Measuring mutagenicity in ecotoxicology: A case study of Cd exposure in Chironomus riparius

• Published in: Environmental pollution (1987) Vol. 272; p. 116004
• Main Authors: Doria, Halina Binde, Waldvogel, Ann-Marie, Pfenninger, Markus
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.03.2021
• Subjects: Animals; Cadmium - toxicity; Chironomidae - genetics; Chronic exposure; Ecotoxicology; Mutagenesis; Mutagenicity assay; Mutagenicity Tests; Mutagens - toxicity; Non-biting midge; Non-biting midge; Mutagenicity assay; Chronic exposure
• ISSN: 0269-7491; 1873-6424
• DOI: 10.1016/j.envpol.2020.116004

Existing mutagenicity tests for metazoans lack the direct observation of enhanced germline mutation rates after exposure to anthropogenic substances, therefore being inefficient. Cadmium (Cd) is a metal described as a mutagen in mammalian cells and listed as a group 1 carcinogenic and mutagenic substance. But Cd mutagenesis mechanism is not yet clear. Therefore, in the present study, we propose a method coupling short-term mutation accumulation (MA) lines with subsequent whole genome sequencing (WGS) and a dedicated data analysis pipeline to investigate if chronic Cd exposure on Chironomus riparius can alter the rate at which de novo point mutations appear. Results show that Cd exposure did not affect the basal germline mutation rate nor the mutational spectrum in C. riparius, thereby arguing that exposed organisms might experience a range of other toxic effects before any mutagenic effect may occur. We show that it is possible to establish a practical and easily implemented pipeline to rapidly detect germ cell mutagens in a metazoan test organism. Furthermore, our data implicate that it is questionable to transfer mutagenicity assessments based on in vitro methods to complex metazoans. [Display omitted] •Chronic exposure to Cd does not exert mutagenicity in germ cells in C. riparius.•It was established a pipeline to detect germ cell mutagens in metazoans.•The pipeline has the potential to fill the existing gap of mutagenicity assays for multicellular organisms.