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A complex human gut microbiome cultured in an anaerobic intestine-on-a-chip. | LitMetric

AI Article Synopsis

  • - The human gut's microbiome, consisting of diverse bacteria, is crucial to our health, and studying it in real-time alongside living intestinal cells can deepen our understanding of how they interact.
  • - Researchers developed a microfluidic "intestine-on-a-chip" that allows scientists to maintain complex microbial communities while simulating oxygen levels found in the human gut.
  • - This setup resulted in improved intestinal barrier function and a diverse microbial population that resembles what is typically found in human feces, suggesting it could be a valuable tool for creating new microbiome-based treatments and products.

Article Abstract

The diverse bacterial populations that comprise the commensal microbiome of the human intestine play a central role in health and disease. A method that sustains complex microbial communities in direct contact with living human intestinal cells and their overlying mucus layer in vitro would thus enable the investigation of host-microbiome interactions. Here, we show the extended coculture of living human intestinal epithelium with stable communities of aerobic and anaerobic human gut microbiota, using a microfluidic intestine-on-a-chip that permits the control and real-time assessment of physiologically relevant oxygen gradients. When compared to aerobic coculture conditions, the establishment of a transluminal hypoxia gradient in the chip increased intestinal barrier function and sustained a physiologically relevant level of microbial diversity, consisting of over 200 unique operational taxonomic units from 11 different genera and an abundance of obligate anaerobic bacteria, with ratios of Firmicutes and Bacteroidetes similar to those observed in human faeces. The intestine-on-a-chip may serve as a discovery tool for the development of microbiome-related therapeutics, probiotics and nutraceuticals.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6658209PMC
http://dx.doi.org/10.1038/s41551-019-0397-0DOI Listing

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