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Diversity in bacterium-host interactions within the species Helicobacter heilmannii sensu stricto

Helicobacter (H.) heilmannii sensu stricto (s.s.) is a zoonotic bacterium that naturally colonizes the stomach of dogs and cats. In humans, this microorganism has been associated with gastritis, peptic ulcer disease and mucosa associated lymphoid tissue (MALT) lymphoma. Little information is availab...

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Autores principales: Joosten, Myrthe, Blaecher, Caroline, Flahou, Bram, Ducatelle, Richard, Haesebrouck, Freddy, Smet, Annemieke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3750284/
https://www.ncbi.nlm.nih.gov/pubmed/23895283
http://dx.doi.org/10.1186/1297-9716-44-65
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author Joosten, Myrthe
Blaecher, Caroline
Flahou, Bram
Ducatelle, Richard
Haesebrouck, Freddy
Smet, Annemieke
author_facet Joosten, Myrthe
Blaecher, Caroline
Flahou, Bram
Ducatelle, Richard
Haesebrouck, Freddy
Smet, Annemieke
author_sort Joosten, Myrthe
collection PubMed
description Helicobacter (H.) heilmannii sensu stricto (s.s.) is a zoonotic bacterium that naturally colonizes the stomach of dogs and cats. In humans, this microorganism has been associated with gastritis, peptic ulcer disease and mucosa associated lymphoid tissue (MALT) lymphoma. Little information is available about the pathogenesis of H. heilmannii s.s. infections in humans and it is unknown whether differences in virulence exist within this species. Therefore, a Mongolian gerbil model was used to study bacterium-host interactions of 9 H. heilmannii s.s. strains. The colonization ability of the strains, the intensity of gastritis and gene expression of various inflammatory cytokines in the stomach were determined at 9 weeks after experimental infection. The induction of an antrum-dominant chronic active gastritis with formation of lymphocytic aggregates was shown for 7 strains. High-level antral colonization was seen for 4 strains, while colonization of 4 other strains was more restricted and one strain was not detected in the stomach at 9 weeks post infection. All strains inducing a chronic active gastritis caused an up-regulation of the pro-inflammatory cytokine IL-1β in the antrum. A reduced antral expression of H(+)/K(+) ATPase was seen in the stomach after infection with 3 highly colonizing strains and 2 highly colonizing strains caused an increased gastrin expression in the fundus. In none of the H. heilmannii s.s.-infected groups, IFN-γ expression was up-regulated. This study demonstrates diversity in bacterium-host interactions within the species H. heilmannii s.s. and that the pathogenesis of gastric infections with this microorganism is not identical to that of an H. pylori infection.
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spelling pubmed-37502842013-08-24 Diversity in bacterium-host interactions within the species Helicobacter heilmannii sensu stricto Joosten, Myrthe Blaecher, Caroline Flahou, Bram Ducatelle, Richard Haesebrouck, Freddy Smet, Annemieke Vet Res Research Helicobacter (H.) heilmannii sensu stricto (s.s.) is a zoonotic bacterium that naturally colonizes the stomach of dogs and cats. In humans, this microorganism has been associated with gastritis, peptic ulcer disease and mucosa associated lymphoid tissue (MALT) lymphoma. Little information is available about the pathogenesis of H. heilmannii s.s. infections in humans and it is unknown whether differences in virulence exist within this species. Therefore, a Mongolian gerbil model was used to study bacterium-host interactions of 9 H. heilmannii s.s. strains. The colonization ability of the strains, the intensity of gastritis and gene expression of various inflammatory cytokines in the stomach were determined at 9 weeks after experimental infection. The induction of an antrum-dominant chronic active gastritis with formation of lymphocytic aggregates was shown for 7 strains. High-level antral colonization was seen for 4 strains, while colonization of 4 other strains was more restricted and one strain was not detected in the stomach at 9 weeks post infection. All strains inducing a chronic active gastritis caused an up-regulation of the pro-inflammatory cytokine IL-1β in the antrum. A reduced antral expression of H(+)/K(+) ATPase was seen in the stomach after infection with 3 highly colonizing strains and 2 highly colonizing strains caused an increased gastrin expression in the fundus. In none of the H. heilmannii s.s.-infected groups, IFN-γ expression was up-regulated. This study demonstrates diversity in bacterium-host interactions within the species H. heilmannii s.s. and that the pathogenesis of gastric infections with this microorganism is not identical to that of an H. pylori infection. BioMed Central 2013 2013-07-29 /pmc/articles/PMC3750284/ /pubmed/23895283 http://dx.doi.org/10.1186/1297-9716-44-65 Text en Copyright © 2013 Joosten et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Joosten, Myrthe
Blaecher, Caroline
Flahou, Bram
Ducatelle, Richard
Haesebrouck, Freddy
Smet, Annemieke
Diversity in bacterium-host interactions within the species Helicobacter heilmannii sensu stricto
title Diversity in bacterium-host interactions within the species Helicobacter heilmannii sensu stricto
title_full Diversity in bacterium-host interactions within the species Helicobacter heilmannii sensu stricto
title_fullStr Diversity in bacterium-host interactions within the species Helicobacter heilmannii sensu stricto
title_full_unstemmed Diversity in bacterium-host interactions within the species Helicobacter heilmannii sensu stricto
title_short Diversity in bacterium-host interactions within the species Helicobacter heilmannii sensu stricto
title_sort diversity in bacterium-host interactions within the species helicobacter heilmannii sensu stricto
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3750284/
https://www.ncbi.nlm.nih.gov/pubmed/23895283
http://dx.doi.org/10.1186/1297-9716-44-65
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