| Literature DB >> 33758343 |
Shira Mandel1, Janna Michaeli1, Noa Nur1, Isabelle Erbetti2, Jonathan Zazoun1, Livia Ferrari2, Antonio Felici2, Moshe Cohen-Kutner1, Niv Bachnoff3.
Abstract
New antimicrobial agents are urgently needed, especially to eliminate multidrug resistant Gram-negative bacteria that stand for most antibiotic-resistant threats. In the following study, we present superior properties of an engineered antimicrobial peptide, OMN6, a 40-amino acid cyclic peptide based on Cecropin A, that presents high efficacy against Gram-negative bacteria with a bactericidal mechanism of action. The target of OMN6 is assumed to be the bacterial membrane in contrast to small molecule-based agents which bind to a specific enzyme or bacterial site. Moreover, OMN6 mechanism of action is effective on Acinetobacter baumannii laboratory strains and clinical isolates, regardless of the bacteria genotype or resistance-phenotype, thus, is by orders-of-magnitude, less likely for mutation-driven development of resistance, recrudescence, or tolerance. OMN6 displays an increase in stability and a significant decrease in proteolytic degradation with full safety margin on erythrocytes and HEK293T cells. Taken together, these results strongly suggest that OMN6 is an efficient, stable, and non-toxic novel antimicrobial agent with the potential to become a therapy for humans.Entities:
Year: 2021 PMID: 33758343 DOI: 10.1038/s41598-021-86155-9
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379