Abstract

Bovine viral diarrhea virus (BVDV) is an important viral disease of cattle that causes immune dysfunction. Macrophages are the key cells for the initiation of the innate immunity and play an important role in viral pathogenesis. In this in vitro study, we studied the effect of the supernatant of BVDV-infected macrophage on immune dysfunction. We infected bovine monocyte-derived macrophages (MDM) with high or low virulence strains of BVDV. The supernatant recovered from BVDV-infected MDM was used to examine the functional activity and surface marker expression of normal macrophages as well as lymphocyte apoptosis. Supernatants from the highly virulent 1373-infected MDM reduced phagocytosis, bactericidal activity and downregulated MHC II and CD14 expression of macrophages. Supernatants from 1373-infected MDM induced apoptosis in MDBK cells, lymphocytes or BL-3 cells. By protein electrophoresis, several protein bands were unique for high-virulence, 1373-infected MDM supernatant. There was no significant difference in the apoptosis-related cytokine mRNA (IL-1beta, IL-6 and TNF-a) of infected MDM. These data suggest that BVDV has an indirect negative effect on macrophage functions that is strain-specific. Further studies are required to determine the identity and mechanism of action of these virulence factors present in the supernatant of the infected macrophages.

Highlights

  • Bovine viral diarrhea virus (BVDV) causes immune dysfunction in cattle and other ruminants, resulting in severe economic losses

  • Our results suggested that the supernatant of infected macrophages with only virulent BVDV strains induced lymphocyte apoptosis

  • BVDV causes immune dysfunction that leads to vaccination failure and secondary bacterial infection with lymphoid depletion associated with BVDV clinical cases

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Summary

Introduction

Bovine viral diarrhea virus (BVDV) causes immune dysfunction in cattle and other ruminants, resulting in severe economic losses. BVDV induces multiple abnormalities to immune cell function and immune mediators that could potentiate viral infection and pathogenesis [5,6]. BVDV infects neutrophils and decreases their microbicidal activity [7]. It infects alveolar macrophage and decreases the expression of complement Fc receptors and chemokine production, reducing their ability to engulf opsonized pathogens [8]. Only cytopathogenic (Cp) strains can induce direct apoptosis to peripheral blood mononuclear cells (PBMCs) [9,10], other studies have suggested that Ncp BVDV induces apoptosis

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