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Wall Teichoic Acid Glycosylation Governs Staphylococcus aureus Nasal Colonization
Nasal colonization by the human pathogen Staphylococcus aureus is a major risk factor for hospital- and community-acquired infections. A key factor required for nasal colonization is a cell surface-exposed zwitterionic glycopolymer, termed wall teichoic acid (WTA). However, the precise mechanisms th...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Microbiology
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4488942/ https://www.ncbi.nlm.nih.gov/pubmed/26126851 http://dx.doi.org/10.1128/mBio.00632-15 |
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author | Winstel, Volker Kühner, Petra Salomon, Ferdinand Larsen, Jesper Skov, Robert Hoffmann, Wolfgang Peschel, Andreas Weidenmaier, Christopher |
author_facet | Winstel, Volker Kühner, Petra Salomon, Ferdinand Larsen, Jesper Skov, Robert Hoffmann, Wolfgang Peschel, Andreas Weidenmaier, Christopher |
author_sort | Winstel, Volker |
collection | PubMed |
description | Nasal colonization by the human pathogen Staphylococcus aureus is a major risk factor for hospital- and community-acquired infections. A key factor required for nasal colonization is a cell surface-exposed zwitterionic glycopolymer, termed wall teichoic acid (WTA). However, the precise mechanisms that govern WTA-mediated nasal colonization have remained elusive. Here, we report that WTA GlcNAcylation is a pivotal requirement for WTA-dependent attachment of community-acquired methicillin-resistant S. aureus (MRSA) and emerging livestock-associated MRSA to human nasal epithelial cells, even under conditions simulating the nutrient composition and dynamic flow of nasal secretions. Depending on the S. aureus strain, WTA O-GlcNAcylation occurs in either α or β configuration, which have similar capacities to mediate attachment to human nasal epithelial cells, suggesting that many S. aureus strains maintain redundant pathways to ensure appropriate WTA glycosylation. Strikingly, a lack of WTA glycosylation significantly abrogated the ability of MRSA to colonize cotton rat nares in vivo. These results indicate that WTA glycosylation modulates S. aureus nasal colonization and may help to develop new strategies for eradicating S. aureus nasal colonization in the future. |
format | Online Article Text |
id | pubmed-4488942 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | American Society of Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-44889422015-07-07 Wall Teichoic Acid Glycosylation Governs Staphylococcus aureus Nasal Colonization Winstel, Volker Kühner, Petra Salomon, Ferdinand Larsen, Jesper Skov, Robert Hoffmann, Wolfgang Peschel, Andreas Weidenmaier, Christopher mBio Research Article Nasal colonization by the human pathogen Staphylococcus aureus is a major risk factor for hospital- and community-acquired infections. A key factor required for nasal colonization is a cell surface-exposed zwitterionic glycopolymer, termed wall teichoic acid (WTA). However, the precise mechanisms that govern WTA-mediated nasal colonization have remained elusive. Here, we report that WTA GlcNAcylation is a pivotal requirement for WTA-dependent attachment of community-acquired methicillin-resistant S. aureus (MRSA) and emerging livestock-associated MRSA to human nasal epithelial cells, even under conditions simulating the nutrient composition and dynamic flow of nasal secretions. Depending on the S. aureus strain, WTA O-GlcNAcylation occurs in either α or β configuration, which have similar capacities to mediate attachment to human nasal epithelial cells, suggesting that many S. aureus strains maintain redundant pathways to ensure appropriate WTA glycosylation. Strikingly, a lack of WTA glycosylation significantly abrogated the ability of MRSA to colonize cotton rat nares in vivo. These results indicate that WTA glycosylation modulates S. aureus nasal colonization and may help to develop new strategies for eradicating S. aureus nasal colonization in the future. American Society of Microbiology 2015-06-30 /pmc/articles/PMC4488942/ /pubmed/26126851 http://dx.doi.org/10.1128/mBio.00632-15 Text en Copyright © 2015 Winstel et al. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-ShareAlike 3.0 Unported license (http://creativecommons.org/licenses/by-nc-sa/3.0/) , which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Winstel, Volker Kühner, Petra Salomon, Ferdinand Larsen, Jesper Skov, Robert Hoffmann, Wolfgang Peschel, Andreas Weidenmaier, Christopher Wall Teichoic Acid Glycosylation Governs Staphylococcus aureus Nasal Colonization |
title | Wall Teichoic Acid Glycosylation Governs Staphylococcus aureus Nasal Colonization |
title_full | Wall Teichoic Acid Glycosylation Governs Staphylococcus aureus Nasal Colonization |
title_fullStr | Wall Teichoic Acid Glycosylation Governs Staphylococcus aureus Nasal Colonization |
title_full_unstemmed | Wall Teichoic Acid Glycosylation Governs Staphylococcus aureus Nasal Colonization |
title_short | Wall Teichoic Acid Glycosylation Governs Staphylococcus aureus Nasal Colonization |
title_sort | wall teichoic acid glycosylation governs staphylococcus aureus nasal colonization |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4488942/ https://www.ncbi.nlm.nih.gov/pubmed/26126851 http://dx.doi.org/10.1128/mBio.00632-15 |
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