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Global gene expression under nitrogen starvation in Xylella fastidiosa: contribution of the σ(54 )regulon

BACKGROUND: Xylella fastidiosa, a Gram-negative fastidious bacterium, grows in the xylem of several plants causing diseases such as citrus variegated chlorosis. As the xylem sap contains low concentrations of amino acids and other compounds, X. fastidiosa needs to cope with nitrogen limitation in it...

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Autores principales: da Silva Neto, José F, Koide, Tie, Gomes, Suely L, Marques, Marilis V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3224663/
https://www.ncbi.nlm.nih.gov/pubmed/20799976
http://dx.doi.org/10.1186/1471-2180-10-231
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author da Silva Neto, José F
Koide, Tie
Gomes, Suely L
Marques, Marilis V
author_facet da Silva Neto, José F
Koide, Tie
Gomes, Suely L
Marques, Marilis V
author_sort da Silva Neto, José F
collection PubMed
description BACKGROUND: Xylella fastidiosa, a Gram-negative fastidious bacterium, grows in the xylem of several plants causing diseases such as citrus variegated chlorosis. As the xylem sap contains low concentrations of amino acids and other compounds, X. fastidiosa needs to cope with nitrogen limitation in its natural habitat. RESULTS: In this work, we performed a whole-genome microarray analysis of the X. fastidiosa nitrogen starvation response. A time course experiment (2, 8 and 12 hours) of cultures grown in defined medium under nitrogen starvation revealed many differentially expressed genes, such as those related to transport, nitrogen assimilation, amino acid biosynthesis, transcriptional regulation, and many genes encoding hypothetical proteins. In addition, a decrease in the expression levels of many genes involved in carbon metabolism and energy generation pathways was also observed. Comparison of gene expression profiles between the wild type strain and the rpoN null mutant allowed the identification of genes directly or indirectly induced by nitrogen starvation in a σ(54)-dependent manner. A more complete picture of the σ(54 )regulon was achieved by combining the transcriptome data with an in silico search for potential σ(54)-dependent promoters, using a position weight matrix approach. One of these σ(54)-predicted binding sites, located upstream of the glnA gene (encoding glutamine synthetase), was validated by primer extension assays, confirming that this gene has a σ(54)-dependent promoter. CONCLUSIONS: Together, these results show that nitrogen starvation causes intense changes in the X. fastidiosa transcriptome and some of these differentially expressed genes belong to the σ(54 )regulon.
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spelling pubmed-32246632011-11-28 Global gene expression under nitrogen starvation in Xylella fastidiosa: contribution of the σ(54 )regulon da Silva Neto, José F Koide, Tie Gomes, Suely L Marques, Marilis V BMC Microbiol Research Article BACKGROUND: Xylella fastidiosa, a Gram-negative fastidious bacterium, grows in the xylem of several plants causing diseases such as citrus variegated chlorosis. As the xylem sap contains low concentrations of amino acids and other compounds, X. fastidiosa needs to cope with nitrogen limitation in its natural habitat. RESULTS: In this work, we performed a whole-genome microarray analysis of the X. fastidiosa nitrogen starvation response. A time course experiment (2, 8 and 12 hours) of cultures grown in defined medium under nitrogen starvation revealed many differentially expressed genes, such as those related to transport, nitrogen assimilation, amino acid biosynthesis, transcriptional regulation, and many genes encoding hypothetical proteins. In addition, a decrease in the expression levels of many genes involved in carbon metabolism and energy generation pathways was also observed. Comparison of gene expression profiles between the wild type strain and the rpoN null mutant allowed the identification of genes directly or indirectly induced by nitrogen starvation in a σ(54)-dependent manner. A more complete picture of the σ(54 )regulon was achieved by combining the transcriptome data with an in silico search for potential σ(54)-dependent promoters, using a position weight matrix approach. One of these σ(54)-predicted binding sites, located upstream of the glnA gene (encoding glutamine synthetase), was validated by primer extension assays, confirming that this gene has a σ(54)-dependent promoter. CONCLUSIONS: Together, these results show that nitrogen starvation causes intense changes in the X. fastidiosa transcriptome and some of these differentially expressed genes belong to the σ(54 )regulon. BioMed Central 2010-08-28 /pmc/articles/PMC3224663/ /pubmed/20799976 http://dx.doi.org/10.1186/1471-2180-10-231 Text en Copyright ©2010 da Silva Neto et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
da Silva Neto, José F
Koide, Tie
Gomes, Suely L
Marques, Marilis V
Global gene expression under nitrogen starvation in Xylella fastidiosa: contribution of the σ(54 )regulon
title Global gene expression under nitrogen starvation in Xylella fastidiosa: contribution of the σ(54 )regulon
title_full Global gene expression under nitrogen starvation in Xylella fastidiosa: contribution of the σ(54 )regulon
title_fullStr Global gene expression under nitrogen starvation in Xylella fastidiosa: contribution of the σ(54 )regulon
title_full_unstemmed Global gene expression under nitrogen starvation in Xylella fastidiosa: contribution of the σ(54 )regulon
title_short Global gene expression under nitrogen starvation in Xylella fastidiosa: contribution of the σ(54 )regulon
title_sort global gene expression under nitrogen starvation in xylella fastidiosa: contribution of the σ(54 )regulon
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3224663/
https://www.ncbi.nlm.nih.gov/pubmed/20799976
http://dx.doi.org/10.1186/1471-2180-10-231
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