Affiliation:
1. Department of Biochemistry, Microbiology and Immunology University of Ottawa Ottawa Ontario Canada
2. Centre for Infection, Immunity and Inflammation University of Ottawa Ottawa Canada
3. These authors contributed equally to this work
Abstract
AbstractIntracellular bacterial pathogens implement a diverse array of strategies to target host cells and establish infection. For vacuolar pathogens, the process of pathogen‐containing vacuole movement within host cells, termed intracellular trafficking, is central to both pathogen survival and infection progression. Typically a process mediated by secreted virulence factors that manipulate the host cytoskeletal machinery, internalized pathogen‐containing vacuoles traffic to the site of replication to establish a unique replicative niche, and if applicable, traffic back toward the host cell periphery for cell‐to‐cell spread. As such, the intracellular positioning of pathogen‐containing vacuoles represents a fundamental measure of infection progression. Here, we describe a fluorescence microscopy‐based method to quantitatively assess bacterial intracellular positioning, using Salmonella enterica serovar Typhimurium infection of epithelial cells as a model. This experimental approach can be modified to study infection in diverse host cell types, and with a broad array of pathogens. The system can also be adapted to examine the kinetics of infection, identify secreted virulence factors that mediate host trafficking, investigate host factors that are targeted by the pathogen for trafficking, and assess functional domains within a virulence factor responsible for mediating the phenotype. Collectively, these tools can provide fundamental insight into the pathogenesis of a diverse array of intracellular bacterial pathogens, and new host factors that are hijacked to mediate infection. © 2024 The Authors. Current Protocols published by Wiley Periodicals LLC.Basic Protocol 1: Culture and preparation of host cellsAlternate Protocol: Culture and preparation of host cells to assess host factor contribution to bacterial positioningBasic Protocol 2: Infection of epithelial cells with S. TyphimuriumBasic Protocol 3: Fluorescence staining for analysis of bacterial positioningBasic Protocol 4: Fluorescence microscopy analysis of bacterial positioning