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Updated: Jun 16, 2026

Non-Invasive Model of Neuropathogenic Escherichia coli Infection in the Neonatal Rat
Published on: October 29, 2014
Neonatal infection with Helicobacter pylori affects stomach and colon microbiome composition and gene expression in
Katrine B Graversen1, Bella Bjarnov-Nicolau1, Sigri Kløve1
1Center for Evolutionary Hologenomics, Globe Institute, University of Copenhagen, Denmark.
Insights
Neonatal Helicobacter pylori (H. pylori) infection in mice alters the gut microbiome and stomach gene expression, potentially accelerating development. This study models early-life infection impacts.
Area of Science:
- Microbiology
- Gastroenterology
- Immunology
Background:
- Helicobacter pylori infection affects millions globally, with health outcomes influenced by age at infection.
- Neonatal H. pylori infection in mice provides a model for studying early-life metabolic and immunological effects.
- The dynamic first month of life is crucial for understanding host-microbe interactions.
Purpose of the Study:
- To compare the gastrointestinal tract microbiome and stomach gene expression in neonatally H. pylori-infected mice versus uninfected controls.
- To investigate the dynamic changes during the first month of life following H. pylori infection.
- To explore the impact of low-level H. pylori colonization on the host.
Main Methods:
- Explorative study design in a mouse model.
- Analysis of gastrointestinal tract microbiome composition (stomach and colon).
- Stomach gene expression profiling using pathway enrichment analysis.
Main Results:
- H. pylori was localized to the stomach, with loads increasing post-weaning.
- Despite low H. pylori abundance (<3%), infection significantly altered gastrointestinal microbiome composition and alpha diversity.
- Stomach gene expression related to extracellular matrix, muscle contraction, and metabolism was affected by H. pylori infection.
Conclusions:
- Neonatal H. pylori infection significantly impacts the developing gastrointestinal microbiome and host gene expression.
- Infected mice showed gene expression patterns resembling later developmental stages, suggesting accelerated development.
- Early-life H. pylori infection warrants further investigation for its long-term health implications.
Abstract:
The stomach bacterium Helicobacter pylori is estimated to infect half of the world's population, and the health implications are affected by the age at infection. Neonatal H. pylori infection of mice is a relevant model to investigate metabolic and immunological effects. We performed an explorative study at the dynamic first month of life, to compare the composition of the gastrointestinal tract microbiome and stomach gene expression of mice neonatally infected with H. pylori with that of uninfected mice. We found that H. pylori was present only in the stomach, and that H. pylori loads increase with age from one week after infection and onwards, especially after weaning. Stomach and colon microbiome composition was strikingly similar between sites at the same sampling time, but changed significantly over one week, with increased diversity at both sites. Despite that the relative abundance of H. pylori in the stomach was low and never exceeded 3%, the composition and alpha diversity of the gastrointestinal microbiome was significantly affected by infection. In a pathway enrichment analysis we found that stomach gene expression related to the extracellular matrix, muscle contraction, and metabolism was affected by infection. Expression of these key processes was, in infected mice, shifted away from that of control mice, towards that of all mice sampled the subsequent week, which we speculate represents accelerated development in infected mice.
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