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Pneumococcal colonization and invasive disease studied in a porcine model
BACKGROUND: Streptococcus pneumoniae, a Gram-positive bacterium carried in the human nasopharynx, is an important human pathogen causing mild diseases such as otitis media and sinusitis as well as severe diseases including pneumonia, meningitis and sepsis. There is a strong resemblance between the a...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4898302/ https://www.ncbi.nlm.nih.gov/pubmed/27276874 http://dx.doi.org/10.1186/s12866-016-0718-3 |
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author | de Greeff, Astrid van Selm, Saskia Buys, Herma Harders-Westerveen, José F. Tunjungputri, Rahajeng N. de Mast, Quirijn van der Ven, Andre J. Stockhofe-Zurwieden, Norbert de Jonge, Marien I. Smith, Hilde E. |
author_facet | de Greeff, Astrid van Selm, Saskia Buys, Herma Harders-Westerveen, José F. Tunjungputri, Rahajeng N. de Mast, Quirijn van der Ven, Andre J. Stockhofe-Zurwieden, Norbert de Jonge, Marien I. Smith, Hilde E. |
author_sort | de Greeff, Astrid |
collection | PubMed |
description | BACKGROUND: Streptococcus pneumoniae, a Gram-positive bacterium carried in the human nasopharynx, is an important human pathogen causing mild diseases such as otitis media and sinusitis as well as severe diseases including pneumonia, meningitis and sepsis. There is a strong resemblance between the anatomy, immunology and physiology of the pig and human species. Furthermore, there are striking similarities between S. suis pathogenesis in piglets and S. pneumoniae pathogenesis in humans. Therefore, we investigated the use of piglets as a model for pneumococcal colonization and invasive disease. RESULTS: Intravenous inoculation of piglets with an invasive pneumococcal isolate led to bacteraemia during 5 days, showing clear bacterial replication in the first two days. Bacteraemia was frequently associated with fever and septic arthritis. Moreover, intranasal inoculation of piglets with a nasopharyngeal isolate led to colonization for at least six consecutive days. CONCLUSIONS: This demonstrates that central aspects of human pneumococcal infections can be modelled in piglets enabling the use of this model for studies on colonization and transmission but also on development of vaccines and host-directed therapies. Moreover this is the first example of an animal model inducing high levels of pneumococcal septic arthritis. |
format | Online Article Text |
id | pubmed-4898302 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48983022016-06-09 Pneumococcal colonization and invasive disease studied in a porcine model de Greeff, Astrid van Selm, Saskia Buys, Herma Harders-Westerveen, José F. Tunjungputri, Rahajeng N. de Mast, Quirijn van der Ven, Andre J. Stockhofe-Zurwieden, Norbert de Jonge, Marien I. Smith, Hilde E. BMC Microbiol Research Article BACKGROUND: Streptococcus pneumoniae, a Gram-positive bacterium carried in the human nasopharynx, is an important human pathogen causing mild diseases such as otitis media and sinusitis as well as severe diseases including pneumonia, meningitis and sepsis. There is a strong resemblance between the anatomy, immunology and physiology of the pig and human species. Furthermore, there are striking similarities between S. suis pathogenesis in piglets and S. pneumoniae pathogenesis in humans. Therefore, we investigated the use of piglets as a model for pneumococcal colonization and invasive disease. RESULTS: Intravenous inoculation of piglets with an invasive pneumococcal isolate led to bacteraemia during 5 days, showing clear bacterial replication in the first two days. Bacteraemia was frequently associated with fever and septic arthritis. Moreover, intranasal inoculation of piglets with a nasopharyngeal isolate led to colonization for at least six consecutive days. CONCLUSIONS: This demonstrates that central aspects of human pneumococcal infections can be modelled in piglets enabling the use of this model for studies on colonization and transmission but also on development of vaccines and host-directed therapies. Moreover this is the first example of an animal model inducing high levels of pneumococcal septic arthritis. BioMed Central 2016-06-08 /pmc/articles/PMC4898302/ /pubmed/27276874 http://dx.doi.org/10.1186/s12866-016-0718-3 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article de Greeff, Astrid van Selm, Saskia Buys, Herma Harders-Westerveen, José F. Tunjungputri, Rahajeng N. de Mast, Quirijn van der Ven, Andre J. Stockhofe-Zurwieden, Norbert de Jonge, Marien I. Smith, Hilde E. Pneumococcal colonization and invasive disease studied in a porcine model |
title | Pneumococcal colonization and invasive disease studied in a porcine model |
title_full | Pneumococcal colonization and invasive disease studied in a porcine model |
title_fullStr | Pneumococcal colonization and invasive disease studied in a porcine model |
title_full_unstemmed | Pneumococcal colonization and invasive disease studied in a porcine model |
title_short | Pneumococcal colonization and invasive disease studied in a porcine model |
title_sort | pneumococcal colonization and invasive disease studied in a porcine model |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4898302/ https://www.ncbi.nlm.nih.gov/pubmed/27276874 http://dx.doi.org/10.1186/s12866-016-0718-3 |
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