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Osteoarticular tissue infection and development of skeletal pathology in murine brucellosis
Brucellosis, a frequent bacterial zoonosis, can produce debilitating chronic disease with involvement of multiple organs in human patients. Whereas acute brucellosis is well studied using the murine animal model, long-term complications of host-pathogen interaction remain largely elusive. Human bruc...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Limited
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3634663/ https://www.ncbi.nlm.nih.gov/pubmed/23519029 http://dx.doi.org/10.1242/dmm.011056 |
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author | Magnani, Diogo M. Lyons, Elizabeth T. Forde, Toni S. Shekhani, Mohammed T. Adarichev, Vyacheslav A. Splitter, Gary A. |
author_facet | Magnani, Diogo M. Lyons, Elizabeth T. Forde, Toni S. Shekhani, Mohammed T. Adarichev, Vyacheslav A. Splitter, Gary A. |
author_sort | Magnani, Diogo M. |
collection | PubMed |
description | Brucellosis, a frequent bacterial zoonosis, can produce debilitating chronic disease with involvement of multiple organs in human patients. Whereas acute brucellosis is well studied using the murine animal model, long-term complications of host-pathogen interaction remain largely elusive. Human brucellosis frequently results in persistent, chronic osteoarticular system involvement, with complications such as arthritis, spondylitis and sacroiliitis. Here, we focused on identifying infectious sites in the mouse that parallel Brucella melitensis foci observed in patients. In vivo imaging showed rapid bacterial dispersal to multiple sites of the murine axial skeleton. In agreement with these findings, immunohistochemistry revealed the presence of bacteria in bones and limbs, and in the lower spine vertebrae of the axial skeleton where they were preferentially located in the bone marrow. Surprisingly, some animals developed arthritis in paws and spine after infection, but without obvious bacteria in these sites. The identification of Brucella in the bones of mice corroborates the findings in humans that these osteoarticular sites are important niches for the persistence of Brucella in the host, but the mechanisms that mediate pathological manifestations in these sites remain unclear. Future studies addressing the immune responses within osteoarticular tissue foci could elucidate important tissue injury mediators and Brucella survival strategies. |
format | Online Article Text |
id | pubmed-3634663 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | The Company of Biologists Limited |
record_format | MEDLINE/PubMed |
spelling | pubmed-36346632013-06-19 Osteoarticular tissue infection and development of skeletal pathology in murine brucellosis Magnani, Diogo M. Lyons, Elizabeth T. Forde, Toni S. Shekhani, Mohammed T. Adarichev, Vyacheslav A. Splitter, Gary A. Dis Model Mech Research Article Brucellosis, a frequent bacterial zoonosis, can produce debilitating chronic disease with involvement of multiple organs in human patients. Whereas acute brucellosis is well studied using the murine animal model, long-term complications of host-pathogen interaction remain largely elusive. Human brucellosis frequently results in persistent, chronic osteoarticular system involvement, with complications such as arthritis, spondylitis and sacroiliitis. Here, we focused on identifying infectious sites in the mouse that parallel Brucella melitensis foci observed in patients. In vivo imaging showed rapid bacterial dispersal to multiple sites of the murine axial skeleton. In agreement with these findings, immunohistochemistry revealed the presence of bacteria in bones and limbs, and in the lower spine vertebrae of the axial skeleton where they were preferentially located in the bone marrow. Surprisingly, some animals developed arthritis in paws and spine after infection, but without obvious bacteria in these sites. The identification of Brucella in the bones of mice corroborates the findings in humans that these osteoarticular sites are important niches for the persistence of Brucella in the host, but the mechanisms that mediate pathological manifestations in these sites remain unclear. Future studies addressing the immune responses within osteoarticular tissue foci could elucidate important tissue injury mediators and Brucella survival strategies. The Company of Biologists Limited 2013-05 2013-03-08 /pmc/articles/PMC3634663/ /pubmed/23519029 http://dx.doi.org/10.1242/dmm.011056 Text en © 2013. Published by The Company of Biologists Ltd This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial Share Alike License (http://creativecommons.org/licenses/by-nc-sa/3.0), which permits unrestricted non-commercial use, distribution and reproduction in any medium provided that the original work is properly cited and all further distributions of the work or adaptation are subject to the same Creative Commons License terms. |
spellingShingle | Research Article Magnani, Diogo M. Lyons, Elizabeth T. Forde, Toni S. Shekhani, Mohammed T. Adarichev, Vyacheslav A. Splitter, Gary A. Osteoarticular tissue infection and development of skeletal pathology in murine brucellosis |
title | Osteoarticular tissue infection and development of skeletal pathology in murine brucellosis |
title_full | Osteoarticular tissue infection and development of skeletal pathology in murine brucellosis |
title_fullStr | Osteoarticular tissue infection and development of skeletal pathology in murine brucellosis |
title_full_unstemmed | Osteoarticular tissue infection and development of skeletal pathology in murine brucellosis |
title_short | Osteoarticular tissue infection and development of skeletal pathology in murine brucellosis |
title_sort | osteoarticular tissue infection and development of skeletal pathology in murine brucellosis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3634663/ https://www.ncbi.nlm.nih.gov/pubmed/23519029 http://dx.doi.org/10.1242/dmm.011056 |
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