Infectious bursa disease virus (IBDV) pathogenesis is characterized by increased numbers of T cells and decreased numbers of B cells in the bursa. Currently, little is about the key factor that affects T migration into bursa. In humans, CC chemokine ligand 19 (CCL19) recruits monocytes and neutrophils and is usually involved in various inflammatory disorders. The aim of this study was to assess the roles of CCL19 in driving peripheral blood cells infiltration into bursa of Fabricius of chickens infected with IBDV. Bursal samples were collected from chickens of the infection group and the control group on day 1, 3, 5, and 7 post infection (dpi) with IBDV. The mRNA or protein levels of ccl19 and ccr7 genes in bursae were determined by real-time PCR and immunohistochemistry (IHC) methods. Moreover, an in vitro chemotaxis assay was performed to evaluate the chemotaxis ability of CCL19 and bursal total protein. The results have displayed that the mRNA levels of ccl19 were significantly increased on 1, 3, 5, and 7 dpi in the infection group. The highest value amounted to 73.4-fold of the control group. Also, the mRNA levels of CCR7, the receptor of CCL19, began to increase on 3 dpi and reached to the highest value of 206.3-fold on 5 dpi after IBDV infection. Then the gene expression of CCR7 in bursae of the infection group returned to the normal level. IHC results of CCL19 protein level accorded with the mRNA levels of CCL19, with the highest value on 5 dpi. Then, in vitro chemotaxis test demonstrated that the total bursal protein had the ability of recruiting peripheral white blood cells (PWBC) and the migration percentage was a little higher than that of the blank control with only basal medium (P < 0.05). Taken together, these data suggest that CCL19 acts as a chicken PWBC chemotactic factor and facilitate the infiltration of PWBC (especially T cells) into the bursae after IBDV infection.
Keywords: CCL19; IBDV; T cell; chemotaxis.
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