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Equine herpesvirus type 2: cell-virus relationship during persistent cell-associated viremia
American Journal of Veterinary Research
|January 1, 1985
Summary
Equine herpesvirus type 2 (EHV-2) establishes a latent infection in leukocytes. A new assay quantifies these infected cells, revealing variations in EHV-2 viremia among horses.
Area of Science:
- Veterinary Virology
- Immunology
- Equine Infectious Diseases
Background:
- Equine herpesvirus type 2 (EHV-2) causes persistent, cell-associated viremia.
- Understanding the latent stage of EHV-2 infection is crucial for managing equine health.
Purpose of the Study:
- To investigate the biology of EHV-2 during its persistent cell-associated viremia stage.
- To develop and validate a method for enumerating latently infected leukocytes.
Main Methods:
- Developed and utilized an infective center (IC) assay to quantify latently EHV-2 infected leukocytes.
- Assessed the relationship between cell density, IC plaque formation, and EHV-2 infection.
- Correlated serum-neutralization titers with IC numbers.
- Attempted transmission of EHV-2 via infected leukocytes to equine fetuses.
Main Results:
- The IC assay was simple, reproducible, and showed a linear relationship between cell number and plaques, except at high cell densities.
- Significant variation in IC counts was observed between different horses, but consistency within individual horses over time.
- A direct correlation was found between serum-neutralization titers and IC counts.
- Transfer of infected leukocytes did not establish EHV-2 infection in fetuses.
- EHV-2 infection did not induce detectable Fc receptors on equine fetal kidney cells.
Conclusions:
- The developed IC assay is a reliable tool for quantifying latent EHV-2 infected leukocytes.
- EHV-2 exhibits significant inter-horse variability in latent viremia.
- Serum-neutralization titers may reflect the level of latent EHV-2 infection.
- Cell-associated EHV-2 viremia in leukocytes may not be efficiently transmitted vertically, and EHV-2 does not induce Fc receptors on equine fetal kidney cells.