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Beneficial effect of Xuebijing against Pseudomonas aeruginosa infection in Caenorhabditis elegans

In the clinical intensive care units (ICU), the traditional Chinese medicine (TCM) formulation of Xuebijing has been frequently used for treating sepsis. Nevertheless, the underlying pharmacological mechanisms of Xuebijing remain largely unclear. Caenorhabditis elegans is an important experimental h...

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Autores principales: Zhang, Le, Wang, Yuxing, Cao, Chang, Zhu, Yike, Huang, Wei, Yang, Yi, Qiu, Haibo, Liu, Songqiao, Wang, Dayong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9470999/
https://www.ncbi.nlm.nih.gov/pubmed/36120363
http://dx.doi.org/10.3389/fphar.2022.949608
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author Zhang, Le
Wang, Yuxing
Cao, Chang
Zhu, Yike
Huang, Wei
Yang, Yi
Qiu, Haibo
Liu, Songqiao
Wang, Dayong
author_facet Zhang, Le
Wang, Yuxing
Cao, Chang
Zhu, Yike
Huang, Wei
Yang, Yi
Qiu, Haibo
Liu, Songqiao
Wang, Dayong
author_sort Zhang, Le
collection PubMed
description In the clinical intensive care units (ICU), the traditional Chinese medicine (TCM) formulation of Xuebijing has been frequently used for treating sepsis. Nevertheless, the underlying pharmacological mechanisms of Xuebijing remain largely unclear. Caenorhabditis elegans is an important experimental host for bacterial infections. Using C. elegans as an animal model, we here examined the potential of Xuebijing treatment against bacterial infection and the underlying mechanisms. Xuebijing treatment could inhibit the reduction tendency of lifespan caused by Pseudomonas aeruginosa infection. For the cellular mechanisms of this antibacterial infection property, we found that Xuebijing treatment rescued C. elegans lifespan to be against P. aeruginosa infection by inhibiting Pseudomonas colonization in the intestinal lumen. Meanwhile, the increase in the expression of antimicrobial genes induced by Pseudomonas infection was also suppressed by Xuebijing treatment. Moreover, the beneficial effect of Xuebijing against Pseudomonas infection depended on insulin, p38 MAPK, Wnt, DBL-1/TGF-β, ELT-2, and programmed cell death (PCD)-related signals. Although Xuebijing did not show obvious antibacterial activity, Xuebijing (100%) treatment could inhibit the Pseudomonas biofilm formation and decrease the expression of virulence genes (lasA, lasB, rhlA, rhlC, phzA, phzM, phzH, and phzS) and quorum sensing (QS)-related genes (lasI, lasR, rhlI, rhlR, pqsA, and pqsR). Our results support the potential role of Xuebijing treatment against bacterial infection in hosts.
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spelling pubmed-94709992022-09-15 Beneficial effect of Xuebijing against Pseudomonas aeruginosa infection in Caenorhabditis elegans Zhang, Le Wang, Yuxing Cao, Chang Zhu, Yike Huang, Wei Yang, Yi Qiu, Haibo Liu, Songqiao Wang, Dayong Front Pharmacol Pharmacology In the clinical intensive care units (ICU), the traditional Chinese medicine (TCM) formulation of Xuebijing has been frequently used for treating sepsis. Nevertheless, the underlying pharmacological mechanisms of Xuebijing remain largely unclear. Caenorhabditis elegans is an important experimental host for bacterial infections. Using C. elegans as an animal model, we here examined the potential of Xuebijing treatment against bacterial infection and the underlying mechanisms. Xuebijing treatment could inhibit the reduction tendency of lifespan caused by Pseudomonas aeruginosa infection. For the cellular mechanisms of this antibacterial infection property, we found that Xuebijing treatment rescued C. elegans lifespan to be against P. aeruginosa infection by inhibiting Pseudomonas colonization in the intestinal lumen. Meanwhile, the increase in the expression of antimicrobial genes induced by Pseudomonas infection was also suppressed by Xuebijing treatment. Moreover, the beneficial effect of Xuebijing against Pseudomonas infection depended on insulin, p38 MAPK, Wnt, DBL-1/TGF-β, ELT-2, and programmed cell death (PCD)-related signals. Although Xuebijing did not show obvious antibacterial activity, Xuebijing (100%) treatment could inhibit the Pseudomonas biofilm formation and decrease the expression of virulence genes (lasA, lasB, rhlA, rhlC, phzA, phzM, phzH, and phzS) and quorum sensing (QS)-related genes (lasI, lasR, rhlI, rhlR, pqsA, and pqsR). Our results support the potential role of Xuebijing treatment against bacterial infection in hosts. Frontiers Media S.A. 2022-08-31 /pmc/articles/PMC9470999/ /pubmed/36120363 http://dx.doi.org/10.3389/fphar.2022.949608 Text en Copyright © 2022 Zhang, Wang, Cao, Zhu, Huang, Yang, Qiu, Liu 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
Zhang, Le
Wang, Yuxing
Cao, Chang
Zhu, Yike
Huang, Wei
Yang, Yi
Qiu, Haibo
Liu, Songqiao
Wang, Dayong
Beneficial effect of Xuebijing against Pseudomonas aeruginosa infection in Caenorhabditis elegans
title Beneficial effect of Xuebijing against Pseudomonas aeruginosa infection in Caenorhabditis elegans
title_full Beneficial effect of Xuebijing against Pseudomonas aeruginosa infection in Caenorhabditis elegans
title_fullStr Beneficial effect of Xuebijing against Pseudomonas aeruginosa infection in Caenorhabditis elegans
title_full_unstemmed Beneficial effect of Xuebijing against Pseudomonas aeruginosa infection in Caenorhabditis elegans
title_short Beneficial effect of Xuebijing against Pseudomonas aeruginosa infection in Caenorhabditis elegans
title_sort beneficial effect of xuebijing against pseudomonas aeruginosa infection in caenorhabditis elegans
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9470999/
https://www.ncbi.nlm.nih.gov/pubmed/36120363
http://dx.doi.org/10.3389/fphar.2022.949608
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