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The synergistic activity of SBC3 in combination with Ebselen against Escherichia coli infection

Escherichia coli ranks as the number one clinical isolate in the past years in China according to The China Antimicrobial Surveillance Network (CHINET), and its multidrug-resistant (MDR) pathogenic strains account for over 160 million cases of dysentery and one million deaths per year. Here, our wor...

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Autores principales: Chen, Hao, Lu, Qianqian, An, Haoyue, Li, Juntong, Shen, Shuchu, Zheng, Xi, Chen, Wei, Wang, Lu, Li, Jihong, Du, Youqin, Wang, Yueqing, Liu, Xiaowen, Baumann, Marcus, Tacke, Matthias, Zou, Lili, Wang, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9797518/
https://www.ncbi.nlm.nih.gov/pubmed/36588729
http://dx.doi.org/10.3389/fphar.2022.1080281
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author Chen, Hao
Lu, Qianqian
An, Haoyue
Li, Juntong
Shen, Shuchu
Zheng, Xi
Chen, Wei
Wang, Lu
Li, Jihong
Du, Youqin
Wang, Yueqing
Liu, Xiaowen
Baumann, Marcus
Tacke, Matthias
Zou, Lili
Wang, Jun
author_facet Chen, Hao
Lu, Qianqian
An, Haoyue
Li, Juntong
Shen, Shuchu
Zheng, Xi
Chen, Wei
Wang, Lu
Li, Jihong
Du, Youqin
Wang, Yueqing
Liu, Xiaowen
Baumann, Marcus
Tacke, Matthias
Zou, Lili
Wang, Jun
author_sort Chen, Hao
collection PubMed
description Escherichia coli ranks as the number one clinical isolate in the past years in China according to The China Antimicrobial Surveillance Network (CHINET), and its multidrug-resistant (MDR) pathogenic strains account for over 160 million cases of dysentery and one million deaths per year. Here, our work demonstrates that E. coli is highly sensitive to the synergistic combination of SBC3 [1,3-Dibenzyl-4,5-diphenyl-imidazol-2-ylidene silver (I) acetate] and Ebselen, which shows no synergistic toxicity on mammalian cells. The proposed mechanism for the synergistic antibacterial effect of SBC3 in combination with Ebselen is based on directly inhibiting E. coli thioredoxin reductase and rapidly depleting glutathione, resulting in the increase of reactive oxygen species that cause bacterial cell death. Furthermore, the bactericidal efficacy of SBC3 in combination with Ebselen has been confirmed in mild and acute peritonitis mice. In addition, the five most difficult to treat Gram-negative bacteria (including E. coli, Acinetobacter baumannii, Enterobacter cloacae, Klebsiella pneumoniae, and Pseudomonas aeruginosa) are also highly sensitive to a synergistic combination of SBC3 and Ebselen. Thus, SBC3 in combination with Ebselen has potential as a treatment for clinically important Gram-negative bacterial infections.
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spelling pubmed-97975182022-12-30 The synergistic activity of SBC3 in combination with Ebselen against Escherichia coli infection Chen, Hao Lu, Qianqian An, Haoyue Li, Juntong Shen, Shuchu Zheng, Xi Chen, Wei Wang, Lu Li, Jihong Du, Youqin Wang, Yueqing Liu, Xiaowen Baumann, Marcus Tacke, Matthias Zou, Lili Wang, Jun Front Pharmacol Pharmacology Escherichia coli ranks as the number one clinical isolate in the past years in China according to The China Antimicrobial Surveillance Network (CHINET), and its multidrug-resistant (MDR) pathogenic strains account for over 160 million cases of dysentery and one million deaths per year. Here, our work demonstrates that E. coli is highly sensitive to the synergistic combination of SBC3 [1,3-Dibenzyl-4,5-diphenyl-imidazol-2-ylidene silver (I) acetate] and Ebselen, which shows no synergistic toxicity on mammalian cells. The proposed mechanism for the synergistic antibacterial effect of SBC3 in combination with Ebselen is based on directly inhibiting E. coli thioredoxin reductase and rapidly depleting glutathione, resulting in the increase of reactive oxygen species that cause bacterial cell death. Furthermore, the bactericidal efficacy of SBC3 in combination with Ebselen has been confirmed in mild and acute peritonitis mice. In addition, the five most difficult to treat Gram-negative bacteria (including E. coli, Acinetobacter baumannii, Enterobacter cloacae, Klebsiella pneumoniae, and Pseudomonas aeruginosa) are also highly sensitive to a synergistic combination of SBC3 and Ebselen. Thus, SBC3 in combination with Ebselen has potential as a treatment for clinically important Gram-negative bacterial infections. Frontiers Media S.A. 2022-12-15 /pmc/articles/PMC9797518/ /pubmed/36588729 http://dx.doi.org/10.3389/fphar.2022.1080281 Text en Copyright © 2022 Chen, Lu, An, Li, Shen, Zheng, Chen, Wang, Li, Du, Wang, Liu, Baumann, Tacke, Zou and Wang. https://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 Pharmacology
Chen, Hao
Lu, Qianqian
An, Haoyue
Li, Juntong
Shen, Shuchu
Zheng, Xi
Chen, Wei
Wang, Lu
Li, Jihong
Du, Youqin
Wang, Yueqing
Liu, Xiaowen
Baumann, Marcus
Tacke, Matthias
Zou, Lili
Wang, Jun
The synergistic activity of SBC3 in combination with Ebselen against Escherichia coli infection
title The synergistic activity of SBC3 in combination with Ebselen against Escherichia coli infection
title_full The synergistic activity of SBC3 in combination with Ebselen against Escherichia coli infection
title_fullStr The synergistic activity of SBC3 in combination with Ebselen against Escherichia coli infection
title_full_unstemmed The synergistic activity of SBC3 in combination with Ebselen against Escherichia coli infection
title_short The synergistic activity of SBC3 in combination with Ebselen against Escherichia coli infection
title_sort synergistic activity of sbc3 in combination with ebselen against escherichia coli infection
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9797518/
https://www.ncbi.nlm.nih.gov/pubmed/36588729
http://dx.doi.org/10.3389/fphar.2022.1080281
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