» Articles » PMID: 29301331

Antimicrobial and Antibiofilm Activity of UP-5, an Ultrashort Antimicrobial Peptide Designed Using Only Arginine and Biphenylalanine

Overview
Publisher MDPI
Specialty Chemistry
Date 2018 Jan 6
PMID 29301331
Citations 23
Authors
Affiliations
Soon will be listed here.
Abstract

The recent upsurge of multidrug resistant bacteria (MDRB) among global communities has become one of the most serious challenges facing health professionals and the human population worldwide. Cationic ultrashort antimicrobial peptides (USAMPs) are a promising group of molecules that meet the required criteria of novel antimicrobial drug development. UP-5, a novel penta-peptide, displayed significant antimicrobial activities against various standard and clinical isolates of MDRB. UP-5 displayed MICs values within the range of (10-15 μM) and (55-65 μM) against Gram-positive and Gram-negative bacteria, respectively. Furthermore, UP-5 displayed antibiofilm activity with minimum biofilm eradication concentration (MBEC) value as equal to twofold higher than MIC value. At the same inhibitory concentrations, UP-5 exhibited very low or negligible toxicity toward human erythrocytes and mammalian cells. Combining UP-5 with conventional antibiotics led to a synergistic or additive mode of action that resulted in the reduction of the MIC values for some of the antibiotics by 99.7% along a significant drop in MIC values of the peptide. The stability profile of UP-5 was evaluated in full mouse plasma and serum with results indicating a more stable pattern in plasma. The present study indicates that USAMPs are promising antimicrobial agents that can avoid the negative characteristics of conventional antimicrobial peptides. Additionally, USAMPs exhibit good to moderate activity against MDRB, negligible toxicity, and synergistic outcomes in combination with conventional antimicrobial agents.

Citing Articles

Evaluating the Antimicrobial Efficacy of a Designed Synthetic peptide against Pathogenic Bacteria.

de Moura Cavalheiro M, de Oliveira C, de Araujo Boleti A, Rocha L, Jacobowski A, Pedron C J Microbiol Biotechnol. 2024; 34(11):2231-2244.

PMID: 39344347 PMC: 11637823. DOI: 10.4014/jmb.2405.05011.


Complementary Activities of Host Defence Peptides and Antibiotics in Combating Antimicrobial Resistant Bacteria.

Lennard P, Hiemstra P, Nibbering P Antibiotics (Basel). 2023; 12(10).

PMID: 37887219 PMC: 10604037. DOI: 10.3390/antibiotics12101518.


Self-Assembling Enzymatic Nanocomplexes with Polypeptides and Low-Weight Organic Compounds: Preparation, Characterization, and Application of New Antibacterials.

Lyagin I, Stepanov N, Presnov D, Trifonov A, Efremenko E Int J Mol Sci. 2023; 24(3).

PMID: 36768158 PMC: 9915939. DOI: 10.3390/ijms24031831.


The design and evaluation of the antimicrobial activity of a novel conjugated penta-ultrashort antimicrobial peptide in combination with conventional antibiotics against sensitive and resistant strains of and .

Darwish R, Almaaytah A, Salama A Res Pharm Sci. 2023; 17(6):612-620.

PMID: 36704429 PMC: 9872186. DOI: 10.4103/1735-5362.359429.


Assessment of New Strategies to Improve the Performance of Antimicrobial Peptides.

Wang L, Liu H, Li X, Yao C Nanomaterials (Basel). 2022; 12(20).

PMID: 36296881 PMC: 9610275. DOI: 10.3390/nano12203691.


References
1.
Chu H, Yu H, Yip B, Chih Y, Liang C, Cheng H . Boosting salt resistance of short antimicrobial peptides. Antimicrob Agents Chemother. 2013; 57(8):4050-2. PMC: 3719776. DOI: 10.1128/AAC.00252-13. View

2.
Glukhov E, Stark M, Burrows L, Deber C . Basis for selectivity of cationic antimicrobial peptides for bacterial versus mammalian membranes. J Biol Chem. 2005; 280(40):33960-7. DOI: 10.1074/jbc.M507042200. View

3.
Makovitzki A, Baram J, Shai Y . Antimicrobial lipopolypeptides composed of palmitoyl Di- and tricationic peptides: in vitro and in vivo activities, self-assembly to nanostructures, and a plausible mode of action. Biochemistry. 2008; 47(40):10630-6. DOI: 10.1021/bi8011675. View

4.
Feng X, Sambanthamoorthy K, Palys T, Paranavitana C . The human antimicrobial peptide LL-37 and its fragments possess both antimicrobial and antibiofilm activities against multidrug-resistant Acinetobacter baumannii. Peptides. 2013; 49:131-7. DOI: 10.1016/j.peptides.2013.09.007. View

5.
Ong Z, Wiradharma N, Yang Y . Strategies employed in the design and optimization of synthetic antimicrobial peptide amphiphiles with enhanced therapeutic potentials. Adv Drug Deliv Rev. 2014; 78:28-45. DOI: 10.1016/j.addr.2014.10.013. View