TY - JOUR
T1 - Delivery of E. coli Nissle to the mouse gut by mucoadhesive microcontainers does not improve its competitive ability against strains linked to ulcerative colitis
AU - Bondegaard, Pi Westi
AU - Torp, Anders Meyer
AU - Guerra, Priscila
AU - Kristensen, Katja Ann
AU - Christfort, Juliane Fjelrad
AU - Krogfelt, Karen Angeliki
AU - Nielsen, Line Hagner
AU - Zor, Kinga
AU - Boisen, Anja
AU - Mortensen, Martin Steen
AU - Bahl, Martin Iain
AU - Licht, Tine Rask
PY - 2023
Y1 - 2023
N2 - For patients with ulcerative colitis (UC), administration of the probiotic E. coli Nissle (EcN) holds promise for alleviation of disease symptoms. The mechanisms are unclear, but it has been hypothesised that a capacity of the probiotic to outcompete potentially detrimental UC-associated E. coli strains plays an important role. However, this could previously not be confirmed in a mouse model of competition between EcN and two UC-associated strains, as reported by Petersen et al. 2011. In the present study, we re-evaluated the idea, hypothesising that delivery of EcN by a micro device dosing system (microcontainers), designed for delivery into the intestinal mucus, could support colonisation and confer a competition advantage compared to classical oral dosing. Six groups of mice were pre-colonised with one of two UC-associated E. coli strains followed by oral delivery of EcN, either in capsules containing microcontainers with freeze-dried EcN powder, capsules containing freeze-dried EcN powder, or as a fresh sucrose suspension. Co-colonisation between the probiotic and the disease-associated strains was observed regardless of dosing method, and no competition advantages linked to microcontainer delivery were identified within this setup. Other approaches are thus needed if the competitive capacity of EcN in the gut should be improved.
AB - For patients with ulcerative colitis (UC), administration of the probiotic E. coli Nissle (EcN) holds promise for alleviation of disease symptoms. The mechanisms are unclear, but it has been hypothesised that a capacity of the probiotic to outcompete potentially detrimental UC-associated E. coli strains plays an important role. However, this could previously not be confirmed in a mouse model of competition between EcN and two UC-associated strains, as reported by Petersen et al. 2011. In the present study, we re-evaluated the idea, hypothesising that delivery of EcN by a micro device dosing system (microcontainers), designed for delivery into the intestinal mucus, could support colonisation and confer a competition advantage compared to classical oral dosing. Six groups of mice were pre-colonised with one of two UC-associated E. coli strains followed by oral delivery of EcN, either in capsules containing microcontainers with freeze-dried EcN powder, capsules containing freeze-dried EcN powder, or as a fresh sucrose suspension. Co-colonisation between the probiotic and the disease-associated strains was observed regardless of dosing method, and no competition advantages linked to microcontainer delivery were identified within this setup. Other approaches are thus needed if the competitive capacity of EcN in the gut should be improved.
KW - Ulcerative colitis
KW - Probiotics
KW - E. coli Nissle
KW - Microcontainer delivery
KW - Bacterial competition
KW - Micro device dosing system
U2 - 10.1093/femsle/fnad110
DO - 10.1093/femsle/fnad110
M3 - Journal article
C2 - 37863838
SN - 0378-1097
VL - 370
JO - FEMS Microbiology Letters
JF - FEMS Microbiology Letters
M1 - fnad110
ER -