4.6 Article

Association between aging-dependent gut microbiome dysbiosis and dry eye severity in C57BL/6 male mouse model: a pilot study

期刊

BMC MICROBIOLOGY
卷 21, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12866-021-02173-7

关键词

Dry eye; Aging; Microbiome; Paraprevotella; 16S rRNA

资金

  1. Cooperative Research Program of Basic Medical Science and Clinical Science from Seoul National University College of Medicine [800-20190256]
  2. National Research Foundation of Korea (NRF) - Korea government (MSIT) [2020R1F1A1072506]
  3. National Research Foundation of Korea [2020R1F1A1072506] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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This pilot study in C57BL/6 male mice found that aging-dependent changes in microbiome composition are associated with the severity of dry eye signs. Corneal staining increased and tear secretion decreased with age, while specific bacterial groups like Firmicutes and Proteobacteria were significantly related to dry eye severity.
Background While aging is a potent risk factor of dry eye disease, age-related gut dysbiosis is associated with inflammation and chronic geriatric diseases. Emerging evidence have demonstrated that gut dysbiosis contributes to the pathophysiology or exacerbation of ocular diseases including dry eye disease. However, the relationship between aging-related changes in gut microbiota and dry eye disease has not been elucidated. In this pilot study, we investigated the association between aging-dependent microbiome changes and dry eye severity in C57BL/6 male mice. Results Eight-week-old (8 W, n = 15), one-year-old (1Y, n = 10), and two-year-old (2Y, n = 8) C57BL/6 male mice were used. Dry eye severity was assessed by corneal staining scores and tear secretion. Bacterial genomic 16 s rRNA from feces was analyzed. Main outcomes were microbiome compositional differences among the groups and their correlation to dry eye severity. In aged mice (1Y and 2Y), corneal staining increased and tear secretion decreased with statistical significance. Gut microbiome alpha-diversity was not different among the groups. However, beta-diversity was significantly different among the groups. In univariate analysis, phylum Firmicutes, Proteobacteria, and Cyanobacteria, Firmicutes/Bacteroidetes ratio, and genus Alistipes, Bacteroides, Prevotella, Paraprevotella, and Helicobacter were significantly related to dry eye severity. After adjustment of age, multivariate analysis revealed phylum Proteobacteria, Firmicutes/Bacteroidetes ratio, and genus Lactobacillus, Alistipes, Prevotella, Paraprevotella, and Helicobacter to be significantly associated with dry eye severity. Conclusions Our pilot study suggests that aging-dependent changes in microbiome composition are related to severity of dry eye signs in C57BL/6 male mice.

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