The global rise in antimicrobial resistance has spurred increased interest in alternative antimicrobial agents, particularly essential oils (EOs). These oils are complex mixtures of volatile compounds that exhibit documented biological activity. This study evaluated antimicrobial and antibiofilm effects of selected EOs against clinically relevant bacterial and fungal pathogens. Antimicrobial activity against planktonic cells was assessed using disc diffusion assays with DMSO-diluted EO solutions against Escherichia coli (E.coli), Staphylococcus aureus (S.aureus), Pseudomonas aeruginosa, Klebsiella pneumoniae, and Candida albicans. Antibiofilm activity of E. coli and S. aureus was examined using ethanol-based EO formulations, with biofilm viability quantified by colony forming unit (CFU) enumeration. Cinnamon (Cinnamomum verum) oil showed the strongest and most consistent activity, inhibiting planktonic and biofilm models. Tea tree (Melaleuca alternifolia), lemongrass (Cymbopogon citratus), rosemary (Rosmarinus officinalis), rose (Rosa damascena), and jasmine (Jasminum officinale) oils showed significant planktonic antimicrobial effects, while jasmine oil (Jasminum officinale) demonstrated pronounced antibiofilm activity against S. aureus, including strong biofilm eradication in several replicates. In contrast, chamomile (Matricaria chamomilla) and sandalwood (Santalum austocaledonicum) oils showed limited or no activity. These findings highlight differences between planktonic and biofilm responses, emphasizing the importance of incorporating biofilm models into antimicrobial evaluation. Overall, Cinnamomum verum and Jasminum officinale oils may serve as complementary antimicrobial agents, warranting further investigation.
Ribačuka et al. (Sun,) studied this question.