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Mucosal vaccination with an attenuated maedi-visna virus clone
Gudmundur Pétursson1, Sigrídur Matthíasdóttir, Vilhjálmur Svansson
1Institute for Experimental Pathology, University of Iceland, Keldur v/Vesturlandsveg, Reykjavik, Iceland. gpet@hi.is
Vaccine
|April 20, 2005
Summary
An attenuated maedi-visna virus (MVV) vaccine did not prevent infection in sheep. However, vaccinated sheep showed reduced virus presence in blood and lungs, suggesting partial protection against pathogenic MVV.
Area of Science:
- Veterinary Virology
- Immunology
- Sheep Diseases
Background:
- Maedi-visna virus (MVV) causes a progressive, debilitating disease in sheep.
- Attenuated viral vaccines are explored to control MVV infections.
- Understanding immune responses to MVV superinfection is crucial for vaccine development.
Purpose of the Study:
- To evaluate the efficacy of an attenuated MVV molecular clone as a vaccine against subsequent challenge with a pathogenic MVV clone.
- To assess the level of protection conferred by the attenuated MVV vaccine in sheep.
Main Methods:
- Intratracheal inoculation of four sheep with an attenuated MVV molecular clone.
- Subsequent intratracheal challenge with a pathogenic MVV clone ten months later.
- Comparison of viral load in blood and lungs between vaccinated and unvaccinated control sheep at sacrifice.
Main Results:
- All sheep, vaccinated and unvaccinated, became infected with the challenge MVV clone.
- Vaccinated sheep exhibited significantly lower virus isolation rates from blood compared to unvaccinated controls.
- Virus was isolated ten times less frequently from the lungs of vaccinated sheep than from unvaccinated sheep at sacrifice.
Conclusions:
- The attenuated MVV vaccine did not provide complete protection against superinfection with a pathogenic MVV clone.
- Partial protection was indicated by reduced viral loads in vaccinated sheep, suggesting a potential role for this vaccine strategy.
- Further research is warranted to enhance vaccine efficacy against maedi-visna virus.