4.7 Article

Oral microbiomes from hunter-gatherers and traditional farmers reveal shifts in commensal balance and pathogen load linked to diet

期刊

MOLECULAR ECOLOGY
卷 27, 期 1, 页码 182-195

出版社

WILEY
DOI: 10.1111/mec.14435

关键词

diet; hunter-gatherers; metagenomics; oral microbiome; Philippines

资金

  1. European Research Council (ERC) [ERC260801]
  2. National Institute for Health Research University College London Hospitals Biomedical Research Centre
  3. UK Medical Research Council [412 MR/N010760/1]
  4. Institut Pasteur-Cenci Bolognetti fellowship
  5. Human Frontiers (HFSP) fellowship
  6. EPSRC [EP/F500351/1]
  7. Reuben Centre for Paediatric Virology and Metagenomics
  8. Leverhulme Trust [RP2011-R-045]
  9. French National Research Agency (ANR) grant Labex IAST
  10. Biotechnology and Biological Sciences Research Council [BB/H008802/1, BB/H008802/2] Funding Source: researchfish
  11. Engineering and Physical Sciences Research Council [1487527] Funding Source: researchfish
  12. Medical Research Council [MR/P007597/1] Funding Source: researchfish
  13. BBSRC [BB/H008802/1, BB/H008802/2] Funding Source: UKRI
  14. MRC [MR/N010760/1, MR/P007597/1] Funding Source: UKRI

向作者/读者索取更多资源

Maladaptation to modern diets has been implicated in several chronic disorders. Given the higher prevalence of disease such as dental caries and chronic gum diseases in industrialized societies, we sought to investigate the impact of different subsistence strategies on oral health and physiology, as documented by the oral microbiome. To control for confounding variables such as environment and host genetics, we sampled saliva from three pairs of populations of hunter-gatherers and traditional farmers living in close proximity in the Philippines. Deep shotgun sequencing of salivary DNA generated high-coverage microbiomes along with human genomes. Comparing these microbiomes with publicly available data from individuals living on a Western diet revealed that abundance ratios of core species were significantly correlated with subsistence strategy, with hunter-gatherers and Westerners occupying either end of a gradient of Neisseria against Haemophilus, and traditional farmers falling in between. Species found preferentially in hunter-gatherers included microbes often considered as oral pathogens, despite their hosts' apparent good oral health. Discriminant analysis of gene functions revealed vitamin B5 autotrophy and urease-mediated pH regulation as candidate adaptations of the microbiome to the hunter-gatherer and Western diets, respectively. These results suggest that major transitions in diet selected for different communities of commensals and likely played a role in the emergence of modern oral pathogens.

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