Synergistic Antibacterial Efficacy of Melittin in Combination with Oxacillin against Methicillin-Resistant Staphylococcus aureus (MRSA).
Ana Flávia Marques PereiraAlessandra Aguirra SaniTatiane Baptista ZapataDébora Silva Marques de SousaBruno César RossiniLucilene Delazari Dos SantosVera Lucia Mores RallCarla Dos Santos RiccardiAry Fernandes JúniorPublished in: Microorganisms (2023)
Methicillin-resistant Staphylococcus aureus (MRSA) often cause infections with high mortality rates. Antimicrobial peptides are a source of molecules for developing antimicrobials; one such peptide is melittin, a fraction from the venom of the Apis mellifera bee. This study aimed to evaluate the antibacterial and antibiofilm activities of melittin and its association with oxacillin (mel+oxa) against MRSA isolates, and to investigate the mechanisms of action of the treatments on MRSA. Minimum inhibitory concentrations (MICs) were determined, and synergistic effects of melittin with oxacillin and cephalothin were assessed. Antibiofilm and cytotoxic activities, as well as their impact on the cell membrane, were evaluated for melittin, oxacillin, and mel+oxa. Proteomics evaluated the effects of the treatments on MRSA. Melittin mean MICs for MRSA was 4.7 μg/mL and 12 μg/mL for oxacillin. Mel+oxa exhibited synergistic effects, reducing biofilm formation, and causing leakage of proteins, nucleic acids, potassium, and phosphate ions, indicating action on cell membrane. Melittin and mel+oxa, at MIC values, did not induce hemolysis and apoptosis in HaCaT cells. The treatments resulted in differential expression of proteins associated with protein synthesis and energy metabolism. Mel+oxa demonstrated antibacterial activity against MRSA, suggesting a potential as a candidate for the development of new antibacterial agents against MRSA.
Keyphrases
- methicillin resistant staphylococcus aureus
- staphylococcus aureus
- biofilm formation
- acinetobacter baumannii
- klebsiella pneumoniae
- pseudomonas aeruginosa
- silver nanoparticles
- cell cycle arrest
- escherichia coli
- oxidative stress
- mass spectrometry
- drug resistant
- cancer therapy
- endoplasmic reticulum stress
- induced apoptosis
- cell proliferation
- cardiovascular disease
- cystic fibrosis
- risk factors
- climate change
- genetic diversity
- anti inflammatory