Abstract

Riemerella anatipestifer is one of the most devastating pathogens affecting the global duck farms. Infection is involved in secretion of proinflammatory cytokines, including interleukin- (IL-) 17A. During the immune response to infection, IL-22 and IL-17A are often produced concurrently and at high levels in inflamed tissues. Little is known about duck IL-22 (duIL-22) during R. anatipestifer infection. We describe the characterization of duIL-22 and its mRNA expression analysis in splenic lymphocytes and macrophages treated with heat-killed R. anatipestifer and in the spleens and livers of R. anatipestifer-infected ducks. Full-length cDNA of duIL-22 encoded 197 amino acids. The deduced amino acid sequence of duIL-22 shared a 30.4–40.5% similarity with piscine counterparts, 57.4–60.1% with mammalian homologs, and 93.4% similarity to the chicken. Duck IL-22 mRNA expression level was relatively high in the skin of normal ducks. It was increased in mitogen-stimulated splenic lymphocytes and in killed R. anatipestifer-activated splenic lymphocytes and macrophages. Compared with healthy ducks, IL-22 transcript expression was significantly upregulated in the livers and spleens on days 1 and 4 postinfection, but not on day 7. IL-17A was significantly increased in the spleens only on day 4 postinfection and in the livers at all time points. When splenic lymphocytes were stimulated with heat-killed R. anatipestifer, CD4+ cells predominantly produced IL-22 while IL-17A was expressed both by CD4+ and CD4− cells. These results suggested that IL-22 and IL-17A are likely expressed in different cell types during R. anatipestifer infection.

Highlights

  • As the originally designated interleukin- (IL-) 10-related T cell-derived inducible factor (IL-10 TIF), IL-22 is one of the best-studied members of the IL-10 cytokine family [1]

  • The full-length cDNA of duck IL-22 (duIL-22) was cloned from ConAstimulated splenic lymphocytes

  • Our previous studies are associated with upregulated expression of IL-17A and IL-17F mRNA in infected ducks and in activated splenic lymphocytes [22, 33]

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Summary

Introduction

As the originally designated interleukin- (IL-) 10-related T cell-derived inducible factor (IL-10 TIF), IL-22 is one of the best-studied members of the IL-10 cytokine family [1]. IL-22 is produced by cells of the adaptive and innate immune system, such as natural killer T cells, natural killer cells, γδ T lymphocytes, type 3 innate lymphoid cells, macrophages, and activated Th1, Th17, and Th22 cells [2, 3]. IL-10R2 is broadly expressed, while IL-22R1 expression is mostly limited to intestinal and respiratory epithelial cells, keratinocytes, hepatocytes, and kidney, but not immune cells [1, 4, 5]. IL-22 induces expression of proinflammatory cytokines, including granulocyte colony-stimulating factor, IL-6, and IL-1β. It promotes production of antimicrobial peptides (AMPs) (e.g., β-defensin-2 and β-defensin-3) and chemokines (CXCL1, CXCL5, and CXCL9) [2, 4, 6]

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