Changes in gut microbiota composition with age and correlations with gut inflammation in rats

PLoS One. 2022 Mar 15;17(3):e0265430. doi: 10.1371/journal.pone.0265430. eCollection 2022.

Abstract

Increasing evidences indicate that gut microbiota composition is associated with multiple inflammatory diseases. However, little is known about how gut microbiota changes with age and correlations with gut inflammation at sexual maturity stage of healthy individuals. Elucidating the dynamic changes of gut microbiota in healthy individuals at the sexual maturity stage and correlations with gut inflammation can provide clues for early risk assessment of gut diseases at the sexual maturity stage. Here, the shift in gut bacteria and its relationship with gut inflammation at the sexual maturity stage were explored. Sprague-Dawley rats at the sexual maturity stage were used in this study. 16S rRNA gene sequencing was performed to decipher gut bacteria shifts from the 7th week to the 9th week, and enzyme-linked immunosorbent assay (ELISA) was used to measure gut inflammation and gut barrier permeability. We found an increase in bacterial richness with age and a decrease in bacterial diversity with age. The gut bacteria were primarily dominated by the phyla Firmicutes and Bacteroides and the genus Prevotella. The relative abundance of Firmicutes increased with age, and the relative abundance of Bacteroides decreased with age. There was a positive correlation between body weight and the Firmicutes:Bacteroides ratio. More and more gut microbiota participated in the host gut inflammation and barrier permeability regulation with age. Ruminococcus was the only gut bacteria participated in gut inflammation and barrier permeability regulation both in the 7th week and the 15th week. These results provide a better understanding of the relationship between gut bacteria and gut inflammation in sexually mature rats and show that Ruminococcus may be a potential indicator for early risk assessment of gut inflammation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacteria / genetics
  • Bacteroides / genetics
  • Firmicutes / genetics
  • Gastrointestinal Microbiome*
  • Inflammation
  • RNA, Ribosomal, 16S / genetics
  • Rats
  • Rats, Sprague-Dawley
  • Ruminococcus / genetics

Substances

  • RNA, Ribosomal, 16S

Grants and funding

This study was supported by the National Natural Science Foundation of China (Grant no. 81871520). Initials of the author who received each award: Hong Liu. Grant numbers awarded to each author: 81871520. URL of funder website: http://www.nsfc.gov.cn/english/site_1/index.html The full name of funder: National Natural Science Foundation of China. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.