Abstract

Three trials were conducted to determine the effects of mannan oligosaccharide (Bio-Mos ®) on the immune responses of marron. In the first trial marron were challenged with Vibrio mimicus infection, in the second with NH 3 exposure and in the third, the marron were exposed to air during a simulated live transportation trial. For V. mimicus infection and live transportation trials, marron (10.44 ± 0.20 g and 4.44 ± 0.20 g initial weights, respectively) were fed three different diets containing 0% (control diet), 0.2% and 0.4% Bio-Mos ® for 30 days and 112 days respectively before challenge, whereas for the NH 3 exposure trial, marron (94 ± 2.17 g initial weight) were reared with the control diet and 0.4% Bio-Mos ® diet for 42 days before exposure to NH 3. Marron were examined for survival and total haemocyte count (THC), differential haemocyte count (DHC), haemolymph clotting time, bacteraemia and lysosomal membrane stability as indicators of immune responses during the course of the challenge. Survival of marron infected with bacteria and exposed to NH 3, were significantly improved when fed Bio-Mos ®. THCs were significantly reduced in marron fed the control diet when they were infected with bacteria and subjected to live transportation while it remained unchanged in the marron fed the Bio-Mos ® supplemented diets. THCs of marron fed any of the diets were reduced when they were exposed to NH 3 but the THCs were higher ( P < 0.05) in marron fed Bio-Mos ® diets. Vibrio spp. in haemolymph of marron fed the control diet significantly increased when they were infected with V. mimicus and challenged with NH 3 but it remained unchanged in the marron fed the Bio-Mos ® diets. Haemolymph clotting time was higher in marron fed the control diets when subjected to live transportation and 3 days of exposure to NH 3. After 96 h infection marron fed the Bio-Mos ® diets had longer NRR time than those fed the control diet. All the findings demonstrated the ability of Bio-Mos ® to improve the survival, health status and immunity of marron under the bacterial infection and stress conditions caused by air and NH 3 exposures.

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