Is Crohn's Disease the Price to Pay Today for Having Survived the Black Death?

J Crohns Colitis. 2019 Sep 27;13(10):1318-1322. doi: 10.1093/ecco-jcc/jjz062.

Abstract

Background and aims: Nucleotide Oligomerisation Domain 2 [NOD2] is a key gene of innate immunity which participates in the host defence against pathogens. Several loss-of-function NOD2 mutations are associated with Crohn's disease [CD]. Their high frequencies in populations of European ancestry suggest a model of balancing selection. Because NOD2 deficiency has been associated with a resistance to Yersinia pseudotuberculosis in mice, we hypothesised that NOD2 mutations have been selected during past plague outbreaks due to the closely related bacterium Yersinia pestis.

Methods: Contemporary frequencies of the main CD-associated NOD2 mutations [R702W, G908R, and 1007fs], measured in healthy people from European and Mediterranean countries, were collected from 60 studies via a PubMed search. Plague exposure was calculated from a dataset providing outbreaks from 1346 to 1860 in Europe and the Mediterranean Bassin. A plague index was built to capture the intensity of plague exposure in the studied geographical areas.

Results: NOD2 mutation frequencies were associated with the past exposure to plague. Statistical significance was obtained for the most frequent mutation [R702W, p = 0.03] and for the pooled three mutations [p = 0.023]. The association remained significant when putative demographic biases were considered.

Conclusions: This result argues for a selection of CD-associated NOD2 mutations by plague outbreaks and further questioned the role of exposure to enteropathogenic Yersinia species in CD.

Keywords: NOD2; Plague; Yersinia.

Publication types

  • Historical Article

MeSH terms

  • Crohn Disease / genetics*
  • Crohn Disease / immunology
  • Disease Outbreaks / history
  • Europe / epidemiology
  • Gene Frequency / genetics
  • Genetic Predisposition to Disease / genetics
  • Genetic Predisposition to Disease / history
  • History, 15th Century
  • History, 16th Century
  • History, 17th Century
  • History, 18th Century
  • History, 19th Century
  • History, Medieval
  • Humans
  • Immunity, Innate / genetics*
  • Models, Statistical
  • Mutation / genetics
  • Nod2 Signaling Adaptor Protein / genetics*
  • Plague / genetics*
  • Plague / history
  • Plague / immunology
  • White People / genetics*

Substances

  • NOD2 protein, human
  • Nod2 Signaling Adaptor Protein