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Tractable Mammalian Cell Infections with Protozoan-primed Bacteria
Published on: April 2, 2013
Differential expression of virulence genes in Legionella pneumophila growing in Acanthamoeba and human monocytes
Qianqian Mou1, Polly H M Leung1
1a Department of Health Technology and Informatics , The Hong Kong Polytechnic University , Kowloon , Hong Kong , China.
Abstract:
Legionella pneumophila, the causative agent of Legionnaires' disease, is widely distributed throughout natural and artificial water systems and can replicate in macrophages and amoebae. Amoebae are the natural hosts of L. pneumophila, whereas macrophages are incidentally infected. The life cycle of L. pneumophila comprises a replicative phase within the Legionella-containing vacuole (LCV) and a transmissive phase during which bacterial cells become motile and are released via killing of the host. Although the host death mechanisms induced by L. pneumophila have been studied, the expression patterns of related L. pneumophila genes have not been reported. The present study compared the expression patterns of host cell death-associated genes in L. pneumophila grown in the human monocytic cell line THP-1 and Acanthamoeba castellanii. Notably, when L. pneumophila was grown in THP-1, expression of the gene flaA, which is involved in the induction of pyroptosis, was downregulated during the course of infection. In contrast, sdhA associated indirectly with host death, was upregulated. Expression of the genes vipD and sidF, which are involved in the induction and suppression of apoptosis, changed by less than 2-fold. Notably, a lower percentage of pyroptotic cells was observed among infected THP-1 cells relative to uninfected cells, and the latter exhibited stronger expression of caspase-1. A different pattern was observed when L. pneumophila was grown in A. castellanii: flaA and vipD were activated, whereas sdhA and sidF were downregulated during the later stage of replication. The percentage of non-viable (annexin-V+ PI+ or annexin-V+PI-) A. castellanii organisms increased with Legionella infection, and the expression of metacaspase-1, which is involved in encystation was up-regulated at late infection time. In summary, L. pneumophila can multiply intracellularly in both amoebae and macrophages to induce cell death and secondary infection, and this characteristic is essential for its survival in water and the lungs. The gene expression profiles observed in this study indicated the increased cytotoxicity of L. pneumophila in A. castellanii, suggesting an increased adaptation of Legionella to this host.
Insights
Legionella pneumophila gene expression differs when infecting amoebae versus human cells. This study reveals distinct host cell death pathways, indicating Legionella
Area of Science:
- Microbiology
- Cell Biology
- Pathogen-Host Interactions
Background:
- Legionella pneumophila causes Legionnaires' disease and replicates in amoebae and macrophages.
- Understanding L. pneumophila's intracellular life cycle and host-cell death induction is crucial.
- Gene expression patterns during host cell infection remain largely uncharacterized.
Purpose of the Study:
- To compare host cell death-associated gene expression of L. pneumophila in Acanthamoeba castellanii and human THP-1 cells.
- To elucidate differential gene regulation in response to distinct host environments.
- To understand L. pneumophila's adaptation and survival strategies.
Main Methods:
- Culturing L. pneumophila in Acanthamoeba castellanii and human THP-1 cell lines.
- Analyzing the expression of specific L. pneumophila genes (flaA, sdhA, vipD, sidF) using quantitative methods.
- Assessing host cell viability and death pathways (pyroptosis, apoptosis, metacaspase-1 activity).
Main Results:
- In THP-1 cells, flaA (pyroptosis) was downregulated, while sdhA was upregulated; vipD and sidF showed minimal change.
- In A. castellanii, flaA and vipD were activated, and sdhA and sidF were downregulated.
- Increased A. castellanii cell death and metacaspase-1 expression were observed with L. pneumophila infection.
Conclusions:
- L. pneumophila exhibits distinct gene expression profiles and host cell interaction strategies in amoebae versus macrophages.
- The bacterium demonstrates increased cytotoxicity and adaptation in Acanthamoeba castellanii.
- Differential gene expression is key to L. pneumophila's survival, replication, and dissemination in diverse environments.
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