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Non-toxicity of Plant Candicidal Peptides for Mammalian Cell Lines and Galleria mellonella Model to Improving Selectivity for Clinical Use

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Abstract

Antimicrobial peptides (AMPs) are promising candidates for the development of new drugs. However, thorough studies on the toxicity of these molecules are scarce, which is a gap, as host toxicity is one of the main reasons for nonapproval of the drug by regulatory agencies. This work aimed to evaluate the toxicity of three AMPs isolated from Capsicum annuum leaves, named CaCPin-II, CaCDef-like and CaCLTP2. The AMP toxicological profile was evaluated by in vitro cytotoxicity against mammalian cells and systemic in vivo toxicity using Galleria mellonella larvae as study model. AMP cytotoxicity was evaluated in a broad panel of human cell lines, namely, vascular endothelium, cervical adenocarcinoma, prostatic epithelium, mammary epithelium and fibroblasts, and in murine macrophages. Cell viability was evaluated through metabolic activity, a gold standard method for assessing viability due to the speed, robustness and reliability of the results. To elucidate the toxicity mechanism of the peptides, their ability to bind to the cell surface and to permeabilize membranes was evaluated by measuring the zeta potential and the absorption of the SYTOX® Green fluorescent probe, respectively. The AMPs did not decrease cell viability or permeabilize the membranes of the cell lines at the tested concentrations. Only CaCLTP2 had the ability to interact with the cell surface, but it was not able to permeabilize them. The in vivo systemic toxicity was evaluated by the survival rate of the G. mellonella larvae inoculated with peptides. CaCPin-II showed in vivo toxicity, as the larval survival rate after the test was 60% lower than that of the controls. The results suggest that these peptides have potential as antimicrobial agents because they have low or no toxicity to mammalian cells and can serve as a framework for drug development.

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No datasets were generated or analysed during the current study.

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Acknowledgements

This work was performed at the Universidade de Lisboa and Universidade Estadual do Norte Fluminense Darcy Ribeiro (UENF).

Funding

We acknowledge the financial support of the Brazilian agencies CNPq (307590/2021-6), FAPERJ (E-26/200567/2023; E-26/210353/2022; E-26/200.127/2023) and European Union H2020-01 (828774). This study was also financed in part by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior – Brazil (CAPES), finance code 001.

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Contributions

The study was conceived by MBC, MARBC and VMG. Experimental procedures were carried out by MBC, GBT, MCC, TZAG, LAS, EOM. Data analyses were performed by MBC, GBT, MCC, VLSN, AOC, MARBC. The paper was written by MBC, MCC, GBT, VMG, MARBC. All authors reviewed the manuscript.

Corresponding author

Correspondence to Valdirene Moreira Gomes.

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Cherene, M.B., Cavaco, M.C., Neves, V.L.S. et al. Non-toxicity of Plant Candicidal Peptides for Mammalian Cell Lines and Galleria mellonella Model to Improving Selectivity for Clinical Use. Int J Pept Res Ther 30, 28 (2024). https://doi.org/10.1007/s10989-024-10607-9

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  • DOI: https://doi.org/10.1007/s10989-024-10607-9

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