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Virulence Differences Among Francisella tularensis Subsp. tularensis Clades in Mice
Francisella tularensis subspecies tularensis (type A) and holarctica (type B) are of clinical importance in causing tularemia. Molecular typing methods have further separated type A strains into three genetically distinct clades, A1a, A1b and A2. Epidemiological analyses of human infections in the U...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2855709/ https://www.ncbi.nlm.nih.gov/pubmed/20419133 http://dx.doi.org/10.1371/journal.pone.0010205 |
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author | Molins, Claudia R. Delorey, Mark J. Yockey, Brook M. Young, John W. Sheldon, Sarah W. Reese, Sara M. Schriefer, Martin E. Petersen, Jeannine M. |
author_facet | Molins, Claudia R. Delorey, Mark J. Yockey, Brook M. Young, John W. Sheldon, Sarah W. Reese, Sara M. Schriefer, Martin E. Petersen, Jeannine M. |
author_sort | Molins, Claudia R. |
collection | PubMed |
description | Francisella tularensis subspecies tularensis (type A) and holarctica (type B) are of clinical importance in causing tularemia. Molecular typing methods have further separated type A strains into three genetically distinct clades, A1a, A1b and A2. Epidemiological analyses of human infections in the United States suggest that A1b infections are associated with a significantly higher mortality rate as compared to infections caused by A1a, A2 and type B. To determine if genetic differences as defined by molecular typing directly correlate with differences in virulence, A1a, A1b, A2 and type B strains were compared in C57BL/6 mice. Here we demonstrate significant differences between survival curves for infections caused by A1b versus A1a, A2 and type B, with A1b infected mice dying earlier than mice infected with A1a, A2 or type B; these results were conserved among multiple strains. Differences were also detected among type A clades as well as between type A clades and type B with respect to bacterial burdens, and gross anatomy in infected mice. Our results indicate that clades defined within F. tularensis subsp. tularensis by molecular typing methods correlate with virulence differences, with A1b strains more virulent than A1a, A2 and type B strains. These findings indicate type A strains are not equivalent with respect to virulence and have important implications for public health as well as basic research programs. |
format | Text |
id | pubmed-2855709 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-28557092010-04-23 Virulence Differences Among Francisella tularensis Subsp. tularensis Clades in Mice Molins, Claudia R. Delorey, Mark J. Yockey, Brook M. Young, John W. Sheldon, Sarah W. Reese, Sara M. Schriefer, Martin E. Petersen, Jeannine M. PLoS One Research Article Francisella tularensis subspecies tularensis (type A) and holarctica (type B) are of clinical importance in causing tularemia. Molecular typing methods have further separated type A strains into three genetically distinct clades, A1a, A1b and A2. Epidemiological analyses of human infections in the United States suggest that A1b infections are associated with a significantly higher mortality rate as compared to infections caused by A1a, A2 and type B. To determine if genetic differences as defined by molecular typing directly correlate with differences in virulence, A1a, A1b, A2 and type B strains were compared in C57BL/6 mice. Here we demonstrate significant differences between survival curves for infections caused by A1b versus A1a, A2 and type B, with A1b infected mice dying earlier than mice infected with A1a, A2 or type B; these results were conserved among multiple strains. Differences were also detected among type A clades as well as between type A clades and type B with respect to bacterial burdens, and gross anatomy in infected mice. Our results indicate that clades defined within F. tularensis subsp. tularensis by molecular typing methods correlate with virulence differences, with A1b strains more virulent than A1a, A2 and type B strains. These findings indicate type A strains are not equivalent with respect to virulence and have important implications for public health as well as basic research programs. Public Library of Science 2010-04-16 /pmc/articles/PMC2855709/ /pubmed/20419133 http://dx.doi.org/10.1371/journal.pone.0010205 Text en This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Molins, Claudia R. Delorey, Mark J. Yockey, Brook M. Young, John W. Sheldon, Sarah W. Reese, Sara M. Schriefer, Martin E. Petersen, Jeannine M. Virulence Differences Among Francisella tularensis Subsp. tularensis Clades in Mice |
title | Virulence Differences Among Francisella tularensis Subsp. tularensis Clades in Mice |
title_full | Virulence Differences Among Francisella tularensis Subsp. tularensis Clades in Mice |
title_fullStr | Virulence Differences Among Francisella tularensis Subsp. tularensis Clades in Mice |
title_full_unstemmed | Virulence Differences Among Francisella tularensis Subsp. tularensis Clades in Mice |
title_short | Virulence Differences Among Francisella tularensis Subsp. tularensis Clades in Mice |
title_sort | virulence differences among francisella tularensis subsp. tularensis clades in mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2855709/ https://www.ncbi.nlm.nih.gov/pubmed/20419133 http://dx.doi.org/10.1371/journal.pone.0010205 |
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