Oxytetracycline induces DNA damage and epigenetic changes: a possible risk for human and animal health?

Author:

Gallo Adriana1,Landi Rosaria2,Rubino Valentina3,Di Cerbo Alessandro4,Giovazzino Angela3,Palatucci Anna Teresa5,Centenaro Sara6,Guidetti Gianandrea6,Canello Sergio6,Cortese Laura7,Ruggiero Giuseppina3,Alessandrini Andrea48,Terrazzano Giuseppe39

Affiliation:

1. Institute of Experimental Endocrinology and Oncology (IEOS), National Research Council (CNR), Naples, Italy

2. Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, Naples, Italy

3. Department of Translational Medical Sciences, University of Naples Federico II, Naples, Italy

4. Department of Physics, Informatics and Mathematics, University of Modena and Reggio Emilia, Modena, Italy

5. PhD School of Science, University of Basilicata, Potenza, Italy

6. Division of Research and Development, Sanypet SpA, Padova, Italy

7. Department of Veterinary Medicine and Animal Productions, University of Naples Federico II, Naples, Italy

8. National Research Council (CNR), Nanoscience Istitute, Modena, Italy

9. Department of Science, University of Basilicata, Potenza, Italy

Abstract

Background Oxytetracycline (OTC), which is largely employed in zootechnical and veterinary practices to ensure wellness of farmed animals, is partially absorbed within the gastrointestinal tract depositing in several tissues. Therefore, the potential OTC toxicity is relevant when considering the putative risk derived by the entry and accumulation of such drug in human and pet food chain supply. Despite scientific literature highlights several OTC-dependent toxic effects on human and animal health, the molecular mechanisms of such toxicity are still poorly understood. Methods Here, we evaluated DNA damages and epigenetic alterations by quantitative reverse transcription polymerase chain reaction, quantitative polymerase chain reaction, chromatin immuno-precipitation and Western blot analysis. Results We observed that human peripheral blood mononuclear cells (PBMCs) expressed DNA damage features (activation of ATM and p53, phosphorylation of H2AX and modifications of histone H3 methylation of lysine K4 in the chromatin) after the in vitro exposure to OTC. These changes are linked to a robust inflammatory response indicated by an increased expression of Interferon (IFN)-γ and type 1 superoxide dismutase (SOD1). Discussion Our data reveal an unexpected biological in vitro activity of OTC able to modify DNA and chromatin in cultured human PBMC. In this regard, OTC presence in foods of animal origin could represent a potential risk for both the human and animal health.

Publisher

PeerJ

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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