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Updated: Dec 29, 2025

Quantifying the Cytotoxicity of Staphylococcus aureus Against Human Polymorphonuclear Leukocytes
Published on: January 3, 2020
Influence of apitoxin and melittin from Apis mellifera bee on Staphylococcus aureus strains
Ana Flávia Marques Pereira1, Mariana Albano1, Fernanda Cristina Bérgamo Alves1
1Department of Microbiology and Immunology, São Paulo State University, 18618-691, Brazil.
Abstract:
The antibacterial activities of apitoxin, a venom produced by Apis mellifera bee, and melittin, an antimicrobial peptide from apitoxin, were tested against planktonic and biofilm states of Staphylococcus aureus methicillin-resistant (MRSA), including clinical, and enterotoxin-producing isolates. Also, the synergism of apitoxin and melittin in combination with oxacillin were evaluated as well. The induced morphological changes on S. aureus cells of both products were detected by transmission electronic microscopy (TEM). The minimum inhibitory concentration (MIC) values were 7.2 μg/mL, and 6.7 μg/mL, for apitoxin and melittin, respectively. The minimum bactericidal concentration (MBC) values were 28.7 μg/mL, and 26 μg/mL for apitoxin and melittin, respectively. The time-kill curve assays of apitoxin or melittin with oxacillin exhibited bactericidal synergism against MRSA isolates. TEM images showed cell distortion, cell disintegration with leakage of cytoplasmic content and loss of cytoplasm content. However, apitoxin and melittin did not interfere with staphylococcal enterotoxin production or release. Thus, apitoxin and melittin are potential agents against MRSA that can serve as possible models for new antibacterial drugs.
Insights
Apitoxin and melittin, derived from bee venom, show potent antibacterial effects against methicillin-resistant Staphylococcus aureus (MRSA). These natural compounds, especially when combined with oxacillin, offer promising potential for new MRSA drug development.
Area of Science:
- Microbiology
- Pharmacology
- Biochemistry
Background:
- Methicillin-resistant Staphylococcus aureus (MRSA) poses a significant global health threat due to its resistance to conventional antibiotics.
- The emergence of multidrug-resistant strains necessitates the exploration of novel therapeutic agents.
- Bee venom (apitoxin) and its primary component, melittin, possess known antimicrobial properties.
Purpose of the Study:
- To evaluate the antibacterial activity of apitoxin and melittin against planktonic and biofilm MRSA.
- To assess the synergistic effects of apitoxin and melittin in combination with oxacillin.
- To investigate the morphological changes induced by apitoxin and melittin in MRSA cells.
Main Methods:
- Minimum Inhibitory Concentration (MIC) and Minimum Bactericidal Concentration (MBC) assays.
- Time-kill curve assays to evaluate synergistic effects with oxacillin.
- Transmission Electron Microscopy (TEM) for morphological analysis of MRSA cells.
Main Results:
- Apitoxin and melittin demonstrated significant antibacterial activity with low MIC and MBC values against MRSA.
- Combination therapy with oxacillin showed bactericidal synergism against MRSA isolates.
- TEM revealed cell distortion, disintegration, and cytoplasmic leakage upon treatment with apitoxin and melittin.
Conclusions:
- Apitoxin and melittin are effective against both planktonic and biofilm MRSA.
- These bee venom components exhibit synergistic effects with oxacillin, enhancing bactericidal activity.
- Apitoxin and melittin represent promising candidates for the development of novel antibacterial agents against MRSA.
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