Lymphoproliferation Assays in Cattle Naturally Infected with Bovine Leukaemia Virus (BLV) and Bovine Immunodeficiency-Like Virus (BIV)

Abstract

Summary Experiments were designed to evaluate the effect of BLV on mitogen‐stimulated peripheral blood mononuclear cells (PBMC) from naturally infected cattle. BIV was also taken into consideration due to a recent report showing that in Costa Rica, most of the BLV‐infected animals are also seropositive for BIV. The methodology was based on a non‐radioactive technique to determine lymphoproliferation. A colourimetric assay using XTT (formazan salt) to measure cell multiplication was adapted for bovine PBMC. ELISA and Western blotting were used to determine the serologic status of the cattle. PCR was only available for BIV detection. Our results show clearly that, dually‐infected cattle (BIV‐BLV) have reduced lymphoproliferative responses to the mitogen Con A. Haematological abnormalities associated with viral infections were also observed, specially leukocytosis and lymphocytosis. Cows with lymphosarcomas are severely affected. The specific antibody response to different viral proteins could not be associated with the suppressive status of the animals. Due to the high rate of dual infections observed in Costa Rica, these results are not sufficient to clarify which virus is responsible for the suppressive activity, if one or both viruses are necessary, or if they act synergistically.

Flow Cytometric Determination of the Expression of gp 51 Protein of Bovine Leukaemia Virus in Experimentally Infected Sheep

“…About 1% to 5% of infected animals develop lymphosarcoma, with or without prior PL (12,14). The primary cellular target of BLV is the B-lymphocyte (15,16).…”