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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...

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Autores principales: Rossi, Mirko, Bolz, Christian, Revez, Joana, Javed, Sundus, El-Najjar, Nahed, Anderl, Florian, Hyytiäinen, Heidi, Vuorela, Pia, Gerhard, Markus, Hänninen, Marja-Liisa
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
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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.
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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
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