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Epigallocatechin-3-Gallate Ameliorates Acute Lung Damage by Inhibiting Quorum-Sensing-Related Virulence Factors of Pseudomonas aeruginosa
The superbug Pseudomonas aeruginosa is among the most formidable antibiotic-resistant pathogens. With declining options for antibiotic-resistant infections, new medicines are of utmost importance to combat with P. aeruginosa. In our previous study, we demonstrated that Epigallocatechin-3-gallate (EG...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9083413/ https://www.ncbi.nlm.nih.gov/pubmed/35547130 http://dx.doi.org/10.3389/fmicb.2022.874354 |
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author | Tang, Huaqiao Hao, Suqi Khan, Muhammad Faraz Zhao, Ling Shi, Fei Li, Yinglun Guo, Hongrui Zou, Yuanfeng Lv, Cheng Luo, Jie Zeng, Ze Wu, Qiang Ye, Gang |
author_facet | Tang, Huaqiao Hao, Suqi Khan, Muhammad Faraz Zhao, Ling Shi, Fei Li, Yinglun Guo, Hongrui Zou, Yuanfeng Lv, Cheng Luo, Jie Zeng, Ze Wu, Qiang Ye, Gang |
author_sort | Tang, Huaqiao |
collection | PubMed |
description | The superbug Pseudomonas aeruginosa is among the most formidable antibiotic-resistant pathogens. With declining options for antibiotic-resistant infections, new medicines are of utmost importance to combat with P. aeruginosa. In our previous study, we demonstrated that Epigallocatechin-3-gallate (EGCG) can inhibit the production of quorum sensing (QS)-regulated virulence factors in vitro. Accordingly, the protective effect and molecular mechanisms of EGCG against P. aeruginosa-induced pneumonia were studied in a mouse model. The results indicated that EGCG significantly lessened histopathological changes and increased the survival rates of mice infected with P. aeruginosa. EGCG effectively alleviated lung injury by reducing the expression of virulence factors and bacterial burden. In addition, EGCG downregulated the production of pro-inflammatory cytokines, such as TNF-α, IL-1, IL-6, and IL-17, and increased the expression of anti-inflammatory cytokines IL-4 and IL-10. Thus, the experimental results supported for the first time that EGCG improved lung damage in P. aeruginosa infection by inhibiting the production of QS-related virulence factors in vivo. |
format | Online Article Text |
id | pubmed-9083413 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90834132022-05-10 Epigallocatechin-3-Gallate Ameliorates Acute Lung Damage by Inhibiting Quorum-Sensing-Related Virulence Factors of Pseudomonas aeruginosa Tang, Huaqiao Hao, Suqi Khan, Muhammad Faraz Zhao, Ling Shi, Fei Li, Yinglun Guo, Hongrui Zou, Yuanfeng Lv, Cheng Luo, Jie Zeng, Ze Wu, Qiang Ye, Gang Front Microbiol Microbiology The superbug Pseudomonas aeruginosa is among the most formidable antibiotic-resistant pathogens. With declining options for antibiotic-resistant infections, new medicines are of utmost importance to combat with P. aeruginosa. In our previous study, we demonstrated that Epigallocatechin-3-gallate (EGCG) can inhibit the production of quorum sensing (QS)-regulated virulence factors in vitro. Accordingly, the protective effect and molecular mechanisms of EGCG against P. aeruginosa-induced pneumonia were studied in a mouse model. The results indicated that EGCG significantly lessened histopathological changes and increased the survival rates of mice infected with P. aeruginosa. EGCG effectively alleviated lung injury by reducing the expression of virulence factors and bacterial burden. In addition, EGCG downregulated the production of pro-inflammatory cytokines, such as TNF-α, IL-1, IL-6, and IL-17, and increased the expression of anti-inflammatory cytokines IL-4 and IL-10. Thus, the experimental results supported for the first time that EGCG improved lung damage in P. aeruginosa infection by inhibiting the production of QS-related virulence factors in vivo. Frontiers Media S.A. 2022-04-25 /pmc/articles/PMC9083413/ /pubmed/35547130 http://dx.doi.org/10.3389/fmicb.2022.874354 Text en Copyright © 2022 Tang, Hao, Khan, Zhao, Shi, Li, Guo, Zou, Lv, Luo, Zeng, Wu and Ye. 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 | Microbiology Tang, Huaqiao Hao, Suqi Khan, Muhammad Faraz Zhao, Ling Shi, Fei Li, Yinglun Guo, Hongrui Zou, Yuanfeng Lv, Cheng Luo, Jie Zeng, Ze Wu, Qiang Ye, Gang Epigallocatechin-3-Gallate Ameliorates Acute Lung Damage by Inhibiting Quorum-Sensing-Related Virulence Factors of Pseudomonas aeruginosa |
title | Epigallocatechin-3-Gallate Ameliorates Acute Lung Damage by Inhibiting Quorum-Sensing-Related Virulence Factors of Pseudomonas aeruginosa |
title_full | Epigallocatechin-3-Gallate Ameliorates Acute Lung Damage by Inhibiting Quorum-Sensing-Related Virulence Factors of Pseudomonas aeruginosa |
title_fullStr | Epigallocatechin-3-Gallate Ameliorates Acute Lung Damage by Inhibiting Quorum-Sensing-Related Virulence Factors of Pseudomonas aeruginosa |
title_full_unstemmed | Epigallocatechin-3-Gallate Ameliorates Acute Lung Damage by Inhibiting Quorum-Sensing-Related Virulence Factors of Pseudomonas aeruginosa |
title_short | Epigallocatechin-3-Gallate Ameliorates Acute Lung Damage by Inhibiting Quorum-Sensing-Related Virulence Factors of Pseudomonas aeruginosa |
title_sort | epigallocatechin-3-gallate ameliorates acute lung damage by inhibiting quorum-sensing-related virulence factors of pseudomonas aeruginosa |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9083413/ https://www.ncbi.nlm.nih.gov/pubmed/35547130 http://dx.doi.org/10.3389/fmicb.2022.874354 |
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