4.8 Article

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

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NATURE COMMUNICATIONS
卷 6, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/ncomms9642

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资金

  1. National Center for Research Resources of the National Institutes of Health [1S10RR026802-01]
  2. NIH [DP2GM111099-01]
  3. NHLBI [R00HL102228-05]
  4. American Cancer Society Research
  5. Kimmel Scholar Award
  6. Edward Mallinckrodt Jr. Foundation
  7. Pew Scholars Program
  8. NSF CAREER award [I0S-1253278]
  9. Packard Fellowship in Science and Engineering and NIAID K22 [AI95375]
  10. NIAID [AI107090, AI109122]
  11. NIH Directors Innovator award [DP2AT008746-01]
  12. [5-P39-DK034987]
  13. [5-P40-0D010995]
  14. [AI-055434]
  15. [GM007464]

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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.

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