Investigation of the cytotoxicity of apidaecin on intestinal epithelial cells of tilapia ( Oreochromis niloticus ) in vitro

Abstract  Antimicrobial peptides (AMPs) are a diverse group of small polypeptides that can inhibit the growth of microbes; the investigation
of their cytotoxicity is critical before they can be considered for use. The purpose of the present study was to examine the
cytotoxicity of apidaecin at different concentrations (0.0, 10.0, 20.0, and 30.0 μg/ml) on tilapia, Oreochromis niloticus, primary intestinal epithelial cells in vitro through cells morphology observation, methylthiazolyldiphenyl-tetrazolium bromide
(MTT) conversion assay, and cellular viability assay. The lactate dehydrogenase (LDH) activity, cytosolic free Ca²⁺ concentration, and phospholipase A₂ (PLA₂) activity of primary cells treated with/without apidaecin were also determined. No significant differences (P > 0.05) in MTT assay and viability were found between the treated and the control cells. LDH activities were slightly increased
when treated with apidaecin for 24 h compared with the control (19.97 ± 1.24 U/l), but not significantly (P > 0.05). When treated with 20.0 μg/ml apidaecin for 24 h, the concentrations of cytosolic free Ca²⁺ was the highest among all the treatments (133.65 ± 9.65 nmol/l), but not the difference was not significant when compared
with the control (P > 0.05). Similar results were found for the activity of cytosolic PLA₂. The current results indicate that apidaecin did not show significant cytotoxicity to primary epithelial cells within 30.0 μg/ml
and that it can be used as a new candidate for infection control in fish culture.