Predictive Analysis Using Chemical-Gene Interaction Networks Consistent with Observed Endocrine Activity and Mutagenicity of U.S. Streams
Author(s) -
Jason P. Berninger,
David M. DeMarini,
Sarah H. Warren,
Jane Ellen Simmons,
Vickie S. Wilson,
Justin M. Conley,
Mikayla D. Armstrong,
Luke R. Iwanowicz,
Dana W. Kolpin,
Kathryn M. Kuivila,
Timothy J. Reilly,
Kristin M. Romanok,
Daniel L. Villeneuve,
Paul M. Bradley
Publication year - 2019
Publication title -
environmental science and technology
Language(s) - English
Resource type - Journals
eISSN - 1520-5851
pISSN - 0013-936X
DOI - 10.1021/acs.est.9b02990
Subject(s) - toxicogenomics , bioassay , adverse outcome pathway , environmental chemistry , estrogen receptor , endocrine system , nonylphenol , endocrine disruptor , biology , chemistry , gene , toxicology , computational biology , genetics , biochemistry , gene expression , hormone , cancer , breast cancer
In a recent U.S. Geological Survey/U.S. Environmental Protection Agency study assessing more than 700 organic compounds in 38 streams, in vitro assays indicated generally low estrogen, androgen, and glucocorticoid receptor activities, with 13 surface waters with 17β-estradiol-equivalent (E2Eq) activities greater than a 1-ng/L estimated effects-based trigger value for estrogenic effects in male fish. Among the 36 samples assayed for mutagenicity in the Salmonella bioassay (reported here), 25% had low mutagenic activity and 75% were not mutagenic. Endocrine and mutagenic activities of the water samples were well correlated with each other and with the total number and cumulative concentrations of detected chemical contaminants. To test the predictive utility of knowledge-base-leveraging approaches, site-specific predicted chemical-gene (pCGA) and predicted analogous pathway-linked (pPLA) association networks identified in the Comparative Toxicogenomics Database were compared with observed endocrine/mutagenic bioactivities. We evaluated pCGA/pPLA patterns among sites by cluster analysis and principal component analysis and grouped the pPLA into broad mode-of-action classes. Measured E2eq and mutagenic activities correlated well with predicted pathways. The pPLA analysis also revealed correlations with signaling, metabolic, and regulatory groups, suggesting that other effects pathways may be associated with chemical contaminants in these waters and indicating the need for broader bioassay coverage to assess potential adverse impacts.
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