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TfmR, a novel TetR‐family transcriptional regulator, modulates the virulence of Xanthomonas citri in response to fatty acids
The type III secretion system (T3SS) is required for Xanthomonas citri subsp. citri (Xcc) virulence by translocating effectors into host cytoplasm to promote disease development. The T3SS is controlled by the master transcriptional regulators HrpG and HrpX. While the function of HrpG and HrpX are we...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6637906/ https://www.ncbi.nlm.nih.gov/pubmed/30919570 http://dx.doi.org/10.1111/mpp.12786 |
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author | Teper, Doron Zhang, Yanan Wang, Nian |
author_facet | Teper, Doron Zhang, Yanan Wang, Nian |
author_sort | Teper, Doron |
collection | PubMed |
description | The type III secretion system (T3SS) is required for Xanthomonas citri subsp. citri (Xcc) virulence by translocating effectors into host cytoplasm to promote disease development. The T3SS is controlled by the master transcriptional regulators HrpG and HrpX. While the function of HrpG and HrpX are well characterized, their upstream regulation remains elusive. By using transposon mutagenesis, we identified XAC3052, a TetR‐family transcriptional regulator, which regulates T3SS gene expression. Deletion of XAC3052 caused significant reduction in the expression of T3SS and effector genes in vitro and in planta; as well as reduction of virulence in sweet orange (Citrus sinensis). Overexpression of hrpG restored the virulence of ∆XAC3052, suggesting that the loss of virulence is caused by reduction of T3SS gene expression. XAC3052 directly binds to the promoter region and represses the transcription of fadE, mhpC and fadH genes. FadE, MhpC and FadH are not involved in T3SS regulation, but involved in fatty acid catabolism. ∆XAC3052 displays altered fatty acid composition and retarded growth in environments limited in fatty acids. Exogenously supplemented long‐chain fatty acids activate the fadE/mhpC promoter and suppress T3SS promoters in wild‐type Xac but not in ∆XAC3052. Moreover, the binding of XAC3052 to its target promoter was disrupted by long‐chain fatty acids in vitro. Herein, XAC3052 is designated as TfmR (T3SS and Fatty acid Mechanism Regulator). This study identifies a novel regulator of fatty acid metabolism and suggests that fatty acids play an important role in the metabolic control of virulence in Xcc. |
format | Online Article Text |
id | pubmed-6637906 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66379062019-09-16 TfmR, a novel TetR‐family transcriptional regulator, modulates the virulence of Xanthomonas citri in response to fatty acids Teper, Doron Zhang, Yanan Wang, Nian Mol Plant Pathol Original Articles The type III secretion system (T3SS) is required for Xanthomonas citri subsp. citri (Xcc) virulence by translocating effectors into host cytoplasm to promote disease development. The T3SS is controlled by the master transcriptional regulators HrpG and HrpX. While the function of HrpG and HrpX are well characterized, their upstream regulation remains elusive. By using transposon mutagenesis, we identified XAC3052, a TetR‐family transcriptional regulator, which regulates T3SS gene expression. Deletion of XAC3052 caused significant reduction in the expression of T3SS and effector genes in vitro and in planta; as well as reduction of virulence in sweet orange (Citrus sinensis). Overexpression of hrpG restored the virulence of ∆XAC3052, suggesting that the loss of virulence is caused by reduction of T3SS gene expression. XAC3052 directly binds to the promoter region and represses the transcription of fadE, mhpC and fadH genes. FadE, MhpC and FadH are not involved in T3SS regulation, but involved in fatty acid catabolism. ∆XAC3052 displays altered fatty acid composition and retarded growth in environments limited in fatty acids. Exogenously supplemented long‐chain fatty acids activate the fadE/mhpC promoter and suppress T3SS promoters in wild‐type Xac but not in ∆XAC3052. Moreover, the binding of XAC3052 to its target promoter was disrupted by long‐chain fatty acids in vitro. Herein, XAC3052 is designated as TfmR (T3SS and Fatty acid Mechanism Regulator). This study identifies a novel regulator of fatty acid metabolism and suggests that fatty acids play an important role in the metabolic control of virulence in Xcc. John Wiley and Sons Inc. 2019-03-27 /pmc/articles/PMC6637906/ /pubmed/30919570 http://dx.doi.org/10.1111/mpp.12786 Text en © 2019 The Authors. Molecular Plant Pathology published by British Society for Plant Pathology and John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Teper, Doron Zhang, Yanan Wang, Nian TfmR, a novel TetR‐family transcriptional regulator, modulates the virulence of Xanthomonas citri in response to fatty acids |
title | TfmR, a novel TetR‐family transcriptional regulator, modulates the virulence of Xanthomonas citri in response to fatty acids |
title_full | TfmR, a novel TetR‐family transcriptional regulator, modulates the virulence of Xanthomonas citri in response to fatty acids |
title_fullStr | TfmR, a novel TetR‐family transcriptional regulator, modulates the virulence of Xanthomonas citri in response to fatty acids |
title_full_unstemmed | TfmR, a novel TetR‐family transcriptional regulator, modulates the virulence of Xanthomonas citri in response to fatty acids |
title_short | TfmR, a novel TetR‐family transcriptional regulator, modulates the virulence of Xanthomonas citri in response to fatty acids |
title_sort | tfmr, a novel tetr‐family transcriptional regulator, modulates the virulence of xanthomonas citri in response to fatty acids |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6637906/ https://www.ncbi.nlm.nih.gov/pubmed/30919570 http://dx.doi.org/10.1111/mpp.12786 |
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