Publication | Open Access
<i>Orthosiphon stamineus</i> protects <i>Caenorhabditis elegans</i> against <i>Staphylococcus aureus</i> infection through immunomodulation
28
Citations
52
References
2014
Year
Drug TargetP38 Map KinaseImmunologyPathogen EffectorChemical BiologyBacterial PathogensCaenorhabditis ElegansS. Aureus InfectionDrug ResistanceMedicinal ChemistrySignaling PathwayInfection ControlAntimicrobial ResistanceHost-pathogen InteractionsPhytoalexinImmune FunctionInfected NematodesAntimicrobial CompoundPharmacologyCell BiologyClinical MicrobiologyNatural SciencesPathogenesisHelminth InfectionMedicineDrug Discovery
Amidst growing concerns over the spread of antibiotic-resistant Staphylococcus aureus strains, the identification of alternative therapeutic molecules has become paramount. Previously, we utilized a Caenorhabditis elegans-S. aureus screening platform to identify potential anti-infective agents from a collection of natural extracts and synthetic compounds. One of the hits obtained from the screen was the aqueous extract of Orthosiphon stamineus leaves (UE-12) that enhanced the survival of infected nematodes without interfering with bacterial growth. In this study, we used a fluorescent transgenic reporter strain and observed that the repressed expression of the lys-7 defense gene in infected nematodes was restored in the presence of UE-12. Analysis of a selected panel of PMK-1 and DAF-16-regulated transcripts and loss-of-function mutants in these pathways indicates that the protective role of UE-12 is mediated via the p38 MAP kinase and insulin-like signaling pathways. Further analysis of a panel of known bioactive compounds of UE-12 proposed eupatorin (C18H16O7) as the possible candidate active molecule contributing to the anti-infective property of UE-12. Taken together, these findings strongly suggest that the O. stamineus leaf extract is a promising anti-infective agent that confers an advantage in survival against S. aureus infection by modulating the immune response of the infected host.
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