4.7 Article

Staphyloxanthin inhibitory potential of thymol impairs antioxidant fitness, enhances neutrophil mediated killing and alters membrane fluidity of methicillin resistant aureus

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BIOMEDICINE & PHARMACOTHERAPY
卷 141, 期 -, 页码 -

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ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.biopha.2021.111933

关键词

MRSA; Thymol; Staphyloxanthin; Neutrophil survival; Membrane fluidity; ROS resistance

资金

  1. DST-FIST [SR/FST/LSI-639/2015 (C)]
  2. UGC-SAP [F.5-1/2018/DRS-II (SAP-II)]
  3. DST-PURSE [SR/PURSE Phase 2/38 (G)]
  4. RUSA 2.0 [Policy (TN Multi-Gen) , Dept. of Edn, GoI] [F.24-51/2014-U]
  5. UGC [F.19-225/2018 (BSR)]
  6. RUSA 2.0

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This study evaluated the inhibitory potential of thymol against MRSA by targeting its production of staphyloxanthin, resulting in increased sensitivity to oxidative stress and neutrophil killing. Thymol was found to interact with CrtM and inhibit staphyloxanthin, making MRSA cells more susceptible to antibiotic treatment. These findings suggest the therapeutic potential of thymol in combating MRSA infections.
Staphylococcus aureus is a leading pathogen responsible for mild to severe invasive infections in humans. Especially, methicillin resistant Staphylococcus aureus (MRSA) is prevalent in hospital and community associated infections. Staphyloxanthin is a golden yellow color eponymous pigment produced by S. aureus and provides resistance to reactive oxygen species (ROS) and host neutrophil-based killing. In addition, this membrane pigment contributes to membrane rigidity and helps MRSA to survive under stress conditions. Targeting virulence of pathogen without exerting selection pressure is the recent approach to fight bacterial infections without developing drug resistance. The present study for the first time evaluated the staphyloxanthin inhibitory potential of thymol against MRSA. Qualitative and quantitative analyses demonstrated 90% of staphyloxanthin inhibition at 100 mu g/mL concentration of thymol without alteration in growth. Molecular docking analysis and in vitro measurement of metabolic intermediates of staphyloxanthin revealed that thymol could possibly interact with CrtM to inhibit staphyloxanthin. Absorbance and infra red spectra further validated the inhibition of staphyloxanthin by thymol. In addition, thymol treatment significantly reduced the resistance of MRSA to ROS and neutrophil-based killing as exhibited by oxidant susceptibility assays and ex vivo innate immune clearance assay using human whole blood and neutrophils. Further, reduction in staphyloxanthin by thymol treatment increased the membrane fluidity and made MRSA cells more susceptible to membrane targeting antibiotic polymyxin B. Especially, thymol was found to be non-cytotoxic to human peripheral blood mononuclear cells. Our study validated the antivirulence potential of thymol against MRSA by inhibiting staphyloxanthin and suggests the prospective therapeutic role of thymol to combat MRSA infections.

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