ORCID

Abstract

Abstract This study was conducted to evaluate the effects of exogenous enzymes on Nile tilapia (Oreochromis niloticus) growth and general health status. Tilapia (38.7 g) were fed one of four plant-based diets (408 g kg−1protein, 78 g kg−1 lipid); one of which was a control and the remaining three were supplemented with exogenous enzymes (phytase, protease and carbohydrase at 300 mg kg−1, 200 mg kg−1, and 300 mg kg−1, respectively). Tilapia fed the phytase supplemented diet displayed higher final body weight, FBW (94.9 g fish−1) and specific growth rate, SGR (2.48% day−1) compared to tilapia fed the control diet (82.6 g fish−1 FBW and 2.11% day−1 SGR) (P < 0.05). In terms of feed conversion ratio, FCR and protein efficiency ratio, PER, tilapia fed diet supplemented with phytase (1.36 FCR and 1.08 PER) performed better (P < 0.05) than tilapia fed the control diet (1.68 FCR and 0.80 PER). However, the dietary treatments had no significant effect on tilapia somatic indices (P ˃ 0.05). The level of circulatory red blood cells was higher (P < 0.05) in tilapia fed the carbohydrase supplemented diet (1.98 × 106 μL−1) compare to those fed the control diet. Dietary treatments did not affect the mid-intestinal perimeter ratio, goblet cell abundance and intraepithelial leucocytes abundance. However, the microvilli density of the mid-intestine was higher (P < 0.05) in tilapia fed the phytase (15.6) and carbohydrase (16.0) supplemented diets compared to those fed the control (10.4) and protease (11.5) supplemented diets. The intestinal bacterial community profile of tilapia fed the carbohydrase supplemented diet was significantly altered in contrast to those fed the control diet (P < 0.05). The supplementation of diets with phytase has the potential to enhance tilapia growth without detrimental impacts on intestinal health.

DOI

10.1016/j.anifeedsci.2016.03.002

Publication Date

2016-03-03

Publication Title

Animal Feed Science and Technology

Volume

215

First Page

133

Last Page

143

ISSN

0377-8401

Embargo Period

2017-03-04

Organisational Unit

School of Biomedical Sciences

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