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Isolation of Salmonella typhimurium-containing Phagosomes from Macrophages
Published on: October 25, 2017
Salmonella enterica infection stimulates macrophages to hemophagocytose
M Carolina Pilonieta1, Sarah M Moreland1, Christopher N English1
1Department of Molecular, Cellular and Developmental Biology, University of Colorado Boulder, Boulder, Colorado, USA.
Unlabelled:
Hemophagocytes are cells of the monocyte lineage that have engulfed erythrocytes and leukocytes. Hemophagocytes frequently accumulate in patients with severe acute bacterial infections, such as those caused by Salmonella enterica, Brucella abortus, and Mycobacterium tuberculosis. The relationship between hemophagocytosis and infection is not well understood. In the murine liver, S. enterica serovar Typhimurium resides within hemophagocytic macrophages containing leukocytes. Here we show that S. Typhimurium also resides within hemophagocytes containing erythrocytes. In cell culture, S. Typhimurium benefits from residence within hemophagocytes by accessing iron, but why macrophages hemophagocytose is unknown. We show that treatment of macrophages with a cocktail of the proinflammatory cytokine interferon gamma (IFN-γ) and lipopolysaccharide (LPS) stimulates engulfment of nonsenescent erythrocytes. Exposure of resting or IFN-γ-treated macrophages to live, but not to heat-killed, S. Typhimurium cells also stimulates erythrocyte engulfment. Single-cell analyses show that S. Typhimurium-infected macrophages are more likely to erythrophagocytose and that infected macrophages engulf more erythrocytes than uninfected macrophages within the same culture well. In addition, macrophages containing erythrocytes harbor more bacteria. However, S. Typhimurium does not promote macrophage engulfment of polystyrene beads, suggesting a role for a ligand on the target cell. Finally, neither of the two S. Typhimurium type 3 secretion systems, T3SS1 or T3SS2, is fully required for hemophagocytosis. These results indicate that infection of macrophages with live S. Typhimurium cells stimulates hemophagocytosis.
Importance:
Macrophages are white blood cells (leukocytes) that engulf and destroy pathogens. Hemophagocytes, a subset of macrophages, are characteristic of severe acute infection in patients with, for instance, typhoid fever, brucellosis, tuberculosis, and leishmaniasis. Each of these diseases has the potential to become chronic. Hemophagocytes (blood-eating cells) engulf and degrade red and white blood cells for unknown reasons. The bacterial pathogen Salmonella acquires the essential nutrient iron from murine hemophagocytes. We report that Salmonella stimulates macrophages to engulf blood cells, indicating that cells of this bacterium actively promote the formation of a specialized cellular niche in which they can acquire nutrients, evade killing by the host immune system, and potentially transition to chronic infection.
Insights
Salmonella Typhimurium infection stimulates macrophages to engulf red blood cells, creating a niche for bacterial growth and nutrient acquisition. This hemophagocytosis process is key for Salmonella to thrive within host cells.
Area of Science:
- Immunology
- Microbiology
- Cell Biology
Background:
- Hemophagocytes, characterized by engulfed blood cells, are observed in severe bacterial infections like typhoid fever.
- The precise mechanisms and reasons behind hemophagocytosis, particularly in the context of Salmonella infection, remain unclear.
- Salmonella Typhimurium utilizes hemophagocytes for nutrient acquisition, specifically iron.
Purpose of the Study:
- To investigate the relationship between Salmonella Typhimurium infection and hemophagocytosis.
- To determine if Salmonella actively stimulates macrophages to engulf erythrocytes.
- To understand the role of hemophagocytosis in bacterial survival and nutrient acquisition.
Main Methods:
- In vitro cell culture experiments using macrophages and Salmonella Typhimurium.
- Treatment of macrophages with cytokines (interferon gamma) and lipopolysaccharide (LPS).
- Analysis of erythrocyte engulfment by macrophages infected with live or heat-killed Salmonella.
- Single-cell analysis to quantify bacterial load and erythrocyte content in macrophages.
- Assessment of Salmonella's interaction with polystyrene beads to investigate ligand involvement.
- Evaluation of the role of Salmonella type 3 secretion systems (T3SS1, T3SS2).
Main Results:
- Live Salmonella Typhimurium, but not heat-killed bacteria, stimulates macrophages to engulf erythrocytes.
- Infected macrophages are more prone to hemophagocytosis and engulf more erythrocytes than uninfected cells.
- Macrophages containing erythrocytes harbor a higher bacterial load, indicating enhanced bacterial survival.
- Salmonella does not induce the engulfment of inert polystyrene beads, suggesting a specific cellular ligand interaction.
- Neither T3SS1 nor T3SS2 is essential for Salmonella-induced hemophagocytosis.
Conclusions:
- Salmonella Typhimurium infection actively stimulates macrophages to perform hemophagocytosis.
- Engulfment of erythrocytes provides a niche for Salmonella, facilitating nutrient access (iron) and immune evasion.
- This process contributes to bacterial proliferation within host cells and may play a role in disease chronicity.
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