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Repositioning of 8-hydroxyquinoline derivatives as a new promising candidate for combating multidrug resistant Neisseria gonorrhoeae

The multidrug resistance of Neisseria gonorrhoeae becomes a public health problem worldwide, especially the strain H041 that showed the decrease susceptibility to ceftriaxone which is the last resort for gonorrhea treatment. Therefore, the simultaneous discovery and development of a new compound to...

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Autores principales: Lawung, Ratana, Cherdtrakulkiat, Rungrot, Nabu, Sunanta, Prachayasittikul, Supaluk, Isarankura-Na-Ayudhya, Chartchalerm, Prachayasittikul, Virapong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Leibniz Research Centre for Working Environment and Human Factors 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6141828/
https://www.ncbi.nlm.nih.gov/pubmed/30233282
http://dx.doi.org/10.17179/excli2018-1602
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author Lawung, Ratana
Cherdtrakulkiat, Rungrot
Nabu, Sunanta
Prachayasittikul, Supaluk
Isarankura-Na-Ayudhya, Chartchalerm
Prachayasittikul, Virapong
author_facet Lawung, Ratana
Cherdtrakulkiat, Rungrot
Nabu, Sunanta
Prachayasittikul, Supaluk
Isarankura-Na-Ayudhya, Chartchalerm
Prachayasittikul, Virapong
author_sort Lawung, Ratana
collection PubMed
description The multidrug resistance of Neisseria gonorrhoeae becomes a public health problem worldwide, especially the strain H041 that showed the decrease susceptibility to ceftriaxone which is the last resort for gonorrhea treatment. Therefore, the simultaneous discovery and development of a new compound to fight this pathogen is urgently required. In this study, 8-hydroxyquinoline (8HQ) and derivatives were evaluated for their antimicrobial activities against the gonococcal pathogen using spectinomycin as the reference drug. The results showed that 8HQ derivatives gave an excellent antimicrobial potency. Particularly, the dihalogenated 8HQ (iodoquinol, clioquinol and 5,7-diCl-8HQ) exerted the high activity with MIC range of 0.08-0.15 μM, 0.10-0.20 μM and 0.28-0.56 µM, respectively, compared with the reference drug (MIC = 16 μg/mL or 48.14 μM). Moreover, these compounds were also shown to be non-cytotoxic/very high safety index. The findings reveal that these three compounds could be further developed as a new antimicrobial agent for fighting the gonorrheal disease.
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spelling pubmed-61418282018-09-19 Repositioning of 8-hydroxyquinoline derivatives as a new promising candidate for combating multidrug resistant Neisseria gonorrhoeae Lawung, Ratana Cherdtrakulkiat, Rungrot Nabu, Sunanta Prachayasittikul, Supaluk Isarankura-Na-Ayudhya, Chartchalerm Prachayasittikul, Virapong EXCLI J Original Article The multidrug resistance of Neisseria gonorrhoeae becomes a public health problem worldwide, especially the strain H041 that showed the decrease susceptibility to ceftriaxone which is the last resort for gonorrhea treatment. Therefore, the simultaneous discovery and development of a new compound to fight this pathogen is urgently required. In this study, 8-hydroxyquinoline (8HQ) and derivatives were evaluated for their antimicrobial activities against the gonococcal pathogen using spectinomycin as the reference drug. The results showed that 8HQ derivatives gave an excellent antimicrobial potency. Particularly, the dihalogenated 8HQ (iodoquinol, clioquinol and 5,7-diCl-8HQ) exerted the high activity with MIC range of 0.08-0.15 μM, 0.10-0.20 μM and 0.28-0.56 µM, respectively, compared with the reference drug (MIC = 16 μg/mL or 48.14 μM). Moreover, these compounds were also shown to be non-cytotoxic/very high safety index. The findings reveal that these three compounds could be further developed as a new antimicrobial agent for fighting the gonorrheal disease. Leibniz Research Centre for Working Environment and Human Factors 2018-08-23 /pmc/articles/PMC6141828/ /pubmed/30233282 http://dx.doi.org/10.17179/excli2018-1602 Text en Copyright © 2018 Lawung et al. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (http://creativecommons.org/licenses/by/4.0/) You are free to copy, distribute and transmit the work, provided the original author and source are credited.
spellingShingle Original Article
Lawung, Ratana
Cherdtrakulkiat, Rungrot
Nabu, Sunanta
Prachayasittikul, Supaluk
Isarankura-Na-Ayudhya, Chartchalerm
Prachayasittikul, Virapong
Repositioning of 8-hydroxyquinoline derivatives as a new promising candidate for combating multidrug resistant Neisseria gonorrhoeae
title Repositioning of 8-hydroxyquinoline derivatives as a new promising candidate for combating multidrug resistant Neisseria gonorrhoeae
title_full Repositioning of 8-hydroxyquinoline derivatives as a new promising candidate for combating multidrug resistant Neisseria gonorrhoeae
title_fullStr Repositioning of 8-hydroxyquinoline derivatives as a new promising candidate for combating multidrug resistant Neisseria gonorrhoeae
title_full_unstemmed Repositioning of 8-hydroxyquinoline derivatives as a new promising candidate for combating multidrug resistant Neisseria gonorrhoeae
title_short Repositioning of 8-hydroxyquinoline derivatives as a new promising candidate for combating multidrug resistant Neisseria gonorrhoeae
title_sort repositioning of 8-hydroxyquinoline derivatives as a new promising candidate for combating multidrug resistant neisseria gonorrhoeae
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6141828/
https://www.ncbi.nlm.nih.gov/pubmed/30233282
http://dx.doi.org/10.17179/excli2018-1602
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