journal article·2025-10-22Open access

Evaluation of the Effects of Carvacrol on Gram-Negative Bacilli Isolated from Wound Infections

Agata Pruss, Anna Lichota, Helena Masiuk, Paweł Kwiatkowski, Mirosława Słaba, Monika Sienkiewicz, Barbara Dołęgowska

Applied Sciences· Volume 15· Issue 21

Abstract

Wound infections pose a significant challenge in modern medicine, driven by multimorbidity, weakened immunity, microbial virulence factors, and resistance to antibiotics and antiseptics. This study aims to evaluate the antibacterial properties of carvacrol (CAR), its impact on biofilm formation, and its capacity to trigger oxidative stress in clinical strains of Pseudomonas aeruginosa, Klebsiella pneumoniae, and Enterobacter cloacae. Carbapenemases in the studied bacteria were detected using culture on CarbaId agar. The presence of genes encoding bacterial virulence factors and carbapenemase production was confirmed using the PCR method. The antimicrobial activity of carvacrol was evaluated using the broth microdilution method. The ability of strains to form biofilm was determined using a modified crystal violet assay. Oxidative stress levels in bacterial cells in response to carvacrol treatment were measured using 2′,7′-dichlorofluorescein diacetate. Real-TimePCR was used to confirm the presence of NDM family carbapenemase genes in K. pneumoniae strains, KPC genes in E. cloacae strains, and VIM genes in P. aeruginosa strains. CAR exhibited a broad spectrum of antibacterial activity against the tested bacteria, with MIC values ranging from 125 to 1000 μg/mL. Treatment with 1/2 MIC of CAR did not significantly influence biofilm formation, except in a K. pneumoniae isolate. At 1/2 MIC, CAR induced an increase in intracellular ROS in most tested strains, with the exception of P. aeruginosa 25521221. This study provides insights into the antimicrobial efficacy of carvacrol against carbapenemase-producing pathogens isolated from wound infections—specifically P. aeruginosa, K. pneumoniae, and E. cloacae. CAR demonstrated promising bactericidal properties, likely mediated through the induction of oxidative stress, as evidenced by increased ROS generation in most studied isolates.
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Research context

OpenAlex topics: Essential Oils and Antimicrobial Activity · Antimicrobial agents and applications · Medicinal Plants and Neuroprotection

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Laboratory Medicine, Pomeranian Medical University, 70-111 Szczecin, Poland

Department of Pharmaceutical Microbiology and Microbiological Diagnostics, Medical University of Lodz, 90-151 Lodz, Poland

Department of Clinical Microbiology, Pomeranian Medical University in Szczecin, 70-111 Szczecin, Poland

Department of Diagnostic Immunology, Pomeranian Medical University in Szczecin, 70-111 Szczecin, Poland

Department of Industrial Microbiology and Biotechnology, Faculty of Biology and Environmental Protection, University of Lodz, 90-237 Lodz, Poland

References (31)

