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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...

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Detalles Bibliográficos
Autores principales: Linz, Bodo, Windsor, Helen M., Gajewski, John P., Hake, Caylie M., Drautz, Daniela I., Schuster, Stephan C., Marshall, Barry J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
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.
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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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