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Rifamycin O, An Alternative Anti-Mycobacterium abscessus Agent

Mycobacterium abscessus is the most difficult-to-treat nontuberculous mycobacteria because of its resistance to many antibiotics. In this study, we screened the Korea Chemical Bank library for a bioluminescent reporter assay to identify molecules capable of acting against M. abscessus. On applicatio...

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Autores principales: Hanh, Bui Thi Bich, Park, June-Woo, Kim, Tae Ho, Kim, Jae-Sung, Yang, Chul-Su, Jang, Kiseok, Cui, Jinsheng, Oh, Dong-Chan, Jang, Jichan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7181020/
https://www.ncbi.nlm.nih.gov/pubmed/32244387
http://dx.doi.org/10.3390/molecules25071597
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author Hanh, Bui Thi Bich
Park, June-Woo
Kim, Tae Ho
Kim, Jae-Sung
Yang, Chul-Su
Jang, Kiseok
Cui, Jinsheng
Oh, Dong-Chan
Jang, Jichan
author_facet Hanh, Bui Thi Bich
Park, June-Woo
Kim, Tae Ho
Kim, Jae-Sung
Yang, Chul-Su
Jang, Kiseok
Cui, Jinsheng
Oh, Dong-Chan
Jang, Jichan
author_sort Hanh, Bui Thi Bich
collection PubMed
description Mycobacterium abscessus is the most difficult-to-treat nontuberculous mycobacteria because of its resistance to many antibiotics. In this study, we screened the Korea Chemical Bank library for a bioluminescent reporter assay to identify molecules capable of acting against M. abscessus. On application of the assay, rifamycin O showed excellent in vitro activity with a narrow range of the minimum inhibitory concentration required to inhibit the growth of 90% of the bacterium (MIC(90) = 4.0–6.2 μM); its in vivo efficacy in the zebrafish (Danio rerio) infection model was comparable to that of rifabutin at 25 μM. Furthermore, rifamycin O did not show significant toxicity in cells and the zebrafish model. These results are the first in vivo indication that rifamycin O may be a drug candidate for treating M. abscessus infections.
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spelling pubmed-71810202020-04-30 Rifamycin O, An Alternative Anti-Mycobacterium abscessus Agent Hanh, Bui Thi Bich Park, June-Woo Kim, Tae Ho Kim, Jae-Sung Yang, Chul-Su Jang, Kiseok Cui, Jinsheng Oh, Dong-Chan Jang, Jichan Molecules Article Mycobacterium abscessus is the most difficult-to-treat nontuberculous mycobacteria because of its resistance to many antibiotics. In this study, we screened the Korea Chemical Bank library for a bioluminescent reporter assay to identify molecules capable of acting against M. abscessus. On application of the assay, rifamycin O showed excellent in vitro activity with a narrow range of the minimum inhibitory concentration required to inhibit the growth of 90% of the bacterium (MIC(90) = 4.0–6.2 μM); its in vivo efficacy in the zebrafish (Danio rerio) infection model was comparable to that of rifabutin at 25 μM. Furthermore, rifamycin O did not show significant toxicity in cells and the zebrafish model. These results are the first in vivo indication that rifamycin O may be a drug candidate for treating M. abscessus infections. MDPI 2020-03-31 /pmc/articles/PMC7181020/ /pubmed/32244387 http://dx.doi.org/10.3390/molecules25071597 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hanh, Bui Thi Bich
Park, June-Woo
Kim, Tae Ho
Kim, Jae-Sung
Yang, Chul-Su
Jang, Kiseok
Cui, Jinsheng
Oh, Dong-Chan
Jang, Jichan
Rifamycin O, An Alternative Anti-Mycobacterium abscessus Agent
title Rifamycin O, An Alternative Anti-Mycobacterium abscessus Agent
title_full Rifamycin O, An Alternative Anti-Mycobacterium abscessus Agent
title_fullStr Rifamycin O, An Alternative Anti-Mycobacterium abscessus Agent
title_full_unstemmed Rifamycin O, An Alternative Anti-Mycobacterium abscessus Agent
title_short Rifamycin O, An Alternative Anti-Mycobacterium abscessus Agent
title_sort rifamycin o, an alternative anti-mycobacterium abscessus agent
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7181020/
https://www.ncbi.nlm.nih.gov/pubmed/32244387
http://dx.doi.org/10.3390/molecules25071597
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