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Published on: January 27, 2021
DRAM1 confers resistance to Salmonella infection
Samrah Masud1, Jiajun Xie1, Bart J M Grijmans1
1Institute of Biology Leiden, Leiden University, Einsteinweg 55, 2333 CC, Leiden, The Netherlands.
Abstract:
DRAM1 is an infection inducible autophagy modulator, previously shown to promote autophagic and lysosomal defense responses against the intracellular pathogen Mycobacterium marinum. However, its possible role in other anti-bacterial autophagic mechanisms remains unknown. Recently, LC3-associated phagocytosis (LAP) has emerged as autophagy-related mechanism that targets bacteria directly in phagosomes. Our previous work established LAP as the main autophagic mechanism by which macrophages restrict growth of Salmonella Typhimurium in a systemically infected zebrafish host. We therefore employed this infection model to investigate the possible role of Dram1 in LAP. Morpholino knockdown or CRISPR/Cas9-mediated mutation of Dram1 led to reduced host survival and increased bacterial burden during S. Typhimurium infection. In contrast, overexpression of dram1 by mRNA injection curtailed Salmonella replication and reduced mortality of the infected host. During the early response to infection, GFP-Lc3-Salmonella associations were reduced in dram1 knockdown or mutant embryos, and increased by dram1 overexpression. Since LAP is known to require the activity of the phagosomal NADPH oxidase, we used a Salmonella biosensor strain to detect bacterial exposure to reactive oxygen species (ROS) and found that the ROS response was largely abolished with deficiency of dram1, while it was increased with dram1 overexpression. Corroborating these results in a mammalian model, the LC3 and ROS responses to Salmonella were similarly reduced or increased by knockdown or overexpression of Dram1, respectively, in murine RAW264.7 macrophages. Together, these results demonstrate the host protective role of Dram1/DRAM1 during S. Typhimurium infection and suggest a functional link between Dram1/DRAM1 and the induction of LAP. Abbreviations: ATG8: Autophagy related protein 8; ATG16: Autophagy related protein 16; CFU: colony-forming unit; DRAM1: DNA damage regulated autophagy modulator gene 1; dpf: days post fertilization; GFP: green fluorescent protein; hpi: hours post infection; LAP: LC3 associated phagocytosis; LC3, microtubule-associated protein 1 light chain 3; NADPH: Nicotinamide dinucleotide phosphate; p53: Tumor suppressor protein 53: ROS; reactive oxygen species; S. Typhimurium: Salmonella enterica serovar Typhimurium; TIPTP: 2(tetrahydroindazolyl) phenoxy-N-(thiadiazolyl)propenamide 2; UVRAG: UV radiation resistance associated protein.
Insights
DNA damage regulated autophagy modulator 1 (DRAM1) plays a host-protective role against Salmonella Typhimurium infection by enhancing LC3-associated phagocytosis (LAP). Dram1 deficiency impairs bacterial clearance and host survival, while its overexpression improves these outcomes.
Area of Science:
- Immunology
- Cell Biology
- Microbiology
Background:
- LC3-associated phagocytosis (LAP) is an autophagy-related mechanism targeting intracellular bacteria.
- The role of DRAM1 (DNA damage regulated autophagy modulator 1) in LAP against Salmonella Typhimurium remains unclear.
- Macrophages utilize LAP to restrict Salmonella Typhimurium growth in zebrafish models.
Purpose of the Study:
- To investigate the role of Dram1 in LC3-associated phagocytosis (LAP) during Salmonella Typhimurium infection.
- To determine the impact of Dram1 on host survival and bacterial burden in a zebrafish infection model.
- To elucidate the functional link between Dram1 and the induction of LAP and reactive oxygen species (ROS) production.
Main Methods:
- Utilized a zebrafish model of systemic Salmonella Typhimurium infection.
- Employed morpholino knockdown and CRISPR/Cas9 mutation to assess Dram1 function.
- Overexpressed Dram1 using mRNA injection.
- Quantified bacterial burden and host survival.
- Assessed GFP-LC3-Salmonella associations and ROS production using a biosensor strain.
- Validated findings in murine RAW264.7 macrophages.
Main Results:
- Dram1 deficiency led to reduced host survival and increased bacterial burden during S. Typhimurium infection.
- Dram1 overexpression curtailed Salmonella replication and reduced host mortality.
- GFP-LC3-Salmonella associations were diminished in Dram1-deficient embryos and increased with Dram1 overexpression.
- Dram1 deficiency abolished ROS response to Salmonella, while overexpression enhanced it.
- Similar effects of Dram1 modulation on LC3 and ROS responses were observed in murine macrophages.
Conclusions:
- Dram1/DRAM1 plays a crucial host-protective role against Salmonella Typhimurium infection.
- Dram1/DRAM1 is functionally linked to the induction of LC3-associated phagocytosis (LAP).
- Dram1/DRAM1 modulates the reactive oxygen species (ROS) response within phagosomes during Salmonella infection.
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