Caspase-12 and the inflammatory response to Yersinia pestis

PLoS One. 2009 Sep 1;4(9):e6870. doi: 10.1371/journal.pone.0006870.

Abstract

Background: Caspase-12 functions as an antiinflammatory enzyme inhibiting caspase-1 and the NOD2/RIP2 pathways. Due to increased susceptibility to sepsis in individuals with functional caspase-12, an early-stop mutation leading to the loss of caspase-12 has replaced the ancient genotype in Eurasia and a significant proportion of individuals from African populations. In African-Americans, it has been shown that caspase-12 inhibits the pro-inflammatory cytokine production.

Methodology/principal findings: We assessed whether similar mechanisms are present in African individuals, and whether evolutionary pressures due to plague may have led to the present caspase-12 genotype population frequencies. No difference in cytokine induction through the caspase-1 and/or NOD2/RIP2 pathways was observed in two independent African populations, among individuals with either an intact or absent caspase-12. In addition, stimulations with Yersinia pestis and two other species of Yersinia were preformed to investigate whether caspase-12 modulates the inflammatory reaction induced by Yersinia. We found that caspase-12 did not modulate cytokine production induced by Yersinia spp.

Conclusions: Our experiments demonstrate for the first time the involvement of the NOD2/RIP2 pathway for recognition of Yersinia. However, caspase-12 does not modulate innate host defense against Y. pestis and alternative explanations for the geographical distribution of caspase-12 should be sought.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Caspase 12 / physiology*
  • Cytokines / metabolism
  • Gene Expression Regulation*
  • Genotype
  • Humans
  • Immunity, Innate
  • Inflammation
  • Interleukin-1beta / metabolism
  • Mali
  • Nod2 Signaling Adaptor Protein / metabolism
  • Receptor-Interacting Protein Serine-Threonine Kinase 2 / metabolism
  • Sepsis / metabolism*
  • Yersinia Infections / metabolism*
  • Yersinia pestis / pathogenicity*

Substances

  • Cytokines
  • Interleukin-1beta
  • NOD2 protein, human
  • Nod2 Signaling Adaptor Protein
  • RIPK2 protein, human
  • Receptor-Interacting Protein Serine-Threonine Kinase 2
  • Caspase 12