This study was designed to appraise the effect of licorice herbal supplement on the immune status of rainbow trout fingerlings. Accordingly, five diets were formulated with different levels of licorice extract (LE) including 0 (control), 0.5 g kg−1 (LE0.5), 1 g kg−1 (LE1), 2 g kg−1 (LE2), and 3 g kg−1 (LE3). The fingerlings (10.0 ± 0.1 g initial mean weight) received the diets in triplicates (30 fish in each replicate) for 56 days. The results showed that the white blood cells and their differential number (lymphocytes and monocytes) were remarkably increased by LE2 supplementation (P < 0.05). The oral administration of LE2 significantly increased the levels of serum immunoglobulin (Ig), lysozyme activity, and complement components (C3 and C4) compared with others. Meanwhile, the serum bactericidal activity against Yersinia ruckeri in LE2 and LE3 treatments was significantly higher than others except for LE1 (P < 0.05). In addition, serum alternative complement activity significantly improved in all treated groups except LE0.5 compared with the control group (P < 0.05). In terms of skin mucosal immunity, the fish fed with LE2 and LE3 diets exhibited notably higher lysozyme activity, alkaline phosphatase activity, and Ig value than other groups (P < 0.05). The highest skin mucus bactericidal activity against Y. ruckeri was obtained in LE2 treatment (P < 0.05). In addition, dietary LE2 significantly increased the relative expression of immune-associated genes including tumor necrosis factor-α, interleukin-1β, interleukin-8, and IgM and the former treatments showed higher values than the control group. The cumulative mortality of fish against Y. ruckeri infection was notably reduced from 53.6% in the control group to 29.0% in LE3 treatment. Overall, the dietary administration of LE at 2 g kg−1 had the best effects on immunocompetence in rainbow trout.
Aflatoxin M1 (AFM1) is a carcinogenic mycotoxin mostly found in dairy products. The aim of this study was to evaluate the anti-aflatoxin effect of Bifidobacterium bifidum and Saccharomyces cerevisiae with two different concentrations (10 8 and 10 10 cfu/mL), alone or mixed, in contaminated skim milk with three concentrations of AFM1 (0.1, 0.25 and 0.5 μg/mL) and incubated at 4, 25 and 37°C for different times (30, 60, 120 min and 24 h). We found that the storage time is a key factor that significantly affects AFM1 removal. Also, removal of AFM1 was dependent on other factors such as micro-organisms' concentration, incubation temperature and toxin concentration. The effective strategy for the highest removal of AFM1 (90%) in contaminated milk spiked with 0.5 μg/mL, which was treated with mixed strains at concentration10 10 cfu/mL and incubated at 37°C after 24 h. The presented methodology can be considered as a potential method for reducing the aflatoxin content of polluted dairy products.
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