Abstract

Combining antibiotics with resistance reversing agents is a key strategy to overcome bacterial resistance. Upon screening antimicrobial activities of plants used in traditional medicine, we found that a leaf dichloromethane extract from the shea butter tree (Vitellaria paradoxa) had antimicrobial activity against methicillin-resistant Staphylococcus aureus (MRSA) with further evidence of synergy when combined with β-lactams. Using HPLC-MS, we identified ursolic (UA) and oleanolic acids (OA) in leaves and twigs of this species, and quantified them by HPLC-UV as the major constituents in leaf extracts (21% and 6% respectively). Both pure triterpenic acids showed antimicrobial activity against reference and clinical strains of MRSA, with MICs ranging from 8–16 mg/L for UA to 32–128 mg/L for OA. They were highly synergistic with β-lactams (ampicillin and oxacillin) at subMIC concentrations. Reversion of MRSA phenotype was attributed to their capacity to delocalize PBP2 from the septal division site, as observed by fluorescence microscopy, and to disturb thereby peptidoglycan synthesis. Moreover, both compounds also inhibited β-lactamases activity of living bacteria (as assessed by inhibition of nitrocefin hydrolysis), but not in bacterial lysates, suggesting an indirect mechanism for this inhibition. In a murine model of subcutaneous MRSA infection, local administration of UA was synergistic with nafcillin to reduce lesion size and inflammatory cytokine (IL-1β) production. Thus, these data highlight the potential interest of triterpenic acids as resistance reversing agents in combination with β-lactams against MRSA.

Highlights

  • During a preliminary screening of the direct and indirect antimicrobial activity of plants used in traditional medicine in Benin, we found that a Vitellaria paradoxa (VP) leaf dichloromethane extract showed the best direct and indirect antimicrobial activities with a Minimal Inhibitory Concentration (MIC) = 250 mg/L and fractional inhibitory concentration indices (FICI) = 0.14–1 and 0.51–1 in combination with ampicillin and oxacillin, respectively, against a strain of methicillin-resistant Staphylococcus aureus (MRSA) [10]

  • We further explored the potential mechanism of action underlying this synergistic combination focusing on the potential effect of those compounds on the two principal β-lactam resistance mechanism of MRSA: β-Lactamases and PBP2A

  • At the highest triterpenic acid concentrations tested, a 1.5–2 log10 decrease from initial inoculum was observed for both β-lactams, indicating that the presence of large concentrations of ursolic acid (UA) and OA in the VP leaf extract could explain the previously described direct and indirect antimicrobial activity against MRSA exposed to this extract alone or combined with β-lactams [10]

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Summary

Introduction

We studied the direct and indirect (in combination with β-lactams) antimicrobial activity of the main components of Vitellaria paradoxa (VP) leaf extract against S. aureus and analyzed their potential mechanism of action. We continued our work on the dichloromethane extracts and identified, for the first time in leaves and twigs, oleanolic (OA) and ursolic (UA) acids as bioactive compounds We quantified these two substances in extracts and studied the direct and indirect antimicrobial activities of these pure compounds in combination with β-lactams (ampicillin, oxacillin or nafcillin) on a panel of S. aureus reference strains as well as clinical MRSA isolates. We assessed the effectiveness of the combination of UA and nafcillin using an in vivo murine skin infection model

Results and Discussion
Antimicrobial of the themain
Effect of OA and UA on PBP2 Recruitment to the Septum
Evaluation of β‐Lactamase
Murine Model of Subcutaneous Infection
Antibacterial
Plant Material
Preparation of Extracts
Reference Compounds
UA and OA Identification
UA and OA Quantification
Bacteria Strains
Time-Kill Assay
3.10. Effect of Compounds on PBP2 Localization
3.11. Effect of Compounds on PBP2 and PBP2A Expression
3.12. Evaluation of β-Lactamase Activity using the Nitrocefin Test
3.13. Murine Model of Subcutaneous Infection
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