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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
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.
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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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