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. 2022 May 12;13:869951. doi: 10.3389/fendo.2022.869951

Table 1.

Animal models and clinical studies assessing the potential association between adipose tissue-derived bacteria and adipose tissue function/glucose homeostasis.

Study Animals/Participants Adipose tissue bacteria Adipose tissue-related findings Glucose homeostasis-related findings
Amar et al. (113) NC/HFD-fed mice Gram-negative bacteria (experimental translocation model). Increased TNF and IFN-γ in MAT, correlating with bacterial DNA concentration. Increasing MAT bacterial DNA concentration in the progression of prediabetes to diabetes. Probiotic treatment reduced mucosal dysbiosis, bacterial translocation, and improved glucose metabolism.
Denou et al. (114) NOD2-/- mice Commensal bacteria (experimental translocation model). Increased inflammation (IL-6, TNF) in visceral adipose tissue. Increased insulin resistance.
Ahnê et al. (115) Subjects with morbid obesity with T2D (n-20) and without T2D (n-20) Different compartmentalization according to specific tissue (MAT, OAT, SAT). Not assessed. More evident T2D signatures in MAT: reduced bacterial diversity and Gram-positive bacteria (i.e., Faecalibacterium) and increased Gram-negative Enterobacteriaceae.
Massier et al. (116) Subjects with obesity with T2D (n-33) and without T2D (n-42) Proteobacteria and Firmicutes were the predominant phyla in adipose tissue (MAT, OAT, SAT). Higher bacterial quantity and diversity in MAT. Bacterial DNA correlated with macrophage infiltration in OAT (especially in T2D), TNF in SAT, and IL-1B in MAT; bacterial DNA induced adipokine secretion. Eighteen genera were shown to present different abundance between subjects with T2D and subjects without T2D.
Bakker et al. (117) Subjects with obesity and metabolic syndrome receiving lean donor FMT (n-8); BMI- matched controls not receiving FMT (n-16) Very low quantity of bacterial DNA in visceral adipose tissue. FMT did not alter bacterial translocation to adipose tissue. No differences in visceral bacterial DNA content/macrophage infiltration between groups. Not assessed.

NC, normal chow; HFD, high-fat diet; MAT, mesenteric adipose tissue; OAT, omental adipose tissue; SAT, subcutaneous adipose tissue; TNF- α, tumor necrosis factor α; IFN- γ, interferon γ; NOD2, oligomerization domain-2; IL-6, interleukin 6; IL-1B, interleukin-1B; TD2, type 2 diabetes mellitus; FMT, fecal microbiota transplantation; BMI, body mass index.