From formulation to in vivo model: A comprehensive study of a synergistic relationship between vancomycin, carvacrol and cuminaldehyde against Enterococcus faecium
dc.cclicence | CC-BY-NC | en |
dc.contributor.author | Owen, Lucy | |
dc.contributor.author | Webb, Joseph P. | |
dc.contributor.author | Green, Jeffrey | |
dc.contributor.author | Smith, Laura J. | |
dc.contributor.author | Laird, Katie | |
dc.date.acceptance | 2020-01-21 | |
dc.date.accessioned | 2020-01-23T15:22:41Z | |
dc.date.available | 2020-01-23T15:22:41Z | |
dc.date.issued | 2020-02-11 | |
dc.description | The file attached to this record is the author's final peer reviewed version | en |
dc.description.abstract | Vancomycin Resistant Enterococcus faecium (VRE) has become endemic in healthcare settings, reducing treatment options for enterococcal infections. New antimicrobials for VRE infections are a high priority, but the development of novel antibiotics is time-consuming and expensive. Essential Oils (EOs) synergistically enhance the activity of some existing antibiotics, suggesting that EO-antibiotic combinations could re-sensitise resistant bacteria and maintain the antibiotic repertoire. The mechanism of re-sensitisation of bacteria to antibiotics by EOs is relatively understudied. Here, the synergistic interactions between carvacrol (1.98 mM) and cuminaldehyde (4.20 mM) were shown to re-establish susceptibility to vancomycin (0.031 mg/L) in VRE, resulting in bactericidal activity (4.73 log10 CFU/mL reduction). Gene expression profiling, coupled with β-galactosidase leakage and salt tolerance assays suggested that cell envelope damage contributes to the synergistic bactericidal effect against VRE. The EO-vancomycin combination was also shown to kill clinical isolates of VRE (2.33-5.25 log10 CFU/mL reduction) and stable resistance did not appear to develop even after multiple passages. The in vivo efficacy of the EO-vancomycin combination was tested in a Galleria mellonella larvae assay; however no antimicrobial action was observed, indicating that further drug development is required for the EO-vancomycin combination to be clinically useful for treatment of VRE infections. | en |
dc.funder | No external funder | en |
dc.identifier.citation | Owen, L., Webb, J.P., Green, J., Smith, L.J. and Laird, K. (2020) From formulation to in vivo model: A comprehensive study of a synergistic relationship between vancomycin, carvacrol and cuminaldehyde against Enterococcus faecium. Phytotherapy Research, 34 (7), pp. 1638-1649 | en |
dc.identifier.doi | https://doi.org/10.1002/ptr.6631 | |
dc.identifier.issn | 0951-418X | |
dc.identifier.uri | https://dora.dmu.ac.uk/handle/2086/19056 | |
dc.language.iso | en | en |
dc.peerreviewed | Yes | en |
dc.publisher | Wiley | en |
dc.researchinstitute | Leicester Institute for Pharmaceutical Innovation - From Molecules to Practice (LIPI) | en |
dc.subject | Enterococcus faecium | en |
dc.subject | essential oil | en |
dc.subject | carvacrol | en |
dc.subject | cuminaldehyde | en |
dc.subject | synergy | en |
dc.subject | vancomycin | en |
dc.title | From formulation to in vivo model: A comprehensive study of a synergistic relationship between vancomycin, carvacrol and cuminaldehyde against Enterococcus faecium | en |
dc.type | Article | en |
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