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Susceptibility of Selected Multi-Drug Resistant Clinical Isolates to Leaves of Carpolobia lutea

BACKGROUND: The decline in the production of new effective antibiotics coupled with the constantly evolving antimicrobial resistance remains a public health concern. This study thus evaluated the antibacterial and antifungal effects of the ethanolic, n-hexane and hot aqueous extracts of Carpolobialu...

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Autores principales: Anibijuwon, Ibikunle, Gbala, Ifeoluwa, Abioye, Jumai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research and Publications Office of Jimma University 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6016348/
https://www.ncbi.nlm.nih.gov/pubmed/29983509
http://dx.doi.org/10.4314/ejhs.v28i2.3
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author Anibijuwon, Ibikunle
Gbala, Ifeoluwa
Abioye, Jumai
author_facet Anibijuwon, Ibikunle
Gbala, Ifeoluwa
Abioye, Jumai
author_sort Anibijuwon, Ibikunle
collection PubMed
description BACKGROUND: The decline in the production of new effective antibiotics coupled with the constantly evolving antimicrobial resistance remains a public health concern. This study thus evaluated the antibacterial and antifungal effects of the ethanolic, n-hexane and hot aqueous extracts of Carpolobialutea leaves. METHODS: The extracts were tested using agar well diffusion method against selected clinical isolates: Pseudomonas aeruginosa, Salmonella typhi, Escherichia coli, Staphylococcus aureus and Candida albicans. Antibiogram profile of the isolates were deduced by disc diffusion method. RESULTS: Multi-drug resistance was confirmed in all bacteria with a notable pandrug resistance in Pseudomonas aeruginosa. Ofloxacin, Erythromycin and Gentamicin were effective on two or three organisms, notably on Salmonella typhi and Escherichia coli. The preliminary antibacterial assay marked the efficacy of the ethanol and n-hexane extracts except on E. coli, with zero activity for hot water extracts at the stock concentration (200 mg/ml). Pseudomonas aeruginosaand Candida albicans were susceptible to lesser concentrations of the ethanol extracts at 5 mg/ml and 25 mg/ml respectively. None of the isolates showed sensitivity to lesser concentrations of n-hexane extract. Carpolobia lutea leaves proved to be effective over the use of antibiotics in inhibiting the activity of Pseudomonas aeruginosa which was resistant to the latter. The Minimum Inhibitory concentration of the ethanolic extract was considerably low (≤5mg/ml for P. aeruginosa and 25mg/ml for C. albicans). However, there was no Minimum Bactericidal concentration for the extracts against the clinical isolates. CONCLUSION: Carpolobia lutea shelters bioactive components with pharmacological potentials that could show efficiency in the treatment of bacterial infections.
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spelling pubmed-60163482018-07-06 Susceptibility of Selected Multi-Drug Resistant Clinical Isolates to Leaves of Carpolobia lutea Anibijuwon, Ibikunle Gbala, Ifeoluwa Abioye, Jumai Ethiop J Health Sci Original Article BACKGROUND: The decline in the production of new effective antibiotics coupled with the constantly evolving antimicrobial resistance remains a public health concern. This study thus evaluated the antibacterial and antifungal effects of the ethanolic, n-hexane and hot aqueous extracts of Carpolobialutea leaves. METHODS: The extracts were tested using agar well diffusion method against selected clinical isolates: Pseudomonas aeruginosa, Salmonella typhi, Escherichia coli, Staphylococcus aureus and Candida albicans. Antibiogram profile of the isolates were deduced by disc diffusion method. RESULTS: Multi-drug resistance was confirmed in all bacteria with a notable pandrug resistance in Pseudomonas aeruginosa. Ofloxacin, Erythromycin and Gentamicin were effective on two or three organisms, notably on Salmonella typhi and Escherichia coli. The preliminary antibacterial assay marked the efficacy of the ethanol and n-hexane extracts except on E. coli, with zero activity for hot water extracts at the stock concentration (200 mg/ml). Pseudomonas aeruginosaand Candida albicans were susceptible to lesser concentrations of the ethanol extracts at 5 mg/ml and 25 mg/ml respectively. None of the isolates showed sensitivity to lesser concentrations of n-hexane extract. Carpolobia lutea leaves proved to be effective over the use of antibiotics in inhibiting the activity of Pseudomonas aeruginosa which was resistant to the latter. The Minimum Inhibitory concentration of the ethanolic extract was considerably low (≤5mg/ml for P. aeruginosa and 25mg/ml for C. albicans). However, there was no Minimum Bactericidal concentration for the extracts against the clinical isolates. CONCLUSION: Carpolobia lutea shelters bioactive components with pharmacological potentials that could show efficiency in the treatment of bacterial infections. Research and Publications Office of Jimma University 2018-03 /pmc/articles/PMC6016348/ /pubmed/29983509 http://dx.doi.org/10.4314/ejhs.v28i2.3 Text en © 2018 Anibijuwon, et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Original Article
Anibijuwon, Ibikunle
Gbala, Ifeoluwa
Abioye, Jumai
Susceptibility of Selected Multi-Drug Resistant Clinical Isolates to Leaves of Carpolobia lutea
title Susceptibility of Selected Multi-Drug Resistant Clinical Isolates to Leaves of Carpolobia lutea
title_full Susceptibility of Selected Multi-Drug Resistant Clinical Isolates to Leaves of Carpolobia lutea
title_fullStr Susceptibility of Selected Multi-Drug Resistant Clinical Isolates to Leaves of Carpolobia lutea
title_full_unstemmed Susceptibility of Selected Multi-Drug Resistant Clinical Isolates to Leaves of Carpolobia lutea
title_short Susceptibility of Selected Multi-Drug Resistant Clinical Isolates to Leaves of Carpolobia lutea
title_sort susceptibility of selected multi-drug resistant clinical isolates to leaves of carpolobia lutea
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6016348/
https://www.ncbi.nlm.nih.gov/pubmed/29983509
http://dx.doi.org/10.4314/ejhs.v28i2.3
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