Contaminant biomonitoring augmented with a qPCR array indicates hepatic mRNA gene expression effects in wild-collected seabird embryos

Sci Total Environ. 2023 Dec 15:904:166784. doi: 10.1016/j.scitotenv.2023.166784. Epub 2023 Sep 4.

Abstract

Birds can bioaccumulate persistent contaminants, and maternal transfer to eggs may expose embryos to concentrations sufficient to cause adverse effects during sensitive early-life stages. However, using tissue residue concentrations alone to infer whether contaminant effects are occurring suffers from uncertainty, and efficient, sensitive biomarkers remain limited in wildlife. We studied relationships between whole embryo contaminant concentrations (total mercury, organochlorine pesticides, perfluoroalkyl substances, polychlorinated biphenyls, and halogenated flame retardants) together with mRNA expression in embryonic liver tissue from a Pacific Ocean seabird, the rhinoceros auklet (Cerorhinca monocerata). Fresh eggs were collected, incubated under controlled conditions, and from the pre-hatch embryo, hepatic RNA was extracted for qPCR array analysis to measure gene expression (2-∆Cq), while the remaining embryo was analyzed for contaminant residues. Contaminant and gene expression data were assessed with a combination of multivariate approaches and linear models. Results indicated correlations between embryonic total mercury and several genes such as sepp1, which encodes selenoprotein P. Correlation between the biotransformation gene cyp1a4 and the C7 perfluoroalkyl carboxylic acid PFHpA was also evident. This study demonstrates that egg collection from free-living populations for contaminant biomonitoring programs can relate chemical residues to in ovo mRNA gene expression effects in embryo hepatic tissue.

Keywords: Avian; Gene array; Marine; Pollution; Surveillance; Transcriptomic.

MeSH terms

  • Animals
  • Biological Monitoring
  • Birds / metabolism
  • Charadriiformes* / metabolism
  • Environmental Monitoring
  • Gene Expression
  • Liver / chemistry
  • Mercury* / analysis
  • Polychlorinated Biphenyls* / analysis
  • RNA, Messenger / metabolism

Substances

  • RNA, Messenger
  • Polychlorinated Biphenyls
  • Mercury