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YdiV regulates Escherichia coli ferric uptake by manipulating the DNA-binding ability of Fur in a SlyD-dependent manner
Iron is essential for all bacteria. In most bacteria, intracellular iron homeostasis is tightly regulated by the ferric uptake regulator Fur. However, how Fur activates the iron-uptake system during iron deficiency is not fully elucidated. In this study, we found that YdiV, the flagella gene inhibit...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7515728/ https://www.ncbi.nlm.nih.gov/pubmed/32813023 http://dx.doi.org/10.1093/nar/gkaa696 |
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author | Zhang, Fengyu Li, Bingqing Dong, Hongjie Chen, Min Yao, Shun Li, Jingwen Zhang, Honghai Liu, Xiangguo Wang, Hongwei Song, Nannan Zhang, Kundi Du, Ning Xu, Sujuan Gu, Lichuan |
author_facet | Zhang, Fengyu Li, Bingqing Dong, Hongjie Chen, Min Yao, Shun Li, Jingwen Zhang, Honghai Liu, Xiangguo Wang, Hongwei Song, Nannan Zhang, Kundi Du, Ning Xu, Sujuan Gu, Lichuan |
author_sort | Zhang, Fengyu |
collection | PubMed |
description | Iron is essential for all bacteria. In most bacteria, intracellular iron homeostasis is tightly regulated by the ferric uptake regulator Fur. However, how Fur activates the iron-uptake system during iron deficiency is not fully elucidated. In this study, we found that YdiV, the flagella gene inhibitor, is involved in iron homeostasis in Escherichia coli. Iron deficiency triggers overexpression of YdiV. High levels of YdiV then transforms Fur into a novel form which does not bind DNA in a peptidyl-prolyl cis-trans isomerase SlyD dependent manner. Thus, the cooperation of YdiV, SlyD and Fur activates the gene expression of iron-uptake systems under conditions of iron deficiency. Bacterial invasion assays also demonstrated that both ydiV and slyD are necessary for the survival and growth of uropathogenic E. coli in bladder epithelial cells. This reveals a mechanism where YdiV not only represses flagella expression to make E. coli invisible to the host immune system, but it also promotes iron acquisition to help E. coli overcome host nutritional immunity. |
format | Online Article Text |
id | pubmed-7515728 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-75157282020-09-30 YdiV regulates Escherichia coli ferric uptake by manipulating the DNA-binding ability of Fur in a SlyD-dependent manner Zhang, Fengyu Li, Bingqing Dong, Hongjie Chen, Min Yao, Shun Li, Jingwen Zhang, Honghai Liu, Xiangguo Wang, Hongwei Song, Nannan Zhang, Kundi Du, Ning Xu, Sujuan Gu, Lichuan Nucleic Acids Res Gene regulation, Chromatin and Epigenetics Iron is essential for all bacteria. In most bacteria, intracellular iron homeostasis is tightly regulated by the ferric uptake regulator Fur. However, how Fur activates the iron-uptake system during iron deficiency is not fully elucidated. In this study, we found that YdiV, the flagella gene inhibitor, is involved in iron homeostasis in Escherichia coli. Iron deficiency triggers overexpression of YdiV. High levels of YdiV then transforms Fur into a novel form which does not bind DNA in a peptidyl-prolyl cis-trans isomerase SlyD dependent manner. Thus, the cooperation of YdiV, SlyD and Fur activates the gene expression of iron-uptake systems under conditions of iron deficiency. Bacterial invasion assays also demonstrated that both ydiV and slyD are necessary for the survival and growth of uropathogenic E. coli in bladder epithelial cells. This reveals a mechanism where YdiV not only represses flagella expression to make E. coli invisible to the host immune system, but it also promotes iron acquisition to help E. coli overcome host nutritional immunity. Oxford University Press 2020-08-19 /pmc/articles/PMC7515728/ /pubmed/32813023 http://dx.doi.org/10.1093/nar/gkaa696 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Gene regulation, Chromatin and Epigenetics Zhang, Fengyu Li, Bingqing Dong, Hongjie Chen, Min Yao, Shun Li, Jingwen Zhang, Honghai Liu, Xiangguo Wang, Hongwei Song, Nannan Zhang, Kundi Du, Ning Xu, Sujuan Gu, Lichuan YdiV regulates Escherichia coli ferric uptake by manipulating the DNA-binding ability of Fur in a SlyD-dependent manner |
title | YdiV regulates Escherichia coli ferric uptake by manipulating the DNA-binding ability of Fur in a SlyD-dependent manner |
title_full | YdiV regulates Escherichia coli ferric uptake by manipulating the DNA-binding ability of Fur in a SlyD-dependent manner |
title_fullStr | YdiV regulates Escherichia coli ferric uptake by manipulating the DNA-binding ability of Fur in a SlyD-dependent manner |
title_full_unstemmed | YdiV regulates Escherichia coli ferric uptake by manipulating the DNA-binding ability of Fur in a SlyD-dependent manner |
title_short | YdiV regulates Escherichia coli ferric uptake by manipulating the DNA-binding ability of Fur in a SlyD-dependent manner |
title_sort | ydiv regulates escherichia coli ferric uptake by manipulating the dna-binding ability of fur in a slyd-dependent manner |
topic | Gene regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7515728/ https://www.ncbi.nlm.nih.gov/pubmed/32813023 http://dx.doi.org/10.1093/nar/gkaa696 |
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