Sublethal Urea Exposure in Nile Tilapia: Morphological, Behavioural, and Histological Alteration

The pace of research efforts has been extraordinarily accelerated across the globe to address the contamination issues caused by pesticides, and fertilizers, especially in the aquatic ecosystem. The sole aim of this study was to assess the effect of urea on Nile Tilapia (Oreochromis niloticus). For this purpose, the fish fingerlings were exposed to increasing concentrations of urea such as 0, 1, 2.5, 5, 10, 20, and 40 g/l for 72 hr. Survival analysis suggested a strong correlation between the increasing doses of urea and the mortality rate among tested fingerlings. This study reported remarkable morphological, and behavioural alternation such as increased operculum movement, bottom-dwelling, lethargy, secretion of mucus, reduction in food intake, and bleeding in the fin and around the mouth in the treated group. Haematological analysis revealed that a significant reduction in RBC count and Hb along with an increase in WBC number is associated with urea toxicity. Our study showed a significant rise in glucose concentration upon urea toxicity in Nile tilapia fingerlings for the first time, emphasizing the adverse effect of fertilizers on carbohydrate metabolism. Significant rises in the enzymatic activity such as alanine aminotransferase (ALT), alkaline phosphatase (ALP), and aspartate aminotransferase (AST) upon urea treatment emphasize the possibilities of liver damage, biliary obstruction, and abnormal glucose metabolism. Histological analysis of urea-treated fish compared to normal fish revealed that urea toxicity drastically altered the tissue architecture of fish's gills, eyes, intestine, and stomach. As the visual systems of mammals and fish resemble in more aspects, our findings may be useful in understanding the impact of pollutants on sensory organs concerning humans. We conclude that our findings highlight the importance of urea toxicity on Nile tilapia fingerlings and invite multidisciplinary research to uncover molecular mechanisms underlying urea toxicity.