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Archives of virology. Supplementum2004; (18); 221-230; doi: 10.1007/978-3-7091-0572-6_20

Recombinant canarypoxvirus vaccine carrying the prM/E genes of West Nile virus protects horses against a West Nile virus-mosquito challenge.

Abstract: An ALVAC (canarypoxvirus)-based recombinant (vCP2017) expressing the prM and E genes derived from a 1999 New York isolate of West Nile virus (WNV) was constructed and assessed for its protective efficacy in horses in two different experiments. In the first trial, a dose titration study was conducted to evaluate both serum neutralising antibody responses to WNV and duration of immunity. In the second trial the onset of protection was determined. Twenty-eight adult horses received two doses of vCP2017 administered intramuscularly at 5-week intervals and sixteen horses comprised age-matched non-vaccinated controls. Individual sera were taken periodically and tested for neutralising antibodies against WNV. Horses were challenged by allowing WNV-infected Aedes albopictus mosquitoes to feed on them two weeks (second trial) or one year (first trial) after the second vaccination. After challenge, horses were monitored for clinical signs of disease, and blood samples were collected for detection of WNV viremia and antibody. In both trials, all vaccinated horses developed neutralising antibodies against WNV. None of the vaccinated or control horses developed clinical signs of WNV disease upon challenge. None of the nine horses challenged 2 weeks after primary vaccination and only one of the ten vaccinated horses challenged 1 year after vaccination developed detectable viremia after challenge, whereas more than 80% of the controls became infected. Results from these studies demonstrated that a primary course of two doses of vCP2017 provides both antibody response and an early immunity in horses against WNV viremia.
Publication Date: 2004-05-04 PubMed ID: 15119777DOI: 10.1007/978-3-7091-0572-6_20Google Scholar: Lookup
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  • Journal Article

Summary

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The research paper explores the creation and efficacy of a recombinant canarypoxvirus vaccine, named vCP2017, which carries two genes from a 1999 New York isolate of West Nile virus (WNV). When administered to horses, the vaccine was shown to elicit an immune response, reducing the risk of WNV infection considerably.

Creation of the vCP2017 Vaccine

  • The researchers constructed the vaccine using ALVAC, a type of canarypoxvirus.
  • From a 1999 New York-isolated strain of West Nile virus, the prM and E genes were taken and used to create the recombinant vaccine vCP2017.

Assessment of the vCP2017 Vaccine

  • Two experiments were conducted to evaluate the vaccine’s protective efficacy in horses.
  • The first experiment was a dose titration study examining serum neutralising antibody responses and duration of immunity against WNV.
  • The second experiment assessed the onset of protection.
  • A total of 28 adult horses received two doses of the vaccine via intramuscular injections at 5-week intervals, while 16 horses were kept as non-vaccinated controls for comparison.

Immunological Response to the vCP2017 Vaccine

  • Horses were periodically tested for neutralising antibodies against WNV, results showing that all vaccinated horses had developed such antibodies.
  • The horses were later exposed to WNV-infected mosquitoes, then monitored for clinical signs of disease, WNV viremia, and the presence of antibodies.
  • Judging by these observations, neither vaccinated nor control horses displayed any clinical symptoms of WNV.
  • Upon examination two weeks after primary vaccination, none of the nine vaccinated horses challenged showed detectable viremia; even one year following vaccination, only one out of ten vaccinated horses showed signs of viremia, compared to over 80% of the control group.

Conclusion

  • The results conclusively demonstrated that a primary course of two doses of vCP2017 can provide an early immune response in horses against WNV viremia, as well as an antibody response; indicating a promising tool for WNV prevention.

Cite This Article

APA
Minke JM, Siger L, Karaca K, Austgen L, Gordy P, Bowen R, Renshaw RW, Loosmore S, Audonnet JC, Nordgren B. (2004). Recombinant canarypoxvirus vaccine carrying the prM/E genes of West Nile virus protects horses against a West Nile virus-mosquito challenge. Arch Virol Suppl(18), 221-230. https://doi.org/10.1007/978-3-7091-0572-6_20

Publication

ISSN: 0939-1983
NlmUniqueID: 9214275
Country: Austria
Language: English
Issue: 18
Pages: 221-230

Researcher Affiliations

Minke, J M
  • Merial SAS, Lyon, France. julius.minke@merial.com
Siger, L
    Karaca, K
      Austgen, L
        Gordy, P
          Bowen, R
            Renshaw, R W
              Loosmore, S
                Audonnet, J C
                  Nordgren, B

                    MeSH Terms

                    • Animals
                    • Base Sequence
                    • Canarypox virus / immunology
                    • Cloning, Molecular
                    • Culicidae / virology
                    • DNA Primers
                    • Horse Diseases / immunology
                    • Horse Diseases / virology
                    • Horses / immunology
                    • Male
                    • Plasmids / genetics
                    • Polymerase Chain Reaction / methods
                    • Vaccines, Attenuated / therapeutic use
                    • Vaccines, Synthetic / therapeutic use
                    • Viral Plaque Assay
                    • Viral Vaccines / therapeutic use
                    • West Nile Fever / immunology
                    • West Nile Fever / veterinary
                    • West Nile virus / immunology
                    • West Nile virus / isolation & purification

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