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A Salmonella Typhimurium-Typhi Genomic Chimera: A Model to Study Vi Polysaccharide Capsule Function In Vivo

The Vi capsular polysaccharide is a virulence-associated factor expressed by Salmonella enterica serotype Typhi but absent from virtually all other Salmonella serotypes. In order to study this determinant in vivo, we characterised a Vi-positive S. Typhimurium (C5.507 Vi(+)), harbouring the Salmonell...

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Autores principales: Jansen, Angela M., Hall, Lindsay J., Clare, Simon, Goulding, David, Holt, Kathryn E., Grant, Andrew J., Mastroeni, Piero, Dougan, Gordon, Kingsley, Robert A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3145788/
https://www.ncbi.nlm.nih.gov/pubmed/21829346
http://dx.doi.org/10.1371/journal.ppat.1002131
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author Jansen, Angela M.
Hall, Lindsay J.
Clare, Simon
Goulding, David
Holt, Kathryn E.
Grant, Andrew J.
Mastroeni, Piero
Dougan, Gordon
Kingsley, Robert A.
author_facet Jansen, Angela M.
Hall, Lindsay J.
Clare, Simon
Goulding, David
Holt, Kathryn E.
Grant, Andrew J.
Mastroeni, Piero
Dougan, Gordon
Kingsley, Robert A.
author_sort Jansen, Angela M.
collection PubMed
description The Vi capsular polysaccharide is a virulence-associated factor expressed by Salmonella enterica serotype Typhi but absent from virtually all other Salmonella serotypes. In order to study this determinant in vivo, we characterised a Vi-positive S. Typhimurium (C5.507 Vi(+)), harbouring the Salmonella pathogenicity island (SPI)-7, which encodes the Vi locus. S. Typhimurium C5.507 Vi(+) colonised and persisted in mice at similar levels compared to the parent strain, S. Typhimurium C5. However, the innate immune response to infection with C5.507 Vi(+) and SGB1, an isogenic derivative not expressing Vi, differed markedly. Infection with C5.507 Vi(+) resulted in a significant reduction in cellular trafficking of innate immune cells, including PMN and NK cells, compared to SGB1 Vi(−) infected animals. C5.507 Vi(+) infection stimulated reduced numbers of TNF-α, MIP-2 and perforin producing cells compared to SGB1 Vi(−). The modulating effect associated with Vi was not observed in MyD88(−/−) and was reduced in TLR4(−/−) mice. The presence of the Vi capsule also correlated with induction of the anti-inflammatory cytokine IL-10 in vivo, a factor that impacted on chemotaxis and the activation of immune cells in vitro.
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spelling pubmed-31457882011-08-09 A Salmonella Typhimurium-Typhi Genomic Chimera: A Model to Study Vi Polysaccharide Capsule Function In Vivo Jansen, Angela M. Hall, Lindsay J. Clare, Simon Goulding, David Holt, Kathryn E. Grant, Andrew J. Mastroeni, Piero Dougan, Gordon Kingsley, Robert A. PLoS Pathog Research Article The Vi capsular polysaccharide is a virulence-associated factor expressed by Salmonella enterica serotype Typhi but absent from virtually all other Salmonella serotypes. In order to study this determinant in vivo, we characterised a Vi-positive S. Typhimurium (C5.507 Vi(+)), harbouring the Salmonella pathogenicity island (SPI)-7, which encodes the Vi locus. S. Typhimurium C5.507 Vi(+) colonised and persisted in mice at similar levels compared to the parent strain, S. Typhimurium C5. However, the innate immune response to infection with C5.507 Vi(+) and SGB1, an isogenic derivative not expressing Vi, differed markedly. Infection with C5.507 Vi(+) resulted in a significant reduction in cellular trafficking of innate immune cells, including PMN and NK cells, compared to SGB1 Vi(−) infected animals. C5.507 Vi(+) infection stimulated reduced numbers of TNF-α, MIP-2 and perforin producing cells compared to SGB1 Vi(−). The modulating effect associated with Vi was not observed in MyD88(−/−) and was reduced in TLR4(−/−) mice. The presence of the Vi capsule also correlated with induction of the anti-inflammatory cytokine IL-10 in vivo, a factor that impacted on chemotaxis and the activation of immune cells in vitro. Public Library of Science 2011-07-28 /pmc/articles/PMC3145788/ /pubmed/21829346 http://dx.doi.org/10.1371/journal.ppat.1002131 Text en Jansen et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Jansen, Angela M.
Hall, Lindsay J.
Clare, Simon
Goulding, David
Holt, Kathryn E.
Grant, Andrew J.
Mastroeni, Piero
Dougan, Gordon
Kingsley, Robert A.
A Salmonella Typhimurium-Typhi Genomic Chimera: A Model to Study Vi Polysaccharide Capsule Function In Vivo
title A Salmonella Typhimurium-Typhi Genomic Chimera: A Model to Study Vi Polysaccharide Capsule Function In Vivo
title_full A Salmonella Typhimurium-Typhi Genomic Chimera: A Model to Study Vi Polysaccharide Capsule Function In Vivo
title_fullStr A Salmonella Typhimurium-Typhi Genomic Chimera: A Model to Study Vi Polysaccharide Capsule Function In Vivo
title_full_unstemmed A Salmonella Typhimurium-Typhi Genomic Chimera: A Model to Study Vi Polysaccharide Capsule Function In Vivo
title_short A Salmonella Typhimurium-Typhi Genomic Chimera: A Model to Study Vi Polysaccharide Capsule Function In Vivo
title_sort salmonella typhimurium-typhi genomic chimera: a model to study vi polysaccharide capsule function in vivo
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3145788/
https://www.ncbi.nlm.nih.gov/pubmed/21829346
http://dx.doi.org/10.1371/journal.ppat.1002131
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