Cargando…
Spatial Segregation of Virulence Gene Expression during Acute Enteric Infection with Salmonella enterica serovar Typhimurium
To establish a replicative niche during its infectious cycle between the intestinal lumen and tissue, the enteric pathogen Salmonella enterica serovar Typhimurium requires numerous virulence genes, including genes for two type III secretion systems (T3SS) and their cognate effectors. To better under...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Microbiology
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3950517/ https://www.ncbi.nlm.nih.gov/pubmed/24496791 http://dx.doi.org/10.1128/mBio.00946-13 |
_version_ | 1782306999392796672 |
---|---|
author | Laughlin, Richard C. Knodler, Leigh A. Barhoumi, Roula Payne, H. Ross Wu, Jing Gomez, Gabriel Pugh, Roberta Lawhon, Sara D. Bäumler, Andreas J. Steele-Mortimer, Olivia Adams, L. Garry |
author_facet | Laughlin, Richard C. Knodler, Leigh A. Barhoumi, Roula Payne, H. Ross Wu, Jing Gomez, Gabriel Pugh, Roberta Lawhon, Sara D. Bäumler, Andreas J. Steele-Mortimer, Olivia Adams, L. Garry |
author_sort | Laughlin, Richard C. |
collection | PubMed |
description | To establish a replicative niche during its infectious cycle between the intestinal lumen and tissue, the enteric pathogen Salmonella enterica serovar Typhimurium requires numerous virulence genes, including genes for two type III secretion systems (T3SS) and their cognate effectors. To better understand the host-pathogen relationship, including early infection dynamics and induction kinetics of the bacterial virulence program in the context of a natural host, we monitored the subcellular localization and temporal expression of T3SS-1 and T3SS-2 using fluorescent single-cell reporters in a bovine, ligated ileal loop model of infection. We observed that the majority of bacteria at 2 h postinfection are flagellated, express T3SS-1 but not T3SS-2, and are associated with the epithelium or with extruding enterocytes. In epithelial cells, S. Typhimurium cells were surrounded by intact vacuolar membranes or present within membrane-compromised vacuoles that typically contained numerous vesicular structures. By 8 h postinfection, T3SS-2-expressing bacteria were detected in the lamina propria and in the underlying mucosa, while T3SS-1-expressing bacteria were in the lumen. Our work identifies for the first time the temporal and spatial regulation of T3SS-1 and -2 expression during an enteric infection in a natural host and provides further support for the concept of cytosolic S. Typhimurium in extruding epithelium as a mechanism for reseeding the lumen. |
format | Online Article Text |
id | pubmed-3950517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Society of Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-39505172014-03-12 Spatial Segregation of Virulence Gene Expression during Acute Enteric Infection with Salmonella enterica serovar Typhimurium Laughlin, Richard C. Knodler, Leigh A. Barhoumi, Roula Payne, H. Ross Wu, Jing Gomez, Gabriel Pugh, Roberta Lawhon, Sara D. Bäumler, Andreas J. Steele-Mortimer, Olivia Adams, L. Garry mBio Research Article To establish a replicative niche during its infectious cycle between the intestinal lumen and tissue, the enteric pathogen Salmonella enterica serovar Typhimurium requires numerous virulence genes, including genes for two type III secretion systems (T3SS) and their cognate effectors. To better understand the host-pathogen relationship, including early infection dynamics and induction kinetics of the bacterial virulence program in the context of a natural host, we monitored the subcellular localization and temporal expression of T3SS-1 and T3SS-2 using fluorescent single-cell reporters in a bovine, ligated ileal loop model of infection. We observed that the majority of bacteria at 2 h postinfection are flagellated, express T3SS-1 but not T3SS-2, and are associated with the epithelium or with extruding enterocytes. In epithelial cells, S. Typhimurium cells were surrounded by intact vacuolar membranes or present within membrane-compromised vacuoles that typically contained numerous vesicular structures. By 8 h postinfection, T3SS-2-expressing bacteria were detected in the lamina propria and in the underlying mucosa, while T3SS-1-expressing bacteria were in the lumen. Our work identifies for the first time the temporal and spatial regulation of T3SS-1 and -2 expression during an enteric infection in a natural host and provides further support for the concept of cytosolic S. Typhimurium in extruding epithelium as a mechanism for reseeding the lumen. American Society of Microbiology 2014-02-04 /pmc/articles/PMC3950517/ /pubmed/24496791 http://dx.doi.org/10.1128/mBio.00946-13 Text en Copyright © 2014 Laughlin et al. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-ShareAlike 3.0 Unported license (http://creativecommons.org/licenses/by-nc-sa/3.0/) , which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Laughlin, Richard C. Knodler, Leigh A. Barhoumi, Roula Payne, H. Ross Wu, Jing Gomez, Gabriel Pugh, Roberta Lawhon, Sara D. Bäumler, Andreas J. Steele-Mortimer, Olivia Adams, L. Garry Spatial Segregation of Virulence Gene Expression during Acute Enteric Infection with Salmonella enterica serovar Typhimurium |
title | Spatial Segregation of Virulence Gene Expression during Acute Enteric Infection with Salmonella enterica serovar Typhimurium |
title_full | Spatial Segregation of Virulence Gene Expression during Acute Enteric Infection with Salmonella enterica serovar Typhimurium |
title_fullStr | Spatial Segregation of Virulence Gene Expression during Acute Enteric Infection with Salmonella enterica serovar Typhimurium |
title_full_unstemmed | Spatial Segregation of Virulence Gene Expression during Acute Enteric Infection with Salmonella enterica serovar Typhimurium |
title_short | Spatial Segregation of Virulence Gene Expression during Acute Enteric Infection with Salmonella enterica serovar Typhimurium |
title_sort | spatial segregation of virulence gene expression during acute enteric infection with salmonella enterica serovar typhimurium |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3950517/ https://www.ncbi.nlm.nih.gov/pubmed/24496791 http://dx.doi.org/10.1128/mBio.00946-13 |
work_keys_str_mv | AT laughlinrichardc spatialsegregationofvirulencegeneexpressionduringacuteentericinfectionwithsalmonellaentericaserovartyphimurium AT knodlerleigha spatialsegregationofvirulencegeneexpressionduringacuteentericinfectionwithsalmonellaentericaserovartyphimurium AT barhoumiroula spatialsegregationofvirulencegeneexpressionduringacuteentericinfectionwithsalmonellaentericaserovartyphimurium AT paynehross spatialsegregationofvirulencegeneexpressionduringacuteentericinfectionwithsalmonellaentericaserovartyphimurium AT wujing spatialsegregationofvirulencegeneexpressionduringacuteentericinfectionwithsalmonellaentericaserovartyphimurium AT gomezgabriel spatialsegregationofvirulencegeneexpressionduringacuteentericinfectionwithsalmonellaentericaserovartyphimurium AT pughroberta spatialsegregationofvirulencegeneexpressionduringacuteentericinfectionwithsalmonellaentericaserovartyphimurium AT lawhonsarad spatialsegregationofvirulencegeneexpressionduringacuteentericinfectionwithsalmonellaentericaserovartyphimurium AT baumlerandreasj spatialsegregationofvirulencegeneexpressionduringacuteentericinfectionwithsalmonellaentericaserovartyphimurium AT steelemortimerolivia spatialsegregationofvirulencegeneexpressionduringacuteentericinfectionwithsalmonellaentericaserovartyphimurium AT adamslgarry spatialsegregationofvirulencegeneexpressionduringacuteentericinfectionwithsalmonellaentericaserovartyphimurium |