Cargando…
Evidence for Conserved Function of γ–Glutamyltranspeptidase in Helicobacter Genus
The confounding consequences of Helicobacter bilis infection in experimental mice populations are well recognized, but the role of this bacterium in human diseases is less known. Limited data are available on virulence determinants of this species. In Helicobacter pylori, γ-glutamyltranspeptidase (γ...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3279353/ https://www.ncbi.nlm.nih.gov/pubmed/22348013 http://dx.doi.org/10.1371/journal.pone.0030543 |
_version_ | 1782223665093410816 |
---|---|
author | Rossi, Mirko Bolz, Christian Revez, Joana Javed, Sundus El-Najjar, Nahed Anderl, Florian Hyytiäinen, Heidi Vuorela, Pia Gerhard, Markus Hänninen, Marja-Liisa |
author_facet | Rossi, Mirko Bolz, Christian Revez, Joana Javed, Sundus El-Najjar, Nahed Anderl, Florian Hyytiäinen, Heidi Vuorela, Pia Gerhard, Markus Hänninen, Marja-Liisa |
author_sort | Rossi, Mirko |
collection | PubMed |
description | The confounding consequences of Helicobacter bilis infection in experimental mice populations are well recognized, but the role of this bacterium in human diseases is less known. Limited data are available on virulence determinants of this species. In Helicobacter pylori, γ-glutamyltranspeptidase (γGT) contributes to the colonization of the gastric mucosa and to the pathogenesis of peptic ulcer. The role of γGT in H. bilis infections remains unknown. The annotated genome sequence of H. bilis revealed two putative ggt genes and our aim was to characterize these H. bilis γGT paralogues. We performed a phylogenetic analysis to understand the evolution of Helicobacter γGTs and to predict functional activities of these two genes. In addition, both copies of H. bilis γGTs were expressed as recombinant proteins and their biochemical characteristics were analysed. Functional complementation of Esherichia coli deficient in γGT activity and deletion of γGT in H. bilis were performed. Finally, the inhibitory effect of T-cell and gastric cell proliferation by H. bilis γGT was assessed. Our results indicated that one gene is responsible for γGT activity, while the other showed no γGT activity due to lack of autoprocessing. Although both H. bilis and H. pylori γGTs exhibited a similar affinity to L-Glutamine and γ-Glutamyl-p-nitroanilide, the H. bilis γGT was significantly less active. Nevertheless, H. bilis γGT inhibited T-cell proliferation at a similar level to that observed for H. pylori. Finally, we showed a similar suppressive influence of both H. bilis and H. pylori γGTs on AGS cell proliferation mediated by an apoptosis-independent mechanism. Our data suggest a conserved function of γGT in the Helicobacter genus. Since γGT is present only in a few enterohepatic Helicobacter species, its expression appears not to be essential for colonization of the lower gastrointestinal tract, but it could provide metabolic advantages in colonization capability of different niches. |
format | Online Article Text |
id | pubmed-3279353 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-32793532012-02-17 Evidence for Conserved Function of γ–Glutamyltranspeptidase in Helicobacter Genus Rossi, Mirko Bolz, Christian Revez, Joana Javed, Sundus El-Najjar, Nahed Anderl, Florian Hyytiäinen, Heidi Vuorela, Pia Gerhard, Markus Hänninen, Marja-Liisa PLoS One Research Article The confounding consequences of Helicobacter bilis infection in experimental mice populations are well recognized, but the role of this bacterium in human diseases is less known. Limited data are available on virulence determinants of this species. In Helicobacter pylori, γ-glutamyltranspeptidase (γGT) contributes to the colonization of the gastric mucosa and to the pathogenesis of peptic ulcer. The role of γGT in H. bilis infections remains unknown. The annotated genome sequence of H. bilis revealed two putative ggt genes and our aim was to characterize these H. bilis γGT paralogues. We performed a phylogenetic analysis to understand the evolution of Helicobacter γGTs and to predict functional activities of these two genes. In addition, both copies of H. bilis γGTs were expressed as recombinant proteins and their biochemical characteristics were analysed. Functional complementation of Esherichia coli deficient in γGT activity and deletion of γGT in H. bilis were performed. Finally, the inhibitory effect of T-cell and gastric cell proliferation by H. bilis γGT was assessed. Our results indicated that one gene is responsible for γGT activity, while the other showed no γGT activity due to lack of autoprocessing. Although both H. bilis and H. pylori γGTs exhibited a similar affinity to L-Glutamine and γ-Glutamyl-p-nitroanilide, the H. bilis γGT was significantly less active. Nevertheless, H. bilis γGT inhibited T-cell proliferation at a similar level to that observed for H. pylori. Finally, we showed a similar suppressive influence of both H. bilis and H. pylori γGTs on AGS cell proliferation mediated by an apoptosis-independent mechanism. Our data suggest a conserved function of γGT in the Helicobacter genus. Since γGT is present only in a few enterohepatic Helicobacter species, its expression appears not to be essential for colonization of the lower gastrointestinal tract, but it could provide metabolic advantages in colonization capability of different niches. Public Library of Science 2012-02-14 /pmc/articles/PMC3279353/ /pubmed/22348013 http://dx.doi.org/10.1371/journal.pone.0030543 Text en Rossi et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Rossi, Mirko Bolz, Christian Revez, Joana Javed, Sundus El-Najjar, Nahed Anderl, Florian Hyytiäinen, Heidi Vuorela, Pia Gerhard, Markus Hänninen, Marja-Liisa Evidence for Conserved Function of γ–Glutamyltranspeptidase in Helicobacter Genus |
title | Evidence for Conserved Function of γ–Glutamyltranspeptidase in Helicobacter Genus |
title_full | Evidence for Conserved Function of γ–Glutamyltranspeptidase in Helicobacter Genus |
title_fullStr | Evidence for Conserved Function of γ–Glutamyltranspeptidase in Helicobacter Genus |
title_full_unstemmed | Evidence for Conserved Function of γ–Glutamyltranspeptidase in Helicobacter Genus |
title_short | Evidence for Conserved Function of γ–Glutamyltranspeptidase in Helicobacter Genus |
title_sort | evidence for conserved function of γ–glutamyltranspeptidase in helicobacter genus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3279353/ https://www.ncbi.nlm.nih.gov/pubmed/22348013 http://dx.doi.org/10.1371/journal.pone.0030543 |
work_keys_str_mv | AT rossimirko evidenceforconservedfunctionofgglutamyltranspeptidaseinhelicobactergenus AT bolzchristian evidenceforconservedfunctionofgglutamyltranspeptidaseinhelicobactergenus AT revezjoana evidenceforconservedfunctionofgglutamyltranspeptidaseinhelicobactergenus AT javedsundus evidenceforconservedfunctionofgglutamyltranspeptidaseinhelicobactergenus AT elnajjarnahed evidenceforconservedfunctionofgglutamyltranspeptidaseinhelicobactergenus AT anderlflorian evidenceforconservedfunctionofgglutamyltranspeptidaseinhelicobactergenus AT hyytiainenheidi evidenceforconservedfunctionofgglutamyltranspeptidaseinhelicobactergenus AT vuorelapia evidenceforconservedfunctionofgglutamyltranspeptidaseinhelicobactergenus AT gerhardmarkus evidenceforconservedfunctionofgglutamyltranspeptidaseinhelicobactergenus AT hanninenmarjaliisa evidenceforconservedfunctionofgglutamyltranspeptidaseinhelicobactergenus |