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Deciphering why Salmonella Gallinarum is less invasive in vitro than Salmonella Enteritidis

Salmonella Gallinarum and Salmonella Enteritidis are genetically closely related however associated with different pathologies. Several studies have suggested that S. Gallinarum is less invasive in vitro than S. Enteritidis. In this study we confirm that the S. Gallinarum strains tested were much le...

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Autores principales: Rossignol, Aurore, Roche, Sylvie M, Virlogeux-Payant, Isabelle, Wiedemann, Agnès, Grépinet, Olivier, Fredlund, Jennifer, Trotereau, Jérôme, Marchès, Olivier, Quéré, Pascale, Enninga, Jost, Velge, Philippe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4154518/
https://www.ncbi.nlm.nih.gov/pubmed/25175996
http://dx.doi.org/10.1186/s13567-014-0081-z
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author Rossignol, Aurore
Roche, Sylvie M
Virlogeux-Payant, Isabelle
Wiedemann, Agnès
Grépinet, Olivier
Fredlund, Jennifer
Trotereau, Jérôme
Marchès, Olivier
Quéré, Pascale
Enninga, Jost
Velge, Philippe
author_facet Rossignol, Aurore
Roche, Sylvie M
Virlogeux-Payant, Isabelle
Wiedemann, Agnès
Grépinet, Olivier
Fredlund, Jennifer
Trotereau, Jérôme
Marchès, Olivier
Quéré, Pascale
Enninga, Jost
Velge, Philippe
author_sort Rossignol, Aurore
collection PubMed
description Salmonella Gallinarum and Salmonella Enteritidis are genetically closely related however associated with different pathologies. Several studies have suggested that S. Gallinarum is less invasive in vitro than S. Enteritidis. In this study we confirm that the S. Gallinarum strains tested were much less invasive than the S. Enteritidis strains tested in cells of avian or human origin. In addition, the S. Gallinarum T3SS-1-dependent ability to invade host cells was delayed by two to three hours compared to S. Enteritidis, indicating that T3SS-1-dependent entry is less efficient in S. Gallinarum than S. Enteritidis. This was neither due to a decreased transcription of T3SS-1 related genes when bacteria come into contact with cells, as transcription of hilA, invF and sipA was similar to that observed for S. Enteritidis, nor to a lack of functionality of the S. Gallinarum T3SS-1 apparatus as this apparatus was able to secrete and translocate effector proteins into host cells. In contrast, genome comparison of four S. Gallinarum and two S. Enteritidis strains revealed that all S. Gallinarum genomes displayed the same point mutations in each of the main T3SS-1 effector genes sipA, sopE, sopE2, sopD and sopA. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13567-014-0081-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-41545182014-09-05 Deciphering why Salmonella Gallinarum is less invasive in vitro than Salmonella Enteritidis Rossignol, Aurore Roche, Sylvie M Virlogeux-Payant, Isabelle Wiedemann, Agnès Grépinet, Olivier Fredlund, Jennifer Trotereau, Jérôme Marchès, Olivier Quéré, Pascale Enninga, Jost Velge, Philippe Vet Res Research Salmonella Gallinarum and Salmonella Enteritidis are genetically closely related however associated with different pathologies. Several studies have suggested that S. Gallinarum is less invasive in vitro than S. Enteritidis. In this study we confirm that the S. Gallinarum strains tested were much less invasive than the S. Enteritidis strains tested in cells of avian or human origin. In addition, the S. Gallinarum T3SS-1-dependent ability to invade host cells was delayed by two to three hours compared to S. Enteritidis, indicating that T3SS-1-dependent entry is less efficient in S. Gallinarum than S. Enteritidis. This was neither due to a decreased transcription of T3SS-1 related genes when bacteria come into contact with cells, as transcription of hilA, invF and sipA was similar to that observed for S. Enteritidis, nor to a lack of functionality of the S. Gallinarum T3SS-1 apparatus as this apparatus was able to secrete and translocate effector proteins into host cells. In contrast, genome comparison of four S. Gallinarum and two S. Enteritidis strains revealed that all S. Gallinarum genomes displayed the same point mutations in each of the main T3SS-1 effector genes sipA, sopE, sopE2, sopD and sopA. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13567-014-0081-z) contains supplementary material, which is available to authorized users. BioMed Central 2014-08-30 2014 /pmc/articles/PMC4154518/ /pubmed/25175996 http://dx.doi.org/10.1186/s13567-014-0081-z Text en © Rossignol et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Rossignol, Aurore
Roche, Sylvie M
Virlogeux-Payant, Isabelle
Wiedemann, Agnès
Grépinet, Olivier
Fredlund, Jennifer
Trotereau, Jérôme
Marchès, Olivier
Quéré, Pascale
Enninga, Jost
Velge, Philippe
Deciphering why Salmonella Gallinarum is less invasive in vitro than Salmonella Enteritidis
title Deciphering why Salmonella Gallinarum is less invasive in vitro than Salmonella Enteritidis
title_full Deciphering why Salmonella Gallinarum is less invasive in vitro than Salmonella Enteritidis
title_fullStr Deciphering why Salmonella Gallinarum is less invasive in vitro than Salmonella Enteritidis
title_full_unstemmed Deciphering why Salmonella Gallinarum is less invasive in vitro than Salmonella Enteritidis
title_short Deciphering why Salmonella Gallinarum is less invasive in vitro than Salmonella Enteritidis
title_sort deciphering why salmonella gallinarum is less invasive in vitro than salmonella enteritidis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4154518/
https://www.ncbi.nlm.nih.gov/pubmed/25175996
http://dx.doi.org/10.1186/s13567-014-0081-z
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