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Mansonone G and its derivatives exhibit membrane permeabilizing activities against bacteria

In an era where the rate of bacteria evolving to be resistant to clinically-used antibiotics far exceeds that of antibiotic discovery, the search for new sources of antibacterial agents has expanded tremendously. In recent years, interest in plant-based natural products as promising sources of antib...

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Autores principales: Htoo, Htut Htut, Tuyet, Nhung Ngo Thi, Nakprasit, Kittiporn, Aonbangkhen, Chanat, Chaikeeratisak, Vorrapon, Chavasiri, Warinthorn, Nonejuie, Poochit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9436067/
https://www.ncbi.nlm.nih.gov/pubmed/36048830
http://dx.doi.org/10.1371/journal.pone.0273614
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author Htoo, Htut Htut
Tuyet, Nhung Ngo Thi
Nakprasit, Kittiporn
Aonbangkhen, Chanat
Chaikeeratisak, Vorrapon
Chavasiri, Warinthorn
Nonejuie, Poochit
author_facet Htoo, Htut Htut
Tuyet, Nhung Ngo Thi
Nakprasit, Kittiporn
Aonbangkhen, Chanat
Chaikeeratisak, Vorrapon
Chavasiri, Warinthorn
Nonejuie, Poochit
author_sort Htoo, Htut Htut
collection PubMed
description In an era where the rate of bacteria evolving to be resistant to clinically-used antibiotics far exceeds that of antibiotic discovery, the search for new sources of antibacterial agents has expanded tremendously. In recent years, interest in plant-based natural products as promising sources of antibacterial agents has taken an upward trend. Mansonones, botanically-derived naphthoqionones, having many uses in Asian traditional medicine–including anti-infective roles–have sparked interest as a possible source of antibacterial agents. Here, we show that mansonone G, extracted from Mansonia gagei Drumm. heartwoods, possessed antibacterial activities towards Bacillus subtilis, Staphylococcus aureus and Escherichia coli lptD4213, inhibiting the growth of the bacteria at 15.6 μM, 62.5 μM and 125 μM, respectively. Fourteen derivatives of mansonone G were synthesized successfully and were found to have a similar antibacterial spectrum to that of the parent compound, with some derivatives possessing improved antibacterial activities. Bacterial cytological profiling analysis showed that mansonone G harbors membrane permeabilizing activities against B. subtilis and E. coli lptD4213. Temporal analysis of SYTOX Green staining among individual cells showed that mansonone G rapidly permeabilized bacterial membrane within 10 min, with SYTOX Green intensity reaching 13-fold above that of the control. Collectively, these findings highlight the importance of mansonone G and its derivatives as potential antibacterial agents, paving the way for further modifications in order to improve their antibacterial spectrum.
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spelling pubmed-94360672022-09-02 Mansonone G and its derivatives exhibit membrane permeabilizing activities against bacteria Htoo, Htut Htut Tuyet, Nhung Ngo Thi Nakprasit, Kittiporn Aonbangkhen, Chanat Chaikeeratisak, Vorrapon Chavasiri, Warinthorn Nonejuie, Poochit PLoS One Research Article In an era where the rate of bacteria evolving to be resistant to clinically-used antibiotics far exceeds that of antibiotic discovery, the search for new sources of antibacterial agents has expanded tremendously. In recent years, interest in plant-based natural products as promising sources of antibacterial agents has taken an upward trend. Mansonones, botanically-derived naphthoqionones, having many uses in Asian traditional medicine–including anti-infective roles–have sparked interest as a possible source of antibacterial agents. Here, we show that mansonone G, extracted from Mansonia gagei Drumm. heartwoods, possessed antibacterial activities towards Bacillus subtilis, Staphylococcus aureus and Escherichia coli lptD4213, inhibiting the growth of the bacteria at 15.6 μM, 62.5 μM and 125 μM, respectively. Fourteen derivatives of mansonone G were synthesized successfully and were found to have a similar antibacterial spectrum to that of the parent compound, with some derivatives possessing improved antibacterial activities. Bacterial cytological profiling analysis showed that mansonone G harbors membrane permeabilizing activities against B. subtilis and E. coli lptD4213. Temporal analysis of SYTOX Green staining among individual cells showed that mansonone G rapidly permeabilized bacterial membrane within 10 min, with SYTOX Green intensity reaching 13-fold above that of the control. Collectively, these findings highlight the importance of mansonone G and its derivatives as potential antibacterial agents, paving the way for further modifications in order to improve their antibacterial spectrum. Public Library of Science 2022-09-01 /pmc/articles/PMC9436067/ /pubmed/36048830 http://dx.doi.org/10.1371/journal.pone.0273614 Text en © 2022 Htoo et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Htoo, Htut Htut
Tuyet, Nhung Ngo Thi
Nakprasit, Kittiporn
Aonbangkhen, Chanat
Chaikeeratisak, Vorrapon
Chavasiri, Warinthorn
Nonejuie, Poochit
Mansonone G and its derivatives exhibit membrane permeabilizing activities against bacteria
title Mansonone G and its derivatives exhibit membrane permeabilizing activities against bacteria
title_full Mansonone G and its derivatives exhibit membrane permeabilizing activities against bacteria
title_fullStr Mansonone G and its derivatives exhibit membrane permeabilizing activities against bacteria
title_full_unstemmed Mansonone G and its derivatives exhibit membrane permeabilizing activities against bacteria
title_short Mansonone G and its derivatives exhibit membrane permeabilizing activities against bacteria
title_sort mansonone g and its derivatives exhibit membrane permeabilizing activities against bacteria
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9436067/
https://www.ncbi.nlm.nih.gov/pubmed/36048830
http://dx.doi.org/10.1371/journal.pone.0273614
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