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Development of persistent gastrointestinal S. aureus carriage in mice

One fifth to one quarter of the human population is asymptomatically, naturally and persistently colonised by Staphylococcus aureus. Observational human studies indicate that although the whole population is intermittently exposed, some individuals lose S. aureus rapidly. Others become persistent ca...

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Autores principales: Flaxman, Amy, van Diemen, Pauline M., Yamaguchi, Yuko, Allen, Elizabeth, Lindemann, Claudia, Rollier, Christine S., Milicic, Anita, Wyllie, David H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5622074/
https://www.ncbi.nlm.nih.gov/pubmed/28963555
http://dx.doi.org/10.1038/s41598-017-12576-0
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author Flaxman, Amy
van Diemen, Pauline M.
Yamaguchi, Yuko
Allen, Elizabeth
Lindemann, Claudia
Rollier, Christine S.
Milicic, Anita
Wyllie, David H.
author_facet Flaxman, Amy
van Diemen, Pauline M.
Yamaguchi, Yuko
Allen, Elizabeth
Lindemann, Claudia
Rollier, Christine S.
Milicic, Anita
Wyllie, David H.
author_sort Flaxman, Amy
collection PubMed
description One fifth to one quarter of the human population is asymptomatically, naturally and persistently colonised by Staphylococcus aureus. Observational human studies indicate that although the whole population is intermittently exposed, some individuals lose S. aureus rapidly. Others become persistent carriers, as assessed by nasal cultures, with many individuals colonised for decades. Current animal models of S. aureus colonisation are expensive and normally require antibiotics. Importantly, these animal models have not yet contributed to our poor understanding of the dichotomy in human colonisation status. Here, we identify a single strain of S. aureus found to be persistently colonising the gastrointestinal tract of BALB/c mice. Phylogenetic analyses suggest it diverged from a human ST15 lineage in the recent past. We show that murine carriage of this organism occurs in the bowel and nares, is acquired early in life, and can persist for months. Importantly, we observe the development of persistent and non-persistent gastrointestinal carriage states in genetically identical mice. We developed a needle- and antibiotic-free model in which we readily induced S. aureus colonisation of the gastrointestinal tract experimentally by environmental exposure. Using our experimental model, impact of adaptive immunity on S. aureus colonisation could be assessed. Vaccine efficacy to eliminate colonisation could also be investigated using this model.
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spelling pubmed-56220742017-10-12 Development of persistent gastrointestinal S. aureus carriage in mice Flaxman, Amy van Diemen, Pauline M. Yamaguchi, Yuko Allen, Elizabeth Lindemann, Claudia Rollier, Christine S. Milicic, Anita Wyllie, David H. Sci Rep Article One fifth to one quarter of the human population is asymptomatically, naturally and persistently colonised by Staphylococcus aureus. Observational human studies indicate that although the whole population is intermittently exposed, some individuals lose S. aureus rapidly. Others become persistent carriers, as assessed by nasal cultures, with many individuals colonised for decades. Current animal models of S. aureus colonisation are expensive and normally require antibiotics. Importantly, these animal models have not yet contributed to our poor understanding of the dichotomy in human colonisation status. Here, we identify a single strain of S. aureus found to be persistently colonising the gastrointestinal tract of BALB/c mice. Phylogenetic analyses suggest it diverged from a human ST15 lineage in the recent past. We show that murine carriage of this organism occurs in the bowel and nares, is acquired early in life, and can persist for months. Importantly, we observe the development of persistent and non-persistent gastrointestinal carriage states in genetically identical mice. We developed a needle- and antibiotic-free model in which we readily induced S. aureus colonisation of the gastrointestinal tract experimentally by environmental exposure. Using our experimental model, impact of adaptive immunity on S. aureus colonisation could be assessed. Vaccine efficacy to eliminate colonisation could also be investigated using this model. Nature Publishing Group UK 2017-09-29 /pmc/articles/PMC5622074/ /pubmed/28963555 http://dx.doi.org/10.1038/s41598-017-12576-0 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Flaxman, Amy
van Diemen, Pauline M.
Yamaguchi, Yuko
Allen, Elizabeth
Lindemann, Claudia
Rollier, Christine S.
Milicic, Anita
Wyllie, David H.
Development of persistent gastrointestinal S. aureus carriage in mice
title Development of persistent gastrointestinal S. aureus carriage in mice
title_full Development of persistent gastrointestinal S. aureus carriage in mice
title_fullStr Development of persistent gastrointestinal S. aureus carriage in mice
title_full_unstemmed Development of persistent gastrointestinal S. aureus carriage in mice
title_short Development of persistent gastrointestinal S. aureus carriage in mice
title_sort development of persistent gastrointestinal s. aureus carriage in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5622074/
https://www.ncbi.nlm.nih.gov/pubmed/28963555
http://dx.doi.org/10.1038/s41598-017-12576-0
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