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Age-Dependent Differences in Pseudorabies Virus Neuropathogenesis and Associated Cytokine Expression
Sara Verpoest1, Brigitte Cay1, Herman Favoreel2
1Operational Direction Viral Diseases, CODA-CERVA, Ukkel, Belgium.
Young pigs infected with pseudorabies virus (PRV) experience severe neurological disease due to immature neurons and inefficient viral suppression. Older pigs show milder symptoms, with neurological disease linked to olfactory bulb replication and immune response.
Area of Science:
- Veterinary Virology
- Immunology
- Neuropathogenesis
Background:
- Alphaherpesvirus infections cause more severe disease in newborns than older individuals.
- Mechanisms underlying age-dependent neuropathogenesis in pseudorabies virus (PRV) infections remain unclear.
- Pigs serve as a natural host model for studying PRV age-related virulence.
Purpose of the Study:
- To investigate the age-dependent mechanisms of pseudorabies virus (PRV) neuropathogenesis in pigs.
- To elucidate the role of viral replication and immune response in PRV-induced neurological disease.
- To compare PRV infection outcomes in 2-week-old versus 15-week-old pigs.
Main Methods:
- Inoculation of 2- and 15-week-old pigs with PRV strain NIA3.
- Quantitative PCR analysis of viral DNA in various organs.
- Analysis of viral and cytokine mRNA expression in key neuropathogenesis sites.
Main Results:
- PRV infection severity and mortality were higher in younger pigs.
- Viral replication was less pronounced in the trigeminal ganglia (TG) and brain stem of older pigs.
- Extensive viral replication and cytokine mRNA expression in the olfactory bulbs correlated with neurological disease in both age groups.
Conclusions:
- Age-dependent differences in PRV clinical signs are linked to enhanced viral replication and immunopathology in immature neurons of young pigs.
- Neurological disease in pigs is associated with extensive viral replication and immune response in the olfactory bulb.
- PRV neuropathogenesis involves complex interactions between viral replication, neuronal development, and immune responses, varying with host age.
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