Emeka John Dingwoke1
,
Fatima Adis Adamude2,
Ikenna Ezeaku3,
Kingsley Onyekachi Moh4,
Judith Chinelo Amailo1,
Maryann Chidimma Enemmuo1,
Chukwuemeka Paul Nweje-Anyalowu5, 6,
Raymond Ogbonna Offiah7,
Chijioke Cyril Ilechukwu8,
Bruno Ikenna Aguh9,
Abdulhadi Abubakar10,
Adaora Chinemelum Onodugo11,
Onyemuche Tochukwu Nnamdi12
For correspondence:- Emeka Dingwoke Email: emeka.jd@unescoicb.org.ng
Received: 4 March 2025 Accepted: 12 June 2025 Published: 03 July 2025
Citation: Dingwoke EJ, Adamude FA, Ezeaku I, Moh KO, Amailo JC, Enemmuo MC, et al. Terminalia avicennioides root bark extract: A promising phytotherapeutic agent against methicillin-resistant Staphylococcus aureus hospital strains. Trop J Pharm Res 2025; 24(6):779-786 doi: https://dx.doi.org/10.4314/tjpr.v24i6.4
© 2025 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..
Purpose: To investigate the antibacterial activity of a partially purified ethyl acetate fraction obtained from methanol
extract of the root bark of Terminalia avicennioides (Family: Combretaceae) against a hospital strain of methicillinresistant
Staphylococcus aureus (MRSA).
Methods: Gas chromatography-mass spectrometry (GC-MS) was used to identify and characterize compounds in
the bioactive fraction of T. avicennioides root bark, while Fourier Transform Infrared (FTIR) spectroscopy was used to
elucidate the functional groups. The MRSA hospital strain was isolated from a clinical sample and the isolate
biochemically characterized by colonial morphology, Gram staining, and strain reaction. Resistance to
methicillin/oxacillin was confirmed by repeat susceptibility testing using oxacillin. The antibacterial efficacy of the
fraction was compared with those of standard antibiotics including meropenem, amoxiclav, nitrofurantoin, ceftriaxone,
nidof, and ciprofloxacin. Antimicrobial activity was evaluated using agar well diffusion method, while the minimum
inhibitory concentration (MIC) was determined using a 10-fold serial broth dilution assay.
Results: Mass spectrometry analysis revealed that the ethyl acetate fraction with anti-MRSA activity comprised a
mixture of seven compounds in varying proportions, viz: n-hexadecanoic acid, 11-octadecenoic acid, oleic acid,
octadecanoic acid, 3,11-tetradecadien-1-ol, 9-octadecenal, and (9Z)-9-tetradecenal. The FTIR spectra indicated the
presence of alkyl halides. At 100 μg/mL, the ethyl acetate fraction exhibited a bacteriostatic effect, with a minimum
bactericidal concentration (MBC) of 9.48 ± 0.90 μg/mL. Based on Kirby-Bauer standard, it demonstrated bactericidal
activity (MBC) at 150 μg/mL, with mean inhibition zone diameter of 14 mm.
Conclusion: The synergistic action of the seven identified compounds in the bioactive fraction may offer a promising
foundation for developing novel drug candidates with potent bactericidal activity against hospital-acquired MRSA
strains.