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Published on: May 24, 2018
Shigella flexneri regulation of ARF6 activation during bacterial entry via an IpgD-mediated positive feedback loop
Anna Cristina Garza-Mayers1, Kelly A Miller2, Brian C Russo2
1Department of Microbiology and Immunobiology, Harvard Medical School, Boston, Massachusetts, USA.
Unlabelled:
Entry into cells is critical for virulence of the human bacterial pathogens Shigella spp. Shigella spp. induce membrane ruffle formation and macropinocytic uptake, but the events instigating this process are incompletely understood. The host small GTPase ADP-ribosylation factor 6 (ARF6) functions in membrane trafficking at the plasma membrane and activates membrane ruffle formation. We demonstrate that ARF6 is required for efficient Shigella flexneri entry, is activated by S. flexneri dependent on the phosphatase activity of the type III secreted effector IpgD, and depends on cytohesin guanine nucleotide exchange factors (GEFs) for recruitment to entry sites. The cytohesin GEF ARF nucleotide binding site opener (ARNO) is recruited to these sites, also dependent on IpgD phosphatase activity. ARNO recruitment is independent of ARF6, indicating that, in addition to the described recruitment of ARNO by ARF6, ARNO is recruited upstream of ARF6. Our data provide evidence that ARF6, IpgD, phosphoinositide species, and ARNO constitute a previously undescribed positive feedback loop that amplifies ARF6 activation at bacterial entry sites, thereby promoting efficient S. flexneri uptake.
Importance:
Shigella spp. cause diarrhea and dysentery by infection of epithelial cells in the human colon. Critical to disease is the ability of Shigella to enter into cells, yet the mechanisms involved in entry are incompletely understood. We demonstrate that the small GTPase ADP-ribosylation factor 6 (ARF6) is required for efficient cellular entry of Shigella flexneri and that activation of ARF6 depends on the phosphatase activity of the Shigella protein IpgD, which is introduced into cells via the bacterial type III secretion system. We further show that IpgD phosphatase activity is required for recruitment of the ARF6 guanine nucleotide exchange factor (GEF) ARF nucleotide binding site opener (ARNO) to bacterial entry sites and that ARNO lies upstream of ARF6 activation. These relationships define a positive feedback loop that contributes to activation of ARF6 at S. flexneri entry sites and leads to local amplification of signals that promote bacterial entry.
Insights
Shigella flexneri entry into host cells requires ADP-ribosylation factor 6 (ARF6). Bacterial effector IpgD activates ARF6 via a positive feedback loop involving ARNO, promoting bacterial uptake.
Area of Science:
- Microbiology
- Cell Biology
- Bacterial Pathogenesis
Background:
- Shigella spp. are human bacterial pathogens that cause diarrhea and dysentery.
- Cell entry is critical for Shigella virulence, but the underlying mechanisms are not fully understood.
- The host small GTPase ADP-ribosylation factor 6 (ARF6) regulates membrane trafficking and ruffle formation.
Purpose of the Study:
- To investigate the role of ARF6 in Shigella flexneri cellular entry.
- To elucidate the mechanism of ARF6 activation by S. flexneri.
- To identify host factors and bacterial effectors involved in bacterial entry.
Main Methods:
- Demonstrated ARF6 requirement for S. flexneri entry.
- Investigated ARF6 activation dependence on the type III secreted effector IpgD.
- Assessed recruitment of cytohesin guanine nucleotide exchange factors (GEFs), specifically ARF nucleotide binding site opener (ARNO), to bacterial entry sites.
- Analyzed the relationship between ARNO recruitment and ARF6 activation.
Main Results:
- ARF6 is essential for efficient Shigella flexneri entry into host cells.
- S. flexneri activates ARF6 through the phosphatase activity of the effector IpgD.
- IpgD phosphatase activity is required for the recruitment of ARNO to bacterial entry sites.
- ARNO recruitment occurs upstream of ARF6 activation, independent of ARF6 itself.
- A positive feedback loop involving ARF6, IpgD, phosphoinositides, and ARNO amplifies ARF6 activation at entry sites.
Conclusions:
- ARF6 is a key host factor mediating Shigella flexneri entry.
- The bacterial effector IpgD initiates a positive feedback loop to amplify ARF6 activation.
- This feedback loop, involving ARNO and phosphoinositides, enhances ARF6 signaling and promotes efficient bacterial uptake.
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