Analysis of the Effects of Emerging Contaminants on the Bottlenose Dolphin (Tursiops truncatus) Skin Transcriptome: Development of Potential Biomarkers
IAAAM 2015
Denise Lunardi1*; Luigi Abelli1; Cristina Panti2; Letizia Marsili2; Maria Cristina Fossi2; Annalaura Mancia1
1Department of Life Sciences and Biotechnology, University of Ferrara, Ferrara, Italy; 2Department of Physical Sciences, Earth and Environment, University of Siena, Siena, Italy

Abstract

Chemical pollution represents one of the main threats for the marine ecosystem conservation. Persistent chemicals can bioaccumulate and biomagnify through the food web, leading to higher levels of exposure in predator species such as fish, cetaceans and humans.1,2 Among the emerging chemical contaminants are perfluorooctanoic acid (PFOA), used to make fluoropolymers, and bisphenol A (BPA), a monomer used in epoxy resins and polycarbonate plastics, present in many hard plastic bottles and metal-based food storage. BPA and PFOA are worldwide distributed compounds and are considered dangerous factors because of their agonist or antagonist effects on the endocrine receptors.3,4

Here, we applied an ex vivo assay using skin biopsy slices from the common bottlenose dolphin (Tursiops truncatus) combined with global gene expression analysis in response to BPA or PFOA chemical exposure.5,6 The skin was collected from a stranded dolphin on the coast of Tuscany. Right after death, small slices of skin biopsy were excised, cultured and independently treated with different concentrations of BPA or PFOA (0.1, 1, and 10 mg/ml). RNA from the different treatments was extracted and hybridized to species-specific custom-made microarray. Genes involved in the activation of immune response, endocrine pathways, lipid homeostasis and adipogenesis pathways were among the genes found to be differentially expressed. The expression of 7 significantly regulated genes was quantified through quantitative real time-PCR to validate the microarray results. The genes were also tested for their potential role of biomarkers of emerging contaminant exposure. Expression levels of 3 genes (BCAP31, MTSS1 and CDC42α) were also quantified on the skin transcriptome of three live cetaceans (Grampus griseus, Stenella coeruleoalba, Balaenoptera physalus) sampled in the Pelagos Sanctuary off the coast of Ligurian and Thyrrenian (Mediterranean Sea) seas on September 2014. Despite the small set analyzed, we could observe major difference in the expression of these genes between the toothed whale (Odontoceti) and the baleen whales (Mysticeti). Balaenoptera physalus showed level of expression much greater than the toothed whales (G. griseus and S. coeruleoalba) for the 3 genes tested: 34.53 fold for BCAP31, 20.53 fold for CDC42α, and 54.48 fold for MTSS1. This difference could be inferred to the different feeding methods and subsequent contaminant accumulation between Odontoceti and Mysticeti, as previously suggested.7 Deeper analysis on a broader group of animals sampled from different contaminated areas is needed in order to better understand genes and pathways mostly affected by emerging contaminants, which will lead to a selection of species-specific biomarkers of exposure.

Acknowledgements

The authors wish to thank the research staff and the volunteers who greatly contributed to the tissue sample collection. In particular we thank the University of Siena and the Istituto Superiore per la Protezione e la Ricerca Ambientale (ISPRA), committed to the study of pollution in the Italian seas, that organized the 'Plastic Pelagos' research cruise for sample collection.

* Presenting author

Literature Cited

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2.  United Nations Environment Programme. UNEP report; 2013. http://www.unep.com (VIN editor: the correct link is http://unep.org)

3.  Casals-Casas C, Desvergne B. Endocrine disruptors: from endocrine to metabolic disruption. Annu Rev Physiol. 2011;73:135–162.

4.  Calhoun KC, Padilla-Banks E, Jefferson WN, Liu L, Gerrish KE, Young SL, Wood CE, Hunt PA, Vandevoort CA, Williams CJ. Bisphenol A exposure alters developmental gene expression in the fetal rhesus macaque uterus. PLoS One. 2014;9(1):e85894.

5.  Fossi MC, Casini S, Maltese S, Panti C, Spinsanti G, Marsili L. An "ex vivo" model to evaluate toxicological responses to mixtures of contaminants in cetaceans: integumentum biopsy slices. Environ Toxicol. 2014;29(10):1107–1121.

6.  Mancia A, Warr GW, Almeida JS, Veloso A, Wells RS, Chapman RW. Transcriptome profiles: diagnostic signature of dolphin population. Estuar Coast. 2010;33:919–929.

7.  Fossi MC, Panti C, Marsili L, Maltese S, Coppola D, Jimenez B, Muñoz-Arnanz J, Finoia MG, Rojas-Bracho L, Urban RJ. Could feeding habit and migratory behaviour be the causes of different toxicological hazard to cetaceans of Gulf of California (Mexico)? Environ Sci Pollut Res. 2014;21:13353–13366.

  

Speaker Information
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Denise Lunardi
Department of Life Sciences and Biotechnology
University of Ferrara
Ferrara, Italy


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