The Legionella pneumophila effector DenR hijacks the host NRas proto-oncoprotein to downregulate MAPK signaling

Cell Rep. 2024 Apr 23;43(4):114033. doi: 10.1016/j.celrep.2024.114033. Epub 2024 Apr 2.

Abstract

Small GTPases of the Ras subfamily are best known for their role as proto-oncoproteins, while their function during microbial infection has remained elusive. Here, we show that Legionella pneumophila hijacks the small GTPase NRas to the Legionella-containing vacuole (LCV) surface. A CRISPR interference screen identifies a single L. pneumophila effector, DenR (Lpg1909), required for this process. Recruitment is specific for NRas, while its homologs KRas and HRas are excluded from LCVs. The C-terminal hypervariable tail of NRas is sufficient for recruitment, and interference with either NRas farnesylation or S-acylation sites abrogates recruitment. Intriguingly, we detect markers of active NRas signaling on the LCV, suggesting it acts as a signaling platform. Subsequent phosphoproteomics analyses show that DenR rewires the host NRas signaling landscape, including dampening of the canonical mitogen-activated protein kinase pathway. These results provide evidence for L. pneumophila targeting NRas and suggest a link between NRas GTPase signaling and microbial infection.

Keywords: CP: Microbiology; cancer; intracellular pathogen; palmitoylation; type IV secretion system; virulence.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins* / genetics
  • Bacterial Proteins* / metabolism
  • Down-Regulation
  • GTP Phosphohydrolases* / metabolism
  • HEK293 Cells
  • Humans
  • Legionella pneumophila* / metabolism
  • Legionella pneumophila* / pathogenicity
  • Legionnaires' Disease / metabolism
  • Legionnaires' Disease / microbiology
  • MAP Kinase Signaling System*
  • Membrane Proteins* / genetics
  • Membrane Proteins* / metabolism
  • Proto-Oncogene Proteins p21(ras) / genetics
  • Proto-Oncogene Proteins p21(ras) / metabolism
  • Vacuoles / metabolism

Substances

  • Membrane Proteins
  • NRAS protein, human
  • GTP Phosphohydrolases
  • Bacterial Proteins
  • Proto-Oncogene Proteins p21(ras)