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Effect of Licochalcone A on Growth and Properties of Streptococcus suis

Streptococcus suis (S.suis) is an important emerging worldwide pig pathogen and zoonotic agent with rapid evolution of virulence and drug resistance. In this study, we wanted to investigate the effect of licochalcone A on growth and properties of Streptococcus suis. The antimicrobial activity of lic...

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Autores principales: Hao, Huaijie, Hui, Wenjia, Liu, Peng, Lv, Qingyu, Zeng, Xiaotao, jiang, Hua, Wang, Yanzi, Zheng, Xin, Zheng, Yuling, Li, Jianchun, Zhou, Xuyu, Jiang, Yongqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3720849/
https://www.ncbi.nlm.nih.gov/pubmed/23935843
http://dx.doi.org/10.1371/journal.pone.0067728
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author Hao, Huaijie
Hui, Wenjia
Liu, Peng
Lv, Qingyu
Zeng, Xiaotao
jiang, Hua
Wang, Yanzi
Zheng, Xin
Zheng, Yuling
Li, Jianchun
Zhou, Xuyu
Jiang, Yongqiang
author_facet Hao, Huaijie
Hui, Wenjia
Liu, Peng
Lv, Qingyu
Zeng, Xiaotao
jiang, Hua
Wang, Yanzi
Zheng, Xin
Zheng, Yuling
Li, Jianchun
Zhou, Xuyu
Jiang, Yongqiang
author_sort Hao, Huaijie
collection PubMed
description Streptococcus suis (S.suis) is an important emerging worldwide pig pathogen and zoonotic agent with rapid evolution of virulence and drug resistance. In this study, we wanted to investigate the effect of licochalcone A on growth and properties of Streptococcus suis. The antimicrobial activity of licochalcone A was tested by growth inhibition assay and the minimal inhibitory concentrations (MICs) also were determined. The effect of licochalcone A on S.suis biofilm formation was characterized by crystal violet staining. The effect of licochalcone A on suilysin secretion was evaluated by titration of hemolytic activity. To understand the antimicrobial effect, gene expression profile of S.suis treated by licochalcone A was analyzed by DNA microarray. Our results demonstrated that licochalcone A showed antimicrobial activity on S.suis with MICs of 4 µg/ml for S.suis serotype 2 strains and 8 µg/ml for S.suis serotype 7 strains. Biofilm formation was inhibited by 30–40% in the presence of licochalcone A (3 µg/ml) and suilysin secretion was also significantly inhibited in the presence of licochalcone A (1.5 µg/ml). The gene expression profile of S.suis in the presence of licochalcone A showed that 132 genes were differentially regulated, and we analyzed the regulated genes in the aspect of the bacterial cell cycle control. Among the deregulated genes, the genes responsible for the mass doubling was increased expression, but the genes responsible for DNA replication and cell division were inhibited the expression. So, we think the regulation of the cell cycle genes might provide a mechanistic understanding of licochalcone A mediated antimicrobial effect against S.suis.
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spelling pubmed-37208492013-08-09 Effect of Licochalcone A on Growth and Properties of Streptococcus suis Hao, Huaijie Hui, Wenjia Liu, Peng Lv, Qingyu Zeng, Xiaotao jiang, Hua Wang, Yanzi Zheng, Xin Zheng, Yuling Li, Jianchun Zhou, Xuyu Jiang, Yongqiang PLoS One Research Article Streptococcus suis (S.suis) is an important emerging worldwide pig pathogen and zoonotic agent with rapid evolution of virulence and drug resistance. In this study, we wanted to investigate the effect of licochalcone A on growth and properties of Streptococcus suis. The antimicrobial activity of licochalcone A was tested by growth inhibition assay and the minimal inhibitory concentrations (MICs) also were determined. The effect of licochalcone A on S.suis biofilm formation was characterized by crystal violet staining. The effect of licochalcone A on suilysin secretion was evaluated by titration of hemolytic activity. To understand the antimicrobial effect, gene expression profile of S.suis treated by licochalcone A was analyzed by DNA microarray. Our results demonstrated that licochalcone A showed antimicrobial activity on S.suis with MICs of 4 µg/ml for S.suis serotype 2 strains and 8 µg/ml for S.suis serotype 7 strains. Biofilm formation was inhibited by 30–40% in the presence of licochalcone A (3 µg/ml) and suilysin secretion was also significantly inhibited in the presence of licochalcone A (1.5 µg/ml). The gene expression profile of S.suis in the presence of licochalcone A showed that 132 genes were differentially regulated, and we analyzed the regulated genes in the aspect of the bacterial cell cycle control. Among the deregulated genes, the genes responsible for the mass doubling was increased expression, but the genes responsible for DNA replication and cell division were inhibited the expression. So, we think the regulation of the cell cycle genes might provide a mechanistic understanding of licochalcone A mediated antimicrobial effect against S.suis. Public Library of Science 2013-07-23 /pmc/articles/PMC3720849/ /pubmed/23935843 http://dx.doi.org/10.1371/journal.pone.0067728 Text en © 2013 Hao et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Hao, Huaijie
Hui, Wenjia
Liu, Peng
Lv, Qingyu
Zeng, Xiaotao
jiang, Hua
Wang, Yanzi
Zheng, Xin
Zheng, Yuling
Li, Jianchun
Zhou, Xuyu
Jiang, Yongqiang
Effect of Licochalcone A on Growth and Properties of Streptococcus suis
title Effect of Licochalcone A on Growth and Properties of Streptococcus suis
title_full Effect of Licochalcone A on Growth and Properties of Streptococcus suis
title_fullStr Effect of Licochalcone A on Growth and Properties of Streptococcus suis
title_full_unstemmed Effect of Licochalcone A on Growth and Properties of Streptococcus suis
title_short Effect of Licochalcone A on Growth and Properties of Streptococcus suis
title_sort effect of licochalcone a on growth and properties of streptococcus suis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3720849/
https://www.ncbi.nlm.nih.gov/pubmed/23935843
http://dx.doi.org/10.1371/journal.pone.0067728
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