Assessing effects of germline exposure to environmental toxicants by high-throughput screening in C. elegans

• DOI: 10.1371/journal.pgen.1007975
• Publication Date: 2019-02-14T18:31:02Z
• Authors: Nara Shin; Luciann Cuenca; Rajendiran Karthi...; Kurunthachalam Ka...; Monica P. Colaiácovo
• Keywords: 0301 basic medicine; Insecticides; Drug Evaluation, Preclinical; Environmental Exposure; QH426-470; Aneugens; Aneuploidy; Dibutyl Phthalate; High-Throughput Screening Assays; 3. Good health; Animals, Genetically Modified; Meiosis; 03 medical and health sciences; Germ Cells; Plasticizers; Genetics; Animals; DNA Breaks, Double-Stranded; Environmental Pollutants; Benzothiazoles; Caenorhabditis elegans; Permethrin; Thiocyanates; Research Article

Chemicals that are highly prevalent in our environment, such as phthalates and pesticides, have been linked to problems associated with reproductive health. However, rapid assessment of their impact on reproductive health and understanding how they cause such deleterious effects, remain challenging due to their fast-growing numbers and the limitations of various current toxicity assessment model systems. Here, we performed a high-throughput screen in C. elegans to identify chemicals inducing aneuploidy as a result of impaired germline function. We screened 46 chemicals that are widely present in our environment, but for which effects in the germline remain poorly understood. These included pesticides, phthalates, and chemicals used in hydraulic fracturing and crude oil processing. Of the 46 chemicals tested, 41% exhibited levels of aneuploidy higher than those detected for bisphenol A (BPA), an endocrine disruptor shown to affect meiosis, at concentrations correlating well with mammalian reproductive endpoints. We further examined three candidates eliciting aneuploidy: dibutyl phthalate (DBP), a likely endocrine disruptor and frequently used plasticizer, and the pesticides 2-(thiocyanomethylthio) benzothiazole (TCMTB) and permethrin. Exposure to these chemicals resulted in increased embryonic lethality, elevated DNA double-strand break (DSB) formation, activation of p53/CEP-1-dependent germ cell apoptosis, chromosomal abnormalities in oocytes at diakinesis, impaired chromosome segregation during early embryogenesis, and germline-specific alterations in gene expression. This study indicates that this high-throughput screening system is highly reliable for the identification of environmental chemicals inducing aneuploidy, and provides new insights into the impact of exposure to three widely used chemicals on meiosis and germline function.