EQUINE GAMMAHERPESVIRUS-2 (EHV2) IS LATENT IN B-LYMPHOCYTES

Peripheral blood leukocytes were collected from 5 Thoroughbred horses and examined for the presence of EHV2 in sub-populations of mononuclea r cells. Peripheral blood mononuclear cells were separated on Percoll gradients and then enriched for plastic adherent cells (predominantly monocytes), surface immunoglobulin positive (sIg(+)) B lymphocytes and T lymphocytes, using panning techniques. The purity of each cell popu lation was assessed by fluorescence activated cell scanning. In an inf ectious centre assay, each cell population was inoculated onto equine foetal kidney monolayer cell cultures which are fully permissive for t he replication of EHV2. Only enrichment for sig + B lymphocytes result ed in a marked increase in the number of infectious centres, indicatin g that EHV2 is present in B lymphocytes. Freeze-thawing of sIg(+) B ly mphocytes, prior to inoculation onto EFK monolayer cell cultures, resu lted in the complete abrogation of infectious centre formation, confir ming that EHV2 is latent in B lymphocytes i.e., infectious free virus was not present in the cells. The number of EHV2 infected B lymphocyte s varied considerably between horses from 4 to 780 per 10(6) cells. Ev idence was also obtained that direct cell to cell contact between the epithelial cells and sIg(+) B lymphocytes was necessary for the produc tion of infectious centres. The data indicate that EHV2, like other me mbers of the Gammaherpesvirinae, is latent within B lymphocytes.