Cargando…
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...
Autores principales: | , , , , , |
---|---|
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 |
_version_ | 1783355780552982528 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6141828 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Leibniz Research Centre for Working Environment and Human Factors |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT lawungratana repositioningof8hydroxyquinolinederivativesasanewpromisingcandidateforcombatingmultidrugresistantneisseriagonorrhoeae AT cherdtrakulkiatrungrot repositioningof8hydroxyquinolinederivativesasanewpromisingcandidateforcombatingmultidrugresistantneisseriagonorrhoeae AT nabusunanta repositioningof8hydroxyquinolinederivativesasanewpromisingcandidateforcombatingmultidrugresistantneisseriagonorrhoeae AT prachayasittikulsupaluk repositioningof8hydroxyquinolinederivativesasanewpromisingcandidateforcombatingmultidrugresistantneisseriagonorrhoeae AT isarankuranaayudhyachartchalerm repositioningof8hydroxyquinolinederivativesasanewpromisingcandidateforcombatingmultidrugresistantneisseriagonorrhoeae AT prachayasittikulvirapong repositioningof8hydroxyquinolinederivativesasanewpromisingcandidateforcombatingmultidrugresistantneisseriagonorrhoeae |