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Who Ate Whom? Adaptive Helicobacter Genomic Changes That Accompanied a Host Jump from Early Humans to Large Felines

Helicobacter pylori infection of humans is so old that its population genetic structure reflects that of ancient human migrations. A closely related species, Helicobacter acinonychis, is specific for large felines, including cheetahs, lions, and tigers, whereas hosts more closely related to humans h...

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Autores principales: Eppinger, Mark, Baar, Claudia, Linz, Bodo, Raddatz, Günter, Lanz, Christa, Keller, Heike, Morelli, Giovanna, Gressmann, Helga, Achtman, Mark, Schuster, Stephan C
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1523251/
https://www.ncbi.nlm.nih.gov/pubmed/16789826
http://dx.doi.org/10.1371/journal.pgen.0020120
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author Eppinger, Mark
Baar, Claudia
Linz, Bodo
Raddatz, Günter
Lanz, Christa
Keller, Heike
Morelli, Giovanna
Gressmann, Helga
Achtman, Mark
Schuster, Stephan C
author_facet Eppinger, Mark
Baar, Claudia
Linz, Bodo
Raddatz, Günter
Lanz, Christa
Keller, Heike
Morelli, Giovanna
Gressmann, Helga
Achtman, Mark
Schuster, Stephan C
author_sort Eppinger, Mark
collection PubMed
description Helicobacter pylori infection of humans is so old that its population genetic structure reflects that of ancient human migrations. A closely related species, Helicobacter acinonychis, is specific for large felines, including cheetahs, lions, and tigers, whereas hosts more closely related to humans harbor more distantly related Helicobacter species. This observation suggests a jump between host species. But who ate whom and when did it happen? In order to resolve this question, we determined the genomic sequence of H. acinonychis strain Sheeba and compared it to genomes from H. pylori. The conserved core genes between the genomes are so similar that the host jump probably occurred within the last 200,000 (range 50,000–400,000) years. However, the Sheeba genome also possesses unique features that indicate the direction of the host jump, namely from early humans to cats. Sheeba possesses an unusually large number of highly fragmented genes, many encoding outer membrane proteins, which may have been destroyed in order to bypass deleterious responses from the feline host immune system. In addition, the few Sheeba-specific genes that were found include a cluster of genes encoding sialylation of the bacterial cell surface carbohydrates, which were imported by horizontal genetic exchange and might also help to evade host immune defenses. These results provide a genomic basis for elucidating molecular events that allow bacteria to adapt to novel animal hosts.
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spelling pubmed-15232512006-07-28 Who Ate Whom? Adaptive Helicobacter Genomic Changes That Accompanied a Host Jump from Early Humans to Large Felines Eppinger, Mark Baar, Claudia Linz, Bodo Raddatz, Günter Lanz, Christa Keller, Heike Morelli, Giovanna Gressmann, Helga Achtman, Mark Schuster, Stephan C PLoS Genet Research Article Helicobacter pylori infection of humans is so old that its population genetic structure reflects that of ancient human migrations. A closely related species, Helicobacter acinonychis, is specific for large felines, including cheetahs, lions, and tigers, whereas hosts more closely related to humans harbor more distantly related Helicobacter species. This observation suggests a jump between host species. But who ate whom and when did it happen? In order to resolve this question, we determined the genomic sequence of H. acinonychis strain Sheeba and compared it to genomes from H. pylori. The conserved core genes between the genomes are so similar that the host jump probably occurred within the last 200,000 (range 50,000–400,000) years. However, the Sheeba genome also possesses unique features that indicate the direction of the host jump, namely from early humans to cats. Sheeba possesses an unusually large number of highly fragmented genes, many encoding outer membrane proteins, which may have been destroyed in order to bypass deleterious responses from the feline host immune system. In addition, the few Sheeba-specific genes that were found include a cluster of genes encoding sialylation of the bacterial cell surface carbohydrates, which were imported by horizontal genetic exchange and might also help to evade host immune defenses. These results provide a genomic basis for elucidating molecular events that allow bacteria to adapt to novel animal hosts. Public Library of Science 2006-07 2006-07-28 /pmc/articles/PMC1523251/ /pubmed/16789826 http://dx.doi.org/10.1371/journal.pgen.0020120 Text en © 2006 Eppinger 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
Eppinger, Mark
Baar, Claudia
Linz, Bodo
Raddatz, Günter
Lanz, Christa
Keller, Heike
Morelli, Giovanna
Gressmann, Helga
Achtman, Mark
Schuster, Stephan C
Who Ate Whom? Adaptive Helicobacter Genomic Changes That Accompanied a Host Jump from Early Humans to Large Felines
title Who Ate Whom? Adaptive Helicobacter Genomic Changes That Accompanied a Host Jump from Early Humans to Large Felines
title_full Who Ate Whom? Adaptive Helicobacter Genomic Changes That Accompanied a Host Jump from Early Humans to Large Felines
title_fullStr Who Ate Whom? Adaptive Helicobacter Genomic Changes That Accompanied a Host Jump from Early Humans to Large Felines
title_full_unstemmed Who Ate Whom? Adaptive Helicobacter Genomic Changes That Accompanied a Host Jump from Early Humans to Large Felines
title_short Who Ate Whom? Adaptive Helicobacter Genomic Changes That Accompanied a Host Jump from Early Humans to Large Felines
title_sort who ate whom? adaptive helicobacter genomic changes that accompanied a host jump from early humans to large felines
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1523251/
https://www.ncbi.nlm.nih.gov/pubmed/16789826
http://dx.doi.org/10.1371/journal.pgen.0020120
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