The human NAIP-NLRC4-inflammasome senses the Pseudomonas aeruginosa T3SS inner-rod protein

Int Immunol. 2017 Aug 1;29(8):377-384. doi: 10.1093/intimm/dxx047.

Abstract

While NLRC4-dependent sensing of intracellular Gram-negative pathogens such as Salmonella enterica serovar typhimurium is a beneficial host response, NLRC4-dependent sensing of the Pseudomonas aeruginosa type 3 secretion system (T3SS) has been shown to be involved in pathogenicity. In mice, different pathogen-associated microbial patterns are sensed by the combination of the NLRC4-inflammasome with different neuronal apoptosis inhibitory proteins (NAIPs). NAIP2 is involved in sensing PscI, an inner-rod protein of the P. aeruginosa T3SS. Surprisingly, only a single human NAIP (hNAIP) has been found. Moreover, there is no description of hNAIP-NLRC4 inflammasome recognition of T3SS inner-rod proteins in humans. Here, we show that the P. aeruginosa T3SS inner-rod protein PscI and needle protein PscF are both sensed by the hNAIP-NLRC4 inflammasome in human macrophages and PBMCs from healthy donors, allowing caspase-1 and IL-1β maturation and resulting in a robust inflammatory response. TLR4 and TLR2 are involved in redundantly sensing these two T3SS components.

Keywords: Innate Immunity; Nod-like receptor; Pathogen-associated microbial pattern; Toll-like receptor.

MeSH terms

  • Animals
  • CARD Signaling Adaptor Proteins / metabolism*
  • Calcium-Binding Proteins / metabolism*
  • Carrier Proteins / metabolism
  • Caspase 1 / metabolism
  • Humans
  • Immunity, Innate
  • Inflammasomes / metabolism*
  • Intercellular Signaling Peptides and Proteins
  • Interleukin-1beta / metabolism
  • Macrophages / immunology*
  • Macrophages / microbiology
  • Mice
  • Neuronal Apoptosis-Inhibitory Protein / metabolism*
  • Pathogen-Associated Molecular Pattern Molecules / immunology
  • Pseudomonas Infections / immunology*
  • Pseudomonas aeruginosa / immunology*
  • THP-1 Cells
  • Toll-Like Receptor 2 / metabolism
  • Toll-Like Receptor 4 / metabolism
  • Type III Secretion Systems / immunology
  • Type III Secretion Systems / metabolism*

Substances

  • CARD Signaling Adaptor Proteins
  • Calcium-Binding Proteins
  • Carrier Proteins
  • Inflammasomes
  • Intercellular Signaling Peptides and Proteins
  • Interleukin-1beta
  • NLRC4 protein, human
  • Naip2 protein, mouse
  • Neuronal Apoptosis-Inhibitory Protein
  • Pathogen-Associated Molecular Pattern Molecules
  • PscF protein, Pseudomonas aeruginosa
  • TLR2 protein, human
  • TLR4 protein, human
  • Toll-Like Receptor 2
  • Toll-Like Receptor 4
  • Type III Secretion Systems
  • Caspase 1