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Single passage in mouse organs enhances the survival and spread of Salmonella enterica
Intravenous inoculation of Salmonella enterica serovar Typhimurium into mice is a prime experimental model of invasive salmonellosis. The use of wild-type isogenic tagged strains (WITS) in this system has revealed that bacteria undergo independent bottlenecks in the liver and spleen before establish...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707846/ https://www.ncbi.nlm.nih.gov/pubmed/26701880 http://dx.doi.org/10.1098/rsif.2015.0702 |
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author | Dybowski, Richard Restif, Olivier Goupy, Alexandre Maskell, Duncan J. Mastroeni, Piero Grant, Andrew J. |
author_facet | Dybowski, Richard Restif, Olivier Goupy, Alexandre Maskell, Duncan J. Mastroeni, Piero Grant, Andrew J. |
author_sort | Dybowski, Richard |
collection | PubMed |
description | Intravenous inoculation of Salmonella enterica serovar Typhimurium into mice is a prime experimental model of invasive salmonellosis. The use of wild-type isogenic tagged strains (WITS) in this system has revealed that bacteria undergo independent bottlenecks in the liver and spleen before establishing a systemic infection. We recently showed that those bacteria that survived the bottleneck exhibited enhanced growth when transferred to naive mice. In this study, we set out to disentangle the components of this in vivo adaptation by inoculating mice with WITS grown either in vitro or in vivo. We developed an original method to estimate the replication and killing rates of bacteria from experimental data, which involved solving the probability-generating function of a non-homogeneous birth–death–immigration process. This revealed a low initial mortality in bacteria obtained from a donor animal. Next, an analysis of WITS distributions in the livers and spleens of recipient animals indicated that in vivo-passaged bacteria started spreading between organs earlier than in vitro-grown bacteria. These results further our understanding of the influence of passage in a host on the fitness and virulence of Salmonella enterica and represent an advance in the power of investigation on the patterns and mechanisms of host–pathogen interactions. |
format | Online Article Text |
id | pubmed-4707846 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-47078462016-01-25 Single passage in mouse organs enhances the survival and spread of Salmonella enterica Dybowski, Richard Restif, Olivier Goupy, Alexandre Maskell, Duncan J. Mastroeni, Piero Grant, Andrew J. J R Soc Interface Research Articles Intravenous inoculation of Salmonella enterica serovar Typhimurium into mice is a prime experimental model of invasive salmonellosis. The use of wild-type isogenic tagged strains (WITS) in this system has revealed that bacteria undergo independent bottlenecks in the liver and spleen before establishing a systemic infection. We recently showed that those bacteria that survived the bottleneck exhibited enhanced growth when transferred to naive mice. In this study, we set out to disentangle the components of this in vivo adaptation by inoculating mice with WITS grown either in vitro or in vivo. We developed an original method to estimate the replication and killing rates of bacteria from experimental data, which involved solving the probability-generating function of a non-homogeneous birth–death–immigration process. This revealed a low initial mortality in bacteria obtained from a donor animal. Next, an analysis of WITS distributions in the livers and spleens of recipient animals indicated that in vivo-passaged bacteria started spreading between organs earlier than in vitro-grown bacteria. These results further our understanding of the influence of passage in a host on the fitness and virulence of Salmonella enterica and represent an advance in the power of investigation on the patterns and mechanisms of host–pathogen interactions. The Royal Society 2015-12-06 /pmc/articles/PMC4707846/ /pubmed/26701880 http://dx.doi.org/10.1098/rsif.2015.0702 Text en © 2015 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Research Articles Dybowski, Richard Restif, Olivier Goupy, Alexandre Maskell, Duncan J. Mastroeni, Piero Grant, Andrew J. Single passage in mouse organs enhances the survival and spread of Salmonella enterica |
title | Single passage in mouse organs enhances the survival and spread of Salmonella enterica |
title_full | Single passage in mouse organs enhances the survival and spread of Salmonella enterica |
title_fullStr | Single passage in mouse organs enhances the survival and spread of Salmonella enterica |
title_full_unstemmed | Single passage in mouse organs enhances the survival and spread of Salmonella enterica |
title_short | Single passage in mouse organs enhances the survival and spread of Salmonella enterica |
title_sort | single passage in mouse organs enhances the survival and spread of salmonella enterica |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707846/ https://www.ncbi.nlm.nih.gov/pubmed/26701880 http://dx.doi.org/10.1098/rsif.2015.0702 |
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