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Enniatin A1, A Natural Compound with Bactericidal Activity against Mycobacterium tuberculosis In Vitro
Background: Tuberculosis remains a global disease that poses a serious threat to human health, but there is lack of new and available anti-tuberculosis agents to prevent the emergence of drug-resistant strains. To address this problem natural products are still potential sources for the development...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6982829/ https://www.ncbi.nlm.nih.gov/pubmed/31861925 http://dx.doi.org/10.3390/molecules25010038 |
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author | Wang, Gaoyan Dong, Wenqi Lu, Hao Lu, Wenjia Feng, Jiajia Wang, Xiangru Chen, Huanchun Liu, Manli Tan, Chen |
author_facet | Wang, Gaoyan Dong, Wenqi Lu, Hao Lu, Wenjia Feng, Jiajia Wang, Xiangru Chen, Huanchun Liu, Manli Tan, Chen |
author_sort | Wang, Gaoyan |
collection | PubMed |
description | Background: Tuberculosis remains a global disease that poses a serious threat to human health, but there is lack of new and available anti-tuberculosis agents to prevent the emergence of drug-resistant strains. To address this problem natural products are still potential sources for the development of novel drugs. Methods: A whole-cell screening approach was utilized to obtain a natural compound enniatin A1 from a natural products library. The target compound’s antibacterial activity against Mycobacterium tuberculosis (M. tuberculosis) was evaluated by using the resazurin reduction micro-plate assay (REMA) method. The cytotoxicity of the compound against Vero cells was measured to calculate the selectivity index. The intracellular inhibition activity of enniatin A1 was determined. We performed its time-kill kinetic assay against M. tuberculosis. We first tested its synergistic effect in combination with the first and second-line anti-tuberculosis drugs. Finally, we measured the membrane potential and intracellular ATP levels of M. tuberculosis after exposure to enniatin A1. Results: We identified enniatinA1 as a potential antibacterial agent against M. tuberculosis, against which it showed strong selectivity. Enniatin A1 exhibited a time-concentration-dependent bactericidal effect against M. tuberculosis, and it displayed synergy with rifamycin, amikacin, and ethambutol. After exposure to enniatinA1, the membrane potential and intracellular ATP levels of M. tuberculosis was significantly decreased. Conclusions: Enniatin A1 exhibits the positive potential anti-tuberculosis agent characteristics. |
format | Online Article Text |
id | pubmed-6982829 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-69828292020-02-06 Enniatin A1, A Natural Compound with Bactericidal Activity against Mycobacterium tuberculosis In Vitro Wang, Gaoyan Dong, Wenqi Lu, Hao Lu, Wenjia Feng, Jiajia Wang, Xiangru Chen, Huanchun Liu, Manli Tan, Chen Molecules Article Background: Tuberculosis remains a global disease that poses a serious threat to human health, but there is lack of new and available anti-tuberculosis agents to prevent the emergence of drug-resistant strains. To address this problem natural products are still potential sources for the development of novel drugs. Methods: A whole-cell screening approach was utilized to obtain a natural compound enniatin A1 from a natural products library. The target compound’s antibacterial activity against Mycobacterium tuberculosis (M. tuberculosis) was evaluated by using the resazurin reduction micro-plate assay (REMA) method. The cytotoxicity of the compound against Vero cells was measured to calculate the selectivity index. The intracellular inhibition activity of enniatin A1 was determined. We performed its time-kill kinetic assay against M. tuberculosis. We first tested its synergistic effect in combination with the first and second-line anti-tuberculosis drugs. Finally, we measured the membrane potential and intracellular ATP levels of M. tuberculosis after exposure to enniatin A1. Results: We identified enniatinA1 as a potential antibacterial agent against M. tuberculosis, against which it showed strong selectivity. Enniatin A1 exhibited a time-concentration-dependent bactericidal effect against M. tuberculosis, and it displayed synergy with rifamycin, amikacin, and ethambutol. After exposure to enniatinA1, the membrane potential and intracellular ATP levels of M. tuberculosis was significantly decreased. Conclusions: Enniatin A1 exhibits the positive potential anti-tuberculosis agent characteristics. MDPI 2019-12-20 /pmc/articles/PMC6982829/ /pubmed/31861925 http://dx.doi.org/10.3390/molecules25010038 Text en © 2019 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 Wang, Gaoyan Dong, Wenqi Lu, Hao Lu, Wenjia Feng, Jiajia Wang, Xiangru Chen, Huanchun Liu, Manli Tan, Chen Enniatin A1, A Natural Compound with Bactericidal Activity against Mycobacterium tuberculosis In Vitro |
title | Enniatin A1, A Natural Compound with Bactericidal Activity against Mycobacterium tuberculosis In Vitro |
title_full | Enniatin A1, A Natural Compound with Bactericidal Activity against Mycobacterium tuberculosis In Vitro |
title_fullStr | Enniatin A1, A Natural Compound with Bactericidal Activity against Mycobacterium tuberculosis In Vitro |
title_full_unstemmed | Enniatin A1, A Natural Compound with Bactericidal Activity against Mycobacterium tuberculosis In Vitro |
title_short | Enniatin A1, A Natural Compound with Bactericidal Activity against Mycobacterium tuberculosis In Vitro |
title_sort | enniatin a1, a natural compound with bactericidal activity against mycobacterium tuberculosis in vitro |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6982829/ https://www.ncbi.nlm.nih.gov/pubmed/31861925 http://dx.doi.org/10.3390/molecules25010038 |
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