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Published on: February 9, 2011
Infection characteristics among Serratia marcescens capsule lineages
Mark T Anderson1, Stephanie D Himpsl1, Leandra G Kingsley1
1Department of Microbiology and Immunology, University of Michigan, Michigan Medicine, Ann Arbor, Michigan, USA.
Serratia marcescens capsule types influence infection severity. Sialylated capsules (KL1 and KL2) resist macrophage uptake, aiding bacterial survival in bloodstream infections.
Area of Science:
- Microbiology and Immunology
- Infectious Diseases
- Bacterial Pathogenesis
Background:
- Serratia marcescens is a significant healthcare-associated pathogen causing severe infections like bacteremia and pneumonia.
- The capsule polysaccharide is crucial for S. marcescens survival during bacteremia, with diverse capsule locus (KL) types identified.
- KL1 and KL2 strains, producing sialylated polysaccharides, are prevalent in clinical isolates.
Purpose of the Study:
- To compare the infection characteristics and contributions to infection fitness of five different Serratia marcescens capsule types.
- To investigate the role of capsule polysaccharides in S. marcescens colonization and dissemination in animal and cellular models.
- To determine the impact of capsule type on resistance to host immune defenses, specifically macrophage phagocytosis.
Main Methods:
- Utilized murine models of primary bacteremia and bacteremic pneumonia to assess capsule-dependent colonization and dissemination.
- Employed tail vein inoculation in mice to study the impact of different KL types on spleen, liver, and kidney colonization.
- Examined the ability of various KL clade capsules to inhibit internalization by bone marrow-derived macrophages in vitro.
Main Results:
- Clinical isolates of multiple KL types demonstrated capsule-dependent colonization of key organs (spleen, liver, kidney) in a bacteremia model.
- All tested clinical S. marcescens strains required capsule for lung infection and subsequent bloodstream dissemination to secondary organs.
- Only sialylated KL1 and KL2 capsules significantly inhibited macrophage internalization, even when produced in a heterologous background.
Conclusions:
- Capsule polysaccharides are essential for Serratia marcescens virulence, mediating organ colonization and systemic spread.
- Lineage-specific resistance to macrophage phagocytosis, particularly by sialylated KL1 and KL2 capsules, enhances bacterial survival.
- Targeting critical genetic lineages with specific capsule types may offer effective strategies against life-threatening S. marcescens infections.
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