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Rapid Lymphatic Dissemination of Encapsulated Group A Streptococci via Lymphatic Vessel Endothelial Receptor-1 Interaction
Author(s) -
Nicola N. Lynskey,
Suneale Banerji,
Louise A. Johnson,
Kayla A. Holder,
Mark Reglinski,
Peter A. C. Wing,
David A Rigby,
David G. Jackson,
Shiranee Sriskandan
Publication year - 2015
Publication title -
plos pathogens
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.719
H-Index - 206
eISSN - 1553-7374
pISSN - 1553-7366
DOI - 10.1371/journal.ppat.1005137
Subject(s) - lymphatic system , lymphatic endothelium , tropism , lymph , lymphatic vessel , biology , endothelium , immunology , lymph node stromal cell , high endothelial venules , tissue tropism , microbiology and biotechnology , pathology , in vivo , medicine , cancer , metastasis , virus , genetics , endocrinology
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.

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