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Published on: October 15, 2013
Dictyostelium discoideum as a model system for identification of Burkholderia pseudomallei virulence factors
Benjamin M Hasselbring1, Maharsh K Patel, Mark A Schell
1Department of Microbiology, 210 Biological Sciences Building, University of Georgia, Athens, GA 30602, USA.
Abstract:
Burkholderia pseudomallei is an emerging bacterial pathogen and category B biothreat. Human infections with B. pseudomallei (called melioidosis) present as a range of manifestations, including acute septicemia and pneumonia. Although melioidosis can be fatal, little is known about the molecular basis of B. pseudomallei pathogenicity, in part because of the lack of simple, genetically tractable eukaryotic models to facilitate en masse identification of virulence determinants or explore host-pathogen interactions. Two assays, one high-throughput and one quantitative, were developed to monitor levels of resistance of B. pseudomallei and the closely related nearly avirulent species Burkholderia thailandensis to predation by the phagocytic amoeba Dictyostelium discoideum. The quantitative assay showed that levels of resistance to, and survival within, amoeba by these bacteria and their known virulence mutants correlate well with their published levels of virulence in animals. Using the high-throughput assay, we screened a 1,500-member B. thailandensis transposon mutant library and identified 13 genes involved in resistance to predation by D. discoideum. Orthologs of these genes were disrupted in B. pseudomallei, and nearly all mutants had similarly decreased resistance to predation by D. discoideum. For some mutants, decreased resistance also correlated with reduced survival in and cytotoxicity toward macrophages, as well as attenuated virulence in mice. These observations suggest that some factors required by B. pseudomallei for resistance to environmental phagocytes also aid in resistance to phagocytic immune cells and contribute to disease in animals. Thus, D. discoideum provides a novel, high-throughput model system for facilitating inquiry into B. pseudomallei virulence.
Insights
Dictyostelium discoideum predation assays reveal bacterial virulence factors. This model system helps identify genes essential for Burkholderia pseudomallei survival against phagocytes and in animal models of melioidosis.
Area of Science:
- Microbiology
- Pathogen Biology
- Biodefense
Background:
- Burkholderia pseudomallei is an emerging bacterial pathogen and biothreat agent.
- Melioidosis, caused by B. pseudomallei, presents with diverse, potentially fatal manifestations.
- Limited understanding of B. pseudomallei pathogenicity due to lack of tractable models for virulence factor identification.
Purpose of the Study:
- Develop novel assays to study B. pseudomallei virulence.
- Utilize Dictyostelium discoideum as a model system for high-throughput screening of bacterial virulence determinants.
- Identify genes involved in B. pseudomallei resistance to phagocytosis and their role in host-pathogen interactions.
Main Methods:
- Developed high-throughput and quantitative assays to measure bacterial resistance to Dictyostelium discoideum predation.
- Screened a 1,500-member Burkholderia thailandensis transposon mutant library using the high-throughput assay.
- Disrupted orthologous genes in B. pseudomallei and assessed their resistance to D. discoideum, macrophage survival, and mouse virulence.
Main Results:
- Quantitative assay results correlated bacterial resistance to amoeba predation with known animal virulence levels.
- Identified 13 genes in B. thailandensis essential for D. discoideum resistance.
- B. pseudomallei mutants lacking these genes showed decreased amoeba resistance, reduced macrophage survival, and attenuated virulence in mice.
Conclusions:
- Dictyostelium discoideum serves as a novel, high-throughput model for studying B. pseudomallei virulence.
- Factors conferring resistance to environmental phagocytes like D. discoideum are also important for evading host immune cells and causing disease.
- This model facilitates the identification of virulence determinants for biodefense applications.

