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Dynamic Growth and Shrinkage of the Salmonella-Containing Vacuole Determines the Intracellular Pathogen Niche
Salmonella is a human and animal pathogen that causes gastro-enteric diseases. The key to Salmonella infection is its entry into intestinal epithelial cells, where the bacterium resides within a Salmonella-containing vacuole (SCV). Salmonella entry also induces the formation of empty macropinosomes,...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6931108/ https://www.ncbi.nlm.nih.gov/pubmed/31851926 http://dx.doi.org/10.1016/j.celrep.2019.11.049 |
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author | Stévenin, Virginie Chang, Yuen-Yan Le Toquin, Yoann Duchateau, Magalie Gianetto, Quentin Giai Luk, Chak Hon Salles, Audrey Sohst, Victoria Matondo, Mariette Reiling, Norbert Enninga, Jost |
author_facet | Stévenin, Virginie Chang, Yuen-Yan Le Toquin, Yoann Duchateau, Magalie Gianetto, Quentin Giai Luk, Chak Hon Salles, Audrey Sohst, Victoria Matondo, Mariette Reiling, Norbert Enninga, Jost |
author_sort | Stévenin, Virginie |
collection | PubMed |
description | Salmonella is a human and animal pathogen that causes gastro-enteric diseases. The key to Salmonella infection is its entry into intestinal epithelial cells, where the bacterium resides within a Salmonella-containing vacuole (SCV). Salmonella entry also induces the formation of empty macropinosomes, distinct from the SCV, in the vicinity of the entering bacteria. A few minutes after its formation, the SCV increases in size through fusions with the surrounding macropinosomes. Salmonella also induces membrane tubules that emanate from the SCV and lead to SCV shrinkage. Here, we show that these antipodal events are utilized by Salmonella to either establish a vacuolar niche or to be released into the cytosol by SCV rupture. We identify the molecular machinery underlying dynamic SCV growth and shrinkage. In particular, the SNARE proteins SNAP25 and STX4 participate in SCV inflation by fusion with macropinosomes. Thus, host compartment size control emerges as a pathogen strategy for intracellular niche regulation. |
format | Online Article Text |
id | pubmed-6931108 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-69311082019-12-30 Dynamic Growth and Shrinkage of the Salmonella-Containing Vacuole Determines the Intracellular Pathogen Niche Stévenin, Virginie Chang, Yuen-Yan Le Toquin, Yoann Duchateau, Magalie Gianetto, Quentin Giai Luk, Chak Hon Salles, Audrey Sohst, Victoria Matondo, Mariette Reiling, Norbert Enninga, Jost Cell Rep Article Salmonella is a human and animal pathogen that causes gastro-enteric diseases. The key to Salmonella infection is its entry into intestinal epithelial cells, where the bacterium resides within a Salmonella-containing vacuole (SCV). Salmonella entry also induces the formation of empty macropinosomes, distinct from the SCV, in the vicinity of the entering bacteria. A few minutes after its formation, the SCV increases in size through fusions with the surrounding macropinosomes. Salmonella also induces membrane tubules that emanate from the SCV and lead to SCV shrinkage. Here, we show that these antipodal events are utilized by Salmonella to either establish a vacuolar niche or to be released into the cytosol by SCV rupture. We identify the molecular machinery underlying dynamic SCV growth and shrinkage. In particular, the SNARE proteins SNAP25 and STX4 participate in SCV inflation by fusion with macropinosomes. Thus, host compartment size control emerges as a pathogen strategy for intracellular niche regulation. Cell Press 2019-12-17 /pmc/articles/PMC6931108/ /pubmed/31851926 http://dx.doi.org/10.1016/j.celrep.2019.11.049 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Stévenin, Virginie Chang, Yuen-Yan Le Toquin, Yoann Duchateau, Magalie Gianetto, Quentin Giai Luk, Chak Hon Salles, Audrey Sohst, Victoria Matondo, Mariette Reiling, Norbert Enninga, Jost Dynamic Growth and Shrinkage of the Salmonella-Containing Vacuole Determines the Intracellular Pathogen Niche |
title | Dynamic Growth and Shrinkage of the Salmonella-Containing Vacuole Determines the Intracellular Pathogen Niche |
title_full | Dynamic Growth and Shrinkage of the Salmonella-Containing Vacuole Determines the Intracellular Pathogen Niche |
title_fullStr | Dynamic Growth and Shrinkage of the Salmonella-Containing Vacuole Determines the Intracellular Pathogen Niche |
title_full_unstemmed | Dynamic Growth and Shrinkage of the Salmonella-Containing Vacuole Determines the Intracellular Pathogen Niche |
title_short | Dynamic Growth and Shrinkage of the Salmonella-Containing Vacuole Determines the Intracellular Pathogen Niche |
title_sort | dynamic growth and shrinkage of the salmonella-containing vacuole determines the intracellular pathogen niche |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6931108/ https://www.ncbi.nlm.nih.gov/pubmed/31851926 http://dx.doi.org/10.1016/j.celrep.2019.11.049 |
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