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Laboratory Mice Are Frequently Colonized with Staphylococcus aureus and Mount a Systemic Immune Response—Note of Caution for In vivo Infection Experiments
Whether mice are an appropriate model for S. aureus infection and vaccination studies is a matter of debate, because they are not considered as natural hosts of S. aureus. We previously identified a mouse-adapted S. aureus strain, which caused infections in laboratory mice. This raised the question...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5411432/ https://www.ncbi.nlm.nih.gov/pubmed/28512627 http://dx.doi.org/10.3389/fcimb.2017.00152 |
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author | Schulz, Daniel Grumann, Dorothee Trübe, Patricia Pritchett-Corning, Kathleen Johnson, Sarah Reppschläger, Kevin Gumz, Janine Sundaramoorthy, Nandakumar Michalik, Stephan Berg, Sabine van den Brandt, Jens Fister, Richard Monecke, Stefan Uy, Benedict Schmidt, Frank Bröker, Barbara M. Wiles, Siouxsie Holtfreter, Silva |
author_facet | Schulz, Daniel Grumann, Dorothee Trübe, Patricia Pritchett-Corning, Kathleen Johnson, Sarah Reppschläger, Kevin Gumz, Janine Sundaramoorthy, Nandakumar Michalik, Stephan Berg, Sabine van den Brandt, Jens Fister, Richard Monecke, Stefan Uy, Benedict Schmidt, Frank Bröker, Barbara M. Wiles, Siouxsie Holtfreter, Silva |
author_sort | Schulz, Daniel |
collection | PubMed |
description | Whether mice are an appropriate model for S. aureus infection and vaccination studies is a matter of debate, because they are not considered as natural hosts of S. aureus. We previously identified a mouse-adapted S. aureus strain, which caused infections in laboratory mice. This raised the question whether laboratory mice are commonly colonized with S. aureus and whether this might impact on infection experiments. Publicly available health reports from commercial vendors revealed that S. aureus colonization is rather frequent, with rates as high as 21% among specific-pathogen-free mice. In animal facilities, S. aureus was readily transmitted from parents to offspring, which became persistently colonized. Among 99 murine S. aureus isolates from Charles River Laboratories half belonged to the lineage CC88 (54.5%), followed by CC15, CC5, CC188, and CC8. A comparison of human and murine S. aureus isolates revealed features of host adaptation. In detail, murine strains lacked hlb-converting phages and superantigen-encoding mobile genetic elements, and were frequently ampicillin-sensitive. Moreover, murine CC88 isolates coagulated mouse plasma faster than human CC88 isolates. Importantly, S. aureus colonization clearly primed the murine immune system, inducing a systemic IgG response specific for numerous S. aureus proteins, including several vaccine candidates. Phospholipase C emerged as a promising test antigen for monitoring S. aureus colonization in laboratory mice. In conclusion, laboratory mice are natural hosts of S. aureus and therefore, could provide better infection models than previously assumed. Pre-exposure to the bacteria is a possible confounder in S. aureus infection and vaccination studies and should be monitored. |
format | Online Article Text |
id | pubmed-5411432 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54114322017-05-16 Laboratory Mice Are Frequently Colonized with Staphylococcus aureus and Mount a Systemic Immune Response—Note of Caution for In vivo Infection Experiments Schulz, Daniel Grumann, Dorothee Trübe, Patricia Pritchett-Corning, Kathleen Johnson, Sarah Reppschläger, Kevin Gumz, Janine Sundaramoorthy, Nandakumar Michalik, Stephan Berg, Sabine van den Brandt, Jens Fister, Richard Monecke, Stefan Uy, Benedict Schmidt, Frank Bröker, Barbara M. Wiles, Siouxsie Holtfreter, Silva Front Cell Infect Microbiol Microbiology Whether mice are an appropriate model for S. aureus infection and vaccination studies is a matter of debate, because they are not considered as natural hosts of S. aureus. We previously identified a mouse-adapted S. aureus strain, which caused infections in laboratory mice. This raised the question whether laboratory mice are commonly colonized with S. aureus and whether this might impact on infection experiments. Publicly available health reports from commercial vendors revealed that S. aureus colonization is rather frequent, with rates as high as 21% among specific-pathogen-free mice. In animal facilities, S. aureus was readily transmitted from parents to offspring, which became persistently colonized. Among 99 murine S. aureus isolates from Charles River Laboratories half belonged to the lineage CC88 (54.5%), followed by CC15, CC5, CC188, and CC8. A comparison of human and murine S. aureus isolates revealed features of host adaptation. In detail, murine strains lacked hlb-converting phages and superantigen-encoding mobile genetic elements, and were frequently ampicillin-sensitive. Moreover, murine CC88 isolates coagulated mouse plasma faster than human CC88 isolates. Importantly, S. aureus colonization clearly primed the murine immune system, inducing a systemic IgG response specific for numerous S. aureus proteins, including several vaccine candidates. Phospholipase C emerged as a promising test antigen for monitoring S. aureus colonization in laboratory mice. In conclusion, laboratory mice are natural hosts of S. aureus and therefore, could provide better infection models than previously assumed. Pre-exposure to the bacteria is a possible confounder in S. aureus infection and vaccination studies and should be monitored. Frontiers Media S.A. 2017-05-02 /pmc/articles/PMC5411432/ /pubmed/28512627 http://dx.doi.org/10.3389/fcimb.2017.00152 Text en Copyright © 2017 Schulz, Grumann, Trübe, Pritchett-Corning, Johnson, Reppschläger, Gumz, Sundaramoorthy, Michalik, Berg, van den Brandt, Fister, Monecke, Uy, Schmidt, Bröker, Wiles and Holtfreter. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Schulz, Daniel Grumann, Dorothee Trübe, Patricia Pritchett-Corning, Kathleen Johnson, Sarah Reppschläger, Kevin Gumz, Janine Sundaramoorthy, Nandakumar Michalik, Stephan Berg, Sabine van den Brandt, Jens Fister, Richard Monecke, Stefan Uy, Benedict Schmidt, Frank Bröker, Barbara M. Wiles, Siouxsie Holtfreter, Silva Laboratory Mice Are Frequently Colonized with Staphylococcus aureus and Mount a Systemic Immune Response—Note of Caution for In vivo Infection Experiments |
title | Laboratory Mice Are Frequently Colonized with Staphylococcus aureus and Mount a Systemic Immune Response—Note of Caution for In vivo Infection Experiments |
title_full | Laboratory Mice Are Frequently Colonized with Staphylococcus aureus and Mount a Systemic Immune Response—Note of Caution for In vivo Infection Experiments |
title_fullStr | Laboratory Mice Are Frequently Colonized with Staphylococcus aureus and Mount a Systemic Immune Response—Note of Caution for In vivo Infection Experiments |
title_full_unstemmed | Laboratory Mice Are Frequently Colonized with Staphylococcus aureus and Mount a Systemic Immune Response—Note of Caution for In vivo Infection Experiments |
title_short | Laboratory Mice Are Frequently Colonized with Staphylococcus aureus and Mount a Systemic Immune Response—Note of Caution for In vivo Infection Experiments |
title_sort | laboratory mice are frequently colonized with staphylococcus aureus and mount a systemic immune response—note of caution for in vivo infection experiments |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5411432/ https://www.ncbi.nlm.nih.gov/pubmed/28512627 http://dx.doi.org/10.3389/fcimb.2017.00152 |
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