Inhibitory effect of Eimeria maxima IFN-γ inhibitory molecules on the immune function of T cell subsets in chickens

Abstract

It has been reported that infection of chicken coccidian could inhibit the production of Th1 cytokine IFN-γ, thereby evading clearance by the host immune system. The present study aimed to have a further investigation into the effects of Eimeria maxima IFN-γ inhibitory molecules (EmHPSP-2 and EmHPSP-3) on the immune function of chicken peripheral blood mononuclear cells ( PBMC) and various T cell subsets. First, separated PBMC or sorted T cell subsets were used for incubation with recombinant proteins of EmHPSP-2 (rEmHPSP-2) and EmHPSP-3 (rEmHPSP-3). Subsequently, the effects of rEmHPSP-2 and rEmHPSP-3 on proliferative capacity, nitric oxide ( NO) release and mRNA levels of cytokines of the above cells were detected. The sorting purity of CD8 ⁺, CD4 ⁺ CD25 ⁻, CD4 ⁺, and CD4 ⁺ CD25 ⁺ T cells was 93.01, 88.88, 87.04, and 81.26%, respectively. The NO release of PBMC was significantly inhibited by rEmHPSP-2 and rEmHPSP-3. The proliferation of PBMC and CD4 ⁺ T cells was significantly inhibited by rEmHPSP-2 and rEmHPSP-3, whereas CD8 ⁺, CD4 ⁺ CD25 ⁻, and CD4 ⁺ CD25 ⁺ T cells was significantly promoted by the 2 proteins. The 2 proteins significantly downregulated interferon-gamma ( IFN-γ) mRNA level, upregulated the transcriptional levels of interleukin-10 ( IL-10) and transforming growth factor-beta1 ( TGF-β1) in PBMC. IFN-γ and IL-2 transcriptional levels were markedly inhibited in CD8 ⁺ T cells. IFN-γ transcriptional level was significantly inhibited, but IL-4 was promoted by rEmHPSP-2 and rEmHPSP-3 in CD4 ⁺ CD25 ⁻ T cells. Meanwhile, the inhibitory effects of rEmHPSP-2 and rEmHPSP-3 on the transcriptional levels of IFN-γ and IL-2 were more obvious in CD4 ⁺ T cells containing CD25 ⁺ cells compared with the CD25 ⁺ cells depletion group. It was found that IL-10, TGF-β1, and cytotoxic T lymphocyte-associated antigen-4 ( CTLA-4) mRNA levels were significantly upregulated upon stimulation of chicken CD4 ⁺ CD25 ⁺ T cells by proteins. This study is not only of great significance to clarify the immune evasion mechanism of chicken coccidia, but also provides candidate antigen molecules for development of a novel vaccine against chicken coccidiosis.