The Array of Antibacterial Action of Protocatechuic Acid Ethyl Ester and Erythromycin on Staphylococcal Strains.
Maria Miklasińska-MajdanikMałgorzata KępaMonika KulczakMaciej OchwatTomasz J WąsikPublished in: Antibiotics (Basel, Switzerland) (2022)
The spread of antibiotic resistance among bacteria has become one of the major health problems worldwide. Methicillin-resistant staphylococcal strains are especially dangerous because they are often resistant to other antibiotics. The increasing insensitivity to macrolides, lincosamides and streptogramin B antibiotics of methicillin-resistant staphylococcal isolates has limited the use of these drugs in therapy. The combination of natural compounds and antibiotics can be considered as an alternative tool to fight multi-drug-resistant pathogen infections. The aim of the presented study was to examine the antibacterial activity of protocatechuic acid ethyl ester-erythromycin combination towards Staphylococcus aureus and Staphylococcus epidermidis strains with various resistance profiles to methicillin and macrolides, lincosamides and streptogramin B (MLS B ) antibiotics. The in-vitro antibacterial potential of the above combination was investigated by minimum inhibitory concentration assays and checkerboard testing. The observed effects were strain dependent, with 8 of 12 tested staphylococcal strains showing an indifferent effect on the natural compound and erythromycin; for 2 strains, the tested combination had an additive effect, while for another 2, the effect was synergistic. Interestingly, the multi-drug-resistant strains were more sensitive to the cooperative action of the protocatechuic acid ethyl ester and the antibiotic.
Keyphrases
- staphylococcus aureus
- drug resistant
- escherichia coli
- biofilm formation
- methicillin resistant staphylococcus aureus
- multidrug resistant
- acinetobacter baumannii
- mental health
- public health
- healthcare
- stem cells
- health information
- high resolution
- mesenchymal stem cells
- social media
- pseudomonas aeruginosa
- cancer therapy
- drug induced
- atomic force microscopy