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Staphylococcus aureus Manganese Transport Protein C Is a Highly Conserved Cell Surface Protein That Elicits Protective Immunity Against S. aureus and Staphylococcus epidermidis
Staphylococcus aureus and other staphylococci cause severe human disease, and there are currently no vaccines available. We evaluated whether manganese transport protein C (MntC), which is conserved across the staphylococcal species group, could confer protection against S. aureus and Staphylococcus...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3348682/ https://www.ncbi.nlm.nih.gov/pubmed/22474033 http://dx.doi.org/10.1093/infdis/jis272 |
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author | Anderson, Annaliesa S. Scully, Ingrid L. Timofeyeva, Yekaterina Murphy, Ellen McNeil, Lisa K. Mininni, Terri Nuñez, Lorna Carriere, Marjolaine Singer, Christine Dilts, Deborah A. Jansen, Kathrin U. |
author_facet | Anderson, Annaliesa S. Scully, Ingrid L. Timofeyeva, Yekaterina Murphy, Ellen McNeil, Lisa K. Mininni, Terri Nuñez, Lorna Carriere, Marjolaine Singer, Christine Dilts, Deborah A. Jansen, Kathrin U. |
author_sort | Anderson, Annaliesa S. |
collection | PubMed |
description | Staphylococcus aureus and other staphylococci cause severe human disease, and there are currently no vaccines available. We evaluated whether manganese transport protein C (MntC), which is conserved across the staphylococcal species group, could confer protection against S. aureus and Staphylococcus epidermidis. In vivo analysis of S. aureus MntC expression revealed that expression occurs very early during the infectious cycle. Active immunization with MntC was effective at reducing the bacterial load associated with S. aureus and S. epidermidis infection in an acute murine bacteremia model. Anti-MntC monoclonal antibodies have been identified that can bind S. aureus and S. epidermidis cells and are protective in an infant rat passive protection model and induce neutrophil respiratory burst activity. This is the first description of a protein that has the potential to provide protection across the staphylococcal species group. |
format | Online Article Text |
id | pubmed-3348682 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-33486822012-05-09 Staphylococcus aureus Manganese Transport Protein C Is a Highly Conserved Cell Surface Protein That Elicits Protective Immunity Against S. aureus and Staphylococcus epidermidis Anderson, Annaliesa S. Scully, Ingrid L. Timofeyeva, Yekaterina Murphy, Ellen McNeil, Lisa K. Mininni, Terri Nuñez, Lorna Carriere, Marjolaine Singer, Christine Dilts, Deborah A. Jansen, Kathrin U. J Infect Dis Major Articles and Brief Reports Staphylococcus aureus and other staphylococci cause severe human disease, and there are currently no vaccines available. We evaluated whether manganese transport protein C (MntC), which is conserved across the staphylococcal species group, could confer protection against S. aureus and Staphylococcus epidermidis. In vivo analysis of S. aureus MntC expression revealed that expression occurs very early during the infectious cycle. Active immunization with MntC was effective at reducing the bacterial load associated with S. aureus and S. epidermidis infection in an acute murine bacteremia model. Anti-MntC monoclonal antibodies have been identified that can bind S. aureus and S. epidermidis cells and are protective in an infant rat passive protection model and induce neutrophil respiratory burst activity. This is the first description of a protein that has the potential to provide protection across the staphylococcal species group. Oxford University Press 2012-06-01 2012-04-02 /pmc/articles/PMC3348682/ /pubmed/22474033 http://dx.doi.org/10.1093/infdis/jis272 Text en © The Author 2012. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved. http://creativecommons.org/licenses/by-nc/2.5/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5/), which permits unrestricted nonommercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Major Articles and Brief Reports Anderson, Annaliesa S. Scully, Ingrid L. Timofeyeva, Yekaterina Murphy, Ellen McNeil, Lisa K. Mininni, Terri Nuñez, Lorna Carriere, Marjolaine Singer, Christine Dilts, Deborah A. Jansen, Kathrin U. Staphylococcus aureus Manganese Transport Protein C Is a Highly Conserved Cell Surface Protein That Elicits Protective Immunity Against S. aureus and Staphylococcus epidermidis |
title | Staphylococcus aureus Manganese Transport Protein C Is a Highly Conserved Cell Surface Protein That Elicits Protective Immunity Against S. aureus and Staphylococcus epidermidis |
title_full | Staphylococcus aureus Manganese Transport Protein C Is a Highly Conserved Cell Surface Protein That Elicits Protective Immunity Against S. aureus and Staphylococcus epidermidis |
title_fullStr | Staphylococcus aureus Manganese Transport Protein C Is a Highly Conserved Cell Surface Protein That Elicits Protective Immunity Against S. aureus and Staphylococcus epidermidis |
title_full_unstemmed | Staphylococcus aureus Manganese Transport Protein C Is a Highly Conserved Cell Surface Protein That Elicits Protective Immunity Against S. aureus and Staphylococcus epidermidis |
title_short | Staphylococcus aureus Manganese Transport Protein C Is a Highly Conserved Cell Surface Protein That Elicits Protective Immunity Against S. aureus and Staphylococcus epidermidis |
title_sort | staphylococcus aureus manganese transport protein c is a highly conserved cell surface protein that elicits protective immunity against s. aureus and staphylococcus epidermidis |
topic | Major Articles and Brief Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3348682/ https://www.ncbi.nlm.nih.gov/pubmed/22474033 http://dx.doi.org/10.1093/infdis/jis272 |
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