Abstract

In the current study, we investigate changes in CD4+CD25+ cells in chickens during infectious bursal disease virus (IBDV) infection. The percentage of CD4+CD25+ cells in lymph organs, e.g., the thymus, spleen, bursa of Fabricius and peripheral blood, during the first 1–5 days post infection (dpi) was assessed by flow cytometry. The data revealed a remarkable decrease in the percentage of CD4+CD25+ cells in the thymus from 1 to 5 dpi and in the spleen during early infection. An increase of the percentage of CD4+CD25+ cells among peripheral blood lymphocytes was observed during the first two days of IBDV infection. Additionally, CD4+CD25+ cells infiltrated the bursa along with CD4+ cells after IBDV infection. Quantitative reverse transcription polymerase chain reaction (qRT-PCR) was used to measure the mRNA levels of immune-related cytokines in IBDV-infected thymus and bursa of Fabricius tissues. The data revealed that IBDV caused a significant increase in interleukin (IL)-10 mRNA levels, with the Harbin-1 strain (vvIBDV) inducing higher IL-10 expression than the Ts strain. Taken together, our data suggest that chicken CD4+CD25+ cells may participate in IBDV pathogenicity by migrating from their sites of origin and storage, the thymus and spleen, to the virally targeted bursa of Fabricius during IBDV infection.

Highlights

  • Infectious bursal disease virus (IBDV) can lead to an acute, highly contagious immunosuppressive response in young chickens

  • Infectious bursal disease (IBD), which is caused by IBDV, can lead to significant economic losses in the poultry industry [1]

  • IBD, which is caused by IBDV, is an acute, highly contagious immunosuppressive disease of young chickens

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Summary

Introduction

Infectious bursal disease virus (IBDV) can lead to an acute, highly contagious immunosuppressive response in young chickens. Mammalian CD4+CD25+ regulatory T cells have been reported to play a critical immunosuppressive role in many diseases; there is limited information regarding the function of CD4+CD25+ cells in chickens during IBDV infection. Infectious bursal disease (IBD), which is caused by IBDV, can lead to significant economic losses in the poultry industry [1]. IBDV belongs to the family Birnaviridae and consists of two segments, segments A (3.2 kb) and B (2.9 kb), which encode five proteins (VP1-VP5) [2,3]. IBDV can be differentiated into two serotypes (serotypes 1 and 2). IBDV infection causes a lymphoid depletion of B cells and the destruction of bursal tissues, which are crucial to its immunosuppressive effect [7]

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