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Identification and Characterization of Helicobacter pylori Genes Essential for Gastric Colonization
Helicobacter pylori causes one of the most common, chronic bacterial infections and is a primary cause of severe gastric disorders. To unravel the bacterial factors necessary for the process of gastric colonization and pathogenesis, signature tagged mutagenesis (STM) was adapted to H. pylori. The Mo...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2003
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2193887/ https://www.ncbi.nlm.nih.gov/pubmed/12668646 http://dx.doi.org/10.1084/jem.20021531 |
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author | Kavermann, Holger Burns, Brendan P. Angermüller, Katrin Odenbreit, Stefan Fischer, Wolfgang Melchers, Klaus Haas, Rainer |
author_facet | Kavermann, Holger Burns, Brendan P. Angermüller, Katrin Odenbreit, Stefan Fischer, Wolfgang Melchers, Klaus Haas, Rainer |
author_sort | Kavermann, Holger |
collection | PubMed |
description | Helicobacter pylori causes one of the most common, chronic bacterial infections and is a primary cause of severe gastric disorders. To unravel the bacterial factors necessary for the process of gastric colonization and pathogenesis, signature tagged mutagenesis (STM) was adapted to H. pylori. The Mongolian gerbil (Meriones unguiculatus) was used as model system to screen a set of 960 STM mutants. This resulted in 47 H. pylori genes, assigned to 9 different functional categories, representing a set of biological functions absolutely essential for gastric colonization, as verified and quantified for many mutants by competition experiments. Identification of previously known colonization factors, such as the urease and motility functions validated this method, but also novel and several hypothetical genes were found. Interestingly, a secreted collagenase, encoded by hp0169, could be identified and functionally verified as a new essential virulence factor for H. pylori stomach colonization. Furthermore, comB4, encoding a putative ATPase being part of a DNA transformation-associated type IV transport system of H. pylori was found to be absolutely essential for colonization, but natural transformation competence was apparently not the essential function. Thus, this first systematic STM application identified a set of previously unknown H. pylori colonization factors and may help to potentiate the development of novel therapies against gastric Helicobacter infections. |
format | Text |
id | pubmed-2193887 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21938872008-04-11 Identification and Characterization of Helicobacter pylori Genes Essential for Gastric Colonization Kavermann, Holger Burns, Brendan P. Angermüller, Katrin Odenbreit, Stefan Fischer, Wolfgang Melchers, Klaus Haas, Rainer J Exp Med Article Helicobacter pylori causes one of the most common, chronic bacterial infections and is a primary cause of severe gastric disorders. To unravel the bacterial factors necessary for the process of gastric colonization and pathogenesis, signature tagged mutagenesis (STM) was adapted to H. pylori. The Mongolian gerbil (Meriones unguiculatus) was used as model system to screen a set of 960 STM mutants. This resulted in 47 H. pylori genes, assigned to 9 different functional categories, representing a set of biological functions absolutely essential for gastric colonization, as verified and quantified for many mutants by competition experiments. Identification of previously known colonization factors, such as the urease and motility functions validated this method, but also novel and several hypothetical genes were found. Interestingly, a secreted collagenase, encoded by hp0169, could be identified and functionally verified as a new essential virulence factor for H. pylori stomach colonization. Furthermore, comB4, encoding a putative ATPase being part of a DNA transformation-associated type IV transport system of H. pylori was found to be absolutely essential for colonization, but natural transformation competence was apparently not the essential function. Thus, this first systematic STM application identified a set of previously unknown H. pylori colonization factors and may help to potentiate the development of novel therapies against gastric Helicobacter infections. The Rockefeller University Press 2003-04-07 /pmc/articles/PMC2193887/ /pubmed/12668646 http://dx.doi.org/10.1084/jem.20021531 Text en Copyright © 2003, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Article Kavermann, Holger Burns, Brendan P. Angermüller, Katrin Odenbreit, Stefan Fischer, Wolfgang Melchers, Klaus Haas, Rainer Identification and Characterization of Helicobacter pylori Genes Essential for Gastric Colonization |
title | Identification and Characterization of Helicobacter pylori Genes Essential for Gastric Colonization |
title_full | Identification and Characterization of Helicobacter pylori Genes Essential for Gastric Colonization |
title_fullStr | Identification and Characterization of Helicobacter pylori Genes Essential for Gastric Colonization |
title_full_unstemmed | Identification and Characterization of Helicobacter pylori Genes Essential for Gastric Colonization |
title_short | Identification and Characterization of Helicobacter pylori Genes Essential for Gastric Colonization |
title_sort | identification and characterization of helicobacter pylori genes essential for gastric colonization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2193887/ https://www.ncbi.nlm.nih.gov/pubmed/12668646 http://dx.doi.org/10.1084/jem.20021531 |
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