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Bioactive extracts of Carum copticum L. enhances efficacy of ciprofloxacin against MDR enteric bacteria

The widespread occurrence of extended spectrum β-lactamases (ESβLs) producing enteric bacteria and their co-resistance with flouroquinolones has impaired the current antimicrobial therapy. This has prompted the search for new alternatives through synergistic approaches with herbal extracts. In this...

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Autores principales: Maheshwari, Meenu, Safar Althubiani, Abdullah, Hasan Abulreesh, Hussein, Abul Qais, Faizan, Shavez Khan, Mohd, Ahmad, Iqbal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6864163/
https://www.ncbi.nlm.nih.gov/pubmed/31762667
http://dx.doi.org/10.1016/j.sjbs.2017.12.008
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author Maheshwari, Meenu
Safar Althubiani, Abdullah
Hasan Abulreesh, Hussein
Abul Qais, Faizan
Shavez Khan, Mohd
Ahmad, Iqbal
author_facet Maheshwari, Meenu
Safar Althubiani, Abdullah
Hasan Abulreesh, Hussein
Abul Qais, Faizan
Shavez Khan, Mohd
Ahmad, Iqbal
author_sort Maheshwari, Meenu
collection PubMed
description The widespread occurrence of extended spectrum β-lactamases (ESβLs) producing enteric bacteria and their co-resistance with flouroquinolones has impaired the current antimicrobial therapy. This has prompted the search for new alternatives through synergistic approaches with herbal extracts. In this study Carum copticum (seeds) was extracted first in methanol and then subsequently extracted in different organic solvents. MIC of plant extracts, ciprofloxacin and thymol was determined by broth micro-dilution method using TTC. Synergism between plant extracts and ciprofloxacin was assayed by the checkerboard method. Chemical constituents of active extracts were analyzed by GC-MS. Methanolic, hexane and ether extract of Carum copticum exhibited significant antibacterial activity with MIC values ranged from 0.25 mg/ml to 2.0 mg/ml. Synergy analysis between Carum copticum extracts and ciprofloxacin combinations revealed FIC index in the range of 0.093–0.25. About 81% ciprofloxacin resistant ESβL producing enteric bacteria were re-sensitized in the presence of 15.6–250 μg/ml of methanolic extract of Carum copticum. Moreover, ciprofloxacin showed 8 to 64 folds reduction in MIC in presence of 250 and 500 μg/ml of hexane extract. Whereas, 4–32 folds reduction in MIC of ciprofloxacin was achieved in the presence of 31.25 and 62.5 μg/ml of ether extract, indicating synergistic enhancement of drug activity. The chemical analysis of hexane and ether extracts by GC-MS revealed the common occurrence of one or more phenolic hydroxyl at different locations on benzene ring. This study demonstrated the potential use of herbal extract of Carum copticum in combination therapy against ESβL producing bacteria.
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spelling pubmed-68641632019-11-22 Bioactive extracts of Carum copticum L. enhances efficacy of ciprofloxacin against MDR enteric bacteria Maheshwari, Meenu Safar Althubiani, Abdullah Hasan Abulreesh, Hussein Abul Qais, Faizan Shavez Khan, Mohd Ahmad, Iqbal Saudi J Biol Sci Article The widespread occurrence of extended spectrum β-lactamases (ESβLs) producing enteric bacteria and their co-resistance with flouroquinolones has impaired the current antimicrobial therapy. This has prompted the search for new alternatives through synergistic approaches with herbal extracts. In this study Carum copticum (seeds) was extracted first in methanol and then subsequently extracted in different organic solvents. MIC of plant extracts, ciprofloxacin and thymol was determined by broth micro-dilution method using TTC. Synergism between plant extracts and ciprofloxacin was assayed by the checkerboard method. Chemical constituents of active extracts were analyzed by GC-MS. Methanolic, hexane and ether extract of Carum copticum exhibited significant antibacterial activity with MIC values ranged from 0.25 mg/ml to 2.0 mg/ml. Synergy analysis between Carum copticum extracts and ciprofloxacin combinations revealed FIC index in the range of 0.093–0.25. About 81% ciprofloxacin resistant ESβL producing enteric bacteria were re-sensitized in the presence of 15.6–250 μg/ml of methanolic extract of Carum copticum. Moreover, ciprofloxacin showed 8 to 64 folds reduction in MIC in presence of 250 and 500 μg/ml of hexane extract. Whereas, 4–32 folds reduction in MIC of ciprofloxacin was achieved in the presence of 31.25 and 62.5 μg/ml of ether extract, indicating synergistic enhancement of drug activity. The chemical analysis of hexane and ether extracts by GC-MS revealed the common occurrence of one or more phenolic hydroxyl at different locations on benzene ring. This study demonstrated the potential use of herbal extract of Carum copticum in combination therapy against ESβL producing bacteria. Elsevier 2019-11 2017-12-22 /pmc/articles/PMC6864163/ /pubmed/31762667 http://dx.doi.org/10.1016/j.sjbs.2017.12.008 Text en © 2017 King Saud University http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Maheshwari, Meenu
Safar Althubiani, Abdullah
Hasan Abulreesh, Hussein
Abul Qais, Faizan
Shavez Khan, Mohd
Ahmad, Iqbal
Bioactive extracts of Carum copticum L. enhances efficacy of ciprofloxacin against MDR enteric bacteria
title Bioactive extracts of Carum copticum L. enhances efficacy of ciprofloxacin against MDR enteric bacteria
title_full Bioactive extracts of Carum copticum L. enhances efficacy of ciprofloxacin against MDR enteric bacteria
title_fullStr Bioactive extracts of Carum copticum L. enhances efficacy of ciprofloxacin against MDR enteric bacteria
title_full_unstemmed Bioactive extracts of Carum copticum L. enhances efficacy of ciprofloxacin against MDR enteric bacteria
title_short Bioactive extracts of Carum copticum L. enhances efficacy of ciprofloxacin against MDR enteric bacteria
title_sort bioactive extracts of carum copticum l. enhances efficacy of ciprofloxacin against mdr enteric bacteria
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6864163/
https://www.ncbi.nlm.nih.gov/pubmed/31762667
http://dx.doi.org/10.1016/j.sjbs.2017.12.008
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