Towards Profiles of Resistance Development and Toxicity for the Small Cationic Hexapeptide RWRWRW-NH2.

Autor:	Wenzel M; Applied Microbiology, Ruhr University Bochum Bochum, Germany., Prochnow P; Applied Microbiology, Ruhr University Bochum Bochum, Germany., Mowbray C; Institute for Cell and Molecular Biosciences, Newcastle University Newcastle upon Tyne, UK., Vuong C; AiCuris Anti-infective Cures GmbH Wuppertal, Germany., Höxtermann S; Clinic for Dermatology and Allergology, St. Josef Hospital Bochum, Germany., Stepanek JJ; Applied Microbiology, Ruhr University Bochum Bochum, Germany., Albada HB; Chair of Inorganic Chemistry I - Bioinorganic Chemistry, Ruhr University Bochum Bochum, Germany., Hall J; Institute for Cell and Molecular Biosciences, Newcastle University Newcastle upon Tyne, UK., Metzler-Nolte N; Chair of Inorganic Chemistry I - Bioinorganic Chemistry, Ruhr University Bochum Bochum, Germany., Bandow JE; Applied Microbiology, Ruhr University Bochum Bochum, Germany.
Jazyk:	angličtina
Zdroj:	Frontiers in cell and developmental biology [Front Cell Dev Biol] 2016 Aug 26; Vol. 4, pp. 86. Date of Electronic Publication: 2016 Aug 26 (Print Publication: 2016).
DOI:	10.3389/fcell.2016.00086
Abstrakt:	RWRWRW-NH2 (MP196) is an amphipathic hexapeptide that targets the bacterial cytoplasmic membrane and inhibits cellular respiration and cell wall synthesis. In previous studies it showed promising activity against Gram-positive bacteria and no significant cytotoxicity or hemolysis. MP196 is therefore used as lead structure for developing more potent antibiotic derivatives. Here we present a more comprehensive study on the parent peptide MP196 with regard to clinically relevant parameters. We found that MP196 acts rapidly bactericidal killing 97% of initial CFU within 10 min at two times MIC. We were unable to detect resistance in standard 24 and 48 h resistance frequency assays. However, MP196 was effective against some but not all MRSA and VISA strains. Serum binding of MP196 was intermediate and we confirmed its low toxicity against mammalian cell lines. MP196 did neither induce NFκB activation nor cause an increase in IL8 levels at 250 μg/mL, and no IgE-dependent activation of basophil granulocytes was detected at 500 μg/mL. Yet, MP196 demonstrated acute toxicity in mice upon injection into the blood stream. Phase contrast microscopy of mouse blood treated with MP196 revealed a shrinking of erythrocytes at 250 μg/mL and severe morphological changes and lysis of erythrocytes at 500 μg/mL. These data suggest that MP196 derivatization directed at further lowering hemolysis could be instrumental in overcoming acute toxicity. The assessment of hemolysis is a critical step in the evaluation of the clinical potential of promising antimicrobial peptides and should be accompanied by microscopy-based morphological analysis of blood cells.
Databáze:	MEDLINE
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