Activation of Bovine Lymphocyte Subpopulations by Staphylococcal Enterotoxin C

Author:

Ferens Witold A.1,Davis William C.2,Hamilton Mary Jo2,Park Yong H.3,Deobald Claudia F.1,Fox Lawrence4,Bohach Gregory1

Affiliation:

1. Department of Microbiology, Molecular Biology and Biochemistry, University of Idaho, Moscow, Idaho 838441;

2. Department of Veterinary Microbiology and Pathology2 and

3. Department of Microbiology, College of Veterinary Medicine, Seoul National University, Suwon 441-744, Korea3

4. Department of Veterinary Clinical Medicine and Surgery,4 Washington State University, Pullman, Washington 99164; and

Abstract

ABSTRACT Staphylococcus aureus is a major mastitis-causing pathogen in cattle. The chronic nature of bovine staphylococcal mastitis suggests that some products or components of S. aureus may interfere with the development of protective immunity. One class of molecules that could be involved are superantigens (SAgs). Although a significant number of mastitis isolates produce SAgs, the effect of these molecules on the bovine immune system is unresolved. To determine if immunosuppression caused by SAgs could play a role in pathogenesis, we monitored bovine lymphocytes exposed to staphylococcal enterotoxin C1 (SEC1). Activation of bovine lymphocytes by either SEC1 or concanavalin A (ConA) was influenced by the γδ/αβ T-cell ratio in the culture. Compared to ConA-induced stimulation, cultures stimulated with SEC1 generated small numbers of CD4 + αβ T cells expressing high levels of interleukin-2 receptor α chain (IL-2Rα) and major histocompatibility complex class II (MHCII), suggesting that SAg exposure does not lead to full activation of these cells. This state of partial activation was most pronounced in cultures with a high γδ/αβ ratio. In contrast, significant numbers of CD8 + αβ T cells expressed high levels of IL-2Rα and MHCII, regardless of the γδ/αβ ratio and the stimulant used. CD8 + blasts in cultures stimulated with SEC1 also expressed another activation marker, ACT3, previously detected predominantly on thymocytes and CD4 + T cells. Although γδ CD2 and CD2 + T cells expressed MHCII and IL-2Rα following stimulation with SEC1, only a few cells increased to blast size, suggesting that they were only partially activated. The results suggest ways in which SAgs might facilitate immunosuppression that promotes the persistence of bacteria in cattle and contributes to chronic intramammary infection.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

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