Intracellular Localization of Brucella abortus and Francisella tularensis in Primary Murine Macrophages
By: Jean Celli3 

| Abstract |
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Intracellular bacterial pathogens have evolved sophisticated strategies to survive and proliferate within cells of their hosts.
Studying their intracellular life cycle is key to understanding virulence and requires methodologies that can identify the
compartments in which they localize and characterize the replicative niche they generate. Here, we describe immunofluorescence-based
microscopy techniques applied to the intracellular pathogens Brucella abortus and Francisella tularensis during their respective intracellular cycles inside murine bone marrow-derived macrophages. Standard immunofluorescence techniques
are used to define the intracellular localization of the pathogens based on their co-localization with specifically labeled
macrophage organelles. In addition, we describe an assay to assess the integrity of Francisella-containing phagosomes and bacterial release into the macrophage cytoplasm, which is a hallmark of Francisella intracellular pathogenesis.
Affiliation(s): (3) Tularemia Pathogenesis Section, Laboratory of Intracellular Parasites, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT
Book Title: Bacterial Pathogenesis: Methods and Protocols
Series: Methods in Molecular Biology | Volume: 431 | Pub. Date: Feb-01-2008 | Page Range: 133-145 | DOI: 10.1007/978-1-60327-032-8_11
Subject: Microbiology
Key Words:
Brucella
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Francisella
- macrophages - intracellular cycle - endosomes, endoplasmic reticulum - confocal immunofluorescence microscopy - digitonin
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