Antimicrobial peptides have attracted attention as alternatives to conventional antibiotics. previously, a novel antimicrobial peptide, melectin, consisting of 18 amino acids was isolated from the venom of a bee, Melecta albifrons. Here, we investigated the antibacterial activity of melectin against drugresistant bacteria. Melectin showed broad-spectrum antimicrobial activity but low cytotoxicity and no hemolytic activity. Melectin maintained its antimicrobial activity at physiological salt concentrations. Melectin is an α-helical structure that binds to the bacterial membrane via electrostatic interactions and kills bacteria in a short time by bacterial membrane targeting. collectively, our results suggest that melectin has antibacterial activity and anti-inflammatory activity. Excessive use of antibiotics leads to the development of drug-resistant bacteria, which threatens human health 1. Drug-resistant bacteria develop rapidly, while novel antibiotics are discovered at a slower rate. To combat drug-resistant bacteria, new antibiotics must be developed. Antimicrobial peptides (AMPs), known as host defense peptides, consist of short amino acid sequences containing both positively charged and hydrophobic amino acids 2. AMPs are attractive candidates as therapeutic agents, as they can kill a broad range of bacteria including antibiotic-resistant strains and do not tend to develop drug resistance 3. Most AMPs display antimicrobial activity by disrupting the bacterial membrane. The cationic charge of AMPs enables an electrostatic interaction with the negatively charged bacterial membrane. The cytoplasmic membrane of bacteria is rich in phospholipids phosphatidylglycerol, cardiolipin, and phosphatidylserine which have negatively charged head groups and bind to positively charged AMPs. Additionally, the presence of lipoteichoic acid (LTA) of gram-positive bacteria and lipopolysaccharide (LPS) of gram-negative bacteria acts as a lipophilic anchor 4,5. AMPs can replace divalent cations such as Mg 2+ and Ca 2+ bound to LPS, causing membrane disruption and eventually bacterial death 6. Some AMPs penetrate the bacterial membrane and kill bacteria without inducing bacterial membrane permeabilization. These AMPs attack DNA and RNA to inhibit protein synthesis 7. Examples of these AMPs include buforin2 8 and indolicidin 9. The salt sensitivity of AMPs is a major limitation to the development of AMPs as treatment agents 10. AMPs interact electrostatically with the microbial membrane in a salt-sensitive manner. Human body fluid has a high salt concentration which interferes with the antimicrobial activity of AMPs 11. Therefore, it is necessary to develop a peptide that maintains its antimicrobial activity even at physiological salt concentration. Bee venoms contain diverse active compounds, including polypeptides, enzymes, and amino acids 12. Bee venom therapy is the therapeutic application of bee venom. The compounds in bee venom are used as traditional medicines for anti-arthritis and pain relief 13. Various antimicrobial pep...