Abstract

Aflatoxin B1 (AFB1) is the most toxic form among the mycotoxins. Cytokines are important mediators of the immune system. T-cell subsets play a crucial role in cell-mediated immunity. The aim of present study was to evaluate the effects of dietary AFB1 on the cytokines expression and T-cell subsets in the cecal tonsil of broiler chickens throughout a 21-day experimental period. One hundred and fifty six one-day-old broiler chickens were randomly divided into control group (0 mg AFB1/kg feed) and AFB1 group (0.6 mg pure AFB1/kg feed). At 7, 14 and 21 days of age, the levels of seven cytokines (IL-2, IL-4, IL-6, IL-10, IL-17, IFN-γ and TNF-α) mRNA expression as well as the proportions of T-cell subsets (CD3+, CD3+CD4+, CD3+CD8+) by qRT-PCR and flow cytometry methods were assessed in the cecal tonsils. The levels of the seven cytokines mRNA expression and the percentages of T-cell subsets significantly decreased at 14 and 21 days of age in the AFB1 group compared with the control group. However, the CD4+/CD8+ ratio was not significantly changed. These results demonstrate that 0.6 mg/kg AFB1 dietary exposure reduced the levels of cytokines mRNA expression and the percentages of T-cell subsets in the cecal tonsils of broiler chickens, suggesting that the cell-mediated immunity of cecal tonsils might be impaired in broilers.

Highlights

  • Aflatoxin B1 (AFB1) is a strong mutagenic, carcinogenic and teratogenic compound (Mohamed & Metwally, 2009) and can be found in foods and fodder in the world as a common contaminant

  • The CD4+/CD8+ ratio was not significantly changed. These results demonstrate that 0.6 mg/kg AFB1 dietary exposure reduced the levels of cytokines mRNA expression and the percentages of T-cell subsets in the cecal tonsils of broiler chickens, suggesting that the cell-mediated immunity of cecal tonsils might be impaired in broilers

  • The purpose of this paper was to investigate the effects of dietary AFB1 at different time points on the cytokines mRNA expression and T-cell subsets in the cecal tonsil of broiler chickens by quantitative real-time PCR and flow cytometry (FCM) analyses in order to provide helpful information for future studies in immunosuppressive effects induced by AFB1 in poultry

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Summary

Introduction

Aflatoxin B1 (AFB1) is a strong mutagenic, carcinogenic and teratogenic compound (Mohamed & Metwally, 2009) and can be found in foods and fodder in the world as a common contaminant. The inhibitory effects of AFB1 on cytokines expression and T-cell subsets have been demonstrated in various studies. The dietary AFB1 can induce inhibitory effects on interleukin-1 (IL-1), interleukin-2 (IL-2) and interleukin-6 (IL-6) production in rats’ splenocytes (Hinton et al, 2003). There is a decrease in contents of serum IL-2 and interferon gamma (IFN-γ) in broilers exposed to AFB1 (Chen et al., 2013a). Meissonnier et al (2008) found linear increases in IFN-γ, IL-6 and interleukin-10 (IL-10) mRNA with increase in dietary levels of AFB1 in pigs. The increase of IFN-γ, IL-6 and tumor necrosis factor alpha (TNF-α) mRNA (proinflammatory cytokines) has been observed in chickens exposed to AFB1 (Li et al, 2014). The percentage of splenic CD8+ T-cells in rats shows dose-dependent decreases with dietary AFB1 increasing (Qian et al, 2014). Intoxicated mice with AFB1 exhibit significant decreases in the percentage of CD4+ T-cells in the spleen and in the number of CD3+ T-cells in the intestinal T-cells (Hatori et al, 1991; Tomková et al, 2002). Chen et al (2014)

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