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Repurposing Ellipticine Hydrochloride to Combat Colistin-Resistant Extraintestinal Pathogenic E. coli (ExPEC)

Extraintestinal pathogenic Escherichia coli (ExPEC) strains are the cause of a majority of human extraintestinal infections globally, resulting in enormous direct economic and medical costs. The plasmid-mediated, colistin-resistant gene mcr-1 has broken through the ultimate defense line against MDR...

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Autores principales: Lu, Hao, Liu, Manli, Lu, Wenjia, Wang, Chenchen, Wang, Gaoyan, Dong, Wenqi, Wang, Xiangru, Chen, Huanchun, Tan, Chen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7262907/
https://www.ncbi.nlm.nih.gov/pubmed/32528422
http://dx.doi.org/10.3389/fmicb.2020.00806
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author Lu, Hao
Liu, Manli
Lu, Wenjia
Wang, Chenchen
Wang, Gaoyan
Dong, Wenqi
Wang, Xiangru
Chen, Huanchun
Tan, Chen
author_facet Lu, Hao
Liu, Manli
Lu, Wenjia
Wang, Chenchen
Wang, Gaoyan
Dong, Wenqi
Wang, Xiangru
Chen, Huanchun
Tan, Chen
author_sort Lu, Hao
collection PubMed
description Extraintestinal pathogenic Escherichia coli (ExPEC) strains are the cause of a majority of human extraintestinal infections globally, resulting in enormous direct economic and medical costs. The plasmid-mediated, colistin-resistant gene mcr-1 has broken through the ultimate defense line against MDR Gram-negative pathogens. There is an urgent need to discover the new compound intended for colistin-resistant E. coli. In this study, antibacterial targets of ellipticine hydrochloride (EH) were confirmed by localized surface plasmon resonance (LSPR) and decatenation assay. The LSPR analysis exhibited good binding between EH and E. coli topoisomerase IV. In this study, a synergistic effect is obvious in the combination of EH and colistin, to which eight of ten strains showed synergy, while two isolates (20%) showed no difference. The bacteria enumeration analysis of EH treatment group suggested that the decreased bacterial titer can be observed in various tissues of infected mice. EH treatment significantly decreased the levels of a variety of pro-inflammatory factors, such as TNF-α and IL-6. Moreover, other related lesions, such as inflammatory cell infiltration, alveolar interstitial congestion, and edema were observed to be relieved to different extents. This study reveals the anti-E. coli potential activities and molecular mechanism of EH and the therapeutical effectiveness of EH application to animals. It provides us with a new option for fighting against multidrug-resistant ExPEC infections in the future.
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spelling pubmed-72629072020-06-10 Repurposing Ellipticine Hydrochloride to Combat Colistin-Resistant Extraintestinal Pathogenic E. coli (ExPEC) Lu, Hao Liu, Manli Lu, Wenjia Wang, Chenchen Wang, Gaoyan Dong, Wenqi Wang, Xiangru Chen, Huanchun Tan, Chen Front Microbiol Microbiology Extraintestinal pathogenic Escherichia coli (ExPEC) strains are the cause of a majority of human extraintestinal infections globally, resulting in enormous direct economic and medical costs. The plasmid-mediated, colistin-resistant gene mcr-1 has broken through the ultimate defense line against MDR Gram-negative pathogens. There is an urgent need to discover the new compound intended for colistin-resistant E. coli. In this study, antibacterial targets of ellipticine hydrochloride (EH) were confirmed by localized surface plasmon resonance (LSPR) and decatenation assay. The LSPR analysis exhibited good binding between EH and E. coli topoisomerase IV. In this study, a synergistic effect is obvious in the combination of EH and colistin, to which eight of ten strains showed synergy, while two isolates (20%) showed no difference. The bacteria enumeration analysis of EH treatment group suggested that the decreased bacterial titer can be observed in various tissues of infected mice. EH treatment significantly decreased the levels of a variety of pro-inflammatory factors, such as TNF-α and IL-6. Moreover, other related lesions, such as inflammatory cell infiltration, alveolar interstitial congestion, and edema were observed to be relieved to different extents. This study reveals the anti-E. coli potential activities and molecular mechanism of EH and the therapeutical effectiveness of EH application to animals. It provides us with a new option for fighting against multidrug-resistant ExPEC infections in the future. Frontiers Media S.A. 2020-05-25 /pmc/articles/PMC7262907/ /pubmed/32528422 http://dx.doi.org/10.3389/fmicb.2020.00806 Text en Copyright © 2020 Lu, Liu, Lu, Wang, Wang, Dong, Wang, Chen and Tan. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Lu, Hao
Liu, Manli
Lu, Wenjia
Wang, Chenchen
Wang, Gaoyan
Dong, Wenqi
Wang, Xiangru
Chen, Huanchun
Tan, Chen
Repurposing Ellipticine Hydrochloride to Combat Colistin-Resistant Extraintestinal Pathogenic E. coli (ExPEC)
title Repurposing Ellipticine Hydrochloride to Combat Colistin-Resistant Extraintestinal Pathogenic E. coli (ExPEC)
title_full Repurposing Ellipticine Hydrochloride to Combat Colistin-Resistant Extraintestinal Pathogenic E. coli (ExPEC)
title_fullStr Repurposing Ellipticine Hydrochloride to Combat Colistin-Resistant Extraintestinal Pathogenic E. coli (ExPEC)
title_full_unstemmed Repurposing Ellipticine Hydrochloride to Combat Colistin-Resistant Extraintestinal Pathogenic E. coli (ExPEC)
title_short Repurposing Ellipticine Hydrochloride to Combat Colistin-Resistant Extraintestinal Pathogenic E. coli (ExPEC)
title_sort repurposing ellipticine hydrochloride to combat colistin-resistant extraintestinal pathogenic e. coli (expec)
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7262907/
https://www.ncbi.nlm.nih.gov/pubmed/32528422
http://dx.doi.org/10.3389/fmicb.2020.00806
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