Helicobacter pylori adaptation in vivo in response to a high-salt diet

Infect Immun. 2015 Dec;83(12):4871-83. doi: 10.1128/IAI.00918-15. Epub 2015 Oct 5.

Abstract

Helicobacter pylori exhibits a high level of intraspecies genetic diversity. In this study, we investigated whether the diversification of H. pylori is influenced by the composition of the diet. Specifically, we investigated the effect of a high-salt diet (a known risk factor for gastric adenocarcinoma) on H. pylori diversification within a host. We analyzed H. pylori strains isolated from Mongolian gerbils fed either a high-salt diet or a regular diet for 4 months by proteomic and whole-genome sequencing methods. Compared to the input strain and output strains from animals fed a regular diet, the output strains from animals fed a high-salt diet produced higher levels of proteins involved in iron acquisition and oxidative-stress resistance. Several of these changes were attributable to a nonsynonymous mutation in fur (fur-R88H). Further experiments indicated that this mutation conferred increased resistance to high-salt conditions and oxidative stress. We propose a model in which a high-salt diet leads to high levels of gastric inflammation and associated oxidative stress in H. pylori-infected animals and that these conditions, along with the high intraluminal concentrations of sodium chloride, lead to selection of H. pylori strains that are most fit for growth in this environment.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adaptation, Physiological / genetics*
  • Animals
  • Bacterial Proteins / genetics*
  • Bacterial Proteins / metabolism
  • Base Sequence
  • Disease Models, Animal
  • Gastric Mucosa
  • Gene Expression Profiling
  • Gene Expression Regulation, Bacterial*
  • Genome, Bacterial*
  • Gerbillinae
  • Helicobacter Infections / immunology
  • Helicobacter Infections / microbiology*
  • Helicobacter Infections / pathology
  • Helicobacter pylori / drug effects*
  • Helicobacter pylori / genetics
  • Helicobacter pylori / pathogenicity
  • Host-Pathogen Interactions
  • Humans
  • Iron / metabolism
  • Molecular Sequence Data
  • Mutation
  • Oxidative Stress
  • Proteome
  • Repressor Proteins / genetics*
  • Repressor Proteins / metabolism
  • Sodium Chloride, Dietary / pharmacology*

Substances

  • Bacterial Proteins
  • Proteome
  • Repressor Proteins
  • Sodium Chloride, Dietary
  • ferric uptake regulating proteins, bacterial
  • Iron