks following the second vaccination.
- The researchers closely observed and recorded clinical signs and virological replication in both the vaccinated and control group.
Research Findings
- The vaccine didn’t cause any adverse events, but it did result in higher levels of complement fixing and virus neutralizing antibodies as compared to the control group.
- However, there were no significant differences in virus-specific nasopharyngeal antibody levels and cytotoxic T lymphocyte responses between the vaccinated and control groups.
- Post exposure, the immune responses in the vaccinated foals were associated with less severe clinical signs and less viral replication, as well as a reduction in pyrexia, nasopharyngeal shedding, and cell-associated viraemia durations.
Research Conclusions and Implications
- Based on the observed results, the researchers concluded that the RacHΔgM MLV vaccine primed EHV-1-specific humoral immune responses in weaned foals.
- However, the vaccine didn’t provide complete virological protection against EHV-1, indicating that more research in this area is necessary.
Cite This Article
APA
Kydd JH, Hannant D, Robinson RS, Bryant N, Osterrieder N.
(2019).
Vaccination of foals with a modified live, equid herpesvirus-1 gM deletion mutant (RacHΔgM) confers partial protection against infection.
Vaccine, 38(2), 388-398.
https://doi.org/10.1016/j.vaccine.2019.09.106 Publication
Researcher Affiliations
- Centre for Preventive Medicine, Animal Health Trust, Lanwades Park, Kentford, Newmarket, Suffolk CB8 7UU, United Kingdom.
- Centre for Preventive Medicine, Animal Health Trust, Lanwades Park, Kentford, Newmarket, Suffolk CB8 7UU, United Kingdom.
- School of Veterinary Medicine and Science, University of Nottingham, Sutton Bonington, Loughborough, Leicestershire LE12 5RD, United Kingdom.
- Centre for Preventive Medicine, Animal Health Trust, Lanwades Park, Kentford, Newmarket, Suffolk CB8 7UU, United Kingdom.
- Institut für Virologie, Robert von Ostertag-Haus, Zentrum für Infektionsmedizin, Robert von Ostertag-Str. 7-13, 14163 Berlin, Germany.
MeSH Terms
- Animals
- Antibodies, Neutralizing / immunology
- Female
- Gene Deletion
- Herpesviridae Infections / immunology
- Herpesviridae Infections / prevention & control
- Herpesviridae Infections / veterinary
- Herpesvirus 1, Equid / immunology
- Horse Diseases / immunology
- Horse Diseases / prevention & control
- Horse Diseases / virology
- Horses
- Immunity, Humoral
- Longitudinal Studies
- Male
- Nasopharynx / virology
- Prospective Studies
- Viral Vaccines / administration & dosage
- Viral Vaccines / immunology
- Virus Replication / immunology
- Virus Shedding
Citations
This article has been cited 1 times.- Li C, Wang M, Cheng A, Wu Y, Tian B, Yang Q, Gao Q, Sun D, Zhang S, Ou X, He Y, Huang J, Zhao X, Chen S, Zhu D, Liu M, Jia R. N-Linked Glycosylation and Expression of Duck Plague Virus pUL10 Promoted by pUL49.5.. Microbiol Spectr 2023 Aug 17;11(4):e0162523.
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