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Ndk, a novel host-responsive regulator, negatively regulates bacterial virulence through quorum sensing in Pseudomonas aeruginosa
Pathogenic bacteria could adjust gene expression to enable their survival in the distinct host environment. However, the mechanism by which bacteria adapt to the host environment is not well described. In this study, we demonstrated that nucleoside diphosphate kinase (Ndk) of Pseudomonas aeruginosa...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4921839/ https://www.ncbi.nlm.nih.gov/pubmed/27345215 http://dx.doi.org/10.1038/srep28684 |
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author | Yu, Hua Xiong, Junzhi Zhang, Rong Hu, Xiaomei Qiu, Jing Zhang, Di Xu, Xiaohui Xin, Rong He, Xiaomei Xie, Wei Sheng, Halei Chen, Qian Zhang, Le Rao, Xiancai Zhang, Kebin |
author_facet | Yu, Hua Xiong, Junzhi Zhang, Rong Hu, Xiaomei Qiu, Jing Zhang, Di Xu, Xiaohui Xin, Rong He, Xiaomei Xie, Wei Sheng, Halei Chen, Qian Zhang, Le Rao, Xiancai Zhang, Kebin |
author_sort | Yu, Hua |
collection | PubMed |
description | Pathogenic bacteria could adjust gene expression to enable their survival in the distinct host environment. However, the mechanism by which bacteria adapt to the host environment is not well described. In this study, we demonstrated that nucleoside diphosphate kinase (Ndk) of Pseudomonas aeruginosa is critical for adjusting the bacterial virulence determinants during infection. Ndk expression was down-regulated in the pulmonary alveoli of a mouse model of acute pneumonia. Knockout of ndk up-regulated transcription factor ExsA-mediated T3S regulon expression and decreased exoproduct-related gene expression through the inhibition of the quorum sensing hierarchy. Moreover, in vitro and in vivo studies demonstrated that the ndk mutant exhibits enhanced cytotoxicity and host pathogenicity by increasing T3SS proteins. Taken together, our data reveal that ndk is a critical novel host-responsive gene required for coordinating P. aeruginosa virulence upon acute infection. |
format | Online Article Text |
id | pubmed-4921839 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49218392016-06-28 Ndk, a novel host-responsive regulator, negatively regulates bacterial virulence through quorum sensing in Pseudomonas aeruginosa Yu, Hua Xiong, Junzhi Zhang, Rong Hu, Xiaomei Qiu, Jing Zhang, Di Xu, Xiaohui Xin, Rong He, Xiaomei Xie, Wei Sheng, Halei Chen, Qian Zhang, Le Rao, Xiancai Zhang, Kebin Sci Rep Article Pathogenic bacteria could adjust gene expression to enable their survival in the distinct host environment. However, the mechanism by which bacteria adapt to the host environment is not well described. In this study, we demonstrated that nucleoside diphosphate kinase (Ndk) of Pseudomonas aeruginosa is critical for adjusting the bacterial virulence determinants during infection. Ndk expression was down-regulated in the pulmonary alveoli of a mouse model of acute pneumonia. Knockout of ndk up-regulated transcription factor ExsA-mediated T3S regulon expression and decreased exoproduct-related gene expression through the inhibition of the quorum sensing hierarchy. Moreover, in vitro and in vivo studies demonstrated that the ndk mutant exhibits enhanced cytotoxicity and host pathogenicity by increasing T3SS proteins. Taken together, our data reveal that ndk is a critical novel host-responsive gene required for coordinating P. aeruginosa virulence upon acute infection. Nature Publishing Group 2016-06-27 /pmc/articles/PMC4921839/ /pubmed/27345215 http://dx.doi.org/10.1038/srep28684 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Yu, Hua Xiong, Junzhi Zhang, Rong Hu, Xiaomei Qiu, Jing Zhang, Di Xu, Xiaohui Xin, Rong He, Xiaomei Xie, Wei Sheng, Halei Chen, Qian Zhang, Le Rao, Xiancai Zhang, Kebin Ndk, a novel host-responsive regulator, negatively regulates bacterial virulence through quorum sensing in Pseudomonas aeruginosa |
title | Ndk, a novel host-responsive regulator, negatively regulates bacterial virulence through quorum sensing in Pseudomonas aeruginosa |
title_full | Ndk, a novel host-responsive regulator, negatively regulates bacterial virulence through quorum sensing in Pseudomonas aeruginosa |
title_fullStr | Ndk, a novel host-responsive regulator, negatively regulates bacterial virulence through quorum sensing in Pseudomonas aeruginosa |
title_full_unstemmed | Ndk, a novel host-responsive regulator, negatively regulates bacterial virulence through quorum sensing in Pseudomonas aeruginosa |
title_short | Ndk, a novel host-responsive regulator, negatively regulates bacterial virulence through quorum sensing in Pseudomonas aeruginosa |
title_sort | ndk, a novel host-responsive regulator, negatively regulates bacterial virulence through quorum sensing in pseudomonas aeruginosa |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4921839/ https://www.ncbi.nlm.nih.gov/pubmed/27345215 http://dx.doi.org/10.1038/srep28684 |
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