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MHC variation sculpts individualized microbial communities that control susceptibility to enteric infection

  • Jason L. Kubinak
  • , W. Zac Stephens
  • , Ray Soto
  • , Charisse Petersen
  • , Tyson Chiaro
  • , Lasha Gogokhia
  • , Rickesha Bell
  • , Nadim J. Ajami
  • , Joseph F. Petrosino
  • , Linda Morrison
  • , Wayne K. Potts
  • , Peter E. Jensen
  • , Ryan M. O'Connell
  • , June L. Round
  • University of Utah
  • Baylor College of Medicine

Research output: Contribution to journalArticlepeer-review

139 Scopus citations

Abstract

The presentation of protein antigens on the cell surface by major histocompatibility complex (MHC) molecules coordinates vertebrate adaptive immune responses, thereby mediating susceptibility to a variety of autoimmune and infectious diseases. The composition of symbiotic microbial communities (the microbiota) is influenced by host immunity and can have a profound impact on host physiology. Here we use an MHC congenic mouse model to test the hypothesis that genetic variation at MHC genes among individuals mediates susceptibility to disease by controlling microbiota composition. We find that MHC genotype significantly influences antibody responses against commensals in the gut, and that these responses are correlated with the establishment of unique microbial communities. Transplantation experiments in germfree mice indicate that MHC-mediated differences in microbiota composition are sufficient to explain susceptibility to enteric infection. Our findings indicate that MHC polymorphisms contribute to defining an individual's unique microbial fingerprint that influences health.

Original languageEnglish
Article number8642
JournalNature Communications
Volume6
DOIs
StatePublished - Oct 23 2015

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