Perivascular adipose tissue harbors distinct bacterial and viral communities that differ dramatically from the fecal microbiome and exhibit significant temporal variability in Dahl SS rats.
Male Dahl SS rats, n=6 (split into two cohorts: 2023 and 2024, n=3 each).
Non-PVAT adipose tissues (subscapular brown adipose tissue, retroperitoneal white adipose tissue) and fecal samples
Microbial relative abundance (bacterial and viral communities) assessed via whole-genome shotgun sequencing and 16S rRNA gene analysissurrogate
This study provides the first evidence of a distinct, temporally variable resident microbiome in perivascular adipose tissue, highlighting its potential role in vascular biology and immune modulation.
Background: Perivascular adipose tissue (PVAT) contains adipocytes and a stromal-vascular fraction with immune cells that modulate the adjacent vasculature. The presence of immune cells in PVAT of vascular beds is poorly understood—are they resident or recruited? We propose a novel resident microbiome present in PVAT, given the immune-rich stromal environment. Hypothesis: We hypothesized the existence of distinct bacterial and viral communities in healthy PVAT compared to non-PVAT adipose tissues. Methods: PVAT samples from thoracic and abdominal aorta, mesenteric resistance arteries, non-PVAT tissues (subscapular brown adipose tissue, retroperitoneal white adipose tissue), and fecal samples were collected one year apart from male Dahl SS rats, split into two cohorts (2023 and 2024, n = 3 each). Whole-genome shotgun sequencing (CosmosID) and 16S rRNA gene analysis assessed microbial relative abundance. Results: PVAT harbored bacterial and viral sequences, and species composition varied significantly between cohorts. Bacterial and viral fecal samples showed lower variability. Conclusions: PVAT microbiome differed dramatically from the fecal microbiome, with temporal influences on bacterial and viral diversity, marking the first such report. Despite inherent limitations, these findings establish the potential of PVAT microbiota in vascular biology and immune modulation, paving the development of microbiome-targeted drugs to address vascular dysfunctions.
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Mahimkar et al. (Tue,) reported a other. Perivascular adipose tissue harbors distinct bacterial and viral communities that differ dramatically from the fecal microbiome and exhibit significant temporal variability in Dahl SS rats.
www.synapsesocial.com/papers/69d8948f6c1944d70ce057d0 — DOI: https://doi.org/10.3390/life16040609
Sameera Mahimkar
Janice Thompson
Christopher B. Blackwood
Life
Michigan State University
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