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Helicobacter pylori Genomic Microevolution during Naturally Occurring Transmission between Adults
The human gastric pathogen Helicobacter pylori is usually acquired during childhood and, in the absence of treatment, chronic infection persists through most of the host's life. However, the frequency and importance of H. pylori transmission between adults is underestimated. Here we sequenced t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3858298/ https://www.ncbi.nlm.nih.gov/pubmed/24340004 http://dx.doi.org/10.1371/journal.pone.0082187 |
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author | Linz, Bodo Windsor, Helen M. Gajewski, John P. Hake, Caylie M. Drautz, Daniela I. Schuster, Stephan C. Marshall, Barry J. |
author_facet | Linz, Bodo Windsor, Helen M. Gajewski, John P. Hake, Caylie M. Drautz, Daniela I. Schuster, Stephan C. Marshall, Barry J. |
author_sort | Linz, Bodo |
collection | PubMed |
description | The human gastric pathogen Helicobacter pylori is usually acquired during childhood and, in the absence of treatment, chronic infection persists through most of the host's life. However, the frequency and importance of H. pylori transmission between adults is underestimated. Here we sequenced the complete genomes of H. pylori strains that were transmitted between spouses and analysed the genomic changes. Similar to H. pylori from chronic infection, a significantly high proportion of the determined 31 SNPs and 10 recombinant DNA fragments affected genes of the hop family of outer membrane proteins, some of which are known to be adhesins. In addition, changes in a fucosyltransferase gene modified the LPS component of the bacterial cell surface, suggesting strong diversifying selection. In contrast, virulence factor genes were not affected by the genomic changes. We propose a model of the genomic changes that are associated with the transmission and adaptation of H. pylori to a new human host. |
format | Online Article Text |
id | pubmed-3858298 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38582982013-12-11 Helicobacter pylori Genomic Microevolution during Naturally Occurring Transmission between Adults Linz, Bodo Windsor, Helen M. Gajewski, John P. Hake, Caylie M. Drautz, Daniela I. Schuster, Stephan C. Marshall, Barry J. PLoS One Research Article The human gastric pathogen Helicobacter pylori is usually acquired during childhood and, in the absence of treatment, chronic infection persists through most of the host's life. However, the frequency and importance of H. pylori transmission between adults is underestimated. Here we sequenced the complete genomes of H. pylori strains that were transmitted between spouses and analysed the genomic changes. Similar to H. pylori from chronic infection, a significantly high proportion of the determined 31 SNPs and 10 recombinant DNA fragments affected genes of the hop family of outer membrane proteins, some of which are known to be adhesins. In addition, changes in a fucosyltransferase gene modified the LPS component of the bacterial cell surface, suggesting strong diversifying selection. In contrast, virulence factor genes were not affected by the genomic changes. We propose a model of the genomic changes that are associated with the transmission and adaptation of H. pylori to a new human host. Public Library of Science 2013-12-10 /pmc/articles/PMC3858298/ /pubmed/24340004 http://dx.doi.org/10.1371/journal.pone.0082187 Text en © 2013 Linz 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 Linz, Bodo Windsor, Helen M. Gajewski, John P. Hake, Caylie M. Drautz, Daniela I. Schuster, Stephan C. Marshall, Barry J. Helicobacter pylori Genomic Microevolution during Naturally Occurring Transmission between Adults |
title |
Helicobacter pylori Genomic Microevolution during Naturally Occurring Transmission between Adults |
title_full |
Helicobacter pylori Genomic Microevolution during Naturally Occurring Transmission between Adults |
title_fullStr |
Helicobacter pylori Genomic Microevolution during Naturally Occurring Transmission between Adults |
title_full_unstemmed |
Helicobacter pylori Genomic Microevolution during Naturally Occurring Transmission between Adults |
title_short |
Helicobacter pylori Genomic Microevolution during Naturally Occurring Transmission between Adults |
title_sort | helicobacter pylori genomic microevolution during naturally occurring transmission between adults |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3858298/ https://www.ncbi.nlm.nih.gov/pubmed/24340004 http://dx.doi.org/10.1371/journal.pone.0082187 |
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