OMN6 a novel bioengineered peptide for the treatment of multidrug resistant Gram negative bacteria

31Citations
Citations of this article
38Readers
Mendeley users who have this article in their library.

This article is free to access.

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.

Cite

CITATION STYLE

APA

Mandel, S., Michaeli, J., Nur, N., Erbetti, I., Zazoun, J., Ferrari, L., … Bachnoff, N. (2021). OMN6 a novel bioengineered peptide for the treatment of multidrug resistant Gram negative bacteria. Scientific Reports, 11(1). https://doi.org/10.1038/s41598-021-86155-9

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free