The effect of Porphyromonas gingivalis on the gut microbiome of mice in relation to aging
The effect of Porphyromonas gingivalis on the gut microbiome of mice in relation to aging
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DOI:
10.1111/jre.13062
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发表时间:
2022-10-17
影响因子:
3.5
通讯作者:
Furuichi, Yasushi
中科院分区:
文献类型:
--
作者:
Giri, Sarita;Uehara, Osamu;Furuichi, Yasushi
Background and Objective The translocation of oral bacteria, including Porphyromonas gingivalis, to the gut has been shown to alter gut microbiome. However, the effect of P. gingivalis on gut microbiome in relation to aging has not been demonstrated. We hypothesize that P. gingivalis has more detrimental effect on gut environment with increased age. The objective of this study is to investigate the effect of P. gingivalis on gut environment using aged mice. Materials and Methods C57BL/6J mice aged 4 weeks (young) or 76 weeks (old) were divided into four groups: control-young, control-old, P. gingivalis-administered young, and P. gingivalis-administered old. P. gingivalis was orally administered thrice weekly for 5 weeks. At 30 days after the last P. gingivalis administration, 16S rRNA sequencing was performed to study the gut microbiome. The mRNA and protein expression of intestinal junctional barrier molecules and the levels of the inflammatory cytokines IL-1 beta and TNF-alpha in the serum were evaluated. Results Significant differences in the gut microbiomes between the groups, in terms of taxonomic abundance, bacterial diversity, and predicted metagenome function, were observed. A significant reduction in the alpha diversity and in the abundance of beneficial bacteria, such as Akkermansia and Clostridiaceae, in the P. gingivalis-administered old mice was observed. The mRNA and protein levels of Claudin-1 and Claudin-2 in the intestine were significantly elevated, while E-cadherin was significantly downregulated in the P. gingivalis-administered old mice, as were the serum levels of IL-1 beta and TNF-alpha. Conclusion The effect of P. gingivalis on the gut environment is more pronounced in old mice than in young mice.