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Rhinoscleroma pathogenesis: The type K3 capsule of Klebsiella rhinoscleromatis is a virulence factor not involved in Mikulicz cells formation
Rhinoscleroma is a human specific chronic granulomatous infection of the nose and upper airways caused by the Gram-negative bacterium Klebsiella pneumoniae subsp. rhinoscleromatis. Although considered a rare disease, it is endemic in low-income countries where hygienic conditions are poor. A hallmar...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5806929/ https://www.ncbi.nlm.nih.gov/pubmed/29381692 http://dx.doi.org/10.1371/journal.pntd.0006201 |
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author | Corelli, Barbara Almeida, Ana S. Sonego, Fabiane Castiglia, Virginia Fevre, Cindy Brisse, Sylvain Sansonetti, Philippe J. Tournebize, Régis |
author_facet | Corelli, Barbara Almeida, Ana S. Sonego, Fabiane Castiglia, Virginia Fevre, Cindy Brisse, Sylvain Sansonetti, Philippe J. Tournebize, Régis |
author_sort | Corelli, Barbara |
collection | PubMed |
description | Rhinoscleroma is a human specific chronic granulomatous infection of the nose and upper airways caused by the Gram-negative bacterium Klebsiella pneumoniae subsp. rhinoscleromatis. Although considered a rare disease, it is endemic in low-income countries where hygienic conditions are poor. A hallmark of this pathology is the appearance of atypical foamy monocytes called Mikulicz cells. However, the pathogenesis of rhinoscleroma remains poorly investigated. Capsule polysaccharide (CPS) is a prominent virulence factor in bacteria. All K. rhinoscleromatis strains are of K3 serotype, suggesting that CPS can be an important driver of rhinoscleroma disease. In this study, we describe the creation of the first mutant of K. rhinoscleromatis, inactivated in its capsule export machinery. Using a murine model recapitulating the formation of Mikulicz cells in lungs, we observed that a K. rhinoscleromatis CPS mutant (KR cps(-)) is strongly attenuated and that mice infected with a high dose of KR cps(-) are still able to induce Mikulicz cells formation, unlike a K. pneumoniae capsule mutant, and to partially recapitulate the characteristic strong production of IL-10. Altogether, the results of this study show that CPS is a virulence factor of K. rhinoscleromatis not involved in the specific appearance of Mikulicz cells. |
format | Online Article Text |
id | pubmed-5806929 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-58069292018-02-23 Rhinoscleroma pathogenesis: The type K3 capsule of Klebsiella rhinoscleromatis is a virulence factor not involved in Mikulicz cells formation Corelli, Barbara Almeida, Ana S. Sonego, Fabiane Castiglia, Virginia Fevre, Cindy Brisse, Sylvain Sansonetti, Philippe J. Tournebize, Régis PLoS Negl Trop Dis Research Article Rhinoscleroma is a human specific chronic granulomatous infection of the nose and upper airways caused by the Gram-negative bacterium Klebsiella pneumoniae subsp. rhinoscleromatis. Although considered a rare disease, it is endemic in low-income countries where hygienic conditions are poor. A hallmark of this pathology is the appearance of atypical foamy monocytes called Mikulicz cells. However, the pathogenesis of rhinoscleroma remains poorly investigated. Capsule polysaccharide (CPS) is a prominent virulence factor in bacteria. All K. rhinoscleromatis strains are of K3 serotype, suggesting that CPS can be an important driver of rhinoscleroma disease. In this study, we describe the creation of the first mutant of K. rhinoscleromatis, inactivated in its capsule export machinery. Using a murine model recapitulating the formation of Mikulicz cells in lungs, we observed that a K. rhinoscleromatis CPS mutant (KR cps(-)) is strongly attenuated and that mice infected with a high dose of KR cps(-) are still able to induce Mikulicz cells formation, unlike a K. pneumoniae capsule mutant, and to partially recapitulate the characteristic strong production of IL-10. Altogether, the results of this study show that CPS is a virulence factor of K. rhinoscleromatis not involved in the specific appearance of Mikulicz cells. Public Library of Science 2018-01-30 /pmc/articles/PMC5806929/ /pubmed/29381692 http://dx.doi.org/10.1371/journal.pntd.0006201 Text en © 2018 Corelli 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Corelli, Barbara Almeida, Ana S. Sonego, Fabiane Castiglia, Virginia Fevre, Cindy Brisse, Sylvain Sansonetti, Philippe J. Tournebize, Régis Rhinoscleroma pathogenesis: The type K3 capsule of Klebsiella rhinoscleromatis is a virulence factor not involved in Mikulicz cells formation |
title | Rhinoscleroma pathogenesis: The type K3 capsule of Klebsiella rhinoscleromatis is a virulence factor not involved in Mikulicz cells formation |
title_full | Rhinoscleroma pathogenesis: The type K3 capsule of Klebsiella rhinoscleromatis is a virulence factor not involved in Mikulicz cells formation |
title_fullStr | Rhinoscleroma pathogenesis: The type K3 capsule of Klebsiella rhinoscleromatis is a virulence factor not involved in Mikulicz cells formation |
title_full_unstemmed | Rhinoscleroma pathogenesis: The type K3 capsule of Klebsiella rhinoscleromatis is a virulence factor not involved in Mikulicz cells formation |
title_short | Rhinoscleroma pathogenesis: The type K3 capsule of Klebsiella rhinoscleromatis is a virulence factor not involved in Mikulicz cells formation |
title_sort | rhinoscleroma pathogenesis: the type k3 capsule of klebsiella rhinoscleromatis is a virulence factor not involved in mikulicz cells formation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5806929/ https://www.ncbi.nlm.nih.gov/pubmed/29381692 http://dx.doi.org/10.1371/journal.pntd.0006201 |
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