Original ArticlePharmacognosy CommunicationsVol. 14 | Issue 1 | 2024 | pp. 24–33Open access
Taraxacum officinale (L.) Weber ex F.H.Wigg Root Extracts Inhibit the Growth Gastrointestinal Bacterial Pathogens and Potentiate the Activity of Conventional Antibiotics
- 1,
- 1,2*
- 1 School of Environment and Science, Nathan Campus, Griffith University, Brisbane, AUSTRALIA.
- 2 Centre for Planetary Health and Food Security, Nathan Campus, Griffith University, Brisbane, AUSTRALIA.
Published in Pharmacognosy Communications
Correspondence: Ian Edwin Cock
School of Environment and Science, Nathan Campus, Griffith University, Brisbane, AUSTRALIA.; Centre for Planetary Health and Food Security, Nathan Campus, Griffith University, Brisbane, AUSTRALIA.
Email: i.cock@griffith.edu.au
Copyright: © 2024 Manuscript Technomedia. This is an open access article.
- Published:
- Feb 10, 2024
- Received:
- Oct 25, 2023
- Accepted:
- Dec 18, 2023
- DOI:
- 10.5530/pc.2024.1.4
How to cite
Jiang, Y., & Cock, I. E. (2024). Taraxacum officinale (L.) Weber ex F.H.Wigg Root Extracts Inhibit the Growth Gastrointestinal Bacterial Pathogens and Potentiate the Activity of Conventional Antibiotics. Pharmacognosy Communications, 14(1), 24–33. https://doi.org/10.5530/pc.2024.1.4
Abstract
Introduction: An increase in antibiotic resistance and a corresponding decrease in antimicrobial discovery have directed researchers towards alternative therapies, including plant-based medicines. However, synergistic combinations of plant extracts with conventional antibiotics may be a far more effective approach in overcoming resistance and potentiating the activity of antibiotics that are otherwise ineffective against resistant bacterial strains. Materials and Methods: The antibacterial activity of Taraxacum officinale (L.) Weber ex F.H. Wigg root extracts was investigated by disc diffusion assays and quantified by liquid dilution and solid phase MIC assays. The extracts were also combined with a range of conventional antibiotics and tested against gastrointestinal disease-causing bacteria. The ΣFIC values obtained from these assays were used to determine the class of combinational effects. Toxicity was evaluated by Artemia nauplii mortality and HDF cytotoxicity assays. Results: Methanolic, aqueous and ethyl acetate T. officinale root extracts showed good inhibitory activity against several gastrointestinal bacterial pathogens. The methanolic were particularly good inhibitors of S. sonneii and S. newport, with MIC values in the range 400-450 μg/mL, whilst the ethyl acetate extract was the most potent inhibitor of S. newport growth (MIC=128 μg/mL). Of further interest, some combinations of the T. officinale root extracts and conventional antibiotics potentiated bacterial growth inhibition compared to the individual components. Five synergistic and two additive interactions were noted. Interestingly, only a single antagonistic interaction was evident, indicating that nearly all combinations could be used without decreasing the antibacterial activity of the components. All extracts were nontoxic in the ALA and HDF assays. Conclusion: Taraxacum officinale root extracts have potential as inhibitors of bacterial gastrointestinal pathogens. Furthermore, extract components may also potentiate the activity of some antibiotics that are relatively ineffective alone. Isolation and identification of these compounds may be beneficial in drug design against several gastrointestinal bacterial pathogens.
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Article metadata
| Title | Taraxacum officinale (L.) Weber ex F.H.Wigg Root Extracts Inhibit the Growth Gastrointestinal Bacterial Pathogens and Potentiate the Activity of Conventional Antibiotics |
|---|---|
| Authors | Yixue Jiang; Ian Edwin Cock |
| Affiliations | School of Environment and Science, Nathan Campus, Griffith University, Brisbane, AUSTRALIA.; Centre for Planetary Health and Food Security, Nathan Campus, Griffith University, Brisbane, AUSTRALIA. |
| Corresponding author | i.cock@griffith.edu.au |
| Journal | Pharmacognosy Communications |
| Volume / Issue | Vol. 14, Issue 1 (2024) |
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