# Antibacterial Activity of Estragole From Ocimum tenuiflorum, and Tagetes lucida and Synergistic Effect With Meropenem and Tobramycin Against Multidrug‐ and Extensively Drug‐Resistant (MDR‐XDR) Gram‐Negative Bacteria

**Authors:** María Araque, Luis B. Rojas

PMC · DOI: 10.1002/mbo3.70253 · MicrobiologyOpen · 2026-02-23

## TL;DR

Estragole from two plants shows strong antibacterial effects and works well with antibiotics to fight drug-resistant bacteria.

## Contribution

Estragole synergizes with antibiotics against MDR/XDR Gram-negative bacteria, reducing antibiotic doses.

## Key findings

- Estragole has bactericidal activity with MICs ≤ 256 μg/mL against MDR/XDR Gram-negative bacteria.
- Combinations with meropenem and tobramycin showed 16-fold MIC reductions in over 88% of strains.
- Estragole could enhance antibiotic efficacy and reduce side effects in treating resistant infections.

## Abstract

Estragole, a prime compound present in the essential oils (EOs) of Ocimum tenuiflorum and Tagetes lucida, shows significant antimicrobial activity against WHO priority bacterial pathogens. This study evaluated the bactericidal effects of estragole, both in its chemically pure form and when isolated from the EOs of these plants, when used alone and in combination with the antibiotics meropenem and tobramycin against multidrug‐resistant (MDR) and extensively drug‐resistant (XDR) Gram‐negative bacteria. Antibacterial activity was evaluated using the minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) methods. The interaction of estragole with the selected antibiotics was analyzed using the checkerboard method, where the fractional inhibitory concentration index (FICI) was calculated. Results showed that estragole has inherent bactericidal properties, with MICs of no more than 256 μg/mL, indicating significant activity regardless of the bacteria's resistance profile. Combinations with meropenem and tobramycin exhibited pronounced synergy, achieving reductions in the MIC of up to 16‐fold in over 88% of the bacteria tested. An additive or partially synergistic effect was evident in only around 11% of cases. These results highlight the potential of estragole as a therapeutic adjuvant capable of enhancing the efficacy of conventional antibiotics, reducing the required doses and the associated side effects and toxicities. Furthermore, this study emphasizes the beneficial potential of phytochemical‐antibiotic combinations as an innovative strategy to address the growing threat posed by antimicrobial resistance.

This study reveals estragole's bactericidal activity against MDR/XDR Gram‐negative pathogens. Synergy with meropenem and tobramycin was observed in > 88% of strains, reducing antibiotic MICs up to 16‐fold. Estragole represents a promising therapeutic adjuvant to enhance antibiotic efficacy and combat antimicrobial resistance.

## Linked entities

- **Chemicals:** Estragole (PubChem CID 8815), meropenem (PubChem CID 441130), tobramycin (PubChem CID 36294)
- **Species:** Ocimum tenuiflorum (taxon 204149), Tagetes lucida (taxon 169606)

## Full-text entities

- **Genes:** metallo-beta-lactamase [NCBI Gene 11934636], Beta-Lactamase [NCBI Gene 18262323], extended spectrum beta-lactamase [NCBI Gene 13982007], beta-lactamase [NCBI Gene 13913583], AmpC [NCBI Gene 5850688]
- **Diseases:** cytotoxicity (MESH:D064420), XDR (MESH:D054908), Infections (MESH:D007239), death (MESH:D003643), infectious diseases (MESH:D003141), bacterial infections (MESH:D001424), cancer (MESH:D009369), AMR (MESH:D060467), inflammatory (MESH:D007249)
- **Chemicals:** amikacin (MESH:D000583), cephalosporin (MESH:D002511), nitrofurantoin (MESH:D009582), penicillin (MESH:D010406), Tetracycline (MESH:D013752), fosfomycin (MESH:D005578), CLF (-), DMSO (MESH:D004121), chloramphenicol (MESH:D002701), PBS (MESH:D007854), trimethoprim-sulfamethoxazole (MESH:D015662), ampicillin (MESH:D000667), ciprofloxacin (MESH:D002939), beta-cyclodextrin (MESH:C031215), aminoglycoside (MESH:D000617), gentamicin (MESH:D005839), TOB (MESH:D014031), MER (MESH:D000077731), EO (MESH:D009822), carbapenem (MESH:D015780), 4-allylanisole (MESH:C007633)
- **Species:** Homo sapiens (human, species) [taxon 9606], Enterobacter cloacae (species) [taxon 550], Ocimum gratissimum (species) [taxon 204144], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Staphylococcus aureus (species) [taxon 1280], Exiguobacterium sp. TL (species) [taxon 474550], Danio rerio (leopard danio, species) [taxon 7955], Drosophila melanogaster (fruit fly, species) [taxon 7227], Aspergillus (genus) [taxon 5052], Acinetobacter baumannii (species) [taxon 470], Aquipseudomonas alcaligenes (species) [taxon 43263], Klebsiella pneumoniae (species) [taxon 573], Pseudomonas aeruginosa (species) [taxon 287], Ocimum (basils, genus) [taxon 39173], Ocimum tenuiflorum (holy basil, species) [taxon 204149], Escherichia coli (E. coli, species) [taxon 562], Penicillium (genus) [taxon 5073], Enterobacterales (order) [taxon 91347], Enterococcus (genus) [taxon 1350], Tagetes lucida (species) [taxon 169606]
- **Mutations:** A717
- **Cell lines:** LMM-179 — Mus musculus (Mouse), Malignant neoplasms of the mouse mammary gland, Cancer cell line (CVCL_D270)

## Full text

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## Figures

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## References

55 references — full list in the complete paper: https://tomesphere.com/paper/PMC12927992/full.md

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Source: https://tomesphere.com/paper/PMC12927992