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Wall teichoic acid structure governs horizontal gene transfer between major bacterial pathogens

Mobile genetic elements (MGEs) encoding virulence and resistance genes are widespread in bacterial pathogens, but it has remained unclear how they occasionally jump to new host species. Staphylococcus aureus clones exchange MGEs such as S. aureus pathogenicity islands (SaPIs) with high frequency via...

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Autores principales: Winstel, Volker, Liang, Chunguang, Sanchez-Carballo, Patricia, Steglich, Matthias, Munar, Marta, Bröker, Barbara M., Penadés, Jose R., Nübel, Ulrich, Holst, Otto, Dandekar, Thomas, Peschel, Andreas, Xia, Guoqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3903184/
https://www.ncbi.nlm.nih.gov/pubmed/23965785
http://dx.doi.org/10.1038/ncomms3345
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author Winstel, Volker
Liang, Chunguang
Sanchez-Carballo, Patricia
Steglich, Matthias
Munar, Marta
Bröker, Barbara M.
Penadés, Jose R.
Nübel, Ulrich
Holst, Otto
Dandekar, Thomas
Peschel, Andreas
Xia, Guoqing
author_facet Winstel, Volker
Liang, Chunguang
Sanchez-Carballo, Patricia
Steglich, Matthias
Munar, Marta
Bröker, Barbara M.
Penadés, Jose R.
Nübel, Ulrich
Holst, Otto
Dandekar, Thomas
Peschel, Andreas
Xia, Guoqing
author_sort Winstel, Volker
collection PubMed
description Mobile genetic elements (MGEs) encoding virulence and resistance genes are widespread in bacterial pathogens, but it has remained unclear how they occasionally jump to new host species. Staphylococcus aureus clones exchange MGEs such as S. aureus pathogenicity islands (SaPIs) with high frequency via helper phages. Here we report that the S. aureus ST395 lineage is refractory to horizontal gene transfer (HGT) with typical S. aureus but exchanges SaPIs with other species and genera including Staphylococcus epidermidis and Listeria monocytogenes. ST395 produces an unusual wall teichoic acid (WTA) resembling that of its HGT partner species. Notably, distantly related bacterial species and genera undergo efficient HGT with typical S. aureus upon ectopic expression of S. aureus WTA. Combined with genomic analyses, these results indicate that a ‘glycocode’ of WTA structures and WTA-binding helper phages permits HGT even across long phylogenetic distances thereby shaping the evolution of Gram-positive pathogens.
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spelling pubmed-39031842014-01-27 Wall teichoic acid structure governs horizontal gene transfer between major bacterial pathogens Winstel, Volker Liang, Chunguang Sanchez-Carballo, Patricia Steglich, Matthias Munar, Marta Bröker, Barbara M. Penadés, Jose R. Nübel, Ulrich Holst, Otto Dandekar, Thomas Peschel, Andreas Xia, Guoqing Nat Commun Article Mobile genetic elements (MGEs) encoding virulence and resistance genes are widespread in bacterial pathogens, but it has remained unclear how they occasionally jump to new host species. Staphylococcus aureus clones exchange MGEs such as S. aureus pathogenicity islands (SaPIs) with high frequency via helper phages. Here we report that the S. aureus ST395 lineage is refractory to horizontal gene transfer (HGT) with typical S. aureus but exchanges SaPIs with other species and genera including Staphylococcus epidermidis and Listeria monocytogenes. ST395 produces an unusual wall teichoic acid (WTA) resembling that of its HGT partner species. Notably, distantly related bacterial species and genera undergo efficient HGT with typical S. aureus upon ectopic expression of S. aureus WTA. Combined with genomic analyses, these results indicate that a ‘glycocode’ of WTA structures and WTA-binding helper phages permits HGT even across long phylogenetic distances thereby shaping the evolution of Gram-positive pathogens. Nature Pub. Group 2013-08-22 /pmc/articles/PMC3903184/ /pubmed/23965785 http://dx.doi.org/10.1038/ncomms3345 Text en Copyright © 2013, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Article
Winstel, Volker
Liang, Chunguang
Sanchez-Carballo, Patricia
Steglich, Matthias
Munar, Marta
Bröker, Barbara M.
Penadés, Jose R.
Nübel, Ulrich
Holst, Otto
Dandekar, Thomas
Peschel, Andreas
Xia, Guoqing
Wall teichoic acid structure governs horizontal gene transfer between major bacterial pathogens
title Wall teichoic acid structure governs horizontal gene transfer between major bacterial pathogens
title_full Wall teichoic acid structure governs horizontal gene transfer between major bacterial pathogens
title_fullStr Wall teichoic acid structure governs horizontal gene transfer between major bacterial pathogens
title_full_unstemmed Wall teichoic acid structure governs horizontal gene transfer between major bacterial pathogens
title_short Wall teichoic acid structure governs horizontal gene transfer between major bacterial pathogens
title_sort wall teichoic acid structure governs horizontal gene transfer between major bacterial pathogens
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3903184/
https://www.ncbi.nlm.nih.gov/pubmed/23965785
http://dx.doi.org/10.1038/ncomms3345
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