Thymol Reduces <i>agr</i>‐Mediated Virulence Factor Phenol‐Soluble Modulin Production in <i>Staphylococcus aureus</i>
Harshad Lade, Sung Hee Chung, Yeon‐Hee Lee, Bajarang Vasant Kumbhar, Hwang‐Soo Joo, Yun‐Gon Kim, Yung‐Hun Yang, Jae‐Seok Kim
Abstract
Staphylococcus aureus is a major human bacterial pathogen that carries a large number of virulence factors. Many virulence factors of S. aureus are regulated by the accessory gene regulator ( agr ) quorum‐sensing system. Phenol‐soluble modulins (PSMs) are one of the agr ‐mediated virulence determinants known to play a significant role in S. aureus pathogenesis. In the present study, the efficacy of thymol to inhibit PSM production including δ ‐toxin in S. aureus was explored. We employed liquid chromatography–mass spectrometry (LC–MS) to quantify the PSMs α 1–PSM α 4, PSM β 1 and PSM β 2, and δ ‐toxin production from culture supernatants. We found that thymol at 0.5 MIC (128 μ g/mL) significantly reduced the PSM α and δ ‐toxin production in S. aureus WKZ‐1, WKZ‐2, LAC USA300, and ATCC29213. Downregulation in transcription by quantitative real‐time (qRT) PCR analysis of response regulator agrA and receptor histidine kinase agrC upon 0.5 MIC thymol treatment affirmed the results of LC–MS quantification of PSMs. In silico molecular docking analysis demonstrated the binding affinity of thymol with receptors AgrA and AgrC. Transmission electron microscopy images revealed no ultrastructural alterations (cell wall and membrane) in thymol‐treated WKZ‐1 and WKZ‐2 S . aureus strains. Here, we demonstrated that thymol reduces various PSM production in S. aureus clinical isolates and reference strains with mass spectrometry.