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Site-directed mutagenesis of Campylobacter concisus respiratory genes provides insight into the pathogen’s growth requirements
Campylobacter concisus is an emerging human pathogen found throughout the entire human oral-gastrointestinal tract. The ability of C. concisus to colonize diverse niches of the human body indicates the pathogen is metabolically versatile. C. concisus is able to grow under both anaerobic conditions a...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155014/ https://www.ncbi.nlm.nih.gov/pubmed/30242194 http://dx.doi.org/10.1038/s41598-018-32509-9 |
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author | Benoit, Stéphane L. Maier, Robert J. |
author_facet | Benoit, Stéphane L. Maier, Robert J. |
author_sort | Benoit, Stéphane L. |
collection | PubMed |
description | Campylobacter concisus is an emerging human pathogen found throughout the entire human oral-gastrointestinal tract. The ability of C. concisus to colonize diverse niches of the human body indicates the pathogen is metabolically versatile. C. concisus is able to grow under both anaerobic conditions and microaerophilic conditions. Hydrogen (H(2)) has been shown to enhance growth and may even be required. Analysis of several C. concisus genome sequences reveals the presence of two sets of genes encoding for distinct hydrogenases: a H(2)-uptake-type (“Hyd”) complex and a H(2)-evolving hydrogenase (“Hyf”). Whole cells hydrogenase assays indicate that the former (H(2)-uptake) activity is predominant in C. concisus, with activity among the highest we have found for pathogenic bacteria. Attempts to generate site-directed chromosomal mutants were partially successful, as we could disrupt hyfB, but not hydB, suggesting that H(2)-uptake, but not H(2)-evolving activity, is an essential respiratory pathway in C. concisus. Furthermore, the tetrathionate reductase ttrA gene was inactivated in various C. concisus genomospecies. Addition of tetrathionate to the medium resulted in a ten-fold increase in cell yield for the WT, while it had no effect on the ttrA mutant growth. To our knowledge, this is the first report of mutants in C. concisus. |
format | Online Article Text |
id | pubmed-6155014 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61550142018-09-28 Site-directed mutagenesis of Campylobacter concisus respiratory genes provides insight into the pathogen’s growth requirements Benoit, Stéphane L. Maier, Robert J. Sci Rep Article Campylobacter concisus is an emerging human pathogen found throughout the entire human oral-gastrointestinal tract. The ability of C. concisus to colonize diverse niches of the human body indicates the pathogen is metabolically versatile. C. concisus is able to grow under both anaerobic conditions and microaerophilic conditions. Hydrogen (H(2)) has been shown to enhance growth and may even be required. Analysis of several C. concisus genome sequences reveals the presence of two sets of genes encoding for distinct hydrogenases: a H(2)-uptake-type (“Hyd”) complex and a H(2)-evolving hydrogenase (“Hyf”). Whole cells hydrogenase assays indicate that the former (H(2)-uptake) activity is predominant in C. concisus, with activity among the highest we have found for pathogenic bacteria. Attempts to generate site-directed chromosomal mutants were partially successful, as we could disrupt hyfB, but not hydB, suggesting that H(2)-uptake, but not H(2)-evolving activity, is an essential respiratory pathway in C. concisus. Furthermore, the tetrathionate reductase ttrA gene was inactivated in various C. concisus genomospecies. Addition of tetrathionate to the medium resulted in a ten-fold increase in cell yield for the WT, while it had no effect on the ttrA mutant growth. To our knowledge, this is the first report of mutants in C. concisus. Nature Publishing Group UK 2018-09-21 /pmc/articles/PMC6155014/ /pubmed/30242194 http://dx.doi.org/10.1038/s41598-018-32509-9 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Benoit, Stéphane L. Maier, Robert J. Site-directed mutagenesis of Campylobacter concisus respiratory genes provides insight into the pathogen’s growth requirements |
title | Site-directed mutagenesis of Campylobacter concisus respiratory genes provides insight into the pathogen’s growth requirements |
title_full | Site-directed mutagenesis of Campylobacter concisus respiratory genes provides insight into the pathogen’s growth requirements |
title_fullStr | Site-directed mutagenesis of Campylobacter concisus respiratory genes provides insight into the pathogen’s growth requirements |
title_full_unstemmed | Site-directed mutagenesis of Campylobacter concisus respiratory genes provides insight into the pathogen’s growth requirements |
title_short | Site-directed mutagenesis of Campylobacter concisus respiratory genes provides insight into the pathogen’s growth requirements |
title_sort | site-directed mutagenesis of campylobacter concisus respiratory genes provides insight into the pathogen’s growth requirements |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155014/ https://www.ncbi.nlm.nih.gov/pubmed/30242194 http://dx.doi.org/10.1038/s41598-018-32509-9 |
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