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Potential Anti-Infectious Activity of Essential Oil Chemotypes of Lippia origanoides Kunth on Antibiotic-Resistant
Andrés Humberto Uc-Cachón1, Luz María Calvo-Irabien2, Angel de Jesús Dzul-Beh1
1Unidad de Investigación Médica Yucatán, Instituto Mexicano del Seguro Social, Mérida 97150, Yucatán, Mexico.
Abstract:
Staphylococcus aureus infections are prevalent in healthcare and community environments. Methicillin-resistant S. aureus is catalogued as a superbug of high priority among the pathogens. This Gram-positive coccus can form biofilms and produce toxins, leading to persistent infection and antibiotic resistance. Limited effective antibiotics have encouraged the development of innovative strategies, with a particular emphasis on resistance mechanisms and/or virulence factors. Medicinal aromatic plants have emerged as promising alternative sources. This study investigated the antimicrobial, antibiofilm, and antihemolysis properties of three different chemotypes of Lippia origanoides essential oil (EO) against susceptible and drug-resistant S. aureus strains. The chemical composition of the EO was analyzed using GC-MS, revealing high monoterpene concentrations, with carvacrol and thymol as the major components in two of the chemotypes. The third chemotype consisted mainly of the sesquiterpene β-caryophyllene. The MIC values for the two monoterpene chemotypes ranged from 62.5 to 500 µg/mL for all strains, whereas the sesquiterpene chemotype showed activity against seven strains at concentrations of 125-500 µg/mL, which is the first report of its anti-S. aureus activity. The phenolic chemotypes inhibited biofilm formation in seven S. aureus strains, whereas the sesquiterpene chemotype only inhibited biofilm formation in four strains. In addition, phenolic chemotypes displayed antihemolysis activity, with IC50 values ranging from 58.9 ± 3.8 to 128.3 ± 9.2 µg/mL. Our study highlights the importance of L. origanoides EO from the Yucatan Peninsula, which has the potential for the development of anti-S. aureus agents.
Insights
Essential oils from Lippia origanoides, particularly phenolic chemotypes rich in carvacrol and thymol, show significant antimicrobial, antibiofilm, and antihemolysis activity against Staphylococcus aureus, including resistant strains.
Area of Science:
- Phytochemistry
- Microbiology
- Natural Product Chemistry
Background:
- Staphylococcus aureus infections, including methicillin-resistant strains (MRSA), pose a significant public health threat due to biofilm formation and antibiotic resistance.
- The limited efficacy of current antibiotics necessitates the exploration of novel therapeutic strategies targeting virulence factors and resistance mechanisms.
- Medicinal aromatic plants offer a promising avenue for discovering new antimicrobial agents.
Purpose of the Study:
- To evaluate the antimicrobial, antibiofilm, and antihemolysis properties of three Lippia origanoides essential oil (EO) chemotypes against susceptible and resistant S. aureus strains.
- To characterize the chemical composition of the L. origanoides EOs.
Main Methods:
- Gas Chromatography-Mass Spectrometry (GC-MS) was used for EO chemical composition analysis.
- Minimum Inhibitory Concentration (MIC) assays determined antimicrobial activity.
- Biofilm inhibition assays and antihemolysis assays were conducted to assess virulence factor inhibition.
Main Results:
- Two phenolic chemotypes, rich in carvacrol and thymol, exhibited potent antimicrobial activity (MIC 62.5–500 µg/mL) and inhibited biofilm formation in S. aureus strains.
- The sesquiterpene-rich chemotype (β-caryophyllene) demonstrated novel anti-S. aureus activity (MIC 125–500 µg/mL) and moderate biofilm inhibition.
- Phenolic chemotypes displayed significant antihemolysis activity (IC50 58.9–128.3 µg/mL).
Conclusions:
- Lippia origanoides essential oil, particularly its phenolic chemotypes, possesses significant potential as a source for developing novel anti-S. aureus agents.
- The study highlights the importance of chemotype variation in L. origanoides for therapeutic applications against S. aureus infections.
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