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Antimicrobial Effect of Asiatic Acid Against Clostridium difficile Is Associated With Disruption of Membrane Permeability
Antibiotic resistance is a major concern in Clostridium difficile, the causative agent of antibiotic-associated diarrhea. Reduced susceptibility to first- and second-line agents is widespread, therefore various attempts have been made to seek alternative preventive and therapeutic strategies against...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6137100/ https://www.ncbi.nlm.nih.gov/pubmed/30245677 http://dx.doi.org/10.3389/fmicb.2018.02125 |
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author | Harnvoravongchai, Phurt Chankhamhaengdecha, Surang Ounjai, Puey Singhakaew, Sombat Boonthaworn, Kanpong Janvilisri, Tavan |
author_facet | Harnvoravongchai, Phurt Chankhamhaengdecha, Surang Ounjai, Puey Singhakaew, Sombat Boonthaworn, Kanpong Janvilisri, Tavan |
author_sort | Harnvoravongchai, Phurt |
collection | PubMed |
description | Antibiotic resistance is a major concern in Clostridium difficile, the causative agent of antibiotic-associated diarrhea. Reduced susceptibility to first- and second-line agents is widespread, therefore various attempts have been made to seek alternative preventive and therapeutic strategies against this pathogen. In this work, the antimicrobial properties of asiatic acid were evaluated against C. difficile. Asiatic acid displayed substantial inhibitory effects on 19 C. difficile isolates collected from different sources with minimal inhibitory concentrations ranging from 10 to 20 μg/ml. Time kill analysis and minimal bactericidal concentration revealed potential bactericidal activity of this compound. Asiatic acid induced membrane damages and alterations in morphological ultrastructure in C. difficile, thereby causing the leakage of intracellular substances. Moreover, asiatic acid also displayed an inhibitory effect on cell motility, but did not interfere with biofilm formation and spore germination. Analysis of drug combination showed no synergistic effect between asiatic acid and vancomycin/metronidazole. Altogether, asiatic acid exhibited strong antimicrobial activity against vegetative cells and could serve as an alternative resource for tackling C. difficile. |
format | Online Article Text |
id | pubmed-6137100 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61371002018-09-21 Antimicrobial Effect of Asiatic Acid Against Clostridium difficile Is Associated With Disruption of Membrane Permeability Harnvoravongchai, Phurt Chankhamhaengdecha, Surang Ounjai, Puey Singhakaew, Sombat Boonthaworn, Kanpong Janvilisri, Tavan Front Microbiol Microbiology Antibiotic resistance is a major concern in Clostridium difficile, the causative agent of antibiotic-associated diarrhea. Reduced susceptibility to first- and second-line agents is widespread, therefore various attempts have been made to seek alternative preventive and therapeutic strategies against this pathogen. In this work, the antimicrobial properties of asiatic acid were evaluated against C. difficile. Asiatic acid displayed substantial inhibitory effects on 19 C. difficile isolates collected from different sources with minimal inhibitory concentrations ranging from 10 to 20 μg/ml. Time kill analysis and minimal bactericidal concentration revealed potential bactericidal activity of this compound. Asiatic acid induced membrane damages and alterations in morphological ultrastructure in C. difficile, thereby causing the leakage of intracellular substances. Moreover, asiatic acid also displayed an inhibitory effect on cell motility, but did not interfere with biofilm formation and spore germination. Analysis of drug combination showed no synergistic effect between asiatic acid and vancomycin/metronidazole. Altogether, asiatic acid exhibited strong antimicrobial activity against vegetative cells and could serve as an alternative resource for tackling C. difficile. Frontiers Media S.A. 2018-09-07 /pmc/articles/PMC6137100/ /pubmed/30245677 http://dx.doi.org/10.3389/fmicb.2018.02125 Text en Copyright © 2018 Harnvoravongchai, Chankhamhaengdecha, Ounjai, Singhakaew, Boonthaworn and Janvilisri. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Harnvoravongchai, Phurt Chankhamhaengdecha, Surang Ounjai, Puey Singhakaew, Sombat Boonthaworn, Kanpong Janvilisri, Tavan Antimicrobial Effect of Asiatic Acid Against Clostridium difficile Is Associated With Disruption of Membrane Permeability |
title | Antimicrobial Effect of Asiatic Acid Against Clostridium difficile Is Associated With Disruption of Membrane Permeability |
title_full | Antimicrobial Effect of Asiatic Acid Against Clostridium difficile Is Associated With Disruption of Membrane Permeability |
title_fullStr | Antimicrobial Effect of Asiatic Acid Against Clostridium difficile Is Associated With Disruption of Membrane Permeability |
title_full_unstemmed | Antimicrobial Effect of Asiatic Acid Against Clostridium difficile Is Associated With Disruption of Membrane Permeability |
title_short | Antimicrobial Effect of Asiatic Acid Against Clostridium difficile Is Associated With Disruption of Membrane Permeability |
title_sort | antimicrobial effect of asiatic acid against clostridium difficile is associated with disruption of membrane permeability |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6137100/ https://www.ncbi.nlm.nih.gov/pubmed/30245677 http://dx.doi.org/10.3389/fmicb.2018.02125 |
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