SHIME can be converted to M-SHIME by the addition of mucin-covered microcosms to the 3 colon regions. Bacteria which can adhere to the mucus layer will colonize the microcosms and create a mucus-compartment in the reactor.
By replacing half of the microcosms every three days, the intestinal replacement of the mucus layer is simulated, allowing continuous modelling of the mucosa compartment. Furthermore, adhered bacteria can be removed from the harvested microcosms, allowing the characterization of the adhered community.
Publications
Possemiers S. et al. (2004) PCR-DGGE-based quantification of stability of the microbial community in a simulator of the human intestinal microbial ecosystem. FEMS Microbiol Ecol. 49(3):495-507
Van den Abbeele P. et al. (2010) Microbial community development in a dynamic gut model is reproducible, colon region specific and selective for Bacteroidetes and Clostridium cluster IX. Appl Environ Microbiol. 76: 5237-5246
Van den Abbeele P. et al. (2012) Incorporating a mucosal environment in a dynamic gut model results in a more representative colonization by lactobacilli. Microb Biotechnol. 5(1):106-15;
Van den Abbeele P. et al. (2013) Butyrate-producing Clostridium cluster XIVa species specifically colonize mucins in an in vitro gut model. ISME J. 6(4):335-40
Sanchez-Patan, F et al. (2015). Comparative in vitro fermentations of cranberry and grape seed polyphenols with colonic microbiota. Food Chem. 183, 273–282.
Giuliani C. et al., (2016). Dietary supplement based on stilbenes: a focus on gut microbial metabolism by the in vitro simulator M-SHIME®. Food Funct. DOI: 10.1039/c6fo00784h.