Evaluation of Novel HLM Peptide Activity and Toxicity against Planktonic and Biofilm Bacteria: Comparison to Standard Antibiotics
- Authors: Masadeh M.1, Alshogran H.1, Alsaggar M.1, Sabi S.2, Al Momany E.3, Masadeh M.4, Alrabadi N.5, Alzoubi K.6
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Affiliations:
- Department of Pharmaceutical Technology, Faculty of Pharmacy, Jordan University of Science and Technology
- Department of Biology, Faculty of Science, The Hashemite University
- Department of Clinical Pharmacy and Pharmacy Practice, Faculty of Pharmaceutical Sciences, The Hashemite University
- Discipline of Clinical Pharmacy, School of Pharmaceutical Sciences, University Sains Malaysia
- Department of Pharmacology, Faculty of Medicine, Jordan University of Science and Technology
- Department of Pharmacy Practice and Pharmacotherapeutics, University of Sharjah
- Issue: Vol 25, No 10 (2024)
- Pages: 826-843
- Section: Life Sciences
- URL: https://ter-arkhiv.ru/1389-2037/article/view/645437
- DOI: https://doi.org/10.2174/0113892037291252240528110516
- ID: 645437
Cite item
Full Text
Abstract
Background:Antibiotic resistance is one of the main concerns of public health, and the whole world is trying to overcome such a challenge by finding novel therapeutic modalities and approaches. This study has applied the sequence hybridization approach to the original sequence of two cathelicidin natural parent peptides (BMAP-28 and LL-37) to design a novel HLM peptide with broad antimicrobial activity.
Methods:The physicochemical characteristics of the newly designed peptide were determined. As well, the new peptides antimicrobial activity (Minimum Inhibitory Concentration (MIC), Minimum Bacterial Eradication Concentration (MBEC), and antibiofilm activity) was tested on two control (Staphylococcus aureus ATCC 29213, Escherichia coli ATCC 25922) and two resistant (Methicillin-resistant Staphylococcus aureus (MRSA) ATCC BAA41, New Delhi metallo-beta- lactamase-1 Escherichia coli ATCC BAA-2452) bacterial strains. Furthermore, synergistic studies have been applied to HLM-hybridized peptides with five conventional antibiotics by checkerboard assays. Also, the toxicity of HLM-hybridized peptide was studied on Vero cell lines to obtain the IC50 value. Besides the percentage of hemolysis action, the peptide was tested in freshly heparinized blood.
Results:The MIC values for the HLM peptide were obtained as 20, 10, 20, and 20 µM, respectively. Also, the results showed no hemolysis action, with low to slightly moderate toxicity action against mammalian cells, with an IC50 value of 10.06. The Biomatik corporate labs, where HLM was manufactured, determined the stability results of the product by Mass Spectrophotometry (MS) and High-performance Liquid Chromatography (HPLC) methods. The HLM-hybridized peptide exhibited a range of synergistic to additive antimicrobial activities upon combination with five commercially available different antibiotics. It has demonstrated the biofilm-killing effects in the same concentration required to eradicate the control strains.
Conclusion:The results indicated that HLM-hybridized peptide displayed a broad-spectrum activity toward different bacterial strains in planktonic and biofilm forms. It showed synergistic or additive antimicrobial activity upon combining with commercially available different antibiotics.
About the authors
Majed Masadeh
Department of Pharmaceutical Technology, Faculty of Pharmacy, Jordan University of Science and Technology
Author for correspondence.
Email: info@benthamscience.net
Haneen Alshogran
Department of Pharmaceutical Technology, Faculty of Pharmacy, Jordan University of Science and Technology
Email: info@benthamscience.net
Mohammad Alsaggar
Department of Pharmaceutical Technology, Faculty of Pharmacy, Jordan University of Science and Technology
Email: info@benthamscience.net
Salsabeel Sabi
Department of Biology, Faculty of Science, The Hashemite University
Email: info@benthamscience.net
Enaam Al Momany
Department of Clinical Pharmacy and Pharmacy Practice, Faculty of Pharmaceutical Sciences, The Hashemite University
Email: info@benthamscience.net
Majd Masadeh
Discipline of Clinical Pharmacy, School of Pharmaceutical Sciences, University Sains Malaysia
Email: info@benthamscience.net
Nasr Alrabadi
Department of Pharmacology, Faculty of Medicine, Jordan University of Science and Technology
Email: info@benthamscience.net
Karem Alzoubi
Department of Pharmacy Practice and Pharmacotherapeutics, University of Sharjah
Email: info@benthamscience.net
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