TY - JOUR
T1 - Wastewater treatment effluent alters nucleotide excision repair in zebrafish (Danio rerio)
AU - Notch, Emily G.
AU - Mayer, Gregory D.
N1 - Funding Information:
Dr. John Giesy of the Aquatic Toxicology Lab at Michigan State University kindly donated MVLN cells to the lab. The research presented in this paper was funded in part by the Maine Department of Environmental Protection Surface Water Ambient Toxicity monitoring program, USGS WRRI program and the United States Environmental Protection Agency (EPA) under the Science to Achieve Results Graduate Fellowship program. EPA has not officially endorsed this publication and the views expressed herein may not reflect the views of the EPA.
PY - 2009/8
Y1 - 2009/8
N2 - Wastewater treatment effluent is a complex mixture of anthropogenic pollutants including estrogenic substances and chemicals, such as polyaromatic hydrocarbons, that cause bulky DNA adducts. Significant research focuses on reproductive effects of aquatic estrogens from wastewater treatment plants. However, other studies suggest genotoxic and immunological effects occur at lower concentrations of wastewater treatment effluent than reproductive endpoints. Recently, effects of estrogen on DNA repair processes in zebrafish have been suggested as a possible mechanism by which estrogen can modulate incidence of DNA mutations. Because wastewater treatment facilities are a significant source of estrogenic compounds, we hypothesized that exposure to whole effluents would also affect DNA repair in zebrafish (Danio rerio). Exposure to effluent from multiple treatment facilities in northern Maine decreased repair of DNA adducts in zebrafish liver cells. Expression of two nucleotide excision repair genes, XPC and XPA, were quantified and showed varied response after exposure in adult male zebrafish. Evidence of estrogen and aryl hydrocarbon receptor activation after exposure varied between treatment plants and temporally within treatment plants when evaluated using a traditional biomarker, vitellogenin-1 (VTG) and, cytochrome p450 1A1 (CYP1A1) mRNA abundance. This research highlights the continuing importance of examining non-reproductive effects of wastewater treatment effluent.
AB - Wastewater treatment effluent is a complex mixture of anthropogenic pollutants including estrogenic substances and chemicals, such as polyaromatic hydrocarbons, that cause bulky DNA adducts. Significant research focuses on reproductive effects of aquatic estrogens from wastewater treatment plants. However, other studies suggest genotoxic and immunological effects occur at lower concentrations of wastewater treatment effluent than reproductive endpoints. Recently, effects of estrogen on DNA repair processes in zebrafish have been suggested as a possible mechanism by which estrogen can modulate incidence of DNA mutations. Because wastewater treatment facilities are a significant source of estrogenic compounds, we hypothesized that exposure to whole effluents would also affect DNA repair in zebrafish (Danio rerio). Exposure to effluent from multiple treatment facilities in northern Maine decreased repair of DNA adducts in zebrafish liver cells. Expression of two nucleotide excision repair genes, XPC and XPA, were quantified and showed varied response after exposure in adult male zebrafish. Evidence of estrogen and aryl hydrocarbon receptor activation after exposure varied between treatment plants and temporally within treatment plants when evaluated using a traditional biomarker, vitellogenin-1 (VTG) and, cytochrome p450 1A1 (CYP1A1) mRNA abundance. This research highlights the continuing importance of examining non-reproductive effects of wastewater treatment effluent.
KW - CYP1A1
KW - Nucleotide excision repair
KW - Vitellogenin
KW - Wastewater
KW - Zebrafish
UR - http://www.scopus.com/inward/record.url?scp=67649482292&partnerID=8YFLogxK
U2 - 10.1016/j.cbpc.2009.05.009
DO - 10.1016/j.cbpc.2009.05.009
M3 - Article
C2 - 19467346
AN - SCOPUS:67649482292
SN - 1532-0456
VL - 150
SP - 307
EP - 313
JO - Comparative Biochemistry and Physiology - C Toxicology and Pharmacology
JF - Comparative Biochemistry and Physiology - C Toxicology and Pharmacology
IS - 2
ER -