Research Paper
The role of extracellular vesicles and genotypic characterization in antibiotic resistance formation of clinical Staphylococcus aureus isolates in causative flora of patients with diabetic foot syndrome
- 1 Department of Surgery No.1, Kharkiv National Medical University, Balakireva Entry, Kharkiv 61103, Ukraine
- 2 Department of Surgery, Macerata Hospital, Macerata 62100, Italy
- 3 Ukraine Association of Biobank Austria, Graz A-8010, Austria
- 4 International Biobanking and Education, Medical University of Graz, Graz 8010, Austria
- 5 University Luisiana, Biotechnology Department, Baton Rouge, LA 70803, USA
- 6 Department of Surgery No. 1, Kharkiv National Medical University, Kharkiv, Nauki 61000, Ukraine
- 7 Biobank, Medical University of Bialystok, Białystok 15-089, Poland
Received: May 28, 2024 Accepted: November 18, 2024
https://doi.org/10.18632/aging.206164How to Cite
Copyright: © 2024 Gramatiuk et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Abstract
It has been suggested that defense against macroorganism immune factors is carried out by forming membrane vesicles with lytic action on Gram-positive bacteria, which in turn may cause antibiotic resistance in microorganisms. Staphylococcus aureus (S. aureus) is a common pathogen causing diabetic foot syndrome (DFS). We described antibiotic resistance and the role of lytic vesicles as antibiotic resistance factors in cultures of S. aureus isolates and S. aureus reference strains. Moreover, we used Bacillus subtilis (B. subtilis) to determine the lytic effect of vesicles in 36 patients of different ages with ischaemic and mixed forms of DFS. As a result of this study, we found that membrane vesicles have a lytic effect, with lysis zones forming both around vesicles of reference strains of S. aureus and their clinical isolates and around vesicles of reference strains of B. subtilis. Among genes encoding resistance to various antibiotics, blaCTX-M-2 were detected in 16.7% of clinical strains, Erm and Tet genes in 11.1%, Mec-1 in 5.5%, VanA and VanB genes in 5.5%. Plasmid-mediated quinoloneresistance genes qnrB were also detected in 5.5% of strains. Meanwhile, multiple resistance was detected in 11.1% of clinical strains of S. aureus. Further studies should analyze the contribution of the described genes to adhesion and membrane vesicle formation and their significance in the pathogenesis of wound healing in patients with DFS and wounds and infections of other origins.