Membrane-active antimicrobial peptide identified in Rana arvalis by targeted DNA sequencing
- Biochim Biophys Acta Biomembr. 2019 Mar 1;1861(3):651-659. doi: 10.1016/j.bbamem.2018.12.014.
- 1. Department of Physics, Faculty of Science, University of Split, Croatia. Electronic address: [email protected].
- 2. Department of Physics, Faculty of Science, University of Split, Croatia. Electronic address: [email protected].
- 3. Department of Life Sciences, University of Trieste, Italy. Electronic address: [email protected].
- 4. Department of Life Sciences, University of Trieste, Italy. Electronic address: [email protected].
- 5. Department of Life Sciences, University of Trieste, Italy. Electronic address: [email protected].
- 6. Department of Life Sciences, University of Trieste, Italy. Electronic address: [email protected].
- 7. Department of Physics, Faculty of Science, University of Split, Croatia. Electronic address: [email protected].
- 8. Department of Medical Chemistry and Biochemistry, School of Medicine, University of Split, Croatia. Electronic address: [email protected].
- 9. Department of Life Sciences, University of Trieste, Italy. Electronic address: [email protected].
- 10. Department of Biology, Faculty of Science, University of Split, Croatia. Electronic address: [email protected].
- 11. Department of Life Sciences, University of Trieste, Italy. Electronic address: [email protected].
Antimicrobial peptides (AMPs) are naturally produced, gene encoded molecules with a direct antimicrobial activity against pathogens, often also showing Other immune-related properties. Anuran skin secretions are rich in bioactive peptides, including AMPs, and we have reported a novel targeted Sequencing approach to identify novel AMPs simultaneously in different frog species, from small quantities of skin tissue. Over a hundred full-length peptides were identified from specimens belonging to five different Ranidae frog species, out of which 29 were novel sequences. Six of these were selected for synthesis and testing against a panel of Gram-negative and Gram-positive bacteria. One peptide, identified in Rana arvalis, proved to be a potent and broad-spectrum antimicrobial, active against ATCC Bacterial strains and a multi-drug resistant clinical isolate. CD spectroscopy suggests it has a helical conformation, while surface plasmon resonance (SPR) that it may self-aggregate/oligomerize at the membrane surface. It was found to disrupt the Bacterial membrane at sub-MIC, MIC and above-MIC concentrations, as observed by flow cytometry and/or visualized by atomic force microscopy (AFM). Only a limited toxicity was observed towards peripheral blood mononuclear cells (PBMC) with a more pronounced effect observed against the MEC-1 cell line.
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