High-resolution mapping reveals that microniches in the gastric glands control Helicobacter pylori colonization of the stomach.

Lifelong infection of the gastric mucosa by Helicobacter pylori can lead to peptic ulcers and gastric cancer. However, how the bacteria maintain chronic colonization in the face of constant mucus and epithelial cell turnover in the stomach is unclear. Here, we present a new model of how H. pylori es...

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Main Authors: Connie Fung, Shumin Tan, Mifuyu Nakajima, Emma C Skoog, Luis Fernando Camarillo-Guerrero, Jessica A Klein, Trevor D Lawley, Jay V Solnick, Tadashi Fukami, Manuel R Amieva
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-05-01
Series:PLoS Biology
Online Access:https://doi.org/10.1371/journal.pbio.3000231
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spelling doaj-4e380ac3d2554b67855ef0a48d1a160b2021-07-02T21:22:08ZengPublic Library of Science (PLoS)PLoS Biology1544-91731545-78852019-05-01175e300023110.1371/journal.pbio.3000231High-resolution mapping reveals that microniches in the gastric glands control Helicobacter pylori colonization of the stomach.Connie FungShumin TanMifuyu NakajimaEmma C SkoogLuis Fernando Camarillo-GuerreroJessica A KleinTrevor D LawleyJay V SolnickTadashi FukamiManuel R AmievaLifelong infection of the gastric mucosa by Helicobacter pylori can lead to peptic ulcers and gastric cancer. However, how the bacteria maintain chronic colonization in the face of constant mucus and epithelial cell turnover in the stomach is unclear. Here, we present a new model of how H. pylori establish and persist in stomach, which involves the colonization of a specialized microenvironment, or microniche, deep in the gastric glands. Using quantitative three-dimensional (3D) confocal microscopy and passive CLARITY technique (PACT), which renders tissues optically transparent, we analyzed intact stomachs from mice infected with a mixture of isogenic, fluorescent H. pylori strains with unprecedented spatial resolution. We discovered that a small number of bacterial founders initially establish colonies deep in the gastric glands and then expand to colonize adjacent glands, forming clonal population islands that persist over time. Gland-associated populations do not intermix with free-swimming bacteria in the surface mucus, and they compete for space and prevent newcomers from establishing in the stomach. Furthermore, bacterial mutants deficient in gland colonization are outcompeted by wild-type (WT) bacteria. Finally, we found that host factors such as the age at infection and T-cell responses control bacterial density within the glands. Collectively, our results demonstrate that microniches in the gastric glands house a persistent H. pylori reservoir, which we propose replenishes the more transient bacterial populations in the superficial mucosa.https://doi.org/10.1371/journal.pbio.3000231
collection DOAJ
language English
format Article
sources DOAJ
author Connie Fung
Shumin Tan
Mifuyu Nakajima
Emma C Skoog
Luis Fernando Camarillo-Guerrero
Jessica A Klein
Trevor D Lawley
Jay V Solnick
Tadashi Fukami
Manuel R Amieva
spellingShingle Connie Fung
Shumin Tan
Mifuyu Nakajima
Emma C Skoog
Luis Fernando Camarillo-Guerrero
Jessica A Klein
Trevor D Lawley
Jay V Solnick
Tadashi Fukami
Manuel R Amieva
High-resolution mapping reveals that microniches in the gastric glands control Helicobacter pylori colonization of the stomach.
PLoS Biology
author_facet Connie Fung
Shumin Tan
Mifuyu Nakajima
Emma C Skoog
Luis Fernando Camarillo-Guerrero
Jessica A Klein
Trevor D Lawley
Jay V Solnick
Tadashi Fukami
Manuel R Amieva
author_sort Connie Fung
title High-resolution mapping reveals that microniches in the gastric glands control Helicobacter pylori colonization of the stomach.
title_short High-resolution mapping reveals that microniches in the gastric glands control Helicobacter pylori colonization of the stomach.
title_full High-resolution mapping reveals that microniches in the gastric glands control Helicobacter pylori colonization of the stomach.
title_fullStr High-resolution mapping reveals that microniches in the gastric glands control Helicobacter pylori colonization of the stomach.
title_full_unstemmed High-resolution mapping reveals that microniches in the gastric glands control Helicobacter pylori colonization of the stomach.
title_sort high-resolution mapping reveals that microniches in the gastric glands control helicobacter pylori colonization of the stomach.
publisher Public Library of Science (PLoS)
series PLoS Biology
issn 1544-9173
1545-7885
publishDate 2019-05-01
description Lifelong infection of the gastric mucosa by Helicobacter pylori can lead to peptic ulcers and gastric cancer. However, how the bacteria maintain chronic colonization in the face of constant mucus and epithelial cell turnover in the stomach is unclear. Here, we present a new model of how H. pylori establish and persist in stomach, which involves the colonization of a specialized microenvironment, or microniche, deep in the gastric glands. Using quantitative three-dimensional (3D) confocal microscopy and passive CLARITY technique (PACT), which renders tissues optically transparent, we analyzed intact stomachs from mice infected with a mixture of isogenic, fluorescent H. pylori strains with unprecedented spatial resolution. We discovered that a small number of bacterial founders initially establish colonies deep in the gastric glands and then expand to colonize adjacent glands, forming clonal population islands that persist over time. Gland-associated populations do not intermix with free-swimming bacteria in the surface mucus, and they compete for space and prevent newcomers from establishing in the stomach. Furthermore, bacterial mutants deficient in gland colonization are outcompeted by wild-type (WT) bacteria. Finally, we found that host factors such as the age at infection and T-cell responses control bacterial density within the glands. Collectively, our results demonstrate that microniches in the gastric glands house a persistent H. pylori reservoir, which we propose replenishes the more transient bacterial populations in the superficial mucosa.
url https://doi.org/10.1371/journal.pbio.3000231
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