Antifouling biocides: Impairment of bivalve immune system by chlorothalonil

• Published in: Aquatic toxicology Vol. 189; pp. 194 - 199
• Main Authors: Guerreiro, Amanda da Silveira, Rola, Regina Coimbra, Rovani, Monique Tomazele, Costa, Simone Rutz da, Sandrini, Juliana Zomer
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.08.2017
• Subjects: Animals; Antifouling paint; Biocide; Cell Adhesion - drug effects; Disinfectants - toxicity; Ecosystem; Environmental Monitoring; Hemocytes; Hemocytes - drug effects; Hemocytes - immunology; Hemolymph - drug effects; Hemolymph - immunology; Immune System - drug effects; Immunity; Mussels; Nitriles - toxicity; Perna - drug effects; Perna - genetics; Perna - immunology; Phagocytes - drug effects; Phagocytes - immunology; Phagocytosis - drug effects; Phagocytosis - genetics; Phagocytosis - immunology; Water Pollutants, Chemical - toxicity; Antifouling paint; Mussels; Biocide; Immunity; Hemocytes
• ISSN: 0166-445X; 1879-1514
• DOI: 10.1016/j.aquatox.2017.06.012

•Chlorothalonil increases cellular adhesion and phagocytic activity of mussels’ hemocytes.•Exposure do chlrothalonil also induces a decrease in hemocyte viability.•The air survival capacity of mussels was reduced after exposure to chlorothalonil. Marine ecosystems are subjected to a variety of contaminants. Antifouling paints, for example, have been extensively used to protect ship surfaces from marine biofouling, but their toxicity has generated great concern. Thus, we evaluated the effect of the biocide chlorothalonil on the immune system of Perna perna mussels. The mussels were exposed to 0 (control), 0.1μg/L and 10μg/L of chlorothalonil for up to 96h. After 24h and 96h of exposure, the following immune-related parameters were analyzed in the hemolymph of mussels: total hemocyte count, cell adhesion, phagocytic activity, level of reactive oxygen species, cell viability and comet assay. After 24h and 96h of chlorothalonil exposure, cellular adhesion increased and the hemocyte viability reduced. Moreover, an increase in phagocytic activity was also observed after 96h of exposure to cholorothalonil. The exposure to 10μg/L of chlorothalonil for 96h reduced the air survival capacity of mussels. Total hemocyte count, ROS generation and DNA damage were not affected by the contaminant exposure. Our results indicate that chlorothalonil affected important immune responses of the bivalves, demonstrating that this biocide has effects on non-target species. This modulation of immune system reduced the health status of mussels, which could compromise their ability to survive in the environment.