Show source-provided references
1. Octenidine: Novel insights into the detailed killing mechanism of Gram-negative bacteria at a cellular and molecular level10.1016/j.ijantimicag.2020.106146 ↗
2. Phylogenetic Analysis of Antibiotic Resistance Genes and Virulence Genes of Klebsiella species in silico10.3329/dujps.v16i1.33389 ↗
3. Bujňáková, D., Puvača, N., and Ćirković, I. (2022). Virulence Factors and Antibiotic Resistance of Enterobacterales. Microorganisms, 10.10.3390/microorganisms10081588 ↗
4. Lazar, D.S., Nica, M., Dascalu, A., Oprisan, C., Albu, O., Codreanu, D.R., Kosa, A.G., Popescu, C.P., and Florescu, S.A. (2024). Carbapenem-Resistant NDM and OXA-48-like Producing K. pneumoniae: From Menacing Superbug to a Mundane Bacteria; A Retrospective Study in a Romanian Tertiary Hospital. Antibiotics, 13.10.3390/antibiotics13050435 ↗
5. Xiang, T., Chen, C., Wen, J., Liu, Y., Zhang, Q., Cheng, N., Wu, X., and Zhang, W. (2020). Resistance of Klebsiella pneumoniae Strains Carrying blaNDM–1 Gene and the Genetic Environment of blaNDM–1. Front. Microbiol., 11.10.3389/fmicb.2020.00700 ↗
6. Verona Integron-Encoded Metallo-β-Lactamase (VIM)-Producing Pseudomonas aeruginosa Pyelonephritis in a Young Adult: A Case Report
7. Antibacterial activity and antibiotic-modifying action of carvacrol against multidrug-resistant bacteria10.1016/j.sampre.2023.100072 ↗
8. Cacciatore, F.A., Maders, C., Alexandre, B., Barreto Pinilla, C.M., Brandelli, A., and da Silva Malheiros, P. (2022). Carvacrol encapsulation into nanoparticles produced from chia and flaxseed mucilage: Characterization, stability and antimicrobial activity against Salmonella and Listeria monocytogenes. Food Microbiol., 108.10.1016/j.fm.2022.104116 ↗
9. Walczak, M., Michalska-Sionkowska, M., Olkiewicz, D., Tarnawska, P., and Warżyńska, O. (2021). Potential of Carvacrol and Thymol in Reducing Biofilm Formation on Technical Surfaces. Molecules, 26.10.3390/molecules26092723 ↗
10. Ghorbani, G., Rahimi, E., and Shakerian, A. (2022). Antibiotic resistance’s Genotypic and Phenotypic Characteristics and the Frequency of Virulence Factors in P. aeruginosa Isolates Isolated from Water Samples in Iran. Biomed. Res. Int., 2022.10.1155/2022/7076433 ↗
11. Wahl, A., Fischer, M.A., Klaper, K., Müller, A., Borgmann, S., Friesen, J., Hunfeld, K.P., Ilmberger, A., Kolbe-Busch, S., and Kresken, M. (2024). Presence of hypervirulence-associated determinants in Klebsiella pneumoniae from hospitalised patients in Germany. Int. J. Med. Microbiol., 314.10.1016/j.ijmm.2024.151601 ↗
12. Reduced Staphylococcus aureus biofilm formation in the presence of chitosan-coated iron oxide nanoparticles10.2147/IJN.S41371 ↗
13. Quantitative and Qualitative Assessment Methods for Biofilm Growth: A Mini-review
14. The effects of chlorhexidine, povidone-iodine and vancomycin on growth and biofilms of pathogens that cause prosthetic joint infections: An in-vitro model10.1016/j.jhin.2024.06.010 ↗
15. Pourhajibagher, M., and Bahador, A. (2024). Periodontal ligament stem cell-derived exosome-loaded Emodin mediated antimicrobial photodynamic therapy against cariogenic bacteria. BMC Oral Health, 24.10.1186/s12903-024-04062-7 ↗
16. Zhang, K., Yang, N., Teng, D., Mao, R., Hao, Y., and Wang, J. (2024). Expression and characterization of the new antimicrobial peptide AP138L-arg26 anti Staphylococcus aureus. Appl. Microbiol. Biotechnol., 108.10.1007/s00253-023-12947-w ↗
17. Antibacterial activity and cytotoxicity of a novel bacteriocin isolated from Pseudomonas sp. strain 16610.1111/1751-7915.14096 ↗
18. Liu, X., Liu, R., Zhao, R., Wang, J., Cheng, Y., Liu, Q., Wang, Y., and Yang, S. (2022). Synergistic Interaction Between Paired Combinations of Natural Antimicrobials Against Poultry-Borne Pathogens. Front. Microbiol., 13.10.3389/fmicb.2022.811784 ↗
19. Vasireddy, L., Bingle, L.E.H., and Davies, M.S. (2018). Antimicrobial activity of essential oils against multidrug-resistant clinical isolates of the Burkholderia cepacia complex. PLoS ONE, 13.10.1371/journal.pone.0201835 ↗
20. Kumar Rai, M., and Volodymyrivna Kon, K. (2013). Chapter 6-Use of Essential Oils and Their Components against Multidrug-Resistant Bacteria. Fighting Multidrug Resistance with Herbal Extracts, Essential Oils and Their Components, Academic Press. [1st ed.].
21. Anti-biofilm and Virulence Factor-Reducing Activities of Essential Oils and Oil Components as a Possible Option for Bacterial Infection Control10.1055/a-1147-4671 ↗
22. Li, Y., and Wu, M.X. (2022). Visualization and elimination of polymicrobial biofilms by a combination of ALA-carvacrol-blue light. J. Photochem. Photobiol. B Biol., 234.10.1016/j.jphotobiol.2022.112525 ↗
23. A comparative study on antibacterial activity of carvacrol and glutaraldehyde on Pseudomonas aeruginosa and Staphylococcus aureus isolates: An in vitro study10.1007/s40201-021-00620-1 ↗
24. Mączka, W., Twardawska, M., Grabarczyk, M., and Wińska, K. (2023). Carvacrol—A Natural Phenolic Compound with Antimicrobial Properties. Antibiotics, 12.10.3390/antibiotics12050824 ↗
25. Carvacrol oil inhibits biofilm formation and exopolysaccharide production of Enterobacter cloacae10.1016/j.foodcont.2020.107473 ↗
26. Farhadi, K., Rajabi, E., Varpaei, H.A., Iranzadasl, M., Khodaparast, S., and Salehi, M. (2024). Thymol andcarvacrol against Klebsiella: Anti-bacterial, antibiofilm, and synergistic activities—Asystematic review. Front. Pharmacol., 15.10.3389/fphar.2024.1487083 ↗
27. The stringent response controls catalases in Pseudomonas aeruginosa and is required for hydrogen peroxide and antibiotic tolerance10.1128/JB.02061-12 ↗
28. Antimicrobial potential of the food-grade additive carvacrol against uropathogenic E. coli based on membrane depolarization, reactive oxygen species generation, and molecular docking analysis10.1016/j.micpath.2020.104046 ↗
29. da Cruz Nizer, W.S., Inkovskiy, V., Versey, Z., Strempel, N., Cassol, E., and Overhage, J. (2021). Oxidative Stress Response in Pseudomonas aeruginosa. Pathogens, 10.10.3390/pathogens10091187 ↗
30. The antibacterial properties of phenolic isomers, carvacrol and thymol10.1080/10408398.2019.1675585 ↗
31. Preliminary Study on the Antibacterial Activity of Essential Oils Alone and in Combination with Gentamicin Against Extended-Spectrum β-Lactamase-Producing and New Delhi Metallo-β-Lactamase-1-Producing Klebsiella pneumoniae Isolates10.1089/mdr.2018.0051 ↗