Abstract

The abuse of antibiotics for disease treatment has led to the emergence of multidrug resistant bacteria. Antimicrobial peptides, found naturally in various organisms, have received increasing interest as alternatives to conventional antibiotics because of their broad spectrum antimicrobial activity and low cytotoxicity. In a previous report, Macropin, isolated from bee venom, exhibited antimicrobial activity against both gram-positive and negative bacteria. In the present study, Macropin was synthesized and its antibacterial and anti-biofilm activities were tested against bacterial strains, including gram-positive and negative bacteria, and drug resistant bacteria. Moreover, Macropin did not exhibit hemolytic activity and cytotoxicity to keratinocytes, whereas Melittin, as a positive control, showed very high toxicity. Circular dichroism assays showed that Macropin has an α-helical structure in membrane mimic environments. Macropin binds to peptidoglycan and lipopolysaccharide and kills the bacteria by disrupting their membranes. Moreover, the fractional inhibitory concentration index indicated that Macropin has additive and partially synergistic effects with conventional antibiotics against drug resistant bacteria. Thus, our study suggested that Macropin has potential for use of an antimicrobial agent for infectious bacteria, including drug resistant bacteria.

Highlights

  • Regions[4,5]

  • Diseases associated with biofilms, such as chronic infections and medical-appliance-related infections, are difficult to treat, which cause problems to public health that require novel solutions[23]

  • AMPs, a vital component of the innate immune system, represent novel therapeutic agents to treat microbial infections, because they are effective against pathogenic microorganisms and are less likely to induce drug resistance[24]

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Summary

Introduction

Regions[4,5] These characteristics promote the interaction of AMPs with the bacterial cell membrane, which comprises negatively charged lipids, such as phosphatidylglycerol (PG), phosphatidylethanolamine (PE), and cardiolipin (CL). The barrel-stave model suggests that AMPs form pores by binding to the membrane surface. AMPs penetrate the membrane lipid layer to form a pore[8,9]. Combinations of conventional antibiotics and AMPs were used to treat certain fungal and bacterial infections[14,15,16]. Macropin was tested for its antimicrobial activity against gram-negative and positive bacteria, including drug resistant bacteria. The synergistic effect of Macropin with conventional antibiotics was evaluated in a combination assay and by flow cytometry. Our results indicated that Macropin could potentially be used as an antimicrobial agent

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