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Rapid Lymphatic Dissemination of Encapsulated Group A Streptococci via Lymphatic Vessel Endothelial Receptor-1 Interaction
The host lymphatic network represents an important conduit for pathogen dissemination. Indeed, the lethal human pathogen group A streptococcus has a predilection to induce pathology in the lymphatic system and draining lymph nodes, however the underlying basis and subsequent consequences for disease...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4564194/ https://www.ncbi.nlm.nih.gov/pubmed/26352587 http://dx.doi.org/10.1371/journal.ppat.1005137 |
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author | Lynskey, Nicola N. Banerji, Suneale Johnson, Louise A. Holder, Kayla A. Reglinski, Mark Wing, Peter A. C. Rigby, David Jackson, David G. Sriskandan, Shiranee |
author_facet | Lynskey, Nicola N. Banerji, Suneale Johnson, Louise A. Holder, Kayla A. Reglinski, Mark Wing, Peter A. C. Rigby, David Jackson, David G. Sriskandan, Shiranee |
author_sort | Lynskey, Nicola N. |
collection | PubMed |
description | The host lymphatic network represents an important conduit for pathogen dissemination. Indeed, the lethal human pathogen group A streptococcus has a predilection to induce pathology in the lymphatic system and draining lymph nodes, however the underlying basis and subsequent consequences for disease outcome are currently unknown. Here we report that the hyaluronan capsule of group A streptococci is a crucial virulence determinant for lymphatic tropism in vivo, and further, we identify the lymphatic vessel endothelial receptor-1 as the critical host receptor for capsular hyaluronan in the lymphatic system. Interference with this interaction in vivo impeded bacterial dissemination to local draining lymph nodes and, in the case of a hyper-encapsulated M18 strain, redirected streptococcal entry into the blood circulation, suggesting a pivotal role in the manifestation of streptococcal infections. Our results reveal a novel function for bacterial capsular polysaccharide in directing lymphatic tropism, with potential implications for disease pathology. |
format | Online Article Text |
id | pubmed-4564194 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-45641942015-09-17 Rapid Lymphatic Dissemination of Encapsulated Group A Streptococci via Lymphatic Vessel Endothelial Receptor-1 Interaction Lynskey, Nicola N. Banerji, Suneale Johnson, Louise A. Holder, Kayla A. Reglinski, Mark Wing, Peter A. C. Rigby, David Jackson, David G. Sriskandan, Shiranee PLoS Pathog Research Article The host lymphatic network represents an important conduit for pathogen dissemination. Indeed, the lethal human pathogen group A streptococcus has a predilection to induce pathology in the lymphatic system and draining lymph nodes, however the underlying basis and subsequent consequences for disease outcome are currently unknown. Here we report that the hyaluronan capsule of group A streptococci is a crucial virulence determinant for lymphatic tropism in vivo, and further, we identify the lymphatic vessel endothelial receptor-1 as the critical host receptor for capsular hyaluronan in the lymphatic system. Interference with this interaction in vivo impeded bacterial dissemination to local draining lymph nodes and, in the case of a hyper-encapsulated M18 strain, redirected streptococcal entry into the blood circulation, suggesting a pivotal role in the manifestation of streptococcal infections. Our results reveal a novel function for bacterial capsular polysaccharide in directing lymphatic tropism, with potential implications for disease pathology. Public Library of Science 2015-09-09 /pmc/articles/PMC4564194/ /pubmed/26352587 http://dx.doi.org/10.1371/journal.ppat.1005137 Text en © 2015 Lynskey 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 Lynskey, Nicola N. Banerji, Suneale Johnson, Louise A. Holder, Kayla A. Reglinski, Mark Wing, Peter A. C. Rigby, David Jackson, David G. Sriskandan, Shiranee Rapid Lymphatic Dissemination of Encapsulated Group A Streptococci via Lymphatic Vessel Endothelial Receptor-1 Interaction |
title | Rapid Lymphatic Dissemination of Encapsulated Group A Streptococci via Lymphatic Vessel Endothelial Receptor-1 Interaction |
title_full | Rapid Lymphatic Dissemination of Encapsulated Group A Streptococci via Lymphatic Vessel Endothelial Receptor-1 Interaction |
title_fullStr | Rapid Lymphatic Dissemination of Encapsulated Group A Streptococci via Lymphatic Vessel Endothelial Receptor-1 Interaction |
title_full_unstemmed | Rapid Lymphatic Dissemination of Encapsulated Group A Streptococci via Lymphatic Vessel Endothelial Receptor-1 Interaction |
title_short | Rapid Lymphatic Dissemination of Encapsulated Group A Streptococci via Lymphatic Vessel Endothelial Receptor-1 Interaction |
title_sort | rapid lymphatic dissemination of encapsulated group a streptococci via lymphatic vessel endothelial receptor-1 interaction |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4564194/ https://www.ncbi.nlm.nih.gov/pubmed/26352587 http://dx.doi.org/10.1371/journal.ppat.1005137 |
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