| Literature DB >> 34043959 |
Audrey Chong1, Kendal G Cooper1, Laszlo Kari1, Olof R Nilsson1, Chad Hillman1, Brittany A Fleming1, Qinlu Wang2, Vinod Nair3, Olivia Steele-Mortimer4.
Abstract
Persistent and intermittent fecal shedding, hallmarks of Salmonella infections, are important for fecal-oral transmission. In the intestine, Salmonella enterica serovar Typhimurium (STm) actively invades intestinal epithelial cells (IECs) and survives in the Salmonella-containing vacuole (SCV) and the cell cytosol. Cytosolic STm replicate rapidly, express invasion factors, and induce extrusion of infected epithelial cells into the intestinal lumen. Here, we engineered STm that self-destruct in the cytosol (STmCytoKill), but replicates normally in the SCV, to examine the role of cytosolic STm in infection. Intestinal expansion and fecal shedding of STmCytoKill are impaired in mouse models of infection. We propose a model whereby repeated rounds of invasion, cytosolic replication, and release of invasive STm from extruded IECs fuels the high luminal density required for fecal shedding. Published by Elsevier Inc.Entities:
Keywords: Salmonella Typhimurium; autolytic; conditional lethal; epithelium; extrusion; intestinal epithelial cell; intracytosolic replication; shedding
Mesh:
Year: 2021 PMID: 34043959 PMCID: PMC8282707 DOI: 10.1016/j.chom.2021.04.017
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 31.316