Anti-Biofilm Effect of Selected Essential Oils and Main Components on Mono- and Polymicrobic Bacterial Cultures

• Main Authors: Erika Beáta Kerekes, Anita Vidács, Miklós Takó, Tamás Petkovits, Csaba Vágvölgyi, Györgyi Horváth, Viktória Lilla Balázs, Judit Krisch
• Format: Article
• Language: English
• Published: MDPI AG 2019-09-01
• Series: Microorganisms
• Subjects: antibacterial activity; biofilm; polymicrobial biofilm; essential oil; food spoilage
• Online Access: https://www.mdpi.com/2076-2607/7/9/345

Biofilms are surface-associated microbial communities resistant to sanitizers and antimicrobials. Various interactions that can contribute to increased resistance occur between the populations in biofilms. These relationships are the focus of a range of studies dealing with biofilm-associated infections and food spoilage. The present study investigated the effects of cinnamon (<i>Cinnamomum zeylanicum</i>), marjoram (<i>Origanum majorana</i>), and thyme (<i>Thymus vulgaris</i>) essential oils (EOs) and their main components, i.e., trans-cinnamaldehyde, terpinen-4-ol, and thymol, respectively, on single- and dual-species biofilms of <i>Escherichia coli</i>, <i>Listeria monocytogenes</i>, <i>Pseudomonas putida,</i> and <i>Staphylococcus aureus</i>. In dual-species biofilms, <i>L. monocytogenes</i> was paired with each of the other three bacteria. Minimum inhibitory concentration (MIC) values for the individual bacteria ranged between 0.25 and 20 mg/mL, and trans-cinnamaldehyde and cinnamon showed the highest growth inhibitory effect. Single-species biofilms of <i>L. monocytogenes</i>, <i>P. putida,</i> and <i>S. aureus</i> were inhibited by the tested EOs and their components at sub-lethal concentrations. Scanning electron microscopy images showed that the three-dimensional structure of mature biofilms embedded in the exopolysaccharide matrix disappeared or was limited to micro-colonies with a simplified structure. In most dual-species biofilms, to eliminate living cells from the matrix, concentrations exceeding the MIC determined for individual bacteria were required.