ER remodeling by the large GTPase atlastin promotes vacuolar growth of Legionella pneumophila. (23rd August 2017)
- Record Type:
- Journal Article
- Title:
- ER remodeling by the large GTPase atlastin promotes vacuolar growth of Legionella pneumophila. (23rd August 2017)
- Main Title:
- ER remodeling by the large GTPase atlastin promotes vacuolar growth of Legionella pneumophila
- Authors:
- Steiner, Bernhard
Swart, Anna Leoni
Welin, Amanda
Weber, Stephen
Personnic, Nicolas
Kaech, Andres
Freyre, Christophe
Ziegler, Urs
Klemm, Robin W
Hilbi, Hubert - Abstract:
- Abstract: The pathogenic bacterium Legionella pneumophila replicates in host cells within a distinct ER‐associated compartment termed the Legionella ‐containing vacuole (LCV). How the dynamic ER network contributes to pathogen proliferation within the nascent LCV remains elusive. A proteomic analysis of purified LCVs identified the ER tubule‐resident large GTPase atlastin3 (Atl3, yeast Sey1p) and the reticulon protein Rtn4 as conserved LCV host components. Here, we report that Sey1/Atl3 and Rtn4 localize to early LCVs and are critical for pathogen vacuole formation. Sey1 overproduction promotes intracellular growth of L. pneumophila, whereas a catalytically inactive, dominant‐negative GTPase mutant protein, or Atl3 depletion, restricts pathogen replication and impairs LCV maturation. Sey1 is not required for initial recruitment of ER to PtdIns(4) P ‐positive LCVs but for subsequent pathogen vacuole expansion. GTP (but not GDP) catalyzes the Sey1‐dependent aggregation of purified, ER‐positive LCVs in vitro . Thus, Sey1/Atl3‐dependent ER remodeling contributes to LCV maturation and intracellular replication of L. pneumophila . Synopsis: The intracellular pathogen Legionella pneumophila replicates within a distinct ER‐associated compartment, the Legionella ‐containing vacuole (LCV). The large, dynamin‐like GTPase atlastin3/Sey1 contributes to LCV maturation and growth by promoting ER tubule dynamics and organelle remodeling. The ER tubule‐resident large GTPase Atlastin3/Sey1Abstract: The pathogenic bacterium Legionella pneumophila replicates in host cells within a distinct ER‐associated compartment termed the Legionella ‐containing vacuole (LCV). How the dynamic ER network contributes to pathogen proliferation within the nascent LCV remains elusive. A proteomic analysis of purified LCVs identified the ER tubule‐resident large GTPase atlastin3 (Atl3, yeast Sey1p) and the reticulon protein Rtn4 as conserved LCV host components. Here, we report that Sey1/Atl3 and Rtn4 localize to early LCVs and are critical for pathogen vacuole formation. Sey1 overproduction promotes intracellular growth of L. pneumophila, whereas a catalytically inactive, dominant‐negative GTPase mutant protein, or Atl3 depletion, restricts pathogen replication and impairs LCV maturation. Sey1 is not required for initial recruitment of ER to PtdIns(4) P ‐positive LCVs but for subsequent pathogen vacuole expansion. GTP (but not GDP) catalyzes the Sey1‐dependent aggregation of purified, ER‐positive LCVs in vitro . Thus, Sey1/Atl3‐dependent ER remodeling contributes to LCV maturation and intracellular replication of L. pneumophila . Synopsis: The intracellular pathogen Legionella pneumophila replicates within a distinct ER‐associated compartment, the Legionella ‐containing vacuole (LCV). The large, dynamin‐like GTPase atlastin3/Sey1 contributes to LCV maturation and growth by promoting ER tubule dynamics and organelle remodeling. The ER tubule‐resident large GTPase Atlastin3/Sey1 localizes to LCVs and enhances intracellular replication of L. pneumophila . Sey1 is dispensable for initial recruitment of ER to PtdIns(4) P ‐positive LCVs but promotes subsequent pathogen vacuole expansion. GTP (but not GDP) triggers the Sey1‐dependent aggregation of purified, ER‐positive LCVs in vitro . Abstract : The intracellular pathogen Legionella pneumophila replicates within a distinct ER‐associated compartment, the Legionella ‐containing vacuole (LCV). The large, dynamin‐like GTPase atlastin3/Sey1 contributes to LCV maturation and growth by promoting ER tubule dynamics and organelle remodeling. … (more)
- Is Part Of:
- EMBO reports. Volume 18:Number 10(2017)
- Journal:
- EMBO reports
- Issue:
- Volume 18:Number 10(2017)
- Issue Display:
- Volume 18, Issue 10 (2017)
- Year:
- 2017
- Volume:
- 18
- Issue:
- 10
- Issue Sort Value:
- 2017-0018-0010-0000
- Page Start:
- 1817
- Page End:
- 1836
- Publication Date:
- 2017-08-23
- Subjects:
- Dictyostelium discoideum -- macrophage -- pathogen vacuole -- phosphoinositide lipid -- type IV secretion
Molecular biology -- Periodicals
Molecular Biology -- Periodicals
Molecular biology
Periodicals
572.8 - Journal URLs:
- http://www.embo-reports.oupjournals.org/ ↗
http://onlinelibrary.wiley.com/ ↗
http://firstsearch.oclc.org ↗
http://firstsearch.oclc.org/journal=1469-221x;screen=info;ECOIP ↗ - DOI:
- 10.15252/embr.201743903 ↗
- Languages:
- English
- ISSNs:
- 1469-221X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3733.086000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 10804.xml