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pdh modulate virulence through reducing stress tolerance and biofilm formation of Streptococcus suis serotype 2

Streptococcus suis serotype 2 (S. suis 2) is a zoonotic pathogen. It causes meningitis, arthritis, pneumonia and sepsis in pigs, leading to extremely high mortality, which seriously affects public health and the development of the pig industry. Pyruvate dehydrogenase (PDH) is an important sugar meta...

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Autores principales: Wang, Yang, Wang, Yuxin, Liu, Baobao, Wang, Shaohui, Li, Jinpeng, Gong, Shenglong, Sun, Liyun, Yi, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6592368/
https://www.ncbi.nlm.nih.gov/pubmed/31232165
http://dx.doi.org/10.1080/21505594.2019.1631661
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author Wang, Yang
Wang, Yuxin
Liu, Baobao
Wang, Shaohui
Li, Jinpeng
Gong, Shenglong
Sun, Liyun
Yi, Li
author_facet Wang, Yang
Wang, Yuxin
Liu, Baobao
Wang, Shaohui
Li, Jinpeng
Gong, Shenglong
Sun, Liyun
Yi, Li
author_sort Wang, Yang
collection PubMed
description Streptococcus suis serotype 2 (S. suis 2) is a zoonotic pathogen. It causes meningitis, arthritis, pneumonia and sepsis in pigs, leading to extremely high mortality, which seriously affects public health and the development of the pig industry. Pyruvate dehydrogenase (PDH) is an important sugar metabolism enzyme that is widely present in microorganisms, mammals and higher plants. It catalyzes the irreversible oxidative decarboxylation of pyruvate to acetyl-CoA and reduces NAD+ to NADH. In this study, we found that the virulence of the S. suis ZY05719 sequence type 7 pdh deletion strain (Δpdh) was significantly lower than the wild-type strain (WT) in the mouse infection model. The distribution of viable bacteria in the blood and organs of mice infected with the Δpdh was significantly lower than those infected with WT. Bacterial survival rates were reduced in response to temperature stress, salt stress and oxidative stress. Additionally, compared to WT, the ability to adhere to and invade PK15 cells, biofilm formation and stress resistance of Δpdh were significantly reduced. Moreover, real-time PCR results showed that pdh deletion reduced the expression of multiple adhesion-related genes. However, there was no significant difference in the correlation biological analysis between the complemented strain (CΔpdh) and WT. Moreover, the survival rate of Δpdh in RAW264.7 macrophages was significantly lower than that of the WT strain. This study shows that PDH is involved in the pathogenesis of S. suis 2 and reduction in virulence of Δpdh may be related to the decreased ability to resist stress of the strain.
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spelling pubmed-65923682019-07-01 pdh modulate virulence through reducing stress tolerance and biofilm formation of Streptococcus suis serotype 2 Wang, Yang Wang, Yuxin Liu, Baobao Wang, Shaohui Li, Jinpeng Gong, Shenglong Sun, Liyun Yi, Li Virulence Research Paper Streptococcus suis serotype 2 (S. suis 2) is a zoonotic pathogen. It causes meningitis, arthritis, pneumonia and sepsis in pigs, leading to extremely high mortality, which seriously affects public health and the development of the pig industry. Pyruvate dehydrogenase (PDH) is an important sugar metabolism enzyme that is widely present in microorganisms, mammals and higher plants. It catalyzes the irreversible oxidative decarboxylation of pyruvate to acetyl-CoA and reduces NAD+ to NADH. In this study, we found that the virulence of the S. suis ZY05719 sequence type 7 pdh deletion strain (Δpdh) was significantly lower than the wild-type strain (WT) in the mouse infection model. The distribution of viable bacteria in the blood and organs of mice infected with the Δpdh was significantly lower than those infected with WT. Bacterial survival rates were reduced in response to temperature stress, salt stress and oxidative stress. Additionally, compared to WT, the ability to adhere to and invade PK15 cells, biofilm formation and stress resistance of Δpdh were significantly reduced. Moreover, real-time PCR results showed that pdh deletion reduced the expression of multiple adhesion-related genes. However, there was no significant difference in the correlation biological analysis between the complemented strain (CΔpdh) and WT. Moreover, the survival rate of Δpdh in RAW264.7 macrophages was significantly lower than that of the WT strain. This study shows that PDH is involved in the pathogenesis of S. suis 2 and reduction in virulence of Δpdh may be related to the decreased ability to resist stress of the strain. Taylor & Francis 2019-06-24 /pmc/articles/PMC6592368/ /pubmed/31232165 http://dx.doi.org/10.1080/21505594.2019.1631661 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Wang, Yang
Wang, Yuxin
Liu, Baobao
Wang, Shaohui
Li, Jinpeng
Gong, Shenglong
Sun, Liyun
Yi, Li
pdh modulate virulence through reducing stress tolerance and biofilm formation of Streptococcus suis serotype 2
title pdh modulate virulence through reducing stress tolerance and biofilm formation of Streptococcus suis serotype 2
title_full pdh modulate virulence through reducing stress tolerance and biofilm formation of Streptococcus suis serotype 2
title_fullStr pdh modulate virulence through reducing stress tolerance and biofilm formation of Streptococcus suis serotype 2
title_full_unstemmed pdh modulate virulence through reducing stress tolerance and biofilm formation of Streptococcus suis serotype 2
title_short pdh modulate virulence through reducing stress tolerance and biofilm formation of Streptococcus suis serotype 2
title_sort pdh modulate virulence through reducing stress tolerance and biofilm formation of streptococcus suis serotype 2
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6592368/
https://www.ncbi.nlm.nih.gov/pubmed/31232165
http://dx.doi.org/10.1080/21505594.2019.1631661
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