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Gene Expression Profiling of Transcription Factors of Helicobacter pylori under Different Environmental Conditions
Helicobacter pylori is a Gram-negative bacterium that colonizes the human gastric mucosa and causes peptic ulcers and gastric carcinoma. H. pylori strain 26695 has a small genome (1.67 Mb), which codes for few known transcriptional regulators that control bacterial metabolism and virulence. We analy...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5385360/ https://www.ncbi.nlm.nih.gov/pubmed/28443084 http://dx.doi.org/10.3389/fmicb.2017.00615 |
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author | De la Cruz, Miguel A. Ares, Miguel A. von Bargen, Kristine Panunzi, Leonardo G. Martínez-Cruz, Jessica Valdez-Salazar, Hilda A. Jiménez-Galicia, César Torres, Javier |
author_facet | De la Cruz, Miguel A. Ares, Miguel A. von Bargen, Kristine Panunzi, Leonardo G. Martínez-Cruz, Jessica Valdez-Salazar, Hilda A. Jiménez-Galicia, César Torres, Javier |
author_sort | De la Cruz, Miguel A. |
collection | PubMed |
description | Helicobacter pylori is a Gram-negative bacterium that colonizes the human gastric mucosa and causes peptic ulcers and gastric carcinoma. H. pylori strain 26695 has a small genome (1.67 Mb), which codes for few known transcriptional regulators that control bacterial metabolism and virulence. We analyzed by qRT-PCR the expression of 16 transcriptional regulators in H. pylori 26695, including the three sigma factors under different environmental conditions. When bacteria were exposed to acidic pH, urea, nickel, or iron, the sigma factors were differentially expressed with a particularly strong induction of fliA. The regulatory genes hrcA, hup, and crdR were highly induced in the presence of urea, nickel, and iron. In terms of biofilm formation fliA, flgR, hp1021, fur, nikR, and crdR were induced in sessile bacteria. Transcriptional expression levels of rpoD, flgR, hspR, hp1043, and cheY were increased in contact with AGS epithelial cells. Kanamycin, chloramphenicol, and tetracycline increased or decreased expression of regulatory genes, showing that these antibiotics affect the transcription of H. pylori. Our data indicate that environmental cues which may be present in the human stomach modulate H. pylori transcription. |
format | Online Article Text |
id | pubmed-5385360 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53853602017-04-25 Gene Expression Profiling of Transcription Factors of Helicobacter pylori under Different Environmental Conditions De la Cruz, Miguel A. Ares, Miguel A. von Bargen, Kristine Panunzi, Leonardo G. Martínez-Cruz, Jessica Valdez-Salazar, Hilda A. Jiménez-Galicia, César Torres, Javier Front Microbiol Microbiology Helicobacter pylori is a Gram-negative bacterium that colonizes the human gastric mucosa and causes peptic ulcers and gastric carcinoma. H. pylori strain 26695 has a small genome (1.67 Mb), which codes for few known transcriptional regulators that control bacterial metabolism and virulence. We analyzed by qRT-PCR the expression of 16 transcriptional regulators in H. pylori 26695, including the three sigma factors under different environmental conditions. When bacteria were exposed to acidic pH, urea, nickel, or iron, the sigma factors were differentially expressed with a particularly strong induction of fliA. The regulatory genes hrcA, hup, and crdR were highly induced in the presence of urea, nickel, and iron. In terms of biofilm formation fliA, flgR, hp1021, fur, nikR, and crdR were induced in sessile bacteria. Transcriptional expression levels of rpoD, flgR, hspR, hp1043, and cheY were increased in contact with AGS epithelial cells. Kanamycin, chloramphenicol, and tetracycline increased or decreased expression of regulatory genes, showing that these antibiotics affect the transcription of H. pylori. Our data indicate that environmental cues which may be present in the human stomach modulate H. pylori transcription. Frontiers Media S.A. 2017-04-10 /pmc/articles/PMC5385360/ /pubmed/28443084 http://dx.doi.org/10.3389/fmicb.2017.00615 Text en Copyright © 2017 De la Cruz, Ares, von Bargen, Panunzi, Martínez-Cruz, Valdez-Salazar, Jiménez-Galicia and Torres. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology De la Cruz, Miguel A. Ares, Miguel A. von Bargen, Kristine Panunzi, Leonardo G. Martínez-Cruz, Jessica Valdez-Salazar, Hilda A. Jiménez-Galicia, César Torres, Javier Gene Expression Profiling of Transcription Factors of Helicobacter pylori under Different Environmental Conditions |
title | Gene Expression Profiling of Transcription Factors of Helicobacter pylori under Different Environmental Conditions |
title_full | Gene Expression Profiling of Transcription Factors of Helicobacter pylori under Different Environmental Conditions |
title_fullStr | Gene Expression Profiling of Transcription Factors of Helicobacter pylori under Different Environmental Conditions |
title_full_unstemmed | Gene Expression Profiling of Transcription Factors of Helicobacter pylori under Different Environmental Conditions |
title_short | Gene Expression Profiling of Transcription Factors of Helicobacter pylori under Different Environmental Conditions |
title_sort | gene expression profiling of transcription factors of helicobacter pylori under different environmental conditions |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5385360/ https://www.ncbi.nlm.nih.gov/pubmed/28443084 http://dx.doi.org/10.3389/fmicb.2017.00615 |
